4,9-Dihydroxy-3a,12c-dihydroperylene-3,10-dione

Details

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Internal ID 2b7f2811-cb36-4c6f-bfdd-71b5cd300972
Taxonomy Benzenoids > Perylenequinones
IUPAC Name 4,9-dihydroxy-3a,12c-dihydroperylene-3,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H12O4/c21-13-5-1-9-10-2-6-15(23)20-16(24)8-4-12(18(10)20)11-3-7-14(22)19(13)17(9)11/h1-8,17,19,21,23H
InChI Key HCOFSOFLCYXNPH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H12O4
Molecular Weight 316.30 g/mol
Exact Mass 316.07355886 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.12
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,9-Dihydroxy-3a,12c-dihydroperylene-3,10-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.5637 56.37%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8316 83.16%
OATP2B1 inhibitior - 0.7099 70.99%
OATP1B1 inhibitior + 0.9179 91.79%
OATP1B3 inhibitior + 0.9439 94.39%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6372 63.72%
P-glycoprotein inhibitior - 0.8735 87.35%
P-glycoprotein substrate - 0.8269 82.69%
CYP3A4 substrate + 0.5604 56.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8573 85.73%
CYP3A4 inhibition - 0.6517 65.17%
CYP2C9 inhibition + 0.8673 86.73%
CYP2C19 inhibition + 0.5336 53.36%
CYP2D6 inhibition - 0.6939 69.39%
CYP1A2 inhibition + 0.8620 86.20%
CYP2C8 inhibition - 0.6321 63.21%
CYP inhibitory promiscuity + 0.7284 72.84%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7906 79.06%
Carcinogenicity (trinary) Non-required 0.4797 47.97%
Eye corrosion - 0.9753 97.53%
Eye irritation + 0.8501 85.01%
Skin irritation + 0.6364 63.64%
Skin corrosion - 0.9607 96.07%
Ames mutagenesis + 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8407 84.07%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.5878 58.78%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.6856 68.56%
Acute Oral Toxicity (c) II 0.4624 46.24%
Estrogen receptor binding - 0.5148 51.48%
Androgen receptor binding + 0.7696 76.96%
Thyroid receptor binding - 0.6501 65.01%
Glucocorticoid receptor binding + 0.7519 75.19%
Aromatase binding - 0.5086 50.86%
PPAR gamma + 0.8552 85.52%
Honey bee toxicity - 0.8779 87.79%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9893 98.93%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.01% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.98% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.30% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.74% 95.56%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.80% 96.67%
CHEMBL2581 P07339 Cathepsin D 85.58% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.17% 99.23%

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 163039649
LOTUS LTS0008538
wikiData Q105025882