(4aS,10R,10aS)-10-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one

Details

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Internal ID 907e46b0-aec7-4505-9176-177df9e78371
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aS,10R,10aS)-10-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H30O3/c1-12(2)13-10-14-15(11-16(13)24-6)21(5)9-7-8-20(3,4)19(21)18(23)17(14)22/h10-12,18-19,23H,7-9H2,1-6H3/t18-,19-,21+/m0/s1
InChI Key BTFARGIVARHEON-IRFCIJBXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O3
Molecular Weight 330.50 g/mol
Exact Mass 330.21949481 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.46
H-Bond Acceptor 3
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 (4aS,10R,10aS)-10-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-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 + 0.9963 99.63%
Caco-2 + 0.7960 79.60%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8666 86.66%
OATP2B1 inhibitior - 0.8621 86.21%
OATP1B1 inhibitior + 0.8863 88.63%
OATP1B3 inhibitior + 0.9662 96.62%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.6980 69.80%
P-glycoprotein inhibitior - 0.6592 65.92%
P-glycoprotein substrate - 0.7457 74.57%
CYP3A4 substrate + 0.6263 62.63%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7011 70.11%
CYP3A4 inhibition - 0.7306 73.06%
CYP2C9 inhibition - 0.5535 55.35%
CYP2C19 inhibition - 0.6257 62.57%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition + 0.8013 80.13%
CYP2C8 inhibition - 0.7368 73.68%
CYP inhibitory promiscuity - 0.8346 83.46%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8620 86.20%
Carcinogenicity (trinary) Non-required 0.5485 54.85%
Eye corrosion - 0.9840 98.40%
Eye irritation - 0.9088 90.88%
Skin irritation - 0.5775 57.75%
Skin corrosion - 0.9426 94.26%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4485 44.85%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5995 59.95%
skin sensitisation - 0.8545 85.45%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6203 62.03%
Acute Oral Toxicity (c) III 0.7247 72.47%
Estrogen receptor binding + 0.7909 79.09%
Androgen receptor binding - 0.5383 53.83%
Thyroid receptor binding + 0.7289 72.89%
Glucocorticoid receptor binding + 0.7097 70.97%
Aromatase binding + 0.7039 70.39%
PPAR gamma + 0.8413 84.13%
Honey bee toxicity - 0.7081 70.81%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.9884 98.84%

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 96.53% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.38% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.98% 96.77%
CHEMBL2581 P07339 Cathepsin D 94.92% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.23% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 92.85% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.53% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.20% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.85% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.13% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.15% 98.75%
CHEMBL1937 Q92769 Histone deacetylase 2 85.96% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.41% 94.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.03% 82.69%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.00% 97.25%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.80% 97.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.33% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.91% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.23% 100.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.58% 93.03%
CHEMBL340 P08684 Cytochrome P450 3A4 80.17% 91.19%

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.
Cryptomeria japonica

Cross-Links

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PubChem 12114760
LOTUS LTS0272650
wikiData Q104945563