(1S,4aS)-5-hydroxy-1-(hydroxymethyl)-8-methoxy-1,4a-dimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one

Details

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Internal ID 8fed5d28-df20-4102-9877-4dd93131422d
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Hydroxysteroids > 1-hydroxysteroids
IUPAC Name (1S,4aS)-5-hydroxy-1-(hydroxymethyl)-8-methoxy-1,4a-dimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one
SMILES (Canonical) CC(C)C1=CC(=C2C(=C1OC)CCC3C2(CCC(=O)C3(C)CO)C)O
SMILES (Isomeric) CC(C)C1=CC(=C2C(=C1OC)CCC3[C@@]2(CCC(=O)[C@]3(C)CO)C)O
InChI InChI=1S/C21H30O4/c1-12(2)14-10-15(23)18-13(19(14)25-5)6-7-16-20(18,3)9-8-17(24)21(16,4)11-22/h10,12,16,22-23H,6-9,11H2,1-5H3/t16?,20-,21+/m0/s1
InChI Key XGRBHDJWRPUKMD-KCECWRNFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O4
Molecular Weight 346.50 g/mol
Exact Mass 346.21440943 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.71
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4aS)-5-hydroxy-1-(hydroxymethyl)-8-methoxy-1,4a-dimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.8549 85.49%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.9091 90.91%
OATP2B1 inhibitior - 0.8624 86.24%
OATP1B1 inhibitior + 0.9223 92.23%
OATP1B3 inhibitior + 0.8146 81.46%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7209 72.09%
P-glycoprotein inhibitior - 0.8245 82.45%
P-glycoprotein substrate - 0.6715 67.15%
CYP3A4 substrate + 0.6470 64.70%
CYP2C9 substrate + 0.6035 60.35%
CYP2D6 substrate - 0.6859 68.59%
CYP3A4 inhibition - 0.5402 54.02%
CYP2C9 inhibition - 0.6312 63.12%
CYP2C19 inhibition - 0.6044 60.44%
CYP2D6 inhibition - 0.9377 93.77%
CYP1A2 inhibition + 0.7966 79.66%
CYP2C8 inhibition - 0.6707 67.07%
CYP inhibitory promiscuity - 0.7572 75.72%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8120 81.20%
Carcinogenicity (trinary) Non-required 0.6913 69.13%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.7856 78.56%
Skin irritation - 0.7689 76.89%
Skin corrosion - 0.9775 97.75%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4282 42.82%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.7851 78.51%
skin sensitisation - 0.8822 88.22%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7151 71.51%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.8210 82.10%
Acute Oral Toxicity (c) III 0.6385 63.85%
Estrogen receptor binding + 0.6225 62.25%
Androgen receptor binding + 0.5357 53.57%
Thyroid receptor binding + 0.7415 74.15%
Glucocorticoid receptor binding + 0.6972 69.72%
Aromatase binding - 0.5210 52.10%
PPAR gamma + 0.7989 79.89%
Honey bee toxicity - 0.8729 87.29%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9860 98.60%

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 99.17% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.74% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.60% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.65% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.27% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.97% 99.15%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 89.61% 92.88%
CHEMBL1937 Q92769 Histone deacetylase 2 89.61% 94.75%
CHEMBL340 P08684 Cytochrome P450 3A4 89.08% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.55% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.52% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.19% 90.71%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.44% 93.03%
CHEMBL2535 P11166 Glucose transporter 87.32% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.99% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.78% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.49% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.53% 93.99%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.38% 91.24%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.25% 94.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.87% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.21% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.84% 99.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.42% 93.56%
CHEMBL1907 P15144 Aminopeptidase N 81.37% 93.31%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.01% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.81% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.79% 100.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.61% 91.03%

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.
Tripterygium wilfordii

Cross-Links

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PubChem 10641327
NPASS NPC285235