delta7-Avenasterol

Details

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Internal ID ecbf7203-b221-4a4d-9dee-13689d2ce898
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Stigmastanes and derivatives
IUPAC Name (3S,5S,9R,10S,13R,14R,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES (Canonical) CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C
SMILES (Isomeric) C/C=C(/CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C)\C(C)C
InChI InChI=1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h7,11,19-20,22-23,25-27,30H,8-10,12-18H2,1-6H3/b21-7-/t20-,22+,23+,25-,26+,27+,28+,29-/m1/s1
InChI Key MCWVPSBQQXUCTB-OQTIOYDCSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C29H48O
Molecular Weight 412.70 g/mol
Exact Mass 412.370516150 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 8.60

Synonyms

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avenasterol
23290-26-8
24Z-Ethylidenelathosterol
I0WYR6393O
Z-24-Ethylidene-5alpha-cholest-7-en-3beta-ol
24Z-ethylidene-cholest-7-en-3beta-ol
Stigmasta-7,24(28)-dien-3-ol, (3beta,5alpha,24Z)-
(3S,5S,9R,10S,13R,14R,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
7212-91-1
(3S,5S,9R,10S,13R,14R,17R)-17-((R)-5-Isopropylhept-5-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of delta7-Avenasterol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

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 98.15% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.17% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.30% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 95.60% 90.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 93.01% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.43% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.31% 94.45%
CHEMBL240 Q12809 HERG 90.14% 89.76%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.30% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.38% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.98% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.44% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.11% 95.56%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.84% 92.88%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.80% 90.71%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 84.26% 94.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.36% 93.56%
CHEMBL226 P30542 Adenosine A1 receptor 82.03% 95.93%
CHEMBL2581 P07339 Cathepsin D 81.80% 98.95%
CHEMBL3055 P50613 Cyclin-dependent kinase 7 81.79% 81.88%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.16% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.55% 93.99%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.54% 92.86%

Cross-Links

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PubChem 12795736
LOTUS LTS0199292
wikiData Q76422902