(8aS)-5,8-dihydroxy-6-(hydroxymethyl)-8aH-anthracen-9-one

Details

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Internal ID d0a8ac45-3005-4d98-9fb6-f563c28104e6
Taxonomy Benzenoids > Anthracenes
IUPAC Name (8aS)-5,8-dihydroxy-6-(hydroxymethyl)-8aH-anthracen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O4/c16-7-9-6-12(17)13-11(14(9)18)5-8-3-1-2-4-10(8)15(13)19/h1-6,13,16-18H,7H2/t13-/m0/s1
InChI Key NUAQAYOQIPDTPV-ZDUSSCGKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O4
Molecular Weight 256.25 g/mol
Exact Mass 256.07355886 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 1.00
Atomic LogP (AlogP) 2.14
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8aS)-5,8-dihydroxy-6-(hydroxymethyl)-8aH-anthracen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 - 0.6978 69.78%
Blood Brain Barrier - 0.7031 70.31%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7640 76.40%
OATP2B1 inhibitior - 0.7126 71.26%
OATP1B1 inhibitior + 0.9021 90.21%
OATP1B3 inhibitior + 0.9400 94.00%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9338 93.38%
BSEP inhibitior - 0.7937 79.37%
P-glycoprotein inhibitior - 0.9327 93.27%
P-glycoprotein substrate - 0.8198 81.98%
CYP3A4 substrate - 0.5375 53.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8288 82.88%
CYP3A4 inhibition - 0.7834 78.34%
CYP2C9 inhibition + 0.5823 58.23%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.7453 74.53%
CYP1A2 inhibition + 0.8397 83.97%
CYP2C8 inhibition - 0.8192 81.92%
CYP inhibitory promiscuity + 0.8003 80.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.7522 75.22%
Eye corrosion - 0.9880 98.80%
Eye irritation + 0.8513 85.13%
Skin irritation - 0.6262 62.62%
Skin corrosion - 0.9571 95.71%
Ames mutagenesis - 0.5854 58.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8706 87.06%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.5791 57.91%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.4859 48.59%
Acute Oral Toxicity (c) III 0.4560 45.60%
Estrogen receptor binding + 0.7503 75.03%
Androgen receptor binding + 0.6276 62.76%
Thyroid receptor binding + 0.5823 58.23%
Glucocorticoid receptor binding + 0.8378 83.78%
Aromatase binding + 0.6398 63.98%
PPAR gamma + 0.8687 86.87%
Honey bee toxicity - 0.8860 88.60%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9643 96.43%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.25% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.92% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.39% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 90.24% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.58% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.58% 82.69%
CHEMBL226 P30542 Adenosine A1 receptor 82.42% 95.93%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.21% 99.23%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Oldenlandia herbacea

Cross-Links

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PubChem 162886622
LOTUS LTS0037203
wikiData Q105185792