22-Dehydroclerosteryl acetate

Details

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Internal ID f45e81e8-920e-46df-8dd8-5ce021ecbb67
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,3E,5S)-5-ethyl-6-methylhepta-3,6-dien-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
SMILES (Canonical) CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(=C)C
SMILES (Isomeric) CC[C@@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)OC(=O)C)C)C)C(=C)C
InChI InChI=1S/C31H48O2/c1-8-23(20(2)3)10-9-21(4)27-13-14-28-26-12-11-24-19-25(33-22(5)32)15-17-30(24,6)29(26)16-18-31(27,28)7/h9-11,21,23,25-29H,2,8,12-19H2,1,3-7H3/b10-9+/t21-,23+,25+,26+,27-,28+,29+,30+,31-/m1/s1
InChI Key MOEVEIGHSLNJAI-RRXMTBKISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H48O2
Molecular Weight 452.70 g/mol
Exact Mass 452.365430770 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 9.20

Synonyms

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28594-00-5
Stigmasta-5,22,25-trien-3-ol, 3-acetate, (3beta,22E,24S)-
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,3E,5S)-5-ethyl-6-methylhepta-3,6-dien-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
DTXSID101210954
AKOS040761029
FS-9715

2D Structure

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2D Structure of 22-Dehydroclerosteryl acetate

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.77% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.57% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.76% 97.25%
CHEMBL2581 P07339 Cathepsin D 96.48% 98.95%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 94.68% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.04% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.65% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.06% 93.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.52% 96.95%
CHEMBL4227 P25090 Lipoxin A4 receptor 87.81% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.68% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 84.44% 91.19%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.28% 95.71%
CHEMBL202 P00374 Dihydrofolate reductase 83.12% 89.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.71% 95.89%
CHEMBL240 Q12809 HERG 82.19% 89.76%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.04% 82.69%
CHEMBL5028 O14672 ADAM10 81.97% 97.50%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.31% 89.50%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.30% 97.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.13% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.74% 99.17%

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.
Cajanus cajan
Prunus zippeliana

Cross-Links

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PubChem 13988623
LOTUS LTS0174920
wikiData Q105168841