Page last updated: 2024-11-05

c.i. 42510

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Rosaniline Dyes: Compounds that contain the triphenylmethane aniline structure found in rosaniline. Many of them have a characteristic magenta color and are used as COLORING AGENTS. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

basic fuchsin : A four-component mixture of chemically related dyes comprising pararosanilin, rosanilin, magenta II and new fuchsin in varying amounts [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]

rosanilin : A hydrochloride that is the monohydrochloride of 4-[(4-aminophenyl)(4-iminocyclohexa-2,5-dien-1-ylidene)methyl]-2-methylaniline. One of the major constituents of Basic fuchsin, together with pararosanilin, magenta II and new fuchsin. [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 CID12447
CHEMBL ID1979636
CHEBI ID87665
SCHEMBL ID23402
MeSH IDM0084885

Synonyms (139)

Synonym
nsc-93739
fuchsin, basic [usp]
benzenamine, 4-((4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl)-2-methyl-, hydrochloride (1:1)
rosaniline dyes
8uuc89lhb2 ,
unii-8uuc89lhb2
violet zasadita 14
4-[(4-aminophenyl)(4-iminocyclohexa-2,5-dien-1-ylidene)methyl]-2-methylaniline hydrochloride
rosaniline.hcl
basic magenta e-200
magenta superfine
2, .alpha.(sup4)-(p-aminophenyl)-.alpha.(sup4)-(4-imino-2,5-cyclohexadien-1-ylidene)-, monohydrochloride
2-methyl-4,5-cyclohexadien-1-ylidene)methylene]dianiline hydrochloride
4-amino-m-tolyl-bis(4-aminophenyl)methane chloride
calcozine magenta xx
magenta large crystals
benzenamine,5-cyclohexadien-1-ylidene)methyl]-2-methyl-, monohydrochloride
diabasic magenta
fuchsine ho
basic violet 14
magenta g
diamond fuchsin
magenta s
magenta e
magenta
cerise b
fuchsine g
astra fuchsine b
magenta pn
fuchsine cs
mitsui magenta
fuchsin basic
rose aniline
calcozine magenta rtn
rosanilinium chloride
fuchsine y
rosaniline chloride
nsc-10466
methyl fuchsin
magenta dp
fuchsin, basic
magenta powder n
aizen magenta
orient basic magenta
fuchsine crystals
wln: l6y dyj auyr dz&r dz c1& dum &gh
basic magenta
calcozine fuchsine ho
c.i. basic violet 14, monohydrochloride
fuchsine n
fuchsine a
fuchsine
diamond fuchsine
fuchsine rtn
rosaniline hydrochloride
basic fuchsine
c.i. basic violet 14
magenta i
rosaniline
c.i. 42510
12418 red
NSC93739 ,
632-99-5
basic fuchsin
nsc10466
rosaniline hcl
(4-(4-aminophenyl)(4-iminocyclohexa-2,5-dienylidene)methyl)-2-methylaniline hydrochloride
fuchsin
rosanilinium hydrochloride
ai3-18324
magenta super fine
hsdb 6192
ci 42510
benzeneamine, 4-((4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl)-2-methyl-, monohydrochloride
4-((4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl)-2- methylbenzenamine monohydrochloride
ci basic violet 14, monohydrochloride
aniline red
c-wr violet 8
basic fuchsine (van)
magenta i [magenta (containing c.i. basic red 9)]
nsc 93739
4-((4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl)-2-methylbenzenamine hcl
magenta supertine
nsc 10466
einecs 211-189-6
manufacture of magenta
c.i. basic violet 14 monohydrochloride
calcozine magenta rin
benzenamine, 4-((4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl)-2-methyl-, monohydrochloride
ci basic violet 14
violet zasadita 14 [czech]
ccris 366
NCGC00166015-01
F-7910
fuchsine basic monohydrochloride
benzenamine, 4-[(4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl]-2-methyl-, hydrochloride (1:1)
basic fuchsin hydrochloride
C19252
tox21_202790
dtxcid101246
tox21_112288
NCGC00260336-01
cas-632-99-5
dtxsid6021246 ,
FT-0626556
58969-01-0
AKOS015902644
SCHEMBL23402
lowacryl violet 14
ci 42510 [inci]
magenta i [mi]
basic violet 14 [inci]
4-[(4-amino-3-methylphenyl)(4-aminophenyl)methylidene]cyclohexa-2,5-dien-1-iminium chloride
rosanilin
CHEMBL1979636
chebi:87665 ,
basic fuchsin, biological stain
magenta crystals
basic violet 14 hydrochloride
fuchsin; 4-[(4-aminophenyl)-(4-iminocyclohexa-2,5-dien-1-ylidene)methyl]-2-methyl-aniline hydrochloride; basic violet 14 hcl; magenta i
4-((4-amino-3-me-ph)(4-amino-ph)methylene)-2,5-cyclohexadien-1-iminium chloride
4-((4-aminophenyl)(4-iminocyclohexa-2,5-dienylidene)methyl)-2-methylaniline hydrochloride
basic blue 14
Q419167
4-((4-aminophenyl)(4-iminocyclohexa-2,5-dien-1-ylidene)methyl)-2-methylaniline hydrochloride
HY-B1539A
fuchsine base (monohydrochloride)
CS-0013370
4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydrochloride
magenta base monohydrochloride;basic fuchsin monohydrochloride;rosaniline base monohydrochloride
benzenamine,4-[(4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl]-2-methyl-, monohydrochloride
magenta o
STARBLD0016617
[4-[bis(4-aminophenyl)methylidene]-2-methylcyclohexa-2,5-dien-1-ylidene]azanium;chloride
basic fuchsin, indicator
CS-0169059
E82121
fucsino
fucsina

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" The ability to induce "shock protein" synthesis obviously seems to be restricted to toxic drugs."( A cell culture assay for the detection of cardiotoxicity.
Löw-Friedrich, I; Schoeppe, W; von Bredow, F, 1991
)
0.28
" A comparison of adverse effects suggests that exposure of rats or mice to leucomalachite green causes a greater number of and more severe changes than exposure to malachite green."( Toxicity and metabolism of malachite green and leucomalachite green during short-term feeding to Fischer 344 rats and B6C3F1 mice.
Beland, FA; Blankenship, LR; Culp, SJ; Doerge, DR; Kusewitt, DF; Mulligan, LT, 1999
)
0.3
"To describe the adverse events associated with the intraoperative injection of isosulfan blue in a large group of patients having a wide range of surgical procedures, and to identify risk factors for these events."( Adverse events associated with the intraoperative injection of isosulfan blue.
Arens, JF; Bui, TP; Daley, MD; Gershenwald, JE; Hunt, KK; Kowalski, AM; Kuerer, HM; Leak, JA; Nguyen, DT; Norman, PH; Popat, K; Srejic, U, 2004
)
0.32
"Incidence, type, severity, onset time, duration, management, and the presence of potential risk factors for adverse events."( Adverse events associated with the intraoperative injection of isosulfan blue.
Arens, JF; Bui, TP; Daley, MD; Gershenwald, JE; Hunt, KK; Kowalski, AM; Kuerer, HM; Leak, JA; Nguyen, DT; Norman, PH; Popat, K; Srejic, U, 2004
)
0.32
"5%) and 14 of these adverse events (0."( Adverse events associated with the intraoperative injection of isosulfan blue.
Arens, JF; Bui, TP; Daley, MD; Gershenwald, JE; Hunt, KK; Kowalski, AM; Kuerer, HM; Leak, JA; Nguyen, DT; Norman, PH; Popat, K; Srejic, U, 2004
)
0.32
" The Vibrio fischeri acute toxicity test showed that the solution remains toxic after MG has completely disappeared."( Photodegradation of malachite green under natural sunlight irradiation: kinetic and toxicity of the transformation products.
Agüera, A; Fernández-Alba, AR; Hernando, MD; Malato, S; Pérez-Estrada, LA, 2008
)
0.35
"All dyes demonstrated relatively safe viability profiles in both cell lines at surgically relevant concentrations and times."( Comparison of the in vitro safety of intraocular dyes using two retinal cell lines: a focus on brilliant blue G and indocyanine green.
Gonder, J; Hutnik, C; Liu, H; Proulx, A; Yuen, D, 2009
)
0.35
" It has been noted to cause skin necrosis, but its more mild adverse effects from intraparenchymal breast injections are not well characterized."( Inflammatory cutaneous adverse effects of methylene blue dye injection for lymphatic mapping/sentinel lymphadenectomy.
Axelrod, P; Bleicher, RJ; Kloth, DD; Robinson, D, 2009
)
0.35
"Gel destaining following Coomassie Brilliant Blue (CBB) staining involves the use of toxic reagents."( Environmentally safe removal/disposal of Coomassie Brilliant Blue from gel destain and used gel stain.
Dorri, Y; Kurien, BT, 2010
)
0.36
" We compared the in vitro toxicity of IfCG, BBG, and BPB with ICG on the retinal pigment epithelial cells and retinal ganglion cells at various concentrations to optimize the safe dose and duration of exposure."( Comparative in vitro safety analysis of dyes for chromovitrectomy: indocyanine green, brilliant blue green, bromophenol blue, and infracyanine green.
Balaiya, S; Brar, VS; Chalam, KV; Murthy, RK, 2011
)
0.37
" Infracyanine green, BBG, and BPB were significantly less toxic on the 2 cell lines at exposure times <15 minutes."( Comparative in vitro safety analysis of dyes for chromovitrectomy: indocyanine green, brilliant blue green, bromophenol blue, and infracyanine green.
Balaiya, S; Brar, VS; Chalam, KV; Murthy, RK, 2011
)
0.37
"Newer vital dyes, IfCG, BBG, and BPB, are significantly less toxic on retinal ganglion cells and retinal pigment epithelial cells' cell lines when compared with ICG."( Comparative in vitro safety analysis of dyes for chromovitrectomy: indocyanine green, brilliant blue green, bromophenol blue, and infracyanine green.
Balaiya, S; Brar, VS; Chalam, KV; Murthy, RK, 2011
)
0.37
" In contrast, BBG and TA appear safe after subretinal injection."( Toxicity profiles of subretinal indocyanine green, Brilliant Blue G, and triamcinolone acetonide: a comparative study.
Ejstrup, R; Heegaard, S; Kiilgaard, JF; la Cour, M, 2012
)
0.38
" Embryo and larval survival were not affected by exposure of parents to MG; however, when exposed directly, MG oxalate was more toxic than MG chloride in both life stages."( Malachite green toxicity and effects on reproductive success in zebrafish Danio rerio.
Davies, SJ; Henry, TB; White, CR, 2012
)
0.38
"Combinations of trypan blue (TB), Brilliant Blue G (BBG) and polyethyleneglycol had been shown before to be less toxic to ARPE retinal pigment epithelial cells than TB alone."( Brilliant Blue G as protective agent against trypan blue toxicity in human retinal pigment epithelial cells in vitro.
Awad, D; Bartok, M; Gabel, D; Mohr, A; Schrader, I; Sudumbrekar, N, 2013
)
0.39
"075 % and higher was toxic to the cells already after 30 min incubation."( Brilliant Blue G as protective agent against trypan blue toxicity in human retinal pigment epithelial cells in vitro.
Awad, D; Bartok, M; Gabel, D; Mohr, A; Schrader, I; Sudumbrekar, N, 2013
)
0.39
"In totally laparoscopic distal gastrectomy, determining the resection line with safe proximal margins is often difficult, particularly for tumors located in a relatively upper area."( Accurate, safe, and rapid method of intraoperative tumor identification for totally laparoscopic distal gastrectomy: injection of mixed fluid of sodium hyaluronate and patent blue.
Ehara, K; Kaida, S; Nakagawa, M; Tanaka, T; Udagawa, H; Ueno, M, 2014
)
0.4
" Adverse retinal staining was not noted and the final visual acuity showed no difference with multiple staining."( Brilliant Blue G double staining enhances successful internal limiting membrane peeling with minimal adverse effect by low cellular permeability into live cells.
Asato, R; Enaida, H; Hisatomi, T; Ikeda, Y; Ishibashi, T; Murakami, Y; Notomi, S; Oishi, S; Sakamoto, T; Tachibana, T; Yamashita, T, 2015
)
0.42
" 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
" Experimental results indicated that both these forms of mercury were toxic to all the neural cells, but at very different degrees."( In vitro evaluation of inorganic and methyl mercury mediated cytotoxic effect on neural cells derived from different animal species.
Lu, Y; Tong, J; Wang, Y, 2016
)
0.43
" However, it may be safe to preserve a clinically non-suspicious ARM node in patients with a positive SLNB who require a completion ALND."( Axillary reverse mapping in patients with breast cancer: Is it oncologically safe?
Elder, EE; French, J; Kilby, CJ; Ngui, NK; Pathmanathan, N, 2016
)
0.43
" To test this, a nontoxic triphenylmethane dye, Brilliant Blue G (BBG), which has been reported to modulate Aβ aggregation and neurotoxicity, was investigated using mouse primary cortical neuronal cultures treated with photoinduced cross-linked toxic Aβ40 oligomers as well as soluble Aβ40 and Aβ42 peptides."( Oligomeric Amyloid-β Toxicity Can Be Inhibited by Blocking Its Cellular Binding in Cortical Neuronal Cultures with Addition of the Triphenylmethane Dye Brilliant Blue G.
Cappai, R; Ciccotosto, GD; Jana, MK, 2016
)
0.43
"1) is an important enzyme in the homeostasis of sulfite levels (present either as a toxic intermediate in the pathway or as a toxic air pollutant that has penetrated the plant tissue via the stomata)."( Determination of Enzymes Associated with Sulfite Toxicity in Plants: Kinetic Assays for SO, APR, SiR, and In-Gel SiR Activity.
Bekturova, A; Brychkova, G; Khozin, I; Kurmanbayeva, A; Sagi, M; Standing, D; Yarmolinsky, D, 2017
)
0.46
" Our study suggests that BNC without scans is safe and effective."( Are pre-operative lymphoscintigrams needed for localization prior to sentinel node biopsy?: An audit to ensure safe practice and to provide another view.
Green, M; Gregg, L; Ives, C; Trust, C, 2018
)
0.48
" We conclude that the temporary hair dyes may have risk to human health, and those who use them should be aware of their potential toxic effects."( The Bio-Safety Concerns of Three Domestic Temporary Hair Dye Molecules: Fuchsin Basic, Victoria Blue B and Basic Red 2.
Deng, SJ; Jin, SF; Li, HC; Liu, B; Sun, XY; Yan, SQ; Zhao, P, 2019
)
0.51
" Thus, investigating the relationship between the gut microbiome and toxic chemicals is a hot topic in toxicology research."( The gut microbiota: a new perspective on the toxicity of malachite green (MG).
Jin, W; Li, H; Li, T; Tian, D; Wu, S; Zhu, Z, 2019
)
0.51
" The toxic effect on cancer cells is correlated to the ionization ability of MG-Xs."( pH-triggered solubility and cytotoxicity changes of malachite green derivatives incorporated in liposomes for killing cancer cells.
Hayashi, K; Iwasaki, T; Uda, RM; Yoshida, N, 2020
)
0.56
" However, BBG dye, though considered safe and nontoxic, can also occasionally lead to macular toxicity."( Brilliant Blue G toxicity in macular hole surgeries: A report on combined phototoxicity and dye-induced macular damage.
Chhablani, J; Dogra, A; Pappuru, RR; Parameswarappa, DC; Sahoo, NK; Soni, A; Tyagi, M, 2022
)
0.72

Pharmacokinetics

ExcerptReferenceRelevance
" Based on these values the intracellular nonenzymatic reduction of TAM+ to TAM-H by endogenous NADH was estimated to proceed with an average half-life of 30 min."( An assessment of the role of intracellular reductive capacity in the biological clearance of triarylmethane dyes.
Ozer, I; Tacal, O, 2007
)
0.34

Compound-Compound Interactions

ExcerptReferenceRelevance
"Sister chromatid exchange (SCE) induced by Indigo carmine (secondary amine containing dye), Fast green FCF (tertiary amine containing dye) and nitrite singly and in combination with nitrite were carried out in vivo in mice following acute exposure."( Sister chromatid exchange induced by secondary and tertiary amine containing dyes and in combination with nitrite in vivo in mice.
Giri, AK; Mukherjee, A, 1990
)
0.28
"This paper describes the application of image analysis combined with a quantitative staining method for the analysis of cervical specimens."( Image analysis combined with quantitative cytochemistry. Results and instrumental developments for cancer diagnosis.
Goyarts-Veldstra, L; Ploem, JS; Ploem-Zaaijer, JJ; van der Zwan, M; van Driel-Kulker, AM; Verwoerd, NP, 1986
)
0.27
"The protein dyes Light Green and Orange II were studied separately and in combination with the Feulgen-Pararosanilin(SO2) and -Thionin(SO2) method for the simultaneous determination of DNA and protein."( The use of Light Green and Orange II as quantitative protein stains, and their combination with the Feulgen method for the simultaneous determination of protein and DNA.
Henderik, JB; Hermkens, HG; Huysmans, AC; James, J; Oud, PS; Pahlplatz, MM; Tas, J; Vooijs, GP, 1984
)
0.27
"An electrochemiluminescence (ECL) inhibition method combined with molecularly imprinted solid phase extraction (MISPE) was developed for quantitative determination of malachite green (MG) residues in fish."( Determination of malachite green residues in fish using a highly sensitive electrochemiluminescence method combined with molecularly imprinted solid phase extraction.
Duan, J; Gai, P; Guo, Z; Hao, T; Wang, S, 2011
)
0.37
" The LAMP assay in combination with an FTA card described here is rapid and sensitive, as well as simple to perform, and has great potential usefulness for diagnosis and surveillance of leishmaniasis in endemic areas."( A rapid molecular diagnosis of cutaneous leishmaniasis by colorimetric malachite green-loop-mediated isothermal amplification (LAMP) combined with an FTA card as a direct sampling tool.
Cáceres, AG; Gomez, EA; Guerrero-Quincho, S; Guevara, AG; Hashiguchi, Y; Katakura, K; Kato, H; Mimori, T; Nzelu, CO; Rodriquez-Delfin, L; Tineo-Villafuerte, E; Uezato, H, 2016
)
0.43

Bioavailability

ExcerptReferenceRelevance
"The spontaneous release of drug payloads in the whole body always results in the compromised drug bioavailability and ultimate therapeutic efficacy."( Molecular structural transformation regulated dynamic disordering of supramolecular vesicles as pH-responsive drug release systems.
Chen, XG; Fan, YS; Gao, FP; Liu, Y; Wang, H; Zhang, D, 2014
)
0.4
" Solubilizing curcumin with Tween 80 would be a useful alternative to increase curcumin bioavailability in clinical studies."( Heat/Pressure Treatment with Detergents Significantly Increases Curcumin Solubility and Stability: Its Use as an Environment-Friendly Protein Gel Stain.
Kurien, BT; Payne, A; Scofield, RH; Thomas, R, 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

Dosage Studied

ExcerptRelevanceReference
", reduced Feulgen-DNA reactivity), irrespective of the dosage employed and the delay prior to sacrifice."( Cytophotometric analysis of magnocellular azure B-RNA and Feulgen-DNA following chronic GABA infusion into the nucleus basalis of rats.
Anthony, A; Ballough, G; Kan, R; Majchrzak, M; Strauss, J; Will, B, 1992
)
0.28
" Using a fixed intensity fluorescent light source and quantitative spectrophotometric analysis, a highly significant dose-response relationship was demonstrated between duration of light exposure and the decrease in ethyl violet concentration."( Photodeactivation of ethyl violet: a potential hazard of Sodasorb.
Andrews, JJ; Arens, JF; Bee, DE; Johnston, RV, 1990
)
0.28
"Trials have been carried out, first on a relatively small scale among patients in Manila and later on a larger scale among domiciliary patients in an area of endemic schistosomiasis in Leyte Province, Philippines, with various dosage schedules of pararosaniline pamoate (CI-403-A) to determine that drug's efficacy and optimum dosage against Schistosoma japonicum infection."( Pararosaniline pamoate (CI-403-A) in the treatment of Schistosoma japonicum infection in the Philippines.
Banzon, TC; Noseñas, J; Pesigan, TP; Santos, AT; Zabala, RG, 1967
)
0.25
" With a dosage of 20 micrograms kg-1 soman, no RNA alterations were evidenced at 1 h whereas at 6-8 h myocardial cells exhibited higher RNA levels and an increase in F-DNA reactivity of chromatin."( Scanning cytophotometric analysis of myocardial nucleic acid and chromatin changes in soman toxicated rabbits.
Anthony, A; Doebler, JA; Martin, LJ; Shih, TM; Swisher, JW, 1984
)
0.27
"005) of the femoral neck at all dosage levels."( Risedronate treatment does not increase microdamage in the canine femoral neck.
Burr, DB; Eastman, DF; Forwood, MR; Schwardt, JD; Smith, PN; Takano, Y, 1995
)
0.29
" In this study we have studied the dose-response effects of MG on free radical formation, lipid peroxidation and DNA damage in SHE cells."( Dose-response effects of malachite green on free radical formation, lipid peroxidation and DNA damage in Syrian hamster embryo cells and their modulation by antioxidants.
Maru, GB; Panandiker, A; Rao, KV, 1994
)
0.29
" The dose-response curve for ATP was biphasic with a first increase in the 1-30 microM concentration range and a further increase at concentrations higher than 100 microM."( Low affinity purinergic receptor modulates the response of rat submandibular glands to carbachol and substance P.
Alzola, E; Amsallem, H; Chaib, N; Dehaye, JP; Elyamani, A; Marino, A; Métioui, M; Moran, A, 1996
)
0.29
" To calculate the dose-response curves we calibrated the relationship between the dye concentration and the photometer voltage output."( Measurement of concentration-response relationships by concentration-ramp application of agonists.
Schmandt, G; Schmidt, KF, 1999
)
0.3
" The present study was focused on the impact of ofloxacin on rat testicular DNA ploidy in a dose-response relationship using an image analysis technique on testicular sections following Fuelgen DNA staining."( The impact of ofloxacin on rat testicular DNA: application of image analysis.
Abd-Allah, AR; Gannam, BB; Hamada, FM, 2000
)
0.31
" The extent of the reduction of SpO2 readings two hours after the administration of PB was relevant to the total accumulative dosage of PB (rs = -0."( Prolonged interference of patent blue on pulse oximetry readings.
Chia, YY; Kao, PF; Liu, K; Sun, GC; Wang, KY, 2001
)
0.31
" The extent of desaturation may be related to the total accumulative dosage of intra-arterial PB injected."( Prolonged interference of patent blue on pulse oximetry readings.
Chia, YY; Kao, PF; Liu, K; Sun, GC; Wang, KY, 2001
)
0.31
" Antibiotic dosed solid CLMs were placed on agar plates streaked with Escherichia coli and incubated."( Local pharmaceutical release from a new hydrogel implant.
Chen, J; Felsen, D; Petratos, PB; Poppas, DP, 2002
)
0.31
"Treatment of Chinese hamster ovary and mouse hybridoma cells with Mega-H brand silica hydride, a marketed antioxidant, after photosensitization with singlet oxygen and hydroxyl/superoxide reactive oxygen species through the use of rose bengal diacetate and malachite green resulted in an effective method of reducing free radical activity by more than 96% against singlet oxygen species and more than 86% for hydroxyl and superoxide free radicals with the dosage recommended by the manufacturer."( Antioxidant capability and efficacy of Mega-H silica hydride, an antioxidant dietary supplement, by in vitro cellular analysis using photosensitization and fluorescence detection.
Flanagan, GP; Stephanson, AM; Stephanson, CJ, 2002
)
0.31
" The effect of adsorption on contact time, concentration of MG and adsorbent dosage of the samples treated or carbonized at different temperatures were investigated."( Adsorption characteristics of malachite green on activated carbon derived from rice husks produced by chemical-thermal process.
Rahman, IA; Saad, B; Shaidan, S; Sya Rizal, ES, 2005
)
0.33
" At low dye concentrations (20-80 mgl(-1)), an increase in the adsorbent dosage resulted in a higher removal percentage of the dye, but a lower amount of dye adsorbed per unit mass (q)."( Removal of basic dye (Astrazon Blue FGRL) using macroalga Caulerpa lentillifera.
Marungrueng, K; Pavasant, P, 2006
)
0.33
" The effect of system variables such as concentration, temperature, pH, contact time, adsorbent dosage and particle size was studied."( Adsorptive removal of basic dyes from aqueous phase onto activated carbon of used tea leaves: a kinetic and thermodynamic study.
Rastogi, K; Singh, DK, 2004
)
0.32
" The operating variables studied are the initial dye concentration, initial solution pH, adsorbent dosage and contact time."( Equilibrium, kinetics and mechanism modeling and simulation of basic and acid dyes sorption onto jute fiber carbon: Eosin yellow, malachite green and crystal violet single component systems.
Porkodi, K; Vasanth Kumar, K, 2007
)
0.34
"Aim of this study to improve the detection rate of parametrial sentinel nodes in patients with early cervical cancer by using a new dosage of blue dye in a randomized trial."( Dilution of dye improves parametrial SLN detection in patients with cervical cancer.
Altgassen, C; Dahmen, G; Diedrich, K; Dimpfl, T; Hertel, H; Paseka, A; Urbanczyk, H, 2007
)
0.34
"5, 3, and 5 times the concentration used for the therapeutic dosage; and at the concentration used for the therapeutic dosage but for 3 or 5 times the recommended exposure time."( Tolerance of benzalkonium chloride, formalin, malachite green, and potassium permanganate in goldfish and zebrafish.
Di Bello, D; Intorre, L; Meucci, V; Monni, G; Pretti, C; Soldani, G, 2007
)
0.34
"In both species, exposure to malachite green at the therapeutic dosage resulted in toxic effects, including death."( Tolerance of benzalkonium chloride, formalin, malachite green, and potassium permanganate in goldfish and zebrafish.
Di Bello, D; Intorre, L; Meucci, V; Monni, G; Pretti, C; Soldani, G, 2007
)
0.34
" The dye removal with the assistance of ultrasound was enhanced with the increase of sorbate initial concentration and temperature, and with the decrease of sorbent dosage and ionic strength."( Ultrasound-assisted removal of malachite green from aqueous solution by dead pine needles.
Chiha, M; Hamdaoui, O; Naffrechoux, E, 2008
)
0.35
" Patent Blue had a linear dose-response effect on the serum indices."( Interference with serum indices measurement, but not chemical analysis, on the Roche Modular by Patent Blue V.
Broomhead, C; Darby, D, 2008
)
0.35
" With the same total dosage of applied H2O2, the multiple steps addition did not show a much higher removal efficiency than that obtained by one step."( [Degradation of malachite green in aqueous solution by Fe3+/H2O2 catalyzed with EDTA].
Li, CJ; Ma, J; Yu, M; Zhang, YJ, 2008
)
0.35
" Dose-response modelling of the data for hepatocellular adenomas and carcinomas in female mice gave a BMDL10 of 20 mg/kg-bw/day."( Application of the margin of exposure (MOE) approach to substances in food that are genotoxic and carcinogenic. Example: leucomalachite green.
Leblanc, JC; Renwick, A; Setzer, RW, 2010
)
0.36
" Adsorbed amount of MG by DCB increased with increasing DCB dosage and initial MG concentration."( Removal of Malachite Green from aqueous solution using degreased coffee bean.
Baek, MH; Ijagbemi, CO; Kim, DS; O, SJ, 2010
)
0.36
" The removal rate of MG increased with the increase of the dosage of catalyst."( [Photo-assisted degradation of dye malachite green solution over Fe3+ C2O4-loaded resin in the presence of H2O2].
Chen, L; Ma, J; Wu, PY; Zhang, YJ; Zhao, J, 2009
)
0.35
" The ZHL was treated with calcined BS to give the BS-ZHL, and its ability to adsorb MG was compared with untreated ZHL, calcined BS and Ca(OH)(2)-treated ZHL under several different conditions: pH (2-8), adsorbent dosage (0."( Utilization of bivalve shell-treated Zea mays L. (maize) husk leaf as a low-cost biosorbent for enhanced adsorption of malachite green.
Adam, SH; Azmi, ZZ; Hameed, BH; Jaafar, NF; Jalil, AA; Kamarudin, NH; Sapawe, N; Setiabudi, HD; Sidik, SM; Triwahyono, S; Yaakob, MR, 2012
)
0.38
" The adsorption kinetics, adsorption capacity of the adsorbent, and the effect of the adsorbent dosage and solution pH on the removal efficiency of pararosaniline were investigated."( A facile one-pot solvothermal method to produce superparamagnetic graphene-Fe3O4 nanocomposite and its application in the removal of dye from aqueous solution.
Feng, C; Wang, C; Wang, Z; Wu, Q, 2013
)
0.39
" The hazardous dyes MG and MB removal studied under the various conditions like contact time, dye concentration, temperature, pH and adsorbent dosage to examine the adsorption characteristics of the newly synthesized mesoporous AlPO(4) molecular sieves."( Hazardous dyes removal from aqueous solution over mesoporous aluminophosphate with textural porosity by adsorption.
Devi, MR; Kannan, C; Muthuraja, K, 2013
)
0.39
" The effects of variables such as pH, initial dye concentration, adsorbent dosage (g), temperature and sonication time on MG removal were studied using central composite design (CCD) and the optimum experimental conditions were found with desirability function (DF) combined response surface methodology (RSM)."( Optimization of the combined ultrasonic assisted/adsorption method for the removal of malachite green by gold nanoparticles loaded on activated carbon: experimental design.
Asghari, A; Daneshfar, A; Ghaedi, M; Roosta, M; Sahraei, R; Shokri, N, 2014
)
0.4
" To overcome these biases, we developed the PROgressive SAmple Dosage (PROSAD) platform and tested it."( PROSAD: a powerful platform for instrument calibration and quantification.
Cristoni, S; Floridia, M, 2014
)
0.4
" The extent of MG adsorption onto modified sawdust increased with increasing organic acid concentrations, pH, contact time, and temperature but decreased with increasing adsorbent dosage and ionic strength."( Removal of malachite green dye from wastewater by different organic acid-modified natural adsorbent: kinetics, equilibriums, mechanisms, practical application, and disposal of dye-loaded adsorbent.
Leng, L; Liao, K; Peng, L; Peng, X; Wang, H; Xiao, Z; Yuan, X; Zeng, G, 2014
)
0.4
" The relation between removal percentages with variables such as solution pH, adsorbent dosage (0."( Isotherm and kinetics study of malachite green adsorption onto copper nanowires loaded on activated carbon: artificial neural network modeling and genetic algorithm optimization.
Ghaedi, AM; Ghaedi, M; Sahraei, R; Shojaeipour, E, 2015
)
0.42
"36mm) and adsorbent dosage (2-12g/L)."( Investigation on removal of malachite green using EM based compost as adsorbent.
Bhagavathi Pushpa, T; Jegan, J; Sardhar Basha, SJ; Sekaran, V; Vijayaraghavan, J; Vijayaraghavan, K, 2015
)
0.42
" Confocal microscopic images and dose-response titration experiments showed that loading of IgG into the film was mediated by pAG(MG) bound to the FAP."( Local retention of antibodies in vivo with an injectable film embedded with a fluorogen-activating protein.
Bagia, C; Fan, Y; Freeman, EC; Gawalt, ES; Liu, W; Meng, WS; Saunders, MJ; Waggoner, AS, 2016
)
0.43
" The addition of an appropriate PS dosage (5 g/L) resulted in remarkable increase in the removal efficiency of MG at lower current density and shorter operating time compared with the conventional EC process."( Removal of malachite green from aqueous solutions by electrocoagulation/peanut shell adsorption coupling in a batch system.
Li, Y; Ni, J; Pang, S; Wang, X, 2017
)
0.46
"008g of adsorbent dosage and 20min of agitation time were utilized in the kinetic and isotherm studies."( Adsorption of malachite green from aqueous solution by using novel chitosan ionic liquid beads.
Hamid, NSA; Mehamod, FS; Naseeruteen, F; Ngah, WSW; Suah, FBM, 2018
)
0.48
" The impact of parameters like initial dye concentration, pH and adsorbent dosage on the dye removal efficiency was confirmed by carrying out Box-Behnken design experiments."( Facile synthesis of carbon-coated layered double hydroxide and its comparative characterisation with Zn-Al LDH: application on crystal violet and malachite green dye adsorption-isotherm, kinetics and Box-Behnken design.
George, G; Saravanakumar, MP, 2018
)
0.48
" The adsorbent dosage and pH effects were studied, as well as kinetic, equilibrium, and thermodynamic curves were constructed."( Preparation of carbonaceous materials from pyrolysis of chicken bones and its application for fuchsine adsorption.
Collazzo, GC; Côrtes, LN; Dotto, GL; Druzian, SP; Sant'anna Cadaval Junior, TR; Streit, AFM, 2019
)
0.51
"The adsorption of malachite green (MG) onto sodium dodecylbenzene sulfonate (SDBS)-modified sepiolite was investigated with respect to pH, oscillation rate, MG dosage and adsorbent dosage."( Adsorption of Malachite Green with Sodium Dodecylbenzene Sulfonate Modified Sepiolite: Characterization, Adsorption Performance and Regeneration.
Liu, B; Yu, J; Zhang, L, 2019
)
0.51
" The presence of ferric ions at an appropriate dosage could promote the deprotonation process and therefore enhance decolorization efficiency, while excess ferric ions in solution might compete with malachite green dye towards reductive sites on tea polyphenols."( Insight into performance and mechanism of tea polyphenols and ferric ions on reductive decolorization of malachite green cationic dye under moderate conditions.
Dong, H; Huang, J; Liu, G; Wu, T; Xie, Y; Yu, L; Yu, Y, 2020
)
0.56
" Therefore, the present study aimed to trial a modified injection regime using more frequent dosing of BBG to improve outcomes in this model of GVHD."( P2X7 receptor antagonism increases regulatory T cells and reduces clinical and histological graft-versus-host disease in a humanised mouse model.
Adhikary, SR; Casolin, S; Cuthbertson, P; Geraghty, NJ; Sluyter, R; Watson, D, 2021
)
0.62
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (18)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
TDP1 proteinHomo sapiens (human)Potency2.82320.000811.382244.6684AID686978; AID686979
GLI family zinc finger 3Homo sapiens (human)Potency2.92250.000714.592883.7951AID1259392
AR proteinHomo sapiens (human)Potency6.41090.000221.22318,912.5098AID1259243; AID1259247; AID743035; AID743042; AID743054; AID743063
progesterone receptorHomo sapiens (human)Potency0.38970.000417.946075.1148AID1346784
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency19.40910.000214.376460.0339AID720691; AID720692
retinoid X nuclear receptor alphaHomo sapiens (human)Potency1.62740.000817.505159.3239AID1159527; AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency2.33990.001530.607315,848.9004AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403
estrogen nuclear receptor alphaHomo sapiens (human)Potency6.14060.000229.305416,493.5996AID1259244; AID1259248; AID743069; AID743078; AID743079; AID743080; AID743091
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency19.53880.001019.414170.9645AID743094; AID743140
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency5.75410.001723.839378.1014AID743083
nuclear receptor subfamily 1, group I, member 2Rattus norvegicus (Norway rat)Potency12.58930.10009.191631.6228AID1346983
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency8.34600.000323.4451159.6830AID743065; AID743067
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency2.35610.000627.21521,122.0200AID743202; AID743219
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency4.90620.001557.789015,848.9004AID1259244
Cellular tumor antigen p53Homo sapiens (human)Potency26.60320.002319.595674.0614AID651631
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency4.90620.001551.739315,848.9004AID1259244
ATPase family AAA domain-containing protein 5Homo sapiens (human)Potency1.88340.011917.942071.5630AID651632
Ataxin-2Homo sapiens (human)Potency1.88340.011912.222168.7989AID651632
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (141)

Processvia Protein(s)Taxonomy
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)
cell population proliferationATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of B cell proliferationATPase family AAA domain-containing protein 5Homo sapiens (human)
nuclear DNA replicationATPase family AAA domain-containing protein 5Homo sapiens (human)
signal transduction in response to DNA damageATPase family AAA domain-containing protein 5Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorATPase family AAA domain-containing protein 5Homo sapiens (human)
isotype switchingATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of DNA replicationATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of isotype switching to IgG isotypesATPase family AAA domain-containing protein 5Homo sapiens (human)
DNA clamp unloadingATPase family AAA domain-containing protein 5Homo sapiens (human)
regulation of mitotic cell cycle phase transitionATPase family AAA domain-containing protein 5Homo sapiens (human)
negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of cell cycle G2/M phase transitionATPase family AAA domain-containing protein 5Homo sapiens (human)
negative regulation of receptor internalizationAtaxin-2Homo sapiens (human)
regulation of translationAtaxin-2Homo sapiens (human)
RNA metabolic processAtaxin-2Homo sapiens (human)
P-body assemblyAtaxin-2Homo sapiens (human)
stress granule assemblyAtaxin-2Homo sapiens (human)
RNA transportAtaxin-2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (40)

Processvia Protein(s)Taxonomy
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)
protein bindingATPase family AAA domain-containing protein 5Homo sapiens (human)
ATP bindingATPase family AAA domain-containing protein 5Homo sapiens (human)
ATP hydrolysis activityATPase family AAA domain-containing protein 5Homo sapiens (human)
DNA clamp unloader activityATPase family AAA domain-containing protein 5Homo sapiens (human)
DNA bindingATPase family AAA domain-containing protein 5Homo sapiens (human)
RNA bindingAtaxin-2Homo sapiens (human)
epidermal growth factor receptor bindingAtaxin-2Homo sapiens (human)
protein bindingAtaxin-2Homo sapiens (human)
mRNA bindingAtaxin-2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (27)

Processvia Protein(s)Taxonomy
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)
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
Elg1 RFC-like complexATPase family AAA domain-containing protein 5Homo sapiens (human)
nucleusATPase family AAA domain-containing protein 5Homo sapiens (human)
cytoplasmAtaxin-2Homo sapiens (human)
Golgi apparatusAtaxin-2Homo sapiens (human)
trans-Golgi networkAtaxin-2Homo sapiens (human)
cytosolAtaxin-2Homo sapiens (human)
cytoplasmic stress granuleAtaxin-2Homo sapiens (human)
membraneAtaxin-2Homo sapiens (human)
perinuclear region of cytoplasmAtaxin-2Homo sapiens (human)
ribonucleoprotein complexAtaxin-2Homo sapiens (human)
cytoplasmic stress granuleAtaxin-2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (3)

Assay IDTitleYearJournalArticle
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.
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.
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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (4,634)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901389 (29.97)18.7374
1990's612 (13.21)18.2507
2000's1130 (24.38)29.6817
2010's1254 (27.06)24.3611
2020's249 (5.37)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 13.67

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index13.67 (24.57)
Research Supply Index8.55 (2.92)
Research Growth Index4.58 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (13.67)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials190 (3.83%)5.53%
Reviews120 (2.42%)6.00%
Case Studies181 (3.65%)4.05%
Observational3 (0.06%)0.25%
Other4,466 (90.04%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]