1-(6,7-dihydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl)-2-hydroxyethanone

Details

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Internal ID 00d5bdb5-7b9e-439b-99c8-d3dfbb9d8eb4
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Oxosteroids
IUPAC Name 1-(6,7-dihydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl)-2-hydroxyethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O4/c1-18(2)15-6-5-12-9-19(3,16(23)11-21)8-7-13(12)20(15,4)10-14(22)17(18)24/h9,13-15,17,21-22,24H,5-8,10-11H2,1-4H3
InChI Key ZVSKFZYNDQVXOH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O4
Molecular Weight 336.50 g/mol
Exact Mass 336.23005950 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.46
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(6,7-dihydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl)-2-hydroxyethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.5558 55.58%
Blood Brain Barrier + 0.5635 56.35%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8836 88.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9276 92.76%
OATP1B3 inhibitior + 0.8627 86.27%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5174 51.74%
BSEP inhibitior + 0.6735 67.35%
P-glycoprotein inhibitior - 0.8055 80.55%
P-glycoprotein substrate - 0.8165 81.65%
CYP3A4 substrate + 0.6134 61.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7991 79.91%
CYP3A4 inhibition - 0.7677 76.77%
CYP2C9 inhibition - 0.8613 86.13%
CYP2C19 inhibition - 0.9060 90.60%
CYP2D6 inhibition - 0.9381 93.81%
CYP1A2 inhibition - 0.9023 90.23%
CYP2C8 inhibition - 0.7097 70.97%
CYP inhibitory promiscuity - 0.9241 92.41%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7396 73.96%
Eye corrosion - 0.9929 99.29%
Eye irritation - 0.9687 96.87%
Skin irritation - 0.5440 54.40%
Skin corrosion - 0.9632 96.32%
Ames mutagenesis - 0.7140 71.40%
Human Ether-a-go-go-Related Gene inhibition - 0.5889 58.89%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6984 69.84%
skin sensitisation - 0.7946 79.46%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6285 62.85%
Acute Oral Toxicity (c) III 0.7556 75.56%
Estrogen receptor binding + 0.6739 67.39%
Androgen receptor binding + 0.6274 62.74%
Thyroid receptor binding + 0.6808 68.08%
Glucocorticoid receptor binding + 0.9002 90.02%
Aromatase binding + 0.6203 62.03%
PPAR gamma - 0.5187 51.87%
Honey bee toxicity - 0.8201 82.01%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9833 98.33%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.40% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.92% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.87% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.03% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.95% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.67% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 85.65% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.58% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.49% 95.56%
CHEMBL5028 O14672 ADAM10 81.16% 97.50%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.98% 86.67%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.66% 91.07%

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.
Milleria quinqueflora

Cross-Links

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PubChem 162849684
LOTUS LTS0126097
wikiData Q105384565