Page last updated: 2024-12-05

congo red

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Description

Congo red is a diazo dye that is used in a variety of applications, including staining biological tissues, as a pH indicator, and as a reagent in analytical chemistry. It was first synthesized in 1884 by Paul Ehrlich, who named it after the Belgian Congo, where it was discovered. Congo red is a bright red dye that is soluble in water and alcohol. It is also known as benzopurpurin 4B. Congo red is synthesized by coupling diazotized benzidine with naphthionic acid. The resulting dye is then converted to the sodium salt. The dye has been used extensively in various industries, including textiles, paper, and leather. It has also been used as a stain in microscopy and as a reagent in analytical chemistry. The use of Congo red has declined in recent years due to concerns about its toxicity. In the body, Congo red binds to amyloid proteins, which are associated with a number of diseases, including Alzheimer’s disease and amyloidosis. This binding ability makes it a useful tool for studying these diseases. Congo red has been investigated as a potential therapeutic agent for amyloidosis, but clinical trials have not been successful. Congo red is known to have a number of toxic effects. It can cause skin irritation, eye irritation, and respiratory problems. In some cases, it can also cause liver damage and cancer. It is important to handle Congo red with care and to avoid contact with the skin, eyes, and mucous membranes.'

Congo Red: An acid dye used in testing for hydrochloric acid in gastric contents. It is also used histologically to test for AMYLOIDOSIS. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Congo Red : An indicator dye that is blue-violet at pH 3.0 and red at pH 5.0. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID11313
CHEMBL ID429694
CHEBI ID34653
SCHEMBL ID25635
MeSH IDM0005003

Synonyms (118)

Synonym
nsc-56651
CHEMBL429694
disodium 3,3'-[biphenyl-4,4'-diyldi(e)diazene-2,1-diyl]bis(4-aminonaphthalene-1-sulfonate)
congazone sodium
congo red ici
nsc-7232
CHEBI:34653
disodium 3,3'-(biphenyl-4,4'-diyldidiazene-2,1-diyl)bis(4-aminonaphthalene-1-sulfonate)
ci direct red 28
congo red 4b
benzo congo red
congo red
direct red c
573-58-0
cotton red l
atul congo red
diacotton congo red
direct congo red
atlantic congo red
kayaku congo red
sugai congo red
azocard red congo
red k
congo red cr
disodium 3,3'-((1,1'-biphenyl)-4,4'-diylbis(azo))bis(4-aminonaphthalene-1-sulphonate)
solucongo
congo red 4bx
3,3'-[[1,1'biphenyl]-4,4'-diylbis(azo)-]bis[4-amino-1-naphthalenesulfonic acid] disodium salt
c.i. 22120
congo red k
congo red r
peeramine congo red
direct red 28
trisulfon congo red
congo red h
vondacel red cl
tertrodirect red c
congo red w
haemonorm
congo red sodium salt
congo red ws
ai3-63036
1-naphthalenesulfonic acid, 3,3'-([1,1'-biphenyl]-4,4'-diyldiazo)bis[4-amino-, disodium salt
brasilamina congo 4b
congo red n
cotton red 5b
direct red dc-cf
haemomedical
sodium diphenyldiazo-bis-alpha-naphthylaminesulfonate
ccris 2277
c.i. direct red 28, disodium salt (8ci)
congo red rs
mitsui congo red
congo red l
direct red k
1-naphthalenesulfonic acid, 3,3'-[[1,1'-biphenyl]-4,4'-diylbis(azo)]bis[4-amino-, disodium salt (9ci)
hemorrhagyl
erie congo 4b
cotton red 4bc
congo red m
hispamin congo 4b
c.i. direct red 28, disodium salt
c.i. direct red 28
einecs 209-358-4
kongorot [german]
cerven kongo [czech]
nsc 7232
natrium-salz der diphenyl-bis-azo-bis-naphthylamin-4-sulfonsaeure [german]
cerven prima 28 [czech]
1-naphthalenesulfonic acid, 3,3'-((1,1'-biphenyl)-4,4'-diylbis(azo))bis(4-amino-, disodium salt
nsc 56651
hsdb 4225
1-naphthalenesulfonic acid, 3,3'-(4,4'-biphenylenebis(azo))bis(4-amino-, disodium salt
congo red, dye content >=35 %
congo red, bioxtra, certified by the biological stain commission
AKOS000282971
sodium 3,3'-(1e,1'e)-biphenyl-4,4'-diylbis(diazene-2,1-diyl)bis(4-aminonaphthalene-1-sulfonate)
tox21_111605
cas-573-58-0
tox21_202934
dtxcid502816
dtxsid4022816 ,
NCGC00260480-01
cerven kongo
1-naphthalenesulfonic acid, 3,3'-((1,1'-biphenyl)-4,4'-diylbis(2,1-diazenediyl))bis(4-amino-, sodium salt (1:2)
3u05fhg59s ,
congo red [usp]
natrium-salz der diphenyl-bis-azo-bis-naphthylamin-4-sulfonsaeure
unii-3u05fhg59s
cerven prima 28
FT-0624037
AKOS016368576
SCHEMBL25635
congo red [mart.]
1-naphthalenesulfonic acid, 3,3'-((1,1'-biphenyl)-4,4'-diyldiazo)bis(4-amino-, disodium salt
congo red [who-dd]
disodium 3,3'-(biphenyl-4,4'-diyldidiazene-2,1-diyl)bis(4-aminonaphthalene-1-sulphonate)
congo red [mi]
congo red [hsdb]
AKOS024285600
W-105472
c32h22n6o6s2.2na
HB0737
congo red (c.i. 22120)
mfcd00004028
congo red, analytical standard
congo red, indicator grade
congo red, for microscopy (bact., bot., hist.), indicator (ph 3.0-5.2), reag. ph. eur.
congo red, jis special grade
congo-red
disodium 4-amino-3-[4-[4-(1-amino-4-sulfonatonaphthalen-2-yl)diazenylphenyl]phenyl]diazenylnaphthalene-1-sulfonate
congo red, high purity - cas 573-58-0
Q114391
sodium 3,3'-([1,1'-biphenyl]-4,4'-diylbis(diazene-2,1-diyl))bis(4-aminonaphthalene-1-sulfonate)
D89267
congo red, certifiable grade
SY010430
c.i.direct red 28

Research Excerpts

Overview

Congo Red is a diazo textile dye that has been used to visualize the production of amyloid fibers for nearly a century. Congo Red (CR) is a histological stain used for the detection of extracellular amyloids mediating various neurodegenerative diseases. Congo red is a hallmarkAmyloid-binding dye and binds to curli, yet also binds to cellulose.

ExcerptReferenceRelevance
"Congo Red (CR) is a typical azo dye with highly toxic and carcinogenic properties. "( Improving the decolorization activity of Bacillus pumilus W3 CotA-laccase to Congo Red by rational modification.
Guan, ZB; Liao, XR; Ma, H; Yan, N; Yang, CX, 2022
)
2.39
"Congo red (CR) is a hazardous pigment, posing increasing dangerous to the environment and human health. "( Plant-derived Ca, N, S-Doped carbon dots for fast universal cell imaging and intracellular Congo red detection.
Durrani, S; Khan, A; Lin, F; Pang, AP; Sayed, SM; Wu, FG; Yang, Z; Zeng, J; Zhang, J; Zhang, Y, 2022
)
2.38
"Congo red (CR) is a genotoxic, sulphonated azo dye and poses significant pollution problem. "( Leveraging molecular docking to understand Congo red degradation by Staphylococcus caprae MB400.
Asghar, S; Basharat, Z; Yasmin, A, 2023
)
2.62
"Congo red (CR) is a typical and widely used azo dye in industries. "( Roles of functional microbial flocculant in dyeing wastewater treatment: Bridging and adsorption.
Fang, L; Tang, X; Wang, T; Zhang, S; Zheng, H; Zheng, J, 2020
)
2
"Congo Red (CR) is an anisotropic organic stain discovered to label amyloid beta (Aβ) plaques in the brain."( Modification of methods to use Congo-red stain to simultaneously visualize amyloid plaques and tangles in human and rodent brain tissue sections.
Cuevas, E; Hanig, J; Raymick, J; Rosas-Hernandez, H; Sarkar, S, 2020
)
1.28
"Congo red is a diazo textile dye that has been used to visualize the production of amyloid fibers for nearly a century. "( Congo Red Stain Identifies Matrix Overproduction and Is an Indirect Measurement for c-di-GMP in Many Species of Bacteria.
Jones, CJ; Wozniak, DJ, 2017
)
3.34
"The Congo Red (CR) assay is a standard biofilm test assessing the colony morphology of bacteria growing on agar plates supplemented with the diazo dye Congo Red. "( Semiquantitative Analysis of the Red, Dry, and Rough Colony Morphology of Salmonella enterica Serovar Typhimurium and Escherichia coli Using Congo Red.
Cimdins, A; Simm, R, 2017
)
1.21
"Congo red (CR) is a histological stain used for the detection of extracellular amyloids mediating various neurodegenerative diseases. "( Evaluation of Congo Red Staining in Degenerating Porcine Photoreceptors In Vitro: Protective Effects by Structural and Trophic Support.
Delbro, D; Johansson, K; Kvanta, A; Mohlin, C, 2018
)
2.28
"Congo red is a hallmark amyloid-binding dye and binds to curli, yet also binds to cellulose."( Influence of the amyloid dye Congo red on curli, cellulose, and the extracellular matrix in E. coli during growth and matrix purification.
Cegelski, L; Lee, J; McCrate, OA; Reichhardt, C; Thongsomboon, W; Zhou, X, 2016
)
1.45
"Congo red (CR) is a known selective amyloid ligand. "( Silver ions as em marker of congo red ligation sites in amyloids and amyloid-like aggregates.
Chłopaś, K; Jagusiak, A; Konieczny, L; Piekarska, B; Piwowar, P; Roterman, I; Rybarska, J; Stopa, B; Woźnicka, O; Zemanek, G, 2017
)
2.19
"Congo red (CR) is a commonly used histological amyloid dye and a weak amyloid inhibitor. "( Binding of Congo red to amyloid protofibrils of the Alzheimer Aβ(9-40) peptide probed by molecular dynamics simulations.
Scott, J; Shea, JE; Wu, C, 2012
)
2.21
"Congo red is a chemically synthesized small molecule that has binding affinity to Abeta."( An Abeta sequestration approach using non-antibody Abeta binding agents.
Aisen, P; Becker, A; Debnath, M; Duff, K; Gray, A; Klunk, W; Lafrancois, J; Mathis, C; Matsuoka, Y; Shao, L, 2005
)
1.05
"Congo red is a commonly used histological dye for amyloid detection. "( Congo red and protein aggregation in neurodegenerative diseases.
Anisimov, SV; Frid, P; Popovic, N, 2007
)
3.23
"Congo red is an azo dye that has been used for many years to detect abnormal prion protein in the brains of diseased patients or animals."( Mechanistic insights into the cure of prion disease by novel antiprion compounds.
Brown, DR; Gilbert, IH; Lekishvili, T; Loeschner, C; Prelli, F; Sellarajah, S; Webb, S; Wisniewski, T, 2007
)
1.06
"Congo red is an acid-base indicator dye. "( Differential Congo red staining: the effects of pH, non-aqueous solvents and the substrate.
Davies, JD; Mera, SL, 1984
)
2.08
"Congo red appears to be a general inhibitor of amyloid fibril toxicity and may therefore be a useful prototype for drugs targeted to the amyloid pathology of AD and adult-onset diabetes."( Amyloid fibril toxicity in Alzheimer's disease and diabetes.
Lorenzo, A; Yankner, BA, 1996
)
1.02
"Congo red (CR) is a histologic dye that binds to many amyloid proteins because of their extensive beta-sheet structure. "( Quantifying amyloid beta-peptide (Abeta) aggregation using the Congo red-Abeta (CR-abeta) spectrophotometric assay.
Jacob, RF; Klunk, WE; Mason, RP, 1999
)
1.99
"Congo red is a pH indicator."( Congo red vital staining of cornea and conjunctiva.
Norn, MS, 1976
)
2.42

Effects

Congo red (CR) has been used for its binding affinity to amyloid fibrils for the better part of a century. Congo red has little therapeutic potential for the treatment of these diseases due to toxicity and poor permeation of the blood-brain barrier.

ExcerptReferenceRelevance
"Congo Red (CR) has been used for its binding affinity to amyloid fibrils for the better part of a century. "( In vivo demonstration of Congo Red labeled amyloid plaques via perfusion in the Alzheimer disease rat model.
Hanig, J; Raymick, J; Sarkar, S; Setti, SE, 2021
)
2.37
"Yet, Congo red has no influence on the isolation of curli from curli-producing cells that do not produce cellulose."( Influence of the amyloid dye Congo red on curli, cellulose, and the extracellular matrix in E. coli during growth and matrix purification.
Cegelski, L; Lee, J; McCrate, OA; Reichhardt, C; Thongsomboon, W; Zhou, X, 2016
)
1.18
"Congo red (CR) has been widely used as a model antiamyloid agent to prevent Aβ aggregation."( Effects of Congo red on aβ(1-40) fibril formation process and morphology.
Arvidsson, PI; Chatterjee, U; Göthelid, E; Johansson, J; Pratim Bose, P; Xie, L, 2010
)
1.47
"Congo red (CR) has been reported to inhibit or enhance amyloid fibril formation by several proteins. "( Congo red populates partially unfolded states of an amyloidogenic protein to enhance aggregation and amyloid fibril formation.
Carpenter, JF; Kim, YS; Manning, MC; Randolph, TW; Stevens, FJ, 2003
)
3.2
"Congo red has been used to identify amyloid fibrils in tissues for more than 80 years and is also a weak inhibitor to both amyloid-beta fibril formation and toxicity. "( Dual binding modes of Congo red to amyloid protofibril surface observed in molecular dynamics simulations.
Duan, Y; Lei, H; Wang, Z; Wu, C; Zhang, W, 2007
)
2.1
"Congo red has little therapeutic potential for the treatment of these diseases due to toxicity and poor permeation of the blood-brain barrier."( Mechanistic insights into the cure of prion disease by novel antiprion compounds.
Brown, DR; Gilbert, IH; Lekishvili, T; Loeschner, C; Prelli, F; Sellarajah, S; Webb, S; Wisniewski, T, 2007
)
1.06
"Congo red (CR) has been shown to inhibit the accumulation in scrapie-infected cells of prion protein (PrP) in the abnormal protease-resistant form (PrP-res). "( Structural aspects of Congo red as an inhibitor of protease-resistant prion protein formation.
Caughey, B; Chesebro, B; Demaimay, R; Gordon, H; Harper, J; Weaver, D, 1998
)
2.06
"The Congo red stain has undergone several modifications since it was first used by Bennhold in 1922 in order to increase the specificity for staining amyloid. "( The congo red stain revisited.
Barr, K; Elghetany, MT; Saleem, A,
)
1.25
"Congo Red, which has been shown to induce shortening of isolated myofibrils, also increases the high-frequency motions of the isolated filaments."( The active cross-bridge motions of isolated thick filaments from myosin-regulated muscles detected by quasi-elastic light scattering.
Chu, B; Colflesh, D; Dewey, MM; Fan, SF; Gaylinn, B; Greguski, RA, 1985
)
0.99

Actions

ExcerptReferenceRelevance
"Congo red was found to inhibit the hemolytic activity of TDH in a dose-dependent manner."( Thermostable direct hemolysin of Vibrio parahaemolyticus is a bacterial reversible amyloid toxin.
Fujiwara, S; Fukui, T; Fukusaki, E; Hamada, D; Hara, K; Honda, T; Iida, T; Imanaka, T; Mayanagi, K; Miyata, T; Shiraki, K; Yanagihara, I; Yanagihara, K, 2005
)
1.05

Treatment

Congo red treatment failed to ameliorate either motor or cognitive deficits in R6/2 mice.

ExcerptReferenceRelevance
"Congo red dye solution treated with mutant Pseudomonas sp."( Evaluation and elimination of inhibitory effects of salts and heavy metal ions on biodegradation of Congo red by Pseudomonas sp. mutant.
Gopinath, KP; Kathiravan, MN; Sankaranarayanan, S; Srinivasan, R, 2011
)
1.31
"Congo red treatment failed to ameliorate either motor or cognitive deficits in R6/2 mice."( Systemic administration of Congo red does not improve motor or cognitive function in R6/2 mice.
Morton, AJ; Pallier, PN; Wanderer, J; Wood, NI, 2007
)
1.36

Toxicity

ExcerptReferenceRelevance
" These findings and our previous demonstration that amylin fibrils are toxic suggest that a common cytopathic effect of amyloid fibrils may contribute to the pathogenesis of Alzheimer disease and other amyloidoses."( Beta-amyloid neurotoxicity requires fibril formation and is inhibited by congo red.
Lorenzo, A; Yankner, BA, 1994
)
0.52
"We recently reported that several sulfate-containing glycosaminoglycans, a class of compounds associated with the beta-amyloid plaques of Alzheimer's disease, attenuate the toxic effects of beta-amyloid fragments beta 25-35 and beta 1-40."( Sulfonated dyes attenuate the toxic effects of beta-amyloid in a structure-specific fashion.
Hawtin, SR; Pollack, SJ; Sadler, II; Shearman, MS; Tailor, VJ, 1995
)
0.29
" Amylin was toxic to rat and human insulin-producing islet cells in the concentration range of fibril formation."( Amyloid fibril toxicity in Alzheimer's disease and diabetes.
Lorenzo, A; Yankner, BA, 1996
)
0.29
"Agents that interfere with the toxic effects of beta-amyloid protein may be therapeutically useful against Alzheimer's disease."( Sulphated compounds attenuate beta-amyloid toxicity by inhibiting its association with cells.
Pollack, SJ; Ragan, CI; Sadler, II; Shearman, MS; Smith, DW; Tailor, VJ, 1995
)
0.29
" To use this test, the toxic concentration(s) of betaA4 must first be established empirically."( Predicting the in vitro toxicity of synthetic beta-amyloid (1-40).
Brining, SK,
)
0.13
" Congo red, a histologic dye that binds to amyloid has previously been shown to diminish the toxic effects of A beta in cell culture."( Chrysamine-G, a lipophilic analogue of Congo red, inhibits A beta-induced toxicity in PC12 cells.
Debnath, ML; Klunk, WE; Koros, AM; Pettegrew, JW, 1998
)
1.48
" As it is highly toxic and forms fibrillar aggregates typical of beta-amyloid, it is suitable as a model for testing inhibitors of aggregation and toxicity."( Inhibition of toxicity in the beta-amyloid peptide fragment beta -(25-35) using N-methylated derivatives: a general strategy to prevent amyloid formation.
Burke, RM; Doig, AJ; Hughes, E, 2000
)
0.31
"Pr-IIGL(a), a derivative of the tetrapeptide beta-amyloid 31-34 (Abeta(31-34)), exerts controversial effects: it is toxic in a neuroblastoma culture, but it protects glial cells from the cytotoxic action of Abeta(1-42)."( Beta-amyloid-derived pentapeptide RIIGLa inhibits Abeta(1-42) aggregation and toxicity.
Datki, Z; Fülöp, L; Penke, B; Soós, K; Zarándi, M, 2004
)
0.32
" DB3 dye was the most toxic of all dyes in the bacterial, algal and protozoan tests."( Comparative use of bacterial, algal and protozoan tests to study toxicity of azo- and anthraquinone dyes.
Dias, N; Itävaara, M; Kapanen, A; Lima, N; Malachová, K; Novotný, C; Vándrovcová, M, 2006
)
0.33
" Because appearance of tau-aggregate bearing lesions correlates with both cognitive decline and neurodegeneration, it has been hypothesized that tau aggregation may be directly toxic to cells that harbor them."( Tau aggregation and toxicity in a cell culture model of tauopathy.
Bandyopadhyay, B; Kuret, J; Li, G; Yin, H, 2007
)
0.34
" Prion protein fragment 90-231(wild type) and the D202N mutant were not toxic in native conformation but induced cell death only after thermal denaturation."( High hydrophobic amino acid exposure is responsible of the neurotoxic effects induced by E200K or D202N disease-related mutations of the human prion protein.
Aceto, A; Bucciarelli, T; Chiovitti, K; Corsaro, A; D'Arrigo, C; Florio, T; Scotti, L; Thellung, S; Villa, V, 2011
)
0.37
" We previously identified the toxic conformer of Aβ42 with a turn at positions 22 and 23 ("toxic turn") by solid-state NMR and demonstrated that a monoclonal antibody (11A1) against the toxic turn in Aβ42 mainly detected the oligomer in the brains of AD patients."( Toxicity in rat primary neurons through the cellular oxidative stress induced by the turn formation at positions 22 and 23 of Aβ42.
Akaike, A; Irie, K; Izumi, Y; Izuo, N; Kume, T; Murakami, K; Sato, M, 2012
)
0.38
" In this study, the toxicity of these dyes was assessed in a zebrafish model, and the underlying toxic mechanisms were investigated."( Toxicity induced by Basic Violet 14, Direct Red 28 and Acid Red 26 in zebrafish larvae.
Eilers, G; Li, CQ; Li, YQ; Liu, HC; Meng, FG; Ou, WB; Shen, B; Zhou, SM, 2015
)
0.42

Pharmacokinetics

ExcerptReferenceRelevance
" The studied pharmacodynamic parameters decreased the surface hydrophobicity of Salmonella sp."( Pharmacodynamic parameters of gentamicin and their effect on biological properties of gram-negative bacteria.
Majtán, V; Majtánová, L, 1998
)
0.3

Compound-Compound Interactions

ExcerptReferenceRelevance
" immobilized polyurethane foam combined with activated carbon and sodium alginate was used for the biodegradation of Congo red dye."( Biodegradation of Congo red dye using polyurethane foam-based biocarrier combined with activated carbon and sodium alginate: Batch and continuous study.
Kumar Sonwani, R; Lal Maurya, K; Sharan Singh, R; Swain, G; Verma, A, 2022
)
1.26

Bioavailability

ExcerptReferenceRelevance
" Given the high bioavailability and brain permeability demonstrated in our pharmacokinetic studies, 8 will provide a novel scaffold for an Aβ-aggregation inhibitor that may offer an alternative treatment for AD."( Discovery of an Orally Bioavailable Benzofuran Analogue That Serves as a β-Amyloid Aggregation Inhibitor for the Potential Treatment of Alzheimer's Disease.
Ann, J; Choi, K; Ha, HJ; Hong, HS; Hyun, HJ; Jo, DG; Kang, DW; Kang, JM; Kim, H; Kim, HM; Kim, SH; Kim, Y; Lee, J; Lee, JH, 2018
)
0.48
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51
" Accordingly, this higher absorption rate by Quasimodo cells resulted in the removal of CR from the culture medium, allowing a subset of conidia to germinate and grow."( Functional Genomic and Biochemical Analysis Reveals Pleiotropic Effect of Congo Red on Aspergillus fumigatus.
Bromley, M; Fontaine, T; Fraczek, M; Latgé, JP; Legendre, R; Liu, Z; Michel, JP; Raj, S; Sismeiro, O; van Rhijn, N; Varet, H, 2021
)
0.85
" It was demonstrated that bioavailability of doxorubicin can be significantly enhanced by applying Congo red."( Congo Red as a Supramolecular Carrier System for Doxorubicin: An Approach to Understanding the Mechanism of Action.
Jagusiak, A; Korchowiec, B; Korchowiec, J; Kwiatek, WM; Kwiecińska, K; Roman, M; Roterman, I; Stachowicz-Kuśnierz, A, 2022
)
2.38

Dosage Studied

Dexorubicin and Congo Red were studied to better understand the effect of these compounds in prion diseases. The effect of different parameters like pH, temperature, contact time, adsorbent dosage and initial concentration of Chromium (Cr(VI) and Congo red (CR) were optimised in batch mode.

ExcerptRelevanceReference
" The applicability of this method for rapid and accurate evaluation of fibrinolytic activity was demonstrated by dose-response curves with purified plasmin, plasmin generated by urokinase in human plasma and euglobulin."( A method using fibrin-fixed Blue Dextran for determining the plasmin and plasmin inhibitor activities in human plasma.
Fujii, S; Kosugi, T; Mori, H; Otsuka, A; Sakurai, E; Sone, K; Sumi, H; Tamura, Y, 1978
)
0.26
" However, detailed dose-response curves were generated for several derivatives and they revealed that, while some compounds showed inhibition of PrP-res accumulation at high concentrations, at low concentrations they actually stimulated levels of PrP-res above control values."( Screening Congo Red and its analogues for their ability to prevent the formation of PrP-res in scrapie-infected cells.
Birkett, CR; Gilbert, IH; Hennion, RM; Hope, J; Rudyk, H; Vasiljevic, S, 2000
)
0.71
" Using this assay, we show that Congo red and chrysamine G can modulate aggregate formation, but show complex dose-response curves."( Inhibition of polyglutamine aggregation in R6/2 HD brain slices-complex dose-response profiles.
Bates, GP; Hockly, E; Klunk, WE; Li, XJ; Mahal, A; Murray, KD; Portier, R; Smith, DL; Wanker, E; Woodman, B, 2001
)
0.59
" The adsorption potential of JPW was observed to be dependent on various parameters such as type of dye, initial dye concentration, pH and dosage of adsorbent."( Use of jute processing wastes for treatment of wastewater contaminated with dye and other organics.
Banerjee, S; Dastidar, MG, 2005
)
0.33
" The effects of contact time, pH, adsorbent dosage and initial dye concentration on the adsorption were investigated."( Removal of congo red from aqueous solution by adsorption onto acid activated red mud.
Cengeloglu, Y; Tor, A, 2006
)
0.72
"Many screening hits inhibit enzymes with steep dose-response curves, which are considered pathological."( Interpreting steep dose-response curves in early inhibitor discovery.
Shoichet, BK, 2006
)
0.33
" The effect of process parameters like contact time, dosage of adsorbent, adsorbate concentration and pH on adsorption was investigated."( Comparative studies on removal of Congo red by native and modified mycelial pellets of Trametes versicolor in various reactor modes.
Binupriya, AR; Kuz, CS; Sathishkumar, M; Swaminathan, K; Yun, SE, 2008
)
0.63
"The effect of doxorubicin and Congo Red on prion protein (PrP) infectivity in experimental scrapie was studied to better understand the effect of these compounds in prion diseases and to establish whether a dose-response correlation exists for Congo Red."( Doxorubicin and congo red effectiveness on prion infectivity in golden Syrian hamster.
Bellotti, V; Ceciliani, F; Cereda, C; Ceroni, M; Corato, M; Cova, E; Merlini, G; Ogliari, P, 2009
)
0.99
" Removal efficiency increased with increase of cattail root dosage and ionic strength, but decreased with increase of temperature."( Removal of Congo Red from aqueous solution by cattail root.
Chen, H; Hu, Z; Ji, F; Yuan, S, 2010
)
0.75
" The effect of shaking time, initial dye concentration, temperature, adsorbent dosage and pH has been investigated."( Treatment of industrial wastewater containing Congo Red and Naphthol Green B using low-cost adsorbent.
Ahmed, IM; Attallah, MF; Hamed, MM, 2013
)
0.65
" The effect of initial dye concentration, adsorbent dosage and pH of solution on the adsorption phenomena was studied by conducting the batch adsorption experiments."( Adsorptive removal of dye using biochar derived from residual algae after in-situ transesterification: Alternate use of waste of biodiesel industry.
Dastidar, MG; Nautiyal, P; Subramanian, KA, 2016
)
0.43
" The effect of different parameters like pH, temperature, contact time, adsorbent dosage and initial concentration of Chromium (Cr(VI)) and Congo Red (CR) were optimised in batch mode."( Surface modification of nanocellulose using polypyrrole for the adsorptive removal of Congo red dye and chromium in binary mixture.
Narayanasamy, S; S, MMF; Shahnaz, T; V C, P, 2020
)
0.98
" The impact of EDB, MNPs/EDB and nZVCu/EDB dosage (1-4 g/L), pH (4-10), initial concentration of CR (20-500 mg/L), interaction time (180 min) and material type to remove CR from water was examined at ambient temperature."( Potential of nanocomposites of zero valent copper and magnetite with Eleocharis dulcis biochar for packed column and batch scale removal of Congo red dye.
Ali, S; Ansar, S; Boczkaj, G; Hafeez, F; Haq Khan, ZU; Imran, M; Murtaza, B; Rizwan, M; Shah, NS, 2022
)
0.92
" With a minimal adsorbent dosage (1 mg) and minimum contact time (10 min), and under different pH conditions, adsorption was efficient and cost-effective (nearly 99, 91 and 88% for BG, MG and CR, respectively)."( Biowaste-Derived, Highly Efficient, Reusable Carbon Nanospheres for Speedy Removal of Organic Dyes from Aqueous Solutions.
Ancy, V; Bhat, VS; Hegde, G; Joshi, JC; Krishnappa, B; Naik, M; S, JM, 2022
)
0.72
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
bis(azo) compoundAny azo compound containing two -N=N- groups.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (39)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
LuciferasePhotinus pyralis (common eastern firefly)Potency39.91490.007215.758889.3584AID1224835
acetylcholinesteraseHomo sapiens (human)Potency53.54890.002541.796015,848.9004AID1347395; AID1347397; AID1347398
hypoxia-inducible factor 1 alpha subunitHomo sapiens (human)Potency48.94823.189029.884159.4836AID1224846
RAR-related orphan receptor gammaMus musculus (house mouse)Potency4.58710.006038.004119,952.5996AID1159521; AID1159523
TDP1 proteinHomo sapiens (human)Potency22.04570.000811.382244.6684AID686978; AID686979
GLI family zinc finger 3Homo sapiens (human)Potency61.06840.000714.592883.7951AID1259392
AR proteinHomo sapiens (human)Potency23.73330.000221.22318,912.5098AID1259243; AID1259247; AID743035; AID743042; AID743054; AID743063
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency54.42730.000657.913322,387.1992AID1259378
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency31.48150.001022.650876.6163AID1224838; AID1224893
cytochrome P450 family 3 subfamily A polypeptide 4Homo sapiens (human)Potency22.38720.01237.983543.2770AID1346984
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency32.69970.000214.376460.0339AID720691; AID720692
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency23.02870.001530.607315,848.9004AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403
estrogen nuclear receptor alphaHomo sapiens (human)Potency27.50020.000229.305416,493.5996AID1259244; AID1259248; AID743079; AID743080; AID743091
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency34.65270.001019.414170.9645AID743094; AID743140
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency29.15660.023723.228263.5986AID743241
aryl hydrocarbon receptorHomo sapiens (human)Potency22.40420.000723.06741,258.9301AID743085; AID743122
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency23.53030.001723.839378.1014AID743083
thyroid stimulating hormone receptorHomo sapiens (human)Potency52.28890.001628.015177.1139AID1224843; AID1259385; AID1259395
activating transcription factor 6Homo sapiens (human)Potency24.53220.143427.612159.8106AID1159516
v-jun sarcoma virus 17 oncogene homolog (avian)Homo sapiens (human)Potency1.70800.057821.109761.2679AID1159526; AID1159528
Histone H2A.xCricetulus griseus (Chinese hamster)Potency50.47720.039147.5451146.8240AID1224845
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency22.65660.000323.4451159.6830AID743065; AID743067
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency27.27830.001557.789015,848.9004AID1259244
Cellular tumor antigen p53Homo sapiens (human)Potency8.01680.002319.595674.0614AID651631
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency27.27830.001551.739315,848.9004AID1259244
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
B2 bradykinin receptorCavia porcellus (domestic guinea pig)IC50 (µMol)4.00000.00112.58648.0000AID43124; AID43125
Dihydrofolate reductaseGallus gallus (chicken)IC50 (µMol)0.40000.00000.12730.4000AID56466
Beta-lactamaseEscherichia coli K-12IC50 (µMol)44.87380.01502.46578.0000AID218575; AID218680; AID218681; AID218682; AID275970; AID275971; AID43124; AID43125
Amyloid-beta precursor proteinHomo sapiens (human)IC50 (µMol)1.30000.00053.889510.0000AID1306099; AID1432628
Amyloid-beta precursor proteinHomo sapiens (human)Ki1.00000.00010.08560.8900AID282856; AID282857; AID459782
5-hydroxytryptamine receptor 1ARattus norvegicus (Norway rat)IC50 (µMol)4.00000.00031.38338.4000AID43124
Choline O-acetyltransferaseHomo sapiens (human)Ki0.10000.10001.30003.0000AID52124
Ectonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)IC50 (µMol)1.31000.00111.095810.0000AID472450
Ectonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)Ki1.89000.10000.93801.8900AID472452
PH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)IC50 (µMol)33.00004.00004.00004.0000AID525943
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Other Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Dihydrofolate reductaseHomo sapiens (human)Concentration0.40000.40000.40000.4000AID55718
Beta-lactamaseEnterobacter cloacaeConcentration3.90003.90003.90003.9000AID44056
5-hydroxytryptamine receptor 2ARattus norvegicus (Norway rat)Concentration0.40000.40000.40000.4000AID55718
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (238)

Processvia Protein(s)Taxonomy
tetrahydrobiopterin biosynthetic processDihydrofolate reductaseHomo sapiens (human)
one-carbon metabolic processDihydrofolate reductaseHomo sapiens (human)
negative regulation of translationDihydrofolate reductaseHomo sapiens (human)
axon regenerationDihydrofolate reductaseHomo sapiens (human)
response to methotrexateDihydrofolate reductaseHomo sapiens (human)
dihydrofolate metabolic processDihydrofolate reductaseHomo sapiens (human)
tetrahydrofolate metabolic processDihydrofolate reductaseHomo sapiens (human)
tetrahydrofolate biosynthetic processDihydrofolate reductaseHomo sapiens (human)
folic acid metabolic processDihydrofolate reductaseHomo sapiens (human)
positive regulation of nitric-oxide synthase activityDihydrofolate reductaseHomo sapiens (human)
regulation of removal of superoxide radicalsDihydrofolate reductaseHomo sapiens (human)
one-carbon metabolic processDihydrofolate reductaseGallus gallus (chicken)
response to methotrexateDihydrofolate reductaseGallus gallus (chicken)
tetrahydrofolate metabolic processDihydrofolate reductaseGallus gallus (chicken)
tetrahydrofolate biosynthetic processDihydrofolate reductaseGallus gallus (chicken)
dihydrofolate metabolic processDihydrofolate reductaseGallus gallus (chicken)
folic acid metabolic processDihydrofolate reductaseGallus gallus (chicken)
digestionChymotrypsinogen ABos taurus (cattle)
antibiotic catabolic processBeta-lactamaseEscherichia coli K-12
response to antibioticBeta-lactamaseEscherichia coli K-12
negative regulation of cell population proliferationCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycleCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycle G2/M phase transitionCellular tumor antigen p53Homo sapiens (human)
DNA damage responseCellular tumor antigen p53Homo sapiens (human)
ER overload responseCellular tumor antigen p53Homo sapiens (human)
cellular response to glucose starvationCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
positive regulation of miRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
negative regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
mitophagyCellular tumor antigen p53Homo sapiens (human)
in utero embryonic developmentCellular tumor antigen p53Homo sapiens (human)
somitogenesisCellular tumor antigen p53Homo sapiens (human)
release of cytochrome c from mitochondriaCellular tumor antigen p53Homo sapiens (human)
hematopoietic progenitor cell differentiationCellular tumor antigen p53Homo sapiens (human)
T cell proliferation involved in immune responseCellular tumor antigen p53Homo sapiens (human)
B cell lineage commitmentCellular tumor antigen p53Homo sapiens (human)
T cell lineage commitmentCellular tumor antigen p53Homo sapiens (human)
response to ischemiaCellular tumor antigen p53Homo sapiens (human)
nucleotide-excision repairCellular tumor antigen p53Homo sapiens (human)
double-strand break repairCellular tumor antigen p53Homo sapiens (human)
regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
protein import into nucleusCellular tumor antigen p53Homo sapiens (human)
autophagyCellular tumor antigen p53Homo sapiens (human)
DNA damage responseCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrestCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediatorCellular tumor antigen p53Homo sapiens (human)
transforming growth factor beta receptor signaling pathwayCellular tumor antigen p53Homo sapiens (human)
Ras protein signal transductionCellular tumor antigen p53Homo sapiens (human)
gastrulationCellular tumor antigen p53Homo sapiens (human)
neuroblast proliferationCellular tumor antigen p53Homo sapiens (human)
negative regulation of neuroblast proliferationCellular tumor antigen p53Homo sapiens (human)
protein localizationCellular tumor antigen p53Homo sapiens (human)
negative regulation of DNA replicationCellular tumor antigen p53Homo sapiens (human)
negative regulation of cell population proliferationCellular tumor antigen p53Homo sapiens (human)
determination of adult lifespanCellular tumor antigen p53Homo sapiens (human)
mRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
rRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
response to salt stressCellular tumor antigen p53Homo sapiens (human)
response to inorganic substanceCellular tumor antigen p53Homo sapiens (human)
response to X-rayCellular tumor antigen p53Homo sapiens (human)
response to gamma radiationCellular tumor antigen p53Homo sapiens (human)
positive regulation of gene expressionCellular tumor antigen p53Homo sapiens (human)
cardiac muscle cell apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of cardiac muscle cell apoptotic processCellular tumor antigen p53Homo sapiens (human)
glial cell proliferationCellular tumor antigen p53Homo sapiens (human)
viral processCellular tumor antigen p53Homo sapiens (human)
glucose catabolic process to lactate via pyruvateCellular tumor antigen p53Homo sapiens (human)
cerebellum developmentCellular tumor antigen p53Homo sapiens (human)
negative regulation of cell growthCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
negative regulation of transforming growth factor beta receptor signaling pathwayCellular tumor antigen p53Homo sapiens (human)
mitotic G1 DNA damage checkpoint signalingCellular tumor antigen p53Homo sapiens (human)
negative regulation of telomere maintenance via telomeraseCellular tumor antigen p53Homo sapiens (human)
T cell differentiation in thymusCellular tumor antigen p53Homo sapiens (human)
tumor necrosis factor-mediated signaling pathwayCellular tumor antigen p53Homo sapiens (human)
regulation of tissue remodelingCellular tumor antigen p53Homo sapiens (human)
cellular response to UVCellular tumor antigen p53Homo sapiens (human)
multicellular organism growthCellular tumor antigen p53Homo sapiens (human)
positive regulation of mitochondrial membrane permeabilityCellular tumor antigen p53Homo sapiens (human)
cellular response to glucose starvationCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
entrainment of circadian clock by photoperiodCellular tumor antigen p53Homo sapiens (human)
mitochondrial DNA repairCellular tumor antigen p53Homo sapiens (human)
regulation of DNA damage response, signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of neuron apoptotic processCellular tumor antigen p53Homo sapiens (human)
transcription initiation-coupled chromatin remodelingCellular tumor antigen p53Homo sapiens (human)
negative regulation of proteolysisCellular tumor antigen p53Homo sapiens (human)
negative regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
positive regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
positive regulation of RNA polymerase II transcription preinitiation complex assemblyCellular tumor antigen p53Homo sapiens (human)
positive regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
response to antibioticCellular tumor antigen p53Homo sapiens (human)
fibroblast proliferationCellular tumor antigen p53Homo sapiens (human)
negative regulation of fibroblast proliferationCellular tumor antigen p53Homo sapiens (human)
circadian behaviorCellular tumor antigen p53Homo sapiens (human)
bone marrow developmentCellular tumor antigen p53Homo sapiens (human)
embryonic organ developmentCellular tumor antigen p53Homo sapiens (human)
positive regulation of peptidyl-tyrosine phosphorylationCellular tumor antigen p53Homo sapiens (human)
protein stabilizationCellular tumor antigen p53Homo sapiens (human)
negative regulation of helicase activityCellular tumor antigen p53Homo sapiens (human)
protein tetramerizationCellular tumor antigen p53Homo sapiens (human)
chromosome organizationCellular tumor antigen p53Homo sapiens (human)
neuron apoptotic processCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycleCellular tumor antigen p53Homo sapiens (human)
hematopoietic stem cell differentiationCellular tumor antigen p53Homo sapiens (human)
negative regulation of glial cell proliferationCellular tumor antigen p53Homo sapiens (human)
type II interferon-mediated signaling pathwayCellular tumor antigen p53Homo sapiens (human)
cardiac septum morphogenesisCellular tumor antigen p53Homo sapiens (human)
positive regulation of programmed necrotic cell deathCellular tumor antigen p53Homo sapiens (human)
protein-containing complex assemblyCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stressCellular tumor antigen p53Homo sapiens (human)
thymocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of thymocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
necroptotic processCellular tumor antigen p53Homo sapiens (human)
cellular response to hypoxiaCellular tumor antigen p53Homo sapiens (human)
cellular response to xenobiotic stimulusCellular tumor antigen p53Homo sapiens (human)
cellular response to ionizing radiationCellular tumor antigen p53Homo sapiens (human)
cellular response to gamma radiationCellular tumor antigen p53Homo sapiens (human)
cellular response to UV-CCellular tumor antigen p53Homo sapiens (human)
stem cell proliferationCellular tumor antigen p53Homo sapiens (human)
signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
cellular response to actinomycin DCellular tumor antigen p53Homo sapiens (human)
positive regulation of release of cytochrome c from mitochondriaCellular tumor antigen p53Homo sapiens (human)
cellular senescenceCellular tumor antigen p53Homo sapiens (human)
replicative senescenceCellular tumor antigen p53Homo sapiens (human)
oxidative stress-induced premature senescenceCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathwayCellular tumor antigen p53Homo sapiens (human)
oligodendrocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of execution phase of apoptosisCellular tumor antigen p53Homo sapiens (human)
negative regulation of mitophagyCellular tumor antigen p53Homo sapiens (human)
regulation of mitochondrial membrane permeability involved in apoptotic processCellular tumor antigen p53Homo sapiens (human)
regulation of intrinsic apoptotic signaling pathway by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of miRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
negative regulation of G1 to G0 transitionCellular tumor antigen p53Homo sapiens (human)
negative regulation of miRNA processingCellular tumor antigen p53Homo sapiens (human)
negative regulation of glucose catabolic process to lactate via pyruvateCellular tumor antigen p53Homo sapiens (human)
negative regulation of pentose-phosphate shuntCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to hypoxiaCellular tumor antigen p53Homo sapiens (human)
regulation of fibroblast apoptotic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of stem cell proliferationCellular tumor antigen p53Homo sapiens (human)
positive regulation of cellular senescenceCellular tumor antigen p53Homo sapiens (human)
positive regulation of intrinsic apoptotic signaling pathwayCellular tumor antigen p53Homo sapiens (human)
regulation of gene expressionAmyloid-beta precursor proteinHomo sapiens (human)
cognitionAmyloid-beta precursor proteinHomo sapiens (human)
G2/M transition of mitotic cell cycleAmyloid-beta precursor proteinHomo sapiens (human)
microglial cell activationAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of protein phosphorylationAmyloid-beta precursor proteinHomo sapiens (human)
suckling behaviorAmyloid-beta precursor proteinHomo sapiens (human)
astrocyte activation involved in immune responseAmyloid-beta precursor proteinHomo sapiens (human)
regulation of translationAmyloid-beta precursor proteinHomo sapiens (human)
protein phosphorylationAmyloid-beta precursor proteinHomo sapiens (human)
intracellular copper ion homeostasisAmyloid-beta precursor proteinHomo sapiens (human)
endocytosisAmyloid-beta precursor proteinHomo sapiens (human)
response to oxidative stressAmyloid-beta precursor proteinHomo sapiens (human)
cell adhesionAmyloid-beta precursor proteinHomo sapiens (human)
regulation of epidermal growth factor-activated receptor activityAmyloid-beta precursor proteinHomo sapiens (human)
Notch signaling pathwayAmyloid-beta precursor proteinHomo sapiens (human)
axonogenesisAmyloid-beta precursor proteinHomo sapiens (human)
learning or memoryAmyloid-beta precursor proteinHomo sapiens (human)
learningAmyloid-beta precursor proteinHomo sapiens (human)
mating behaviorAmyloid-beta precursor proteinHomo sapiens (human)
locomotory behaviorAmyloid-beta precursor proteinHomo sapiens (human)
axo-dendritic transportAmyloid-beta precursor proteinHomo sapiens (human)
cholesterol metabolic processAmyloid-beta precursor proteinHomo sapiens (human)
negative regulation of cell population proliferationAmyloid-beta precursor proteinHomo sapiens (human)
adult locomotory behaviorAmyloid-beta precursor proteinHomo sapiens (human)
visual learningAmyloid-beta precursor proteinHomo sapiens (human)
regulation of gene expressionAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of gene expressionAmyloid-beta precursor proteinHomo sapiens (human)
negative regulation of gene expressionAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of peptidyl-threonine phosphorylationAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of G2/M transition of mitotic cell cycleAmyloid-beta precursor proteinHomo sapiens (human)
microglia developmentAmyloid-beta precursor proteinHomo sapiens (human)
axon midline choice point recognitionAmyloid-beta precursor proteinHomo sapiens (human)
neuron remodelingAmyloid-beta precursor proteinHomo sapiens (human)
dendrite developmentAmyloid-beta precursor proteinHomo sapiens (human)
regulation of Wnt signaling pathwayAmyloid-beta precursor proteinHomo sapiens (human)
extracellular matrix organizationAmyloid-beta precursor proteinHomo sapiens (human)
forebrain developmentAmyloid-beta precursor proteinHomo sapiens (human)
neuron projection developmentAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of chemokine productionAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of interleukin-1 beta productionAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of interleukin-6 productionAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of tumor necrosis factor productionAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of peptidyl-serine phosphorylationAmyloid-beta precursor proteinHomo sapiens (human)
ionotropic glutamate receptor signaling pathwayAmyloid-beta precursor proteinHomo sapiens (human)
regulation of multicellular organism growthAmyloid-beta precursor proteinHomo sapiens (human)
negative regulation of neuron differentiationAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of glycolytic processAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of mitotic cell cycleAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of transcription by RNA polymerase IIAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of JNK cascadeAmyloid-beta precursor proteinHomo sapiens (human)
astrocyte activationAmyloid-beta precursor proteinHomo sapiens (human)
regulation of long-term neuronal synaptic plasticityAmyloid-beta precursor proteinHomo sapiens (human)
collateral sprouting in absence of injuryAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of inflammatory responseAmyloid-beta precursor proteinHomo sapiens (human)
regulation of peptidyl-tyrosine phosphorylationAmyloid-beta precursor proteinHomo sapiens (human)
regulation of synapse structure or activityAmyloid-beta precursor proteinHomo sapiens (human)
synapse organizationAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of calcium-mediated signalingAmyloid-beta precursor proteinHomo sapiens (human)
neuromuscular process controlling balanceAmyloid-beta precursor proteinHomo sapiens (human)
synaptic assembly at neuromuscular junctionAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of protein metabolic processAmyloid-beta precursor proteinHomo sapiens (human)
neuron apoptotic processAmyloid-beta precursor proteinHomo sapiens (human)
smooth endoplasmic reticulum calcium ion homeostasisAmyloid-beta precursor proteinHomo sapiens (human)
neuron cellular homeostasisAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of ERK1 and ERK2 cascadeAmyloid-beta precursor proteinHomo sapiens (human)
response to interleukin-1Amyloid-beta precursor proteinHomo sapiens (human)
modulation of excitatory postsynaptic potentialAmyloid-beta precursor proteinHomo sapiens (human)
NMDA selective glutamate receptor signaling pathwayAmyloid-beta precursor proteinHomo sapiens (human)
regulation of spontaneous synaptic transmissionAmyloid-beta precursor proteinHomo sapiens (human)
cytosolic mRNA polyadenylationAmyloid-beta precursor proteinHomo sapiens (human)
negative regulation of long-term synaptic potentiationAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of long-term synaptic potentiationAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of non-canonical NF-kappaB signal transductionAmyloid-beta precursor proteinHomo sapiens (human)
cellular response to amyloid-betaAmyloid-beta precursor proteinHomo sapiens (human)
regulation of presynapse assemblyAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of amyloid fibril formationAmyloid-beta precursor proteinHomo sapiens (human)
amyloid fibril formationAmyloid-beta precursor proteinHomo sapiens (human)
neuron projection maintenanceAmyloid-beta precursor proteinHomo sapiens (human)
positive regulation of T cell migrationAmyloid-beta precursor proteinHomo sapiens (human)
central nervous system developmentAmyloid-beta precursor proteinHomo sapiens (human)
carbohydrate metabolic processBeta-galactosidaseHomo sapiens (human)
galactose catabolic processBeta-galactosidaseHomo sapiens (human)
heparan sulfate proteoglycan catabolic processBeta-galactosidaseHomo sapiens (human)
keratan sulfate catabolic processBeta-galactosidaseHomo sapiens (human)
glycosphingolipid catabolic processBeta-galactosidaseHomo sapiens (human)
response to cortisoneBeta-galactosidaseHomo sapiens (human)
response to Thyroglobulin triiodothyronineBeta-galactosidaseHomo sapiens (human)
phosphatidylcholine biosynthetic processCholine O-acetyltransferaseHomo sapiens (human)
neurotransmitter transportCholine O-acetyltransferaseHomo sapiens (human)
neuromuscular synaptic transmissionCholine O-acetyltransferaseHomo sapiens (human)
acetylcholine biosynthetic processCholine O-acetyltransferaseHomo sapiens (human)
chemotaxisEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
immune responseEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
phospholipid catabolic processEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
positive regulation of epithelial cell migrationEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
vesicle-mediated transportEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
sphingolipid catabolic processEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
regulation of cell migrationEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
phosphatidylcholine catabolic processEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
cell motilityEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
positive regulation of peptidyl-tyrosine phosphorylationEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
positive regulation of lamellipodium morphogenesisEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
hippocampus developmentPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
signal transductionPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
protein dephosphorylationPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
proteolysisChymotrypsin-CHomo sapiens (human)
intracellular calcium ion homeostasisChymotrypsin-CHomo sapiens (human)
proteolysisChymotrypsin-CHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (68)

Processvia Protein(s)Taxonomy
mRNA regulatory element binding translation repressor activityDihydrofolate reductaseHomo sapiens (human)
mRNA bindingDihydrofolate reductaseHomo sapiens (human)
dihydrofolate reductase activityDihydrofolate reductaseHomo sapiens (human)
folic acid bindingDihydrofolate reductaseHomo sapiens (human)
NADPH bindingDihydrofolate reductaseHomo sapiens (human)
sequence-specific mRNA bindingDihydrofolate reductaseHomo sapiens (human)
NADP bindingDihydrofolate reductaseHomo sapiens (human)
mRNA bindingDihydrofolate reductaseGallus gallus (chicken)
dihydrofolate reductase activityDihydrofolate reductaseGallus gallus (chicken)
NADP bindingDihydrofolate reductaseGallus gallus (chicken)
protein bindingChymotrypsinogen ABos taurus (cattle)
serpin family protein bindingChymotrypsinogen ABos taurus (cattle)
beta-lactamase activityBeta-lactamaseEscherichia coli K-12
hydrolase activityBeta-lactamaseEscherichia coli K-12
transcription cis-regulatory region bindingCellular tumor antigen p53Homo sapiens (human)
RNA polymerase II cis-regulatory region sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription factor activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
cis-regulatory region sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
core promoter sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
TFIID-class transcription factor complex bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription repressor activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription activator activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
protease bindingCellular tumor antigen p53Homo sapiens (human)
p53 bindingCellular tumor antigen p53Homo sapiens (human)
DNA bindingCellular tumor antigen p53Homo sapiens (human)
chromatin bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription factor activityCellular tumor antigen p53Homo sapiens (human)
mRNA 3'-UTR bindingCellular tumor antigen p53Homo sapiens (human)
copper ion bindingCellular tumor antigen p53Homo sapiens (human)
protein bindingCellular tumor antigen p53Homo sapiens (human)
zinc ion bindingCellular tumor antigen p53Homo sapiens (human)
enzyme bindingCellular tumor antigen p53Homo sapiens (human)
receptor tyrosine kinase bindingCellular tumor antigen p53Homo sapiens (human)
ubiquitin protein ligase bindingCellular tumor antigen p53Homo sapiens (human)
histone deacetylase regulator activityCellular tumor antigen p53Homo sapiens (human)
ATP-dependent DNA/DNA annealing activityCellular tumor antigen p53Homo sapiens (human)
identical protein bindingCellular tumor antigen p53Homo sapiens (human)
histone deacetylase bindingCellular tumor antigen p53Homo sapiens (human)
protein heterodimerization activityCellular tumor antigen p53Homo sapiens (human)
protein-folding chaperone bindingCellular tumor antigen p53Homo sapiens (human)
protein phosphatase 2A bindingCellular tumor antigen p53Homo sapiens (human)
RNA polymerase II-specific DNA-binding transcription factor bindingCellular tumor antigen p53Homo sapiens (human)
14-3-3 protein bindingCellular tumor antigen p53Homo sapiens (human)
MDM2/MDM4 family protein bindingCellular tumor antigen p53Homo sapiens (human)
disordered domain specific bindingCellular tumor antigen p53Homo sapiens (human)
general transcription initiation factor bindingCellular tumor antigen p53Homo sapiens (human)
molecular function activator activityCellular tumor antigen p53Homo sapiens (human)
promoter-specific chromatin bindingCellular tumor antigen p53Homo sapiens (human)
RNA polymerase II cis-regulatory region sequence-specific DNA bindingAmyloid-beta precursor proteinHomo sapiens (human)
DNA bindingAmyloid-beta precursor proteinHomo sapiens (human)
serine-type endopeptidase inhibitor activityAmyloid-beta precursor proteinHomo sapiens (human)
signaling receptor bindingAmyloid-beta precursor proteinHomo sapiens (human)
protein bindingAmyloid-beta precursor proteinHomo sapiens (human)
heparin bindingAmyloid-beta precursor proteinHomo sapiens (human)
enzyme bindingAmyloid-beta precursor proteinHomo sapiens (human)
identical protein bindingAmyloid-beta precursor proteinHomo sapiens (human)
transition metal ion bindingAmyloid-beta precursor proteinHomo sapiens (human)
receptor ligand activityAmyloid-beta precursor proteinHomo sapiens (human)
PTB domain bindingAmyloid-beta precursor proteinHomo sapiens (human)
protein serine/threonine kinase bindingAmyloid-beta precursor proteinHomo sapiens (human)
signaling receptor activator activityAmyloid-beta precursor proteinHomo sapiens (human)
beta-galactosidase activityBeta-galactosidaseHomo sapiens (human)
protein bindingBeta-galactosidaseHomo sapiens (human)
galactoside bindingBeta-galactosidaseHomo sapiens (human)
protein homodimerization activityBeta-galactosidaseHomo sapiens (human)
choline O-acetyltransferase activityCholine O-acetyltransferaseHomo sapiens (human)
nucleic acid bindingEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
lysophospholipase activityEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
scavenger receptor activityEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
calcium ion bindingEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
zinc ion bindingEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
hydrolase activityEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
polysaccharide bindingEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
alkylglycerophosphoethanolamine phosphodiesterase activityEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
phosphodiesterase I activityEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
protein bindingPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
myosin phosphatase activityPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
metal ion bindingPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
protein serine/threonine phosphatase activityPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
protein bindingChymotrypsin-CHomo sapiens (human)
peptidase activityChymotrypsin-CHomo sapiens (human)
serine-type endopeptidase activityChymotrypsin-CHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (70)

Processvia Protein(s)Taxonomy
mitochondrionDihydrofolate reductaseHomo sapiens (human)
cytosolDihydrofolate reductaseHomo sapiens (human)
mitochondrionDihydrofolate reductaseHomo sapiens (human)
mitochondrionDihydrofolate reductaseGallus gallus (chicken)
extracellular regionChymotrypsinogen ABos taurus (cattle)
serine protease inhibitor complexChymotrypsinogen ABos taurus (cattle)
outer membrane-bounded periplasmic spaceBeta-lactamaseEscherichia coli K-12
periplasmic spaceBeta-lactamaseEscherichia coli K-12
nuclear bodyCellular tumor antigen p53Homo sapiens (human)
nucleusCellular tumor antigen p53Homo sapiens (human)
nucleoplasmCellular tumor antigen p53Homo sapiens (human)
replication forkCellular tumor antigen p53Homo sapiens (human)
nucleolusCellular tumor antigen p53Homo sapiens (human)
cytoplasmCellular tumor antigen p53Homo sapiens (human)
mitochondrionCellular tumor antigen p53Homo sapiens (human)
mitochondrial matrixCellular tumor antigen p53Homo sapiens (human)
endoplasmic reticulumCellular tumor antigen p53Homo sapiens (human)
centrosomeCellular tumor antigen p53Homo sapiens (human)
cytosolCellular tumor antigen p53Homo sapiens (human)
nuclear matrixCellular tumor antigen p53Homo sapiens (human)
PML bodyCellular tumor antigen p53Homo sapiens (human)
transcription repressor complexCellular tumor antigen p53Homo sapiens (human)
site of double-strand breakCellular tumor antigen p53Homo sapiens (human)
germ cell nucleusCellular tumor antigen p53Homo sapiens (human)
chromatinCellular tumor antigen p53Homo sapiens (human)
transcription regulator complexCellular tumor antigen p53Homo sapiens (human)
protein-containing complexCellular tumor antigen p53Homo sapiens (human)
extracellular spaceAmyloid-beta precursor proteinHomo sapiens (human)
dendriteAmyloid-beta precursor proteinHomo sapiens (human)
extracellular regionAmyloid-beta precursor proteinHomo sapiens (human)
extracellular spaceAmyloid-beta precursor proteinHomo sapiens (human)
nuclear envelope lumenAmyloid-beta precursor proteinHomo sapiens (human)
cytoplasmAmyloid-beta precursor proteinHomo sapiens (human)
mitochondrial inner membraneAmyloid-beta precursor proteinHomo sapiens (human)
endosomeAmyloid-beta precursor proteinHomo sapiens (human)
early endosomeAmyloid-beta precursor proteinHomo sapiens (human)
endoplasmic reticulumAmyloid-beta precursor proteinHomo sapiens (human)
endoplasmic reticulum lumenAmyloid-beta precursor proteinHomo sapiens (human)
smooth endoplasmic reticulumAmyloid-beta precursor proteinHomo sapiens (human)
Golgi apparatusAmyloid-beta precursor proteinHomo sapiens (human)
Golgi lumenAmyloid-beta precursor proteinHomo sapiens (human)
Golgi-associated vesicleAmyloid-beta precursor proteinHomo sapiens (human)
cytosolAmyloid-beta precursor proteinHomo sapiens (human)
plasma membraneAmyloid-beta precursor proteinHomo sapiens (human)
clathrin-coated pitAmyloid-beta precursor proteinHomo sapiens (human)
cell-cell junctionAmyloid-beta precursor proteinHomo sapiens (human)
synaptic vesicleAmyloid-beta precursor proteinHomo sapiens (human)
cell surfaceAmyloid-beta precursor proteinHomo sapiens (human)
membraneAmyloid-beta precursor proteinHomo sapiens (human)
COPII-coated ER to Golgi transport vesicleAmyloid-beta precursor proteinHomo sapiens (human)
axonAmyloid-beta precursor proteinHomo sapiens (human)
growth coneAmyloid-beta precursor proteinHomo sapiens (human)
platelet alpha granule lumenAmyloid-beta precursor proteinHomo sapiens (human)
neuromuscular junctionAmyloid-beta precursor proteinHomo sapiens (human)
endosome lumenAmyloid-beta precursor proteinHomo sapiens (human)
trans-Golgi network membraneAmyloid-beta precursor proteinHomo sapiens (human)
ciliary rootletAmyloid-beta precursor proteinHomo sapiens (human)
dendritic spineAmyloid-beta precursor proteinHomo sapiens (human)
dendritic shaftAmyloid-beta precursor proteinHomo sapiens (human)
perikaryonAmyloid-beta precursor proteinHomo sapiens (human)
membrane raftAmyloid-beta precursor proteinHomo sapiens (human)
apical part of cellAmyloid-beta precursor proteinHomo sapiens (human)
synapseAmyloid-beta precursor proteinHomo sapiens (human)
perinuclear region of cytoplasmAmyloid-beta precursor proteinHomo sapiens (human)
presynaptic active zoneAmyloid-beta precursor proteinHomo sapiens (human)
spindle midzoneAmyloid-beta precursor proteinHomo sapiens (human)
recycling endosomeAmyloid-beta precursor proteinHomo sapiens (human)
extracellular exosomeAmyloid-beta precursor proteinHomo sapiens (human)
receptor complexAmyloid-beta precursor proteinHomo sapiens (human)
early endosomeAmyloid-beta precursor proteinHomo sapiens (human)
membrane raftAmyloid-beta precursor proteinHomo sapiens (human)
cell surfaceAmyloid-beta precursor proteinHomo sapiens (human)
Golgi apparatusAmyloid-beta precursor proteinHomo sapiens (human)
plasma membraneAmyloid-beta precursor proteinHomo sapiens (human)
extracellular regionBeta-galactosidaseHomo sapiens (human)
cytoplasmBeta-galactosidaseHomo sapiens (human)
Golgi apparatusBeta-galactosidaseHomo sapiens (human)
azurophil granule lumenBeta-galactosidaseHomo sapiens (human)
lysosomal lumenBeta-galactosidaseHomo sapiens (human)
intracellular membrane-bounded organelleBeta-galactosidaseHomo sapiens (human)
perinuclear region of cytoplasmBeta-galactosidaseHomo sapiens (human)
extracellular exosomeBeta-galactosidaseHomo sapiens (human)
ficolin-1-rich granule lumenBeta-galactosidaseHomo sapiens (human)
vacuoleBeta-galactosidaseHomo sapiens (human)
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
nucleusCholine O-acetyltransferaseHomo sapiens (human)
cytosolCholine O-acetyltransferaseHomo sapiens (human)
synapseCholine O-acetyltransferaseHomo sapiens (human)
cytoplasmCholine O-acetyltransferaseHomo sapiens (human)
neuron projectionCholine O-acetyltransferaseHomo sapiens (human)
extracellular spaceEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
plasma membraneEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
extracellular spaceEctonucleotide pyrophosphatase/phosphodiesterase family member 2Homo sapiens (human)
photoreceptor inner segmentPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
nucleoplasmPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
cytoplasmPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
cytosolPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
photoreceptor outer segment membranePH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
intercellular bridgePH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
mitotic spindlePH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
cytoplasmPH domain leucine-rich repeat-containing protein phosphatase 2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (127)

Assay IDTitleYearJournalArticle
AID43124Inhibitory activity against Amp C beta-Lactamase2003Journal of medicinal chemistry, Sep-25, Volume: 46, Issue:20
A specific mechanism of nonspecific inhibition.
AID1057864Ratio of LC50 for dividing mouse ScN2a-cl3 cells to EC50 for inhibition of RML prion protein2013Bioorganic & medicinal chemistry, Dec-15, Volume: 21, Issue:24
Antiprion compounds that reduce PrP(Sc) levels in dividing and stationary-phase cells.
AID228517Aggregates forming ability by dynamic light scattering(DLS).2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID289397Inhibition of Electrophorus electricus AchE-induced beta amyloid protein 1-42 co-aggregation at 1 uM by thioflavin T assay2007Bioorganic & medicinal chemistry, Oct-15, Volume: 15, Issue:20
Synthesis, in vitro assay, and molecular modeling of new piperidine derivatives having dual inhibitory potency against acetylcholinesterase and Abeta1-42 aggregation for Alzheimer's disease therapeutics.
AID1057862Inhibition of RML prion protein infected in mouse dividing ScN2a-cl3 cells expressing full length mouse PrP assessed as reduction of PrPsc level after 5 days by ELISA2013Bioorganic & medicinal chemistry, Dec-15, Volume: 21, Issue:24
Antiprion compounds that reduce PrP(Sc) levels in dividing and stationary-phase cells.
AID335875Protection against beta-amyloid (25 to 35) insult in rat PC12 cells assessed as viable cells after 24 hrs by MTT assay2002Journal of natural products, Sep, Volume: 65, Issue:9
Discovery of natural products from Curcuma longa that protect cells from beta-amyloid insult: a drug discovery effort against Alzheimer's disease.
AID472456Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 0.003 uM2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID619269Inhibition of Electrophorus electricus AChE-induced amyloid beta (1 to 42) aggregation at 100 uM after 8 hrs by thioflavin T fluorescence method2011European journal of medicinal chemistry, Oct, Volume: 46, Issue:10
Hybrids of oxoisoaporphine-tacrine congeners: novel acetylcholinesterase and acetylcholinesterase-induced β-amyloid aggregation inhibitors.
AID744314Inhibition of acetylcholinesterase (unknown origin)-induced amyloid beta(1 to 42) aggregation at 25 uM after 48 hrs by ThT fluorescence assay relative to control2013European journal of medicinal chemistry, May, Volume: 63Synthesis and evaluation of 7,8-dehydrorutaecarpine derivatives as potential multifunctional agents for the treatment of Alzheimer's disease.
AID472454Inhibition of human recombinant C-terminal FLAG-tagged NPP7 expressed in baculovirus-infected Sf9 cells assessed as pNPPC hydrolysis at 10 uM relative to control2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID525943Inhibition of PHLPP2 phosphatase domain expressed in Escherichia coli2010Journal of medicinal chemistry, Oct-14, Volume: 53, Issue:19
Discovery of small molecule inhibitors of the PH domain leucine-rich repeat protein phosphatase (PHLPP) by chemical and virtual screening.
AID322955Inhibition of synthetic amyloid beta-42 oligomerization by ELISA2007The Journal of biological chemistry, Apr-06, Volume: 282, Issue:14
Small molecule inhibitors of aggregation indicate that amyloid beta oligomerization and fibrillization pathways are independent and distinct.
AID497669Inhibition of Beta-lactamase at 4 uM by nitrocefin hydrolysis assay2008Nature chemical biology, Mar, Volume: 4, Issue:3
Small-molecule aggregates inhibit amyloid polymerization.
AID620401Inhibition of equine serum BChE using acetylthiocholine chloride as substrate after 15 mins by Ellman's method2011European journal of medicinal chemistry, Oct, Volume: 46, Issue:10
Hybrids of oxoisoaporphine-tacrine congeners: novel acetylcholinesterase and acetylcholinesterase-induced β-amyloid aggregation inhibitors.
AID300748Displacement of [125I]DMIC from amyloid beta 1-42 aggregates2007Bioorganic & medicinal chemistry, Oct-01, Volume: 15, Issue:19
Structure-activity relationship of chalcones and related derivatives as ligands for detecting of beta-amyloid plaques in the brain.
AID301579Displacement of [125I](E)-3-(4-(Dimethylamino-phenyl)-1-(4-iodophenyl)prop-2-en-1-one from beta amyloid(1-42) aggregates2007Bioorganic & medicinal chemistry, Nov-01, Volume: 15, Issue:21
Novel chalcones as probes for in vivo imaging of beta-amyloid plaques in Alzheimer's brains.
AID345208Inhibition of self-induced amyloid beta (1-40) aggregation at 10 uM by thioflavin T formation assay2008Journal of medicinal chemistry, Nov-27, Volume: 51, Issue:22
Structure-activity relationships of acetylcholinesterase noncovalent inhibitors based on a polyamine backbone. 4. Further investigation on the inner spacer.
AID628027Inhibition of VGLUT in rat synaptic vesicles assessed as glutamate uptake at 5 mM relative to control2011Bioorganic & medicinal chemistry letters, Jul-15, Volume: 21, Issue:14
Use of the hydantoin isostere to produce inhibitors showing selectivity toward the vesicular glutamate transporter versus the obligate exchange transporter system x(c)(-).
AID44056Concentration required for the inhibition of beta-lactamase2003Journal of medicinal chemistry, Jul-31, Volume: 46, Issue:16
Effect of detergent on "promiscuous" inhibitors.
AID620400Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins by Ellman's method2011European journal of medicinal chemistry, Oct, Volume: 46, Issue:10
Hybrids of oxoisoaporphine-tacrine congeners: novel acetylcholinesterase and acetylcholinesterase-induced β-amyloid aggregation inhibitors.
AID1190811Inhibition of Amyloid beta (1 to 42) (unknown origin) self aggregation at 5 uM pre-incubated for 24 hrs by Thioflavin T-based fluorometric assay2015Bioorganic & medicinal chemistry letters, Feb-15, Volume: 25, Issue:4
Synthesis and pharmacological evaluation of multifunctional tacrine derivatives against several disease pathways of AD.
AID472459Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 0.1 uM2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID472450Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID472460Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 0.3 uM2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID522115Antimicrobial activity against Candida glabrata TG162 containing calcineurin deltacnb1 mutant at 1 mg/ml after 48 hrs2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Roles of calcineurin and Crz1 in antifungal susceptibility and virulence of Candida glabrata.
AID275972Inhibition of 20 nM AmpC beta lactamase2006Journal of medicinal chemistry, Dec-14, Volume: 49, Issue:25
Interpreting steep dose-response curves in early inhibitor discovery.
AID628028Inhibition of cystine/glutamate transporter in human SNB19 cells assessed as [3H]glutamate uptake at 500 uM2011Bioorganic & medicinal chemistry letters, Jul-15, Volume: 21, Issue:14
Use of the hydantoin isostere to produce inhibitors showing selectivity toward the vesicular glutamate transporter versus the obligate exchange transporter system x(c)(-).
AID322957Inhibition of synthetic amyloid beta-42 fibrillation by ThT fluorescence analysis relative to control2007The Journal of biological chemistry, Apr-06, Volume: 282, Issue:14
Small molecule inhibitors of aggregation indicate that amyloid beta oligomerization and fibrillization pathways are independent and distinct.
AID744300Cytotoxicity against human SH-SY5Y cells assessed as cell viability after 48 hrs by MTT assay2013European journal of medicinal chemistry, May, Volume: 63Synthesis and evaluation of 7,8-dehydrorutaecarpine derivatives as potential multifunctional agents for the treatment of Alzheimer's disease.
AID475504Binding affinity to amyloid beta (1 to 42) fibrils by change in fluorescence at 100 uM after 10 mins2009Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
A chemical screening approach reveals that indole fluorescence is quenched by pre-fibrillar but not fibrillar amyloid-beta.
AID497651Inhibition of polyhistidine tagged yeast prion protein Sup35 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of amyloid polymerization at 5 uM in presence of 5 mg/ml BSA by thioflavin T fluorescence assay relative to untreated control2008Nature chemical biology, Mar, Volume: 4, Issue:3
Small-molecule aggregates inhibit amyloid polymerization.
AID290817Inhibition of Escherichia coli RecA by ADP-linked fluorescent ATPase assay2007Bioorganic & medicinal chemistry letters, Jun-15, Volume: 17, Issue:12
Directed molecular screening for RecA ATPase inhibitors.
AID322958Inhibition of synthetic amyloid beta-42 fibrillation by light scattering analysis relative to control2007The Journal of biological chemistry, Apr-06, Volume: 282, Issue:14
Small molecule inhibitors of aggregation indicate that amyloid beta oligomerization and fibrillization pathways are independent and distinct.
AID43249Percentage inhibition against beta-Lactamase in the absence of detergent Triton X-100 was determined at a concentration of 10 uM2003Journal of medicinal chemistry, Sep-25, Volume: 46, Issue:20
A specific mechanism of nonspecific inhibition.
AID56466Inhibitory activity against cloned Dihydrofolate reductase (cDHFR)2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID218680Inhibitory activity against beta-lactamase in the presence of 500 mMKPi concentration of buffer2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID1057863Cytotoxicity against mouse dividing ScN2a-cl3 cells assessed as cell viability after 5 days by calcein-AM staining-based fluorescence assay2013Bioorganic & medicinal chemistry, Dec-15, Volume: 21, Issue:24
Antiprion compounds that reduce PrP(Sc) levels in dividing and stationary-phase cells.
AID416747Inhibition of Escherichia coli AmpC assessed as induction of protein unfolding measured by trypsin mediated degradation of compound-AmpC enzyme complex at 250 uM after 15 mins by gel electrophoresis2009Journal of medicinal chemistry, Apr-09, Volume: 52, Issue:7
Promiscuous aggregate-based inhibitors promote enzyme unfolding.
AID744309Antioxidant activity of the compound assessed as trolox equivalent of APPH-induced radical scavenging activity at 1 uM incubated for 15 mins measured every 1 min for 240 mins by ORAC-FL assay2013European journal of medicinal chemistry, May, Volume: 63Synthesis and evaluation of 7,8-dehydrorutaecarpine derivatives as potential multifunctional agents for the treatment of Alzheimer's disease.
AID282856Displacement of [125I]6-iodo-4'-dimethyaminofl avone from beta amyloid (1-40) protein aggregates2005Journal of medicinal chemistry, Nov-17, Volume: 48, Issue:23
Radioiodinated flavones for in vivo imaging of beta-amyloid plaques in the brain.
AID283207Growth inhibition of Candida glabrata 21231 isolate in YEPD agar plates at 4 mg/ml2007Antimicrobial agents and chemotherapy, Mar, Volume: 51, Issue:3
Reduced susceptibility to polyenes associated with a missense mutation in the ERG6 gene in a clinical isolate of Candida glabrata with pseudohyphal growth.
AID55718Concentration required for the inhibition of dihydrofolate reductase2003Journal of medicinal chemistry, Jul-31, Volume: 46, Issue:16
Effect of detergent on "promiscuous" inhibitors.
AID23987Partition coefficient (logP)1999Journal of medicinal chemistry, Jul-29, Volume: 42, Issue:15
Synthesis and amyloid binding properties of rhenium complexes: preliminary progress toward a reagent for SPECT imaging of Alzheimer's disease brain.
AID218689The effect of 10-fold increase in enzyme concentration on beta-lactamase inhibition.2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID1863781Antifungal activity against Candida albicans SN152 harboring CAS5 mutant assessed as inhibition of fungal growth by broth microdilution method2022European journal of medicinal chemistry, Oct-05, Volume: 240β-Nitrostyrene derivatives as broad range potential antifungal agents targeting fungal cell wall.
AID744315Inhibition of amyloid beta(1 to 42) (unknown origin) self-aggregation at 25 uM after 48 hrs by ThT fluorescence assay relative to control2013European journal of medicinal chemistry, May, Volume: 63Synthesis and evaluation of 7,8-dehydrorutaecarpine derivatives as potential multifunctional agents for the treatment of Alzheimer's disease.
AID320067Binding affinity to immobilized amyloid beta 25-35 by Surface plasmon resonance2008Bioorganic & medicinal chemistry letters, Mar-15, Volume: 18, Issue:6
Synthesis and biological properties of beta-turned Abeta(31-35) constrained analogues.
AID52780Inhibitory activity against chymotrypsinogen2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID289395Inhibition of beta amyloid protein 1-42 aggregation by thioflavin T assay2007Bioorganic & medicinal chemistry, Oct-15, Volume: 15, Issue:20
Synthesis, in vitro assay, and molecular modeling of new piperidine derivatives having dual inhibitory potency against acetylcholinesterase and Abeta1-42 aggregation for Alzheimer's disease therapeutics.
AID52124Inhibition of choline acetyltransferase isolated from squid head ganglia1981Journal of medicinal chemistry, Dec, Volume: 24, Issue:12
Interaction of aromatic dyes with the coenzyme A binding site of choline acetyltransferase.
AID43125Inhibitory activity against Beta-lactamase from DMSO stock was determined2003Journal of medicinal chemistry, Sep-25, Volume: 46, Issue:20
A specific mechanism of nonspecific inhibition.
AID577834Antiprion activity in human transmissible spongiform encephalopathies agent Fukuoka-1 prion infected GT1-7 cells assessed as proteinase K-resistant proteins after 3 days Western blotting analysis2011Bioorganic & medicinal chemistry letters, Mar-01, Volume: 21, Issue:5
Synthesis of GN8 derivatives and evaluation of their antiprion activity in TSE-infected cells.
AID1190812Inhibition of Amyloid beta (1 to 42) (unknown origin) self aggregation at 50 uM pre-incubated for 24 hrs by Thioflavin T-based fluorometric assay2015Bioorganic & medicinal chemistry letters, Feb-15, Volume: 25, Issue:4
Synthesis and pharmacological evaluation of multifunctional tacrine derivatives against several disease pathways of AD.
AID1480852Inhibition of human erythrocyte AChE-induced amyloid beta (1 to 42) aggregation at 20 uM after 6 hrs by thioflavin T fluorescence assay relative to control2017European journal of medicinal chemistry, Apr-21, Volume: 130Design, synthesis and evaluation of 2-arylethenyl-N-methylquinolinium derivatives as effective multifunctional agents for Alzheimer's disease treatment.
AID43259Percentage inhibition against beta-Lactamase in the presence of detergent 0.01% Triton X-100 was determined at a concentration of 10 uM2003Journal of medicinal chemistry, Sep-25, Volume: 46, Issue:20
A specific mechanism of nonspecific inhibition.
AID667505Inhibition of Escherichia coli R67 DHFR2012Journal of medicinal chemistry, Apr-12, Volume: 55, Issue:7
Fragment-based design of symmetrical bis-benzimidazoles as selective inhibitors of the trimethoprim-resistant, type II R67 dihydrofolate reductase.
AID459782Displacement of [125I-N-Methyl-4-(4-bromoanilino)phthalimide from beta-amyloid plaques isolated from Alzheimer's disease patient brain2010Bioorganic & medicinal chemistry, Feb, Volume: 18, Issue:3
Novel anilinophthalimide derivatives as potential probes for beta-amyloid plaque in the brain.
AID1884937Inhibition of amyloid beta (unknown origin) assessed as decrease in amyloid beta monomers2022Journal of medicinal chemistry, 07-14, Volume: 65, Issue:13
Near-Infrared Fluorescent Probes as Imaging and Theranostic Modalities for Amyloid-Beta and Tau Aggregates in Alzheimer's Disease.
AID522112Antimicrobial activity against Candida glabrata TG172 containing deltacrz1 mutant at 1 mg/ml after 48 hrs2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Roles of calcineurin and Crz1 in antifungal susceptibility and virulence of Candida glabrata.
AID43269Percentage inhibition of Beta-lactamase at KPi (Potassium Phosphate) stock concentration of 4 uM2003Journal of medicinal chemistry, Sep-25, Volume: 46, Issue:20
A specific mechanism of nonspecific inhibition.
AID282857Displacement of [125I]6-iodo-4'-dimethyaminofl avone from beta amyloid (1-42) protein aggregates2005Journal of medicinal chemistry, Nov-17, Volume: 48, Issue:23
Radioiodinated flavones for in vivo imaging of beta-amyloid plaques in the brain.
AID218575Inhibitory activity against beta-lactamase2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID497646Inhibition of polyhistidine tagged yeast prion protein Sup35 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of amyloid polymerization at 5 uM by thioflavin T fluorescence assay relative to untreated control2008Nature chemical biology, Mar, Volume: 4, Issue:3
Small-molecule aggregates inhibit amyloid polymerization.
AID218682Inhibitory activity against beta-lactamase in the presence of 5 mM KPi concentration of buffer2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID275970Inhibition of 1 nM AmpC beta lactamase2006Journal of medicinal chemistry, Dec-14, Volume: 49, Issue:25
Interpreting steep dose-response curves in early inhibitor discovery.
AID283208Growth inhibition of polyene-resistant Candida glabrata 21229 isolate in YEPD agar plates at 4 mg/ml2007Antimicrobial agents and chemotherapy, Mar, Volume: 51, Issue:3
Reduced susceptibility to polyenes associated with a missense mutation in the ERG6 gene in a clinical isolate of Candida glabrata with pseudohyphal growth.
AID472464Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 30 uM2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID648661Inhibition of Electrophorus electricus AChE-induced beta-amyloid (1 to 40) aggregation at 100 uM after 8 hrs by thioflavin-T based fluorescence assay2012Bioorganic & medicinal chemistry letters, Mar-15, Volume: 22, Issue:6
Novel oxoisoaporphine-based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation.
AID298280Inhibition of human AChE-induced amyloid beta (1-40) aggregation at 100 uM2007Journal of medicinal chemistry, Oct-04, Volume: 50, Issue:20
Novel class of quinone-bearing polyamines as multi-target-directed ligands to combat Alzheimer's disease.
AID40277Inhibition of Beta-galactosidase2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID275971Inhibition of 10 nM AmpC beta lactamase2006Journal of medicinal chemistry, Dec-14, Volume: 49, Issue:25
Interpreting steep dose-response curves in early inhibitor discovery.
AID472458Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 0.03 uM2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID472449Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 10 uM relative to control2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID525944Inhibition of PHLPP in human HT20 cells assessed as increase of phosphorylation of Akt on Ser 473 at 100 to 250 uM after 24 hrs by immunoblotting relative to control2010Journal of medicinal chemistry, Oct-14, Volume: 53, Issue:19
Discovery of small molecule inhibitors of the PH domain leucine-rich repeat protein phosphatase (PHLPP) by chemical and virtual screening.
AID298278Inhibition of human recombinant acetylcholinesterase2007Journal of medicinal chemistry, Oct-04, Volume: 50, Issue:20
Novel class of quinone-bearing polyamines as multi-target-directed ligands to combat Alzheimer's disease.
AID648658Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method2012Bioorganic & medicinal chemistry letters, Mar-15, Volume: 22, Issue:6
Novel oxoisoaporphine-based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation.
AID227958Apparent dissociation constant was measured at 10 mM salt1999Journal of medicinal chemistry, Jul-29, Volume: 42, Issue:15
Synthesis and amyloid binding properties of rhenium complexes: preliminary progress toward a reagent for SPECT imaging of Alzheimer's disease brain.
AID497655Inhibition of mouse prion protein (89-230) assessed as inhibition of amyloid polymerization at 50 uM by thioflavin T fluorescence assay relative to untreated control2008Nature chemical biology, Mar, Volume: 4, Issue:3
Small-molecule aggregates inhibit amyloid polymerization.
AID472452Noncompetitive inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis by Michaelis-Menten method2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID648659Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method2012Bioorganic & medicinal chemistry letters, Mar-15, Volume: 22, Issue:6
Novel oxoisoaporphine-based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation.
AID475505Binding affinity to amyloid beta (1 to 42) oligomers by change in fluorescence at 100 uM after 10 mins2009Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
A chemical screening approach reveals that indole fluorescence is quenched by pre-fibrillar but not fibrillar amyloid-beta.
AID690971Inhibition of HFIP pretreated self-mediated amyloid beta (1 to 40) aggregation at 20 uM after 24 hrs by thioflavin-T based fluorimetric assay2012Bioorganic & medicinal chemistry letters, Oct-15, Volume: 22, Issue:20
Design, synthesis and pharmacological evaluation of novel tacrine-caffeic acid hybrids as multi-targeted compounds against Alzheimer's disease.
AID227959Apparent dissociation constant was measured at 110 mM salt1999Journal of medicinal chemistry, Jul-29, Volume: 42, Issue:15
Synthesis and amyloid binding properties of rhenium complexes: preliminary progress toward a reagent for SPECT imaging of Alzheimer's disease brain.
AID1477859Induction of HFIP-pretreated amyloid beta (1 to 42) (unknown origin) disaggregation after 48 hrs by silver staining-based SDS-PAGE analysis2018Journal of medicinal chemistry, 01-11, Volume: 61, Issue:1
Discovery of an Orally Bioavailable Benzofuran Analogue That Serves as a β-Amyloid Aggregation Inhibitor for the Potential Treatment of Alzheimer's Disease.
AID345207Inhibition of human recombinant AChE-induced amyloid beta (1-40) aggregation at 100 uM by thioflavin T formation assay2008Journal of medicinal chemistry, Nov-27, Volume: 51, Issue:22
Structure-activity relationships of acetylcholinesterase noncovalent inhibitors based on a polyamine backbone. 4. Further investigation on the inner spacer.
AID298279Inhibition of human recombinant butyrylcholinesterase2007Journal of medicinal chemistry, Oct-04, Volume: 50, Issue:20
Novel class of quinone-bearing polyamines as multi-target-directed ligands to combat Alzheimer's disease.
AID472457Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 0.01 uM2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID744310Antioxidant activity of the compound assessed as trolox equivalent of APPH-induced radical scavenging activity at 5 uM incubated for 15 mins measured every 1 min for 240 mins by ORAC-FL assay2013European journal of medicinal chemistry, May, Volume: 63Synthesis and evaluation of 7,8-dehydrorutaecarpine derivatives as potential multifunctional agents for the treatment of Alzheimer's disease.
AID227745Bmax value was measured on A-beta-40 fibrils at high salt1999Journal of medicinal chemistry, Jul-29, Volume: 42, Issue:15
Synthesis and amyloid binding properties of rhenium complexes: preliminary progress toward a reagent for SPECT imaging of Alzheimer's disease brain.
AID335876Protection against beta-amyloid (1 to 42) insult in rat PC12 cells assessed as viable cells after 24 hrs by MTT assay2002Journal of natural products, Sep, Volume: 65, Issue:9
Discovery of natural products from Curcuma longa that protect cells from beta-amyloid insult: a drug discovery effort against Alzheimer's disease.
AID1338171Inhibition of HFIP-pretreated amyloid beta (1 to 42) (unknown origin) self-induced aggregation at 10 uM after 24 hrs by thioflavin-T fluorescence assay relative to control2017European journal of medicinal chemistry, Jan-05, Volume: 125Discovery of novel rivastigmine-hydroxycinnamic acid hybrids as multi-targeted agents for Alzheimer's disease.
AID218566Preincubated with beta-lactamase, inhibitory activity expressed as fold decrease in IC50(ie. improved activity)2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID690972Inhibition of HFIP pretreated AChE-induced amyloid beta (1 to 40) aggregation at 100 uM after 24 hrs by thioflavin-T based fluorimetric assay2012Bioorganic & medicinal chemistry letters, Oct-15, Volume: 22, Issue:20
Design, synthesis and pharmacological evaluation of novel tacrine-caffeic acid hybrids as multi-targeted compounds against Alzheimer's disease.
AID628029Inhibition of VGLUT in rat synaptic vesicles assessed as glutamate uptake at 500 uM relative to control2011Bioorganic & medicinal chemistry letters, Jul-15, Volume: 21, Issue:14
Use of the hydantoin isostere to produce inhibitors showing selectivity toward the vesicular glutamate transporter versus the obligate exchange transporter system x(c)(-).
AID345205Inhibition of human recombinant AChE by Ellman's assay2008Journal of medicinal chemistry, Nov-27, Volume: 51, Issue:22
Structure-activity relationships of acetylcholinesterase noncovalent inhibitors based on a polyamine backbone. 4. Further investigation on the inner spacer.
AID52770Concentration required for the inhibition of Chymotrypsinogen2003Journal of medicinal chemistry, Jul-31, Volume: 46, Issue:16
Effect of detergent on "promiscuous" inhibitors.
AID1306099Inhibition of Abeta42 (unknown origin) aggregation measured after 24 hrs by ThT fluorescence assay2016Bioorganic & medicinal chemistry letters, 07-15, Volume: 26, Issue:14
Synthesis and structure-activity relationship of 2,6-disubstituted pyridine derivatives as inhibitors of β-amyloid-42 aggregation.
AID218681Inhibitory activity against beta-lactamase in the presence of 50 mM KPi concentration of buffer2002Journal of medicinal chemistry, Apr-11, Volume: 45, Issue:8
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening.
AID289396Inhibition of Electrophorus electricus AchE-induced beta amyloid protein 1-42 co-aggregation at 100 uM by thioflavin T assay2007Bioorganic & medicinal chemistry, Oct-15, Volume: 15, Issue:20
Synthesis, in vitro assay, and molecular modeling of new piperidine derivatives having dual inhibitory potency against acetylcholinesterase and Abeta1-42 aggregation for Alzheimer's disease therapeutics.
AID328833Suppression of aggregation of poly Q102-GFP mutant expressed in zebrafish embryo by filter trap assay2007The Journal of biological chemistry, Mar-23, Volume: 282, Issue:12
Identification of anti-prion compounds as efficient inhibitors of polyglutamine protein aggregation in a zebrafish model.
AID648662Inhibition of Electrophorus electricus AChE-induced beta-amyloid (1 to 40) aggregation at 10 uM after 8 hrs by thioflavin-T based fluorescence assay2012Bioorganic & medicinal chemistry letters, Mar-15, Volume: 22, Issue:6
Novel oxoisoaporphine-based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation.
AID472462Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 3 uM2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID1432628Inhibition of HFIP-pretreated amyloid beta (1 to 42 residues) (unknown origin) aggregation after 24 hrs by ThT fluorescence assay2017Bioorganic & medicinal chemistry letters, 03-15, Volume: 27, Issue:6
Discovery and characterization of novel indole and 7-azaindole derivatives as inhibitors of β-amyloid-42 aggregation for the treatment of Alzheimer's disease.
AID472461Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 1 uM2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID472463Inhibition of human recombinant C-terminal FLAG-tagged autotaxin expressed in baculovirus-infected Sf9 cells assessed as FS-3 hydrolysis at 10 uM2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID345206Inhibition of human serum BChE by Ellman's assay2008Journal of medicinal chemistry, Nov-27, Volume: 51, Issue:22
Structure-activity relationships of acetylcholinesterase noncovalent inhibitors based on a polyamine backbone. 4. Further investigation on the inner spacer.
AID227746max value was measured on A-beta-40 fibrils at low salt1999Journal of medicinal chemistry, Jul-29, Volume: 42, Issue:15
Synthesis and amyloid binding properties of rhenium complexes: preliminary progress toward a reagent for SPECT imaging of Alzheimer's disease brain.
AID40276Concentration required for the inhibition of beta-galactosidase2003Journal of medicinal chemistry, Jul-31, Volume: 46, Issue:16
Effect of detergent on "promiscuous" inhibitors.
AID475772Inhibition of VGLUT in rat brain synaptic vesicles assessed as [3H]L-glutamate uptake at 5 mM after 24 hrs by liquid scintillation counting2010Bioorganic & medicinal chemistry letters, Apr-15, Volume: 20, Issue:8
Conformationally-restricted amino acid analogues bearing a distal sulfonic acid show selective inhibition of system x(c)(-) over the vesicular glutamate transporter.
AID619268Inhibition of self-mediated amyloid beta (1 to 42) aggregation at 10 uM after 48 hrs by thioflavin T fluorescence method2011European journal of medicinal chemistry, Oct, Volume: 46, Issue:10
Hybrids of oxoisoaporphine-tacrine congeners: novel acetylcholinesterase and acetylcholinesterase-induced β-amyloid aggregation inhibitors.
AID1863780Antifungal activity against wild type Candida albicans SN152 assessed as inhibition of fungal growth by broth microdilution method2022European journal of medicinal chemistry, Oct-05, Volume: 240β-Nitrostyrene derivatives as broad range potential antifungal agents targeting fungal cell wall.
AID322956Inhibition of synthetic amyloid beta42 oligomer formation by Western blot2007The Journal of biological chemistry, Apr-06, Volume: 282, Issue:14
Small molecule inhibitors of aggregation indicate that amyloid beta oligomerization and fibrillization pathways are independent and distinct.
AID275973Inhibition of 30 nM AmpC beta lactamase2006Journal of medicinal chemistry, Dec-14, Volume: 49, Issue:25
Interpreting steep dose-response curves in early inhibitor discovery.
AID298281Inhibition of self-induced amyloid beta (1-40) aggregation at 10 uM by thioflavin T based fluorometric assay2007Journal of medicinal chemistry, Oct-04, Volume: 50, Issue:20
Novel class of quinone-bearing polyamines as multi-target-directed ligands to combat Alzheimer's disease.
AID472453Inhibition of human recombinant C-terminal FLAG-tagged NPP6 expressed in baculovirus-infected Sf9 cells assessed as pNPPC hydrolysis at 10 uM relative to control2010Journal of medicinal chemistry, Apr-22, Volume: 53, Issue:8
Pharmacophore development and application toward the identification of novel, small-molecule autotaxin inhibitors.
AID497674Inhibition of Beta-lactamase at 4 uM in presence of 0.01% Triton X-100 by nitrocefin hydrolysis assay2008Nature chemical biology, Mar, Volume: 4, Issue:3
Small-molecule aggregates inhibit amyloid polymerization.
AID1347161Confirmatory screen NINDS Rhodamine qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347156DAPI mCherry counterscreen qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347157Confirmatory screen GU Rhodamine qHTS for Zika virus inhibitors qHTS2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1347158ZIKV-mCherry secondary qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347169Tertiary RLuc qRT-PCR qHTS assay for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1347164384 well plate NINDS Rhodamine confirmatory qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1347163384 well plate NINDS AMC confirmatory qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347149Furin counterscreen qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (2,214)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990506 (22.85)18.7374
1990's239 (10.79)18.2507
2000's594 (26.83)29.6817
2010's555 (25.07)24.3611
2020's320 (14.45)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 56.00

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index56.00 (24.57)
Research Supply Index7.76 (2.92)
Research Growth Index4.72 (4.65)
Search Engine Demand Index96.53 (26.88)
Search Engine Supply Index2.01 (0.95)

This Compound (56.00)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials7 (0.30%)5.53%
Reviews87 (3.73%)6.00%
Case Studies155 (6.65%)4.05%
Observational1 (0.04%)0.25%
Other2,080 (89.27%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]