10-Methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione

Details

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Internal ID ad35b580-48ff-4067-a3bc-0104444a2097
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 10-methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H30O3/c1-12(2)13-10-14-15(24-6)11-16-20(3,4)8-7-9-21(16,5)17(14)19(23)18(13)22/h10,12,15-16H,7-9,11H2,1-6H3
InChI Key PGEGRYFGUKEQBL-UHFFFAOYSA-N
Popularity 0 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) 43.40 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8575 85.75%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8555 85.55%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9273 92.73%
OATP1B3 inhibitior + 0.9776 97.76%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.5273 52.73%
P-glycoprotein inhibitior - 0.5652 56.52%
P-glycoprotein substrate - 0.8178 81.78%
CYP3A4 substrate + 0.6123 61.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8482 84.82%
CYP3A4 inhibition - 0.7195 71.95%
CYP2C9 inhibition - 0.7745 77.45%
CYP2C19 inhibition - 0.6308 63.08%
CYP2D6 inhibition - 0.9395 93.95%
CYP1A2 inhibition - 0.8973 89.73%
CYP2C8 inhibition - 0.7196 71.96%
CYP inhibitory promiscuity - 0.8596 85.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9163 91.63%
Carcinogenicity (trinary) Non-required 0.5249 52.49%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9027 90.27%
Skin irritation - 0.6063 60.63%
Skin corrosion - 0.9743 97.43%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4714 47.14%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.5299 52.99%
skin sensitisation - 0.5733 57.33%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5123 51.23%
Acute Oral Toxicity (c) III 0.6715 67.15%
Estrogen receptor binding + 0.6782 67.82%
Androgen receptor binding + 0.5703 57.03%
Thyroid receptor binding + 0.7479 74.79%
Glucocorticoid receptor binding + 0.7225 72.25%
Aromatase binding - 0.6677 66.77%
PPAR gamma + 0.7588 75.88%
Honey bee toxicity - 0.6384 63.84%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5500 55.00%
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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.56% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 95.78% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.05% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.84% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.25% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.90% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.67% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.54% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.61% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.64% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.15% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.91% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.89% 99.23%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.78% 96.38%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 82.47% 94.08%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.16% 90.08%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.99% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.17% 94.00%

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 73009332
LOTUS LTS0047302
wikiData Q105208340