7beta-Hydroxysteroid

Details

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Internal ID ef8f0edf-09fe-491c-bd3a-f691cd005fb9
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Androstane steroids
IUPAC Name (7S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-7-ol
SMILES (Canonical) CC12CCCC1C3C(CC2)C4(CCCCC4CC3O)C
SMILES (Isomeric) CC12CCCC1C3[C@H](CC4CCCCC4(C3CC2)C)O
InChI InChI=1S/C19H32O/c1-18-9-5-7-14(18)17-15(8-11-18)19(2)10-4-3-6-13(19)12-16(17)20/h13-17,20H,3-12H2,1-2H3/t13?,14?,15?,16-,17?,18?,19?/m0/s1
InChI Key GUCUXPJTVXMEKL-JHBQCQMPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H32O
Molecular Weight 276.50 g/mol
Exact Mass 276.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.30
Atomic LogP (AlogP) 4.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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SCHEMBL27883392
C02956

2D Structure

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2D Structure of 7beta-Hydroxysteroid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.7483 74.83%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.6908 69.08%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.8953 89.53%
OATP1B3 inhibitior + 0.9610 96.10%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.6106 61.06%
P-glycoprotein inhibitior - 0.8468 84.68%
P-glycoprotein substrate - 0.8514 85.14%
CYP3A4 substrate + 0.6466 64.66%
CYP2C9 substrate - 0.5774 57.74%
CYP2D6 substrate - 0.6695 66.95%
CYP3A4 inhibition - 0.9168 91.68%
CYP2C9 inhibition - 0.7912 79.12%
CYP2C19 inhibition - 0.8356 83.56%
CYP2D6 inhibition - 0.9620 96.20%
CYP1A2 inhibition - 0.5606 56.06%
CYP2C8 inhibition - 0.7659 76.59%
CYP inhibitory promiscuity - 0.9345 93.45%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5535 55.35%
Eye corrosion - 0.9572 95.72%
Eye irritation - 0.5102 51.02%
Skin irritation + 0.6861 68.61%
Skin corrosion - 0.8253 82.53%
Ames mutagenesis - 0.6270 62.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6604 66.04%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.8011 80.11%
skin sensitisation + 0.5286 52.86%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7209 72.09%
Acute Oral Toxicity (c) III 0.8819 88.19%
Estrogen receptor binding + 0.6762 67.62%
Androgen receptor binding + 0.6068 60.68%
Thyroid receptor binding + 0.5956 59.56%
Glucocorticoid receptor binding + 0.6139 61.39%
Aromatase binding - 0.5802 58.02%
PPAR gamma - 0.8302 83.02%
Honey bee toxicity - 0.8209 82.09%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.8685 86.85%

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 96.93% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.21% 96.09%
CHEMBL237 P41145 Kappa opioid receptor 93.05% 98.10%
CHEMBL259 P32245 Melanocortin receptor 4 91.85% 95.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.54% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.27% 82.69%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 89.82% 93.04%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 89.41% 95.58%
CHEMBL221 P23219 Cyclooxygenase-1 86.88% 90.17%
CHEMBL226 P30542 Adenosine A1 receptor 86.81% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.42% 100.00%
CHEMBL206 P03372 Estrogen receptor alpha 85.41% 97.64%
CHEMBL3012 Q13946 Phosphodiesterase 7A 83.73% 99.29%
CHEMBL1871 P10275 Androgen Receptor 83.65% 96.43%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 83.47% 98.99%
CHEMBL233 P35372 Mu opioid receptor 81.81% 97.93%
CHEMBL238 Q01959 Dopamine transporter 80.71% 95.88%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.53% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.50% 95.89%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.46% 95.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.24% 92.94%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 80.19% 96.03%

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.
Arachniodes carvifolia

Cross-Links

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PubChem 439865
NPASS NPC56854