3,4,8-Trihydroxy-3-methyl-2,4-dihydrobenzo[a]anthracene-1,7,12-trione

Details

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Internal ID ea769cb4-df3e-465d-b34a-fabf4e7a6481
Taxonomy Phenylpropanoids and polyketides > Angucyclines
IUPAC Name 3,4,8-trihydroxy-3-methyl-2,4-dihydrobenzo[a]anthracene-1,7,12-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H14O6/c1-19(25)7-12(21)13-10(18(19)24)6-5-9-15(13)17(23)8-3-2-4-11(20)14(8)16(9)22/h2-6,18,20,24-25H,7H2,1H3
InChI Key DEZAYIZEKGKNAC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H14O6
Molecular Weight 338.30 g/mol
Exact Mass 338.07903816 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.54
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,4,8-Trihydroxy-3-methyl-2,4-dihydrobenzo[a]anthracene-1,7,12-trione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 - 0.7474 74.74%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7651 76.51%
OATP2B1 inhibitior - 0.5678 56.78%
OATP1B1 inhibitior + 0.9205 92.05%
OATP1B3 inhibitior + 0.9664 96.64%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6490 64.90%
P-glycoprotein inhibitior - 0.9144 91.44%
P-glycoprotein substrate - 0.6599 65.99%
CYP3A4 substrate + 0.6222 62.22%
CYP2C9 substrate - 0.7943 79.43%
CYP2D6 substrate - 0.8219 82.19%
CYP3A4 inhibition - 0.8638 86.38%
CYP2C9 inhibition - 0.9132 91.32%
CYP2C19 inhibition - 0.9215 92.15%
CYP2D6 inhibition - 0.9038 90.38%
CYP1A2 inhibition + 0.5488 54.88%
CYP2C8 inhibition - 0.8203 82.03%
CYP inhibitory promiscuity - 0.9774 97.74%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8732 87.32%
Carcinogenicity (trinary) Warning 0.4744 47.44%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.8043 80.43%
Skin irritation - 0.5655 56.55%
Skin corrosion - 0.8429 84.29%
Ames mutagenesis + 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8465 84.65%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.7307 73.07%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.7679 76.79%
Acute Oral Toxicity (c) III 0.6352 63.52%
Estrogen receptor binding + 0.7152 71.52%
Androgen receptor binding + 0.6478 64.78%
Thyroid receptor binding - 0.6801 68.01%
Glucocorticoid receptor binding + 0.8210 82.10%
Aromatase binding - 0.5464 54.64%
PPAR gamma + 0.8424 84.24%
Honey bee toxicity - 0.9250 92.50%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9803 98.03%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 98.61% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.02% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.11% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.01% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.31% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.79% 96.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 90.95% 93.03%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.57% 89.00%
CHEMBL284 P27487 Dipeptidyl peptidase IV 89.36% 95.69%
CHEMBL240 Q12809 HERG 87.25% 89.76%
CHEMBL226 P30542 Adenosine A1 receptor 86.90% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.44% 100.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.03% 85.30%
CHEMBL1937 Q92769 Histone deacetylase 2 85.36% 94.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.58% 85.14%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.28% 96.38%
CHEMBL2056 P21728 Dopamine D1 receptor 83.27% 91.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.98% 96.67%
CHEMBL221 P23219 Cyclooxygenase-1 82.73% 90.17%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.69% 91.24%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.65% 99.15%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.57% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.98% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.99% 95.89%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.92% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.76% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.58% 93.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.11% 97.25%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 72776607
LOTUS LTS0100924
wikiData Q104977680