Page last updated: 2024-11-05

anthracene

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

Description

acene : A polycyclic aromatic hydrocarbon consisting of fused benzene rings in a rectilinear arrangement. [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]

acenes : Polycyclic aromatic hydrocarbons consisting of fused benzene rings in a rectilinear arrangement and their substitution derivatives. [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 CID8418
CHEMBL ID333179
CHEBI ID35298
CHEBI ID35297
MeSH IDM0105136

Synonyms (103)

Synonym
AC-5799
paranaphthalene
wln: l c666j
anthracen
anthracin
nsc7958
nsc-7958
120-12-7
anthracene ,
tetra olive n2g
ccris 767
AN3 ,
141062_sial
hsdb 702
einecs 204-371-1
ai3-00155
nsc 7958
10580_fluka
CHEBI:35298 ,
anthrazen
hracene
46051_riedel
anthracen [german]
ncgc00163972-01 ,
acene
CHEBI:35297
acen
azen
acenes
inchi=1/c14h10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10
c14315 ,
coal tar pitch volatiles: anthracene
anthracene, pure
48567_supelco ,
anthracene, analytical standard
a89200_aldrich ,
anthracene, reagent grade, 97%
48647_supelco ,
40076_supelco ,
anthracene, zone-refined, >=99%
331481_aldrich ,
STK398386
anthracene, reagentplus(r), 99%
A0992
A0495
A0405
CHEMBL333179
FT-0662238
bdbm50060894
AKOS000119970
A804437
NCGC00163972-02
NCGC00163972-03
NCGC00259775-01
tox21_202226
dtxcid203878
NCGC00254204-01
dtxsid0023878 ,
tox21_300014
cas-120-12-7
unii-eh46a1tld7
eh46a1tld7 ,
ec 204-371-1
FT-0622409
deuterated anthracene
54261-80-2
anthracene, labeled with deuterium
EPITOPE ID:119716
anthracene [mi]
anthracene [hsdb]
anthracene [iarc]
p-naphthalene
sterilite hop defoliant
coal tar pitch volatiles:anthracene
J-200085
anthraxcene
mfcd00001240
anthracene, sublimed grade, >=99%
F0001-0328
antraceno
anthracene, certified reference material, tracecert(r)
anthracene, suitable for scintillation, >=99.0% (gc)
anthracene, vial of 250 mg, analytical standard
anthracene, puriss., 99.0%
anthracene 100 microg/ml in acetonitrile
anthracene 10 microg/ml in acetonitrile
Q422152
anthracene, practical
anthracene zone refined (number of passes:30)
anthracene, reagent
anthracene, zone refined (number of passes:30)
AS-14635
EN300-18023
anthracene (1,2,3,4,5,6,7,8,9,10-d10)
9-anthracene
antracene
D88363
anthracene (purified by sublimation)
anthracene technical
paranapthalene
anthracene polycyclic aromatic compound
anthracene (iarc)
34f - wfd f

Research Excerpts

Overview

Anthracene (AC) is a non-mutagenic and non-carcinogenic, low-molecular-weight polycyclic aromatic hydrocarbon present in the environment. Anthracene is a PAH that is not readily degraded, plus its degradation mechanism is still not clear.

ExcerptReferenceRelevance
"Anthracene is a simple PAH that can be oxidized by laccases, copper-containing oxidase enzymes, produced by some plants, fungi, and bacteria."( Profile of natural redox mediators production of laccase-producing fungus Pleurotus ostreatus.
Cheng, Q; Feng, F; La, G; Li, X; Wang, F; Zhang, B; Zhang, Z, 2014
)
1.12
"Anthracene is an ideal benchmark to test these effects."( Vertical and adiabatic excitations in anthracene from quantum Monte Carlo: Constrained energy minimization for structural and electronic excited-state properties in the JAGP ansatz.
Bouaouli, S; Casula, M; Dupuy, N; Mauri, F; Sorella, S, 2015
)
1.41
"Anthracene (AC) is a non-mutagenic and non-carcinogenic, low-molecular-weight polycyclic aromatic hydrocarbon present in the environment. "( Involvement of Tetrahymena pyriformis and selected fungi in the elimination of anthracene, and toxicity assessment of the biotransformation products.
Bohatier, J; Bonnet, JL; Boumendjel, A; Dusser, M; Guiraud, P; Kadri-Dakir, M; Steiman, R, 2008
)
2.02
"Anthracene is a PAH that is not readily degraded, plus its degradation mechanism is still not clear. "( Effect of rhamnolipids on degradation of anthracene by two newly isolated strains, Sphingomonas sp. 12A and Pseudomonas sp. 12B.
Chen, D; Cui, CZ; Shen, P; Wan, X; Zeng, C; Zhang, JY, 2008
)
2.05
"Anthracene is a photodynamic compound in vitro. "( Light-dependent cytotoxic reactions of anthracene.
Kagan, J; Tuveson, RW; Wang, GR; Wang, TP, 1990
)
1.99
"Anthracene is a fluorescent and photoactivatable (dimerization) group which can be used for investigating the lateral distribution and dynamics of lipids in membranes. "( Continuous fluorescence microphotolysis of anthracene-labeled phospholipids in membranes. Theoretical approach of the simultaneous determination of their photodimerization and lateral diffusion rates.
Altibelli, A; Dupou-Cezanne, L; Ferrières, X; Lagouanelle, JL; Lopez, A; Tocanne, JF, 1989
)
1.98

Toxicity

Polycyclic aromatic hydrocarbons (PAHs) constituents, such as phenanthrene (PH) and anthracene (AN), are considered toxic for plants. The present study illustrates the protection of Photosystem I and Photosystem II complexes of wheat plant by Bacillus subtilis (NCIM 5594) from toxic effects of anthracenes.

ExcerptReferenceRelevance
"The authors previously demonstrated that simulated solar radiation (SSR), with a fluence rate of only 40 mumol m-2 sec-1, increased polycyclic aromatic hydrocarbon (PAH) toxicity to the duckweed Lemna gibba and that PAHs photomodified in SSR (generally oxygenation of the ring system) are more toxic than the parent compounds (Huang et al."( Increased polycyclic aromatic hydrocarbon toxicity following their photomodification in natural sunlight: impacts on the duckweed Lemna gibba L. G-3.
Dixon, DG; Greenberg, BM; Huang, XD, 1995
)
0.29
" However, the net effect was still for AHA to ameliorate PAH photo-induced toxicity even though UV has the potential to photooxidize AHA and enhance the production of potentially toxic reactive oxygen species from AHA photosensitization."( Amelioration of the photo-induced toxicity of polycyclic aromatic hydrocarbons by a commercial humic acid.
Dixon, DG; Gensemer, RW; Greenberg, BM, 1998
)
0.3
", oxidation) to more toxic compounds."( Impacts of structural photomodification on the toxicity of environmental contaminants: anthracene photooxidation products.
Dixon, DG; Greenberg, BM; Mallakin, A; McConkey, BJ; McKibben, B; Miao, G; Snieckus, V, 1999
)
0.53
" The mechanism of toxic action starts with inhibition of photosystem I (PSI) or the cytochrome-b6/f complex, followed by photooxidative damage to photosystem II (PSII)."( Sites of toxicity of specific photooxidation products of anthracene to higher plants: inhibition of photosynthetic activity and electron transport in Lemna gibba L. G-3 (duckweed).
Babu, TS; Dixon, DG; Greenberg, BM; Mallakin, A, 2002
)
0.56
" A small amount of any of 5 polynuclear aromatic hydrocarbons or of an aromatic amine given before the highly toxic dose of 7,12-DMBA resulted in survival for more than 2 months and the specific atrophy of testis which follows 7,12-DMBA was largely prevented."( AROMATIC-INDUCED PREVENTION OF FETAL TOXICITY OF 7,12-DIMETHYLBENZ(ALPHA)ANTHRACENE.
FORD, E; FUKUNISHI, R; HUGGINS, C; JENSEN, EV, 1964
)
0.47
" The carcinogenicity of the pitches, evaluated on the basis of benzo[a]pyrene toxic equivalency factors, also followed the same tendency."( Preparation of low toxicity pitches by thermal oxidative condensation of anthracene oil.
Alvarez, P; Blanco, C; Granda, M; José Fernández, J; Menéndez, R; Santamaría, R; Sutil, J; Viña, JA, 2009
)
0.58
"The aim of this study was to compare the toxic effects of selected two- and three-ringed PAHs (naphthalene, phenanthrene, and anthracene) and their N-heterocyclic analogs with one (quinoline, acridine, and phenanthridine) or two (quinoxaline, phenazine, and 1,10-phenanthroline) nitrogen atoms on the survival and reproduction of Enchytraeus crypticus in artificial soil."( Toxic effects of nine polycyclic aromatic compounds on Enchytraeus crypticus in artificial soil in relation to their properties.
Brezovský, J; Hofman, J; Kobetičová, K; Simek, Z, 2011
)
0.58
"Polycyclic aromatic hydrocarbons (PAHs) constituents, such as phenanthrene (PH) and anthracene (AN), are considered toxic for marine organisms, including bivalve mollusks."( Generation of free radicals in haemocytes of mussels after exposure to low molecular weight PAH components: immune activation, oxidative and genotoxic effects.
Dailianis, S; Giannapas, M; Karnis, L, 2012
)
0.6
" Photo-enhanced toxicity from co-exposure to ultraviolet (UV) radiation and PAHs enhanced the toxicity and exhibited toxic effects at PAH concentrations orders of magnitude below effects observed in the absence of UV."( Acute photo-induced toxicity and toxicokinetics of single compounds and mixtures of polycyclic aromatic hydrocarbons in zebrafish.
Oris, JT; Willis, AM, 2014
)
0.4
" Based on the prevalence of signs of blue sac disease (BSD), as expressed by median effective concentrations (EC50s), benz[a]anthracene (B[a]A) was more toxic than chrysene."( Quantitative structure-activity relationships for chronic toxicity of alkyl-chrysenes and alkyl-benz[a]anthracenes to Japanese medaka embryos (Oryzias latipes).
Brown, RS; Hodson, PV; Jørgensen, KB; Lin, H; Morandi, GD; Rantanen, T; Snieckus, V, 2015
)
0.84
"A decrease in photosynthetic efficiency may indicate the toxic effects of environmental pollutants on higher plants."( Assessment of phytotoxicity of anthracene in soybean (Glycine max) with a quick method of chlorophyll fluorescence.
Jajoo, A; Sharma, A; Tomar, RS, 2015
)
0.7
" Therefore, we aimed to determine the toxic effects of PAHs on earthworms."( Determination of biomarkers for polycyclic aromatic hydrocarbons (PAHs) toxicity to earthworm (Eisenia fetida).
Cho, K; Jeon, HJ; Lee, SE; Mo, HH; Nam, TH; Ok, YS, 2015
)
0.42
" In the oral administration study, both known phototoxic compounds and 5 drugs induced phototoxic reactions in both species; one compound each was found to be toxic only in SD rats or guinea pigs."( Evaluation of skin phototoxicity study using SD rats by transdermal and oral administration.
Hashimoto, K; Kataoka, A; Miyashita, T; Nejishima, H; Ogawa, H; Ohsumi, T; Yonezawa, Y, 2015
)
0.42
" In the present study, we have made comparisons of constitutive androstane receptor (CAR) activation and toxic effects on the liver between these two isomers."( Phenanthrene, but not its isomer anthracene, effectively activates both human and mouse nuclear receptor constitutive androstane receptor (CAR) and induces hepatotoxicity in mice.
Cheng, R; Deng, W; Lu, M; Shi, Z; Wang, XX; Yang, H; Zeng, Y; Zhang, SY; Zhao, LY; Zhu, J, 2019
)
0.8
" The present study illustrates the protection of Photosystem I and Photosystem II complexes of wheat plant by Bacillus subtilis (NCIM 5594) from toxic effects of anthracene (ANT)."( Protection of PSI and PSII complexes of wheat from toxic effect of anthracene by Bacillus subtilis (NCIM 5594).
Jain, L; Jajoo, A, 2020
)
0.99
" Thus, type I PDT sensitizers could here overcome traditional type II molecular systems that rely on the photo-initiated production of toxic singlet oxygen."( Influence of Polymer Charge on the Localization and Dark- and Photo-Induced Toxicity of a Potential Type I Photosensitizer in Cancer Cell Models.
Andraud, C; Chen, L; Gederaas, OA; Hansen, TA; Lindgren, M; Mettra, B; Monnereau, C; Siksjø, M, 2020
)
0.56
" Using the model organism Eisenia fetida, we compared the adverse effects among anthracene (ANT), anthraquinone (ANQ), and EPFRs induced by ANT transformation on clay surfaces."( The overlooked toxicity of environmentally persistent free radicals (EPFRs) induced by anthracene transformation to earthworms (Eisenia fetida).
Jia, H; Liu, J; Liu, Z; Ni, Z; Wu, X; Yang, K; Zhou, J; Zhu, L, 2022
)
1.17
"The size of microplastics (MPs) plays an important role in combined toxic effects including synergistic or antagonistic effects."( Combined effects of microplastics and benz[a]anthracene on cardiotoxicity in zebrafish (Danio rerio) larvae: Size matters.
Cho, HJ; Jeong, J; Kim, H; Lee, JS; Lee, WS; Sim, Y, 2023
)
1.17

Bioavailability

The surface concentration as depicted using three-dimensional plots showed that there is occlusion of the aromatics (naphthalene and anthracene) within the soil micropores. This limited their bioavailability and in the long run increasing their toxicity.

ExcerptReferenceRelevance
" These highly lipophilic compounds are well absorbed in the intestine."( The influence of bile on the bioavailability of polynuclear aromatic hydrocarbons from the rat intestine.
Barrowman, JA; Rahimtula, A; Rahman, A, 1986
)
0.27
" Bioavailability of sediment-sorbed PAHs declined with contact time between sediment and animals."( Accumulation kinetics of polycyclic aromatic hydrocarbons adsorbed to sediment by the mollusk Corbicula fluminea.
Djomo, JE; Ferrier, V; Garrigues, P; Narbonne, JF; Ribera, D, 1999
)
0.3
" The influence of substrate bioavailability on microbial growth was predicted successfully by a dynamic, flux-based approach (Best-Equation), which combines substrate dissolution from crystals into solution, substrate uptake by microorganisms from solution, and concurrent biomass formation."( Kinetics of mass transfer-limited bacterial growth on solid PAHs.
Colangelo, T; Harms, H; Wick, LY, 2001
)
0.31
"Several recent reports have indicated that some bacteria may have adapted to the low bioavailability of hydrophobic environmental chemicals and that generalizations about the bioavailability of compounds such as polycyclic aromatic hydrocarbons (PAHs) may be inappropriate."( Responses of Mycobacterium sp. LB501T to the low bioavailability of solid anthracene.
de, MA; Harms, H; Ruiz de Munain, A; Springael, D; Wick, LY, 2002
)
0.55
" Bacteria were cultivated on either anthracene or glucose (one culture with successively amended small doses of this substrate and one with excess concentrations) to distinguish between influences of the chemical structure and the bioavailability of the growth substrate."( Influence of the growth substrate on ester-linked phospho- and glycolipid fatty acids of PAH-degrading Mycobacterium sp. LB501T.
Andersen, N; Bernasconi, SM; Harms, H; Pelz, O; Wick, LY, 2003
)
0.59
"Polycyclic aromatic hydrocarbon (PAHs)-degrading bacteria may enhance the bioavailability of PAHs by excreting biosurfactants, by production of extracellular polymeric substances, or by forming biofilms."( Evaluation of bacterial strategies to promote the bioavailability of polycyclic aromatic hydrocarbons.
Johnsen, AR; Karlson, U, 2004
)
0.32
" Their bioavailability is limited by a low aqueous solubility, which causes specific adaptations in degrading bacteria."( Degradation of anthracene and pyrene supplied by microcrystals and non-aqueous-phase liquids.
Kaestner, M; Mutnuri, S; Vasudevan, N, 2005
)
0.68
"Iron may enhance polycyclic aromatic hydrocarbons (PAHs) degradation directly by increasing the activity of the enzymes involved in the aerobic biodegradation pathways for hydrocarbons, and indirectly by increasing the PAHs bioavailability due to the stimulation of biosurfactant production."( Anthracene biodegradation and surface activity by an iron-stimulated Pseudomonas sp.
Bento, FM; Camargo, FA; Jacques, RJ; Peralba, Mdo C; Sá, EL; Santos, EC; Selbach, PA, 2008
)
1.79
" The surface concentration as depicted using three-dimensional plots showed that there is occlusion of the aromatics (naphthalene and anthracene) within the soil micropores, thereby limiting their bioavailability and in the long run increasing their toxicity."( Estimation of transport and degradation parameters for naphthalene and anthracene: influence of mass transfer on kinetics.
Ogbeide, SE; Owabor, CN; Susu, AA, 2010
)
0.8
"The bioavailability of PAHs in sedimentary pore waters can be accurately determined by application of PDMS fibers (without requiring negligible depletion) in the presence of natural DOM with different sorption affinity for PAHs."( Influence of temperature and origin of dissolved organic matter on the partitioning behavior of polycyclic aromatic hydrocarbons.
Govers, HA; Haftka, JJ; Parsons, JR, 2010
)
0.36
"Laboratory experiments were conducted to assess the effects of soil sterilization on the bioavailability of spiked p,p'-DDE and anthracene to the earthworms Eisenia fetida and Lumbricus terrestris."( Sterilization affects soil organic matter chemistry and bioaccumulation of spiked p,p'-DDE and anthracene by earthworms.
Kelsey, JW; Melnick, AM; Peters, RD; Slizovskiy, IB, 2010
)
0.78
"The nature of bioavailability of DNA-intercalated PAHs in aqueous solution was investigated."( Nature of bioavailability of DNA-intercalated polycyclic aromatic hydrocarbons to Sphingomonas sp.
Ichikawa, H; Iimura, Y; Navarro, RR; Tatsumi, K, 2010
)
0.36
"Polycyclic aromatic hydrocarbon (PAH) bioavailability from ingested soils will vary between soils; however, the nature of this variation is not well characterized."( Is received dose from ingested soil independent of soil PAH concentrations?-Animal model results.
Cave, M; James, K; Peters, RE; Siciliano, SD; Wickstrom, M, 2016
)
0.43
"Recent studies investigating the influence of carbon nanotubes (CNTs) on the bioavailability of organic contaminants have mostly focused on single-solute systems; however, a more likely scenario in the natural environment is a multisolute system where chemical interactions at the surface of the CNT may alter the bioavailability of these chemicals."( Competitive Adsorption of Polycyclic Aromatic Hydrocarbons to Carbon Nanotubes and the Impact on Bioavailability to Fathead Minnow (Pimephales promelas).
Karanfil, T; Lee, CM; Linard, EN; van den Hurk, P, 2020
)
0.56
" In this degradation study, the biosurfactant production aptitude of the isolated strains plays an essential role in increasing the bioavailability of hydrophobic hydrocarbons."( Impact of biosurfactant produced by Bacillus spp. on biodegradation efficiency of crude oil and anthracene.
AlSalhi, MS; Balaji, T; Devanesan, S; Kokila, D; Parthipan, P; Rajamohan, R; Rajasekar, A; Thirumurugan, D, 2023
)
1.13

Dosage Studied

The cell age was 36 h. strain PYR-1 were dosed with anthracene or phenanthrene. After 14 days of incubation had degraded 92 and 90% of the added Anthracene and Phenanthrene, respectively.

ExcerptRelevanceReference
" strain PYR-1 were dosed with anthracene or phenanthrene and after 14 days of incubation had degraded 92 and 90% of the added anthracene and phenanthrene, respectively."( Degradation of phenanthrene and anthracene by cell suspensions of Mycobacterium sp. strain PYR-1.
Cerniglia, CE; Doerge, DR; Freeman, JP; Moody, JD, 2001
)
0.88
" dl-Ethionine under appropriate conditions of time and dosage eliminated the adrenal protection induced by aromatics and also delayed the induction of menadione reductase while depressing the amount of this enzyme which was synthesized."( INDUCED PROTECTION OF ADRENAL CORTEX AGAINST 7,12-DIMETHYLBENZ(ALPHA)ANTHRACENE. INFLUENCE OF ETHIONINE. INDUCTION OF MENADIONE REDUCTASE. INCORPORATION OF THYMIDINE-H3.
FUKUNISHI, R; HUGGINS, C, 1964
)
0.48
" The absorbance decreased significantly over time following treatment with each endocrine disruptor at the concentration confirmed by the dose-response analysis."( Effects of polycyclic aromatic hydrocarbons on the proliferation and differentiation of placental cells.
Choi, SK; Jo, HG; Jo, YS; Kim, AY; Kim, WJ; Ko, HS, 2022
)
0.72
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (3)

ClassDescription
aceneA polycyclic aromatic hydrocarbon consisting of fused benzene rings in a rectilinear arrangement.
ortho-fused tricyclic hydrocarbon
anthracenesCompounds containing an anthracene skeleton.
[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 (23)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
hypoxia-inducible factor 1 alpha subunitHomo sapiens (human)Potency56.70683.189029.884159.4836AID1224846
RAR-related orphan receptor gammaMus musculus (house mouse)Potency5.20150.006038.004119,952.5996AID1159521; AID1159523
GLI family zinc finger 3Homo sapiens (human)Potency70.75760.000714.592883.7951AID1259369
AR proteinHomo sapiens (human)Potency34.49620.000221.22318,912.5098AID1259243; AID1259247
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency25.10570.000657.913322,387.1992AID1259378
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency13.73390.001022.650876.6163AID1224838; AID1224839; AID1224893
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency9.26100.003041.611522,387.1992AID1159552; AID1159553; AID1159555
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency17.07290.001530.607315,848.9004AID1224848; AID1224849; AID1259401; AID1259403
pregnane X nuclear receptorHomo sapiens (human)Potency42.64910.005428.02631,258.9301AID1346982; AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency15.10500.000229.305416,493.5996AID1259244; AID1259248; AID588513; AID743069; AID743078; AID743079; AID743080; AID743091
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency50.11870.001024.504861.6448AID588534
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency0.00200.023723.228263.5986AID588543
aryl hydrocarbon receptorHomo sapiens (human)Potency40.52620.000723.06741,258.9301AID743085; AID743122
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency14.81450.001723.839378.1014AID743083
activating transcription factor 6Homo sapiens (human)Potency54.77650.143427.612159.8106AID1159516; AID1159519
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 (p105), isoform CRA_aHomo sapiens (human)Potency49.753119.739145.978464.9432AID1159509
Histone H2A.xCricetulus griseus (Chinese hamster)Potency73.56610.039147.5451146.8240AID1224845
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency68.58960.000323.4451159.6830AID743065
histone deacetylase 9 isoform 3Homo sapiens (human)Potency13.78770.037617.082361.1927AID1259364; AID1259388
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency17.22890.000627.21521,122.0200AID720636
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency9.25170.001557.789015,848.9004AID1259244
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency9.25170.001551.739315,848.9004AID1259244
[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)
5-lipoxygenase Bos taurus (cattle)IC50 (µMol)30.00000.18001.75824.0000AID160507
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Ceullar Components (1)

Processvia Protein(s)Taxonomy
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID19630Partition coefficient (logP)1997Journal of medicinal chemistry, Nov-07, Volume: 40, Issue:23
Simple analogues of anthralin: unusual specificity of structure and antiproliferative activity.
AID231071Peroxidant property was expressed as ratio of uMol of malondialdehyde and mMol of deoxyribose released by 75 uM test compound1997Journal of medicinal chemistry, Nov-07, Volume: 40, Issue:23
Simple analogues of anthralin: unusual specificity of structure and antiproliferative activity.
AID1605075-LO inhibitory activity was determined by inhibition of LTB4 biosynthesis in bovine polymorphonuclear leukocytes (PMNL)1997Journal of medicinal chemistry, Nov-07, Volume: 40, Issue:23
Simple analogues of anthralin: unusual specificity of structure and antiproliferative activity.
AID1149946Inhibition of alpha-chymotrypsin (unknown origin)1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
Quantitative structure-activity relationship of chymotrypsin-ligand interactions.
AID85482Antiproliferative (inhibition of cell growth) activity against HaCaT cells (human keratinocyte line)1997Journal of medicinal chemistry, Nov-07, Volume: 40, Issue:23
Simple analogues of anthralin: unusual specificity of structure and antiproliferative activity.
AID603957Octanol-water partition coefficient, log P of the compound2008European journal of medicinal chemistry, Apr, Volume: 43, Issue:4
QSPR modeling of octanol/water partition coefficient for vitamins by optimal descriptors calculated with SMILES.
AID85486Cytotoxic activity (2 uM) was measured by the amount of LDH (mU) release in HaCaT cells.1997Journal of medicinal chemistry, Nov-07, Volume: 40, Issue:23
Simple analogues of anthralin: unusual specificity of structure and antiproliferative activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (1,018)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990199 (19.55)18.7374
1990's51 (5.01)18.2507
2000's259 (25.44)29.6817
2010's422 (41.45)24.3611
2020's87 (8.55)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 76.80

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 Index76.80 (24.57)
Research Supply Index6.97 (2.92)
Research Growth Index5.05 (4.65)
Search Engine Demand Index136.32 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (76.80)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (0.09%)5.53%
Reviews11 (1.04%)6.00%
Case Studies1 (0.09%)4.05%
Observational0 (0.00%)0.25%
Other1,047 (98.77%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]