(7-Ethenyl-1,4a,8-trimethyl-2,3,4,4b,5,8,8a,9,10,10a-decahydrophenanthren-1-yl)methanol

Details

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Internal ID dfa5c6b2-f7ef-4b20-9811-069cee622a8a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Isocopalane and spongiane diterpenoids
IUPAC Name (7-ethenyl-1,4a,8-trimethyl-2,3,4,4b,5,8,8a,9,10,10a-decahydrophenanthren-1-yl)methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O/c1-5-15-7-9-17-16(14(15)2)8-10-18-19(3,13-21)11-6-12-20(17,18)4/h5,7,14,16-18,21H,1,6,8-13H2,2-4H3
InChI Key FWRHLIVXPRUHSD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O
Molecular Weight 288.50 g/mol
Exact Mass 288.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.97
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (7-Ethenyl-1,4a,8-trimethyl-2,3,4,4b,5,8,8a,9,10,10a-decahydrophenanthren-1-yl)methanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.8538 85.38%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.7526 75.26%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.8276 82.76%
OATP1B3 inhibitior + 0.8045 80.45%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.7038 70.38%
P-glycoprotein inhibitior - 0.8971 89.71%
P-glycoprotein substrate - 0.8224 82.24%
CYP3A4 substrate + 0.5979 59.79%
CYP2C9 substrate - 0.7951 79.51%
CYP2D6 substrate - 0.7745 77.45%
CYP3A4 inhibition - 0.5488 54.88%
CYP2C9 inhibition - 0.5185 51.85%
CYP2C19 inhibition - 0.5870 58.70%
CYP2D6 inhibition - 0.8987 89.87%
CYP1A2 inhibition - 0.7840 78.40%
CYP2C8 inhibition - 0.6206 62.06%
CYP inhibitory promiscuity - 0.5626 56.26%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6447 64.47%
Eye corrosion - 0.9646 96.46%
Eye irritation - 0.9458 94.58%
Skin irritation - 0.7488 74.88%
Skin corrosion - 0.9678 96.78%
Ames mutagenesis - 0.8082 80.82%
Human Ether-a-go-go-Related Gene inhibition + 0.7894 78.94%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6923 69.23%
skin sensitisation + 0.5456 54.56%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.8371 83.71%
Acute Oral Toxicity (c) III 0.6766 67.66%
Estrogen receptor binding + 0.7817 78.17%
Androgen receptor binding + 0.6324 63.24%
Thyroid receptor binding + 0.6470 64.70%
Glucocorticoid receptor binding + 0.6346 63.46%
Aromatase binding + 0.6663 66.63%
PPAR gamma - 0.5075 50.75%
Honey bee toxicity - 0.7692 76.92%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9974 99.74%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.00% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.73% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.65% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 92.36% 94.75%
CHEMBL325 Q13547 Histone deacetylase 1 89.09% 95.92%
CHEMBL233 P35372 Mu opioid receptor 87.27% 97.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.93% 100.00%
CHEMBL2581 P07339 Cathepsin D 86.13% 98.95%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 85.50% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.08% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.50% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.00% 86.33%

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.
Dichrostachys cinerea

Cross-Links

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PubChem 75068886
LOTUS LTS0058144
wikiData Q105003544