2-Hydroxyandrost-1,4-dien-3,16-dione

Details

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Internal ID 282d1e8f-7842-46dd-b2d0-fe0ec1a6ebdf
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Androstane steroids > Androgens and derivatives
IUPAC Name (8S,9S,10S,13R,14S)-2-hydroxy-10,13-dimethyl-7,8,9,11,12,14,15,17-octahydro-6H-cyclopenta[a]phenanthrene-3,16-dione
SMILES (Canonical) CC12CCC3C(C1CC(=O)C2)CCC4=CC(=O)C(=CC34C)O
SMILES (Isomeric) C[C@]12CC[C@H]3[C@H]([C@@H]1CC(=O)C2)CCC4=CC(=O)C(=C[C@]34C)O
InChI InChI=1S/C19H24O3/c1-18-6-5-14-13(15(18)8-12(20)9-18)4-3-11-7-16(21)17(22)10-19(11,14)2/h7,10,13-15,22H,3-6,8-9H2,1-2H3/t13-,14+,15+,18-,19+/m1/s1
InChI Key SYSRWPPDCRIMSN-LKKZHYCFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O3
Molecular Weight 300.40 g/mol
Exact Mass 300.17254462 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.75
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Hydroxyandrost-1,4-dien-3,16-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.8436 84.36%
Blood Brain Barrier + 0.6830 68.30%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8095 80.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8811 88.11%
OATP1B3 inhibitior + 0.9847 98.47%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.7000 70.00%
BSEP inhibitior - 0.5919 59.19%
P-glycoprotein inhibitior - 0.6042 60.42%
P-glycoprotein substrate - 0.8021 80.21%
CYP3A4 substrate + 0.6915 69.15%
CYP2C9 substrate - 0.8170 81.70%
CYP2D6 substrate - 0.8714 87.14%
CYP3A4 inhibition - 0.8496 84.96%
CYP2C9 inhibition - 0.9480 94.80%
CYP2C19 inhibition - 0.9625 96.25%
CYP2D6 inhibition - 0.9376 93.76%
CYP1A2 inhibition - 0.8942 89.42%
CYP2C8 inhibition - 0.5924 59.24%
CYP inhibitory promiscuity - 0.9120 91.20%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4493 44.93%
Eye corrosion - 0.9940 99.40%
Eye irritation - 0.9615 96.15%
Skin irritation + 0.6471 64.71%
Skin corrosion - 0.9401 94.01%
Ames mutagenesis - 0.7528 75.28%
Human Ether-a-go-go-Related Gene inhibition + 0.6660 66.60%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.6081 60.81%
Respiratory toxicity + 0.9333 93.33%
Reproductive toxicity + 1.0000 100.00%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.7282 72.82%
Acute Oral Toxicity (c) IV 0.6033 60.33%
Estrogen receptor binding + 0.8403 84.03%
Androgen receptor binding + 0.8318 83.18%
Thyroid receptor binding + 0.6788 67.88%
Glucocorticoid receptor binding + 0.8829 88.29%
Aromatase binding + 0.7749 77.49%
PPAR gamma - 0.5090 50.90%
Honey bee toxicity - 0.8308 83.08%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9917 99.17%

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 93.46% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 93.37% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.01% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.30% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.00% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.33% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 87.27% 94.75%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 87.08% 97.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.67% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.02% 93.04%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.76% 93.40%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.17% 93.03%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.60% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.17% 92.94%
CHEMBL1871 P10275 Androgen Receptor 81.84% 96.43%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.09% 94.78%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.99% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.74% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.73% 93.99%

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.
Trichilia hirta

Cross-Links

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PubChem 10614174
LOTUS LTS0261634
wikiData Q105263762