(4aR)-5-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-2,4-dihydrophenanthrene-3,6-dione

Details

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Internal ID 9a436385-a776-4845-a616-c20e0f0b2ad7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aR)-5-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-2,4-dihydrophenanthrene-3,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O3/c1-11(2)14-8-12-6-7-15-19(3,4)9-13(21)10-20(15,5)16(12)18(23)17(14)22/h6-8,11,23H,9-10H2,1-5H3/t20-/m1/s1
InChI Key VRXNUYDBZCMQCD-HXUWFJFHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O3
Molecular Weight 312.40 g/mol
Exact Mass 312.17254462 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 3.00
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 3
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 (4aR)-5-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-2,4-dihydrophenanthrene-3,6-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.8315 83.15%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8442 84.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9048 90.48%
OATP1B3 inhibitior + 0.9609 96.09%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.5632 56.32%
P-glycoprotein inhibitior - 0.8735 87.35%
P-glycoprotein substrate - 0.7880 78.80%
CYP3A4 substrate + 0.5405 54.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8714 87.14%
CYP3A4 inhibition - 0.7573 75.73%
CYP2C9 inhibition - 0.7924 79.24%
CYP2C19 inhibition - 0.7593 75.93%
CYP2D6 inhibition - 0.9143 91.43%
CYP1A2 inhibition - 0.8725 87.25%
CYP2C8 inhibition - 0.9116 91.16%
CYP inhibitory promiscuity - 0.7835 78.35%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9343 93.43%
Carcinogenicity (trinary) Non-required 0.5063 50.63%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.8049 80.49%
Skin irritation - 0.5533 55.33%
Skin corrosion - 0.9488 94.88%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6607 66.07%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5247 52.47%
skin sensitisation + 0.5866 58.66%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4606 46.06%
Acute Oral Toxicity (c) III 0.6892 68.92%
Estrogen receptor binding + 0.7886 78.86%
Androgen receptor binding - 0.5341 53.41%
Thyroid receptor binding + 0.7058 70.58%
Glucocorticoid receptor binding + 0.7191 71.91%
Aromatase binding + 0.7361 73.61%
PPAR gamma + 0.8799 87.99%
Honey bee toxicity - 0.7842 78.42%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9816 98.16%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.67% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 95.52% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.94% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.29% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.73% 93.40%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.53% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.39% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.25% 99.23%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.51% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.25% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.42% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.22% 90.71%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.08% 93.03%

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.
Premna herbacea

Cross-Links

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PubChem 56659752
LOTUS LTS0249181
wikiData Q105292034