(5R,8S,10S,13R,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-5,5,6-trimethylheptan-2-yl]-1,2,5,6,7,8,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one

Details

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Internal ID 8278c7b9-0960-4e7d-97ab-72fc6933c05b
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (5R,8S,10S,13R,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-5,5,6-trimethylheptan-2-yl]-1,2,5,6,7,8,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H54O/c1-21(2)28(4,5)17-13-22(3)23-14-19-32(10)25-11-12-26-29(6,7)27(33)16-18-30(26,8)24(25)15-20-31(23,32)9/h15,21-23,25-26H,11-14,16-20H2,1-10H3/t22-,23-,25-,26+,30-,31-,32+/m1/s1
InChI Key SLGYSWKMTFVUMJ-FATXZUKSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H54O
Molecular Weight 454.80 g/mol
Exact Mass 454.417466342 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 10.00

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5R,8S,10S,13R,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-5,5,6-trimethylheptan-2-yl]-1,2,5,6,7,8,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one

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 98.34% 97.25%
CHEMBL2581 P07339 Cathepsin D 96.99% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.93% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.03% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.83% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.40% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 88.61% 94.75%
CHEMBL2996 Q05655 Protein kinase C delta 88.18% 97.79%
CHEMBL2179 P04062 Beta-glucocerebrosidase 87.87% 85.31%
CHEMBL325 Q13547 Histone deacetylase 1 87.80% 95.92%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.95% 89.34%
CHEMBL1907 P15144 Aminopeptidase N 85.75% 93.31%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.25% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.98% 82.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.91% 90.71%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.17% 95.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.18% 93.99%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.53% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.37% 93.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.19% 93.56%

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.
Pinalia acervata

Cross-Links

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PubChem 14589230
LOTUS LTS0062804
wikiData Q105255330