(4S,4aS,4bS,7R,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-4-ol

Details

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Internal ID 0bb71ee4-4eb6-4360-8597-ddba16aa24fe
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4S,4aS,4bS,7R,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-4-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O/c1-6-19(4)12-9-15-14(13-19)7-8-16-18(2,3)11-10-17(21)20(15,16)5/h6,13,15-17,21H,1,7-12H2,2-5H3/t15-,16-,17-,19-,20+/m0/s1
InChI Key FYBCOTZHIIDSOQ-VDWQKOAOSA-N
Popularity 5 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) 5.11
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4S,4aS,4bS,7R,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.7836 78.36%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.4915 49.15%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.9339 93.39%
OATP1B3 inhibitior + 0.8814 88.14%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.6873 68.73%
P-glycoprotein inhibitior - 0.8610 86.10%
P-glycoprotein substrate - 0.8533 85.33%
CYP3A4 substrate + 0.5723 57.23%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8432 84.32%
CYP2C9 inhibition - 0.7704 77.04%
CYP2C19 inhibition - 0.6222 62.22%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition - 0.8535 85.35%
CYP2C8 inhibition - 0.7352 73.52%
CYP inhibitory promiscuity - 0.8082 80.82%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5996 59.96%
Eye corrosion - 0.9841 98.41%
Eye irritation - 0.9234 92.34%
Skin irritation + 0.6324 63.24%
Skin corrosion - 0.9408 94.08%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7453 74.53%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5751 57.51%
skin sensitisation + 0.6109 61.09%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7584 75.84%
Acute Oral Toxicity (c) III 0.8798 87.98%
Estrogen receptor binding + 0.5825 58.25%
Androgen receptor binding + 0.5955 59.55%
Thyroid receptor binding + 0.5863 58.63%
Glucocorticoid receptor binding + 0.6453 64.53%
Aromatase binding - 0.5382 53.82%
PPAR gamma - 0.5574 55.74%
Honey bee toxicity - 0.8705 87.05%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9940 99.40%

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 94.65% 91.11%
CHEMBL1977 P11473 Vitamin D receptor 88.37% 99.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.08% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.27% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.09% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.78% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 84.55% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.04% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.14% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.71% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.15% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 80.07% 90.17%

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.
Kaempferia marginata

Cross-Links

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PubChem 73946812
LOTUS LTS0153861
wikiData Q105004391