[14-hydroxy-10,13-dimethyl-6-oxo-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] benzoate

Details

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Internal ID 47742b75-d078-49b7-87cd-ce3218ee5b58
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Bile acids, alcohols and derivatives > Hydroxy bile acids, alcohols and derivatives > Tetrahydroxy bile acids, alcohols and derivatives
IUPAC Name [14-hydroxy-10,13-dimethyl-6-oxo-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H48O7/c1-30(2,38)15-14-28(36)33(5,39)27-13-18-34(40)24-20-26(35)25-19-22(41-29(37)21-9-7-6-8-10-21)11-16-31(25,3)23(24)12-17-32(27,34)4/h6-10,20,22-23,25,27-28,36,38-40H,11-19H2,1-5H3
InChI Key YPJCFUQHVHIYDL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H48O7
Molecular Weight 568.70 g/mol
Exact Mass 568.34000387 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP 3.70

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [14-hydroxy-10,13-dimethyl-6-oxo-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] benzoate

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
CHEMBL2581 P07339 Cathepsin D 97.97% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.27% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.19% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 96.05% 82.69%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 96.04% 94.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.30% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.29% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.76% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.69% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.80% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.24% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.21% 97.14%
CHEMBL5028 O14672 ADAM10 87.76% 97.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.28% 85.14%
CHEMBL3524 P56524 Histone deacetylase 4 86.23% 92.97%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.81% 99.23%
CHEMBL2179 P04062 Beta-glucocerebrosidase 83.54% 85.31%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 83.35% 92.67%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 83.20% 94.08%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.06% 96.47%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.02% 91.07%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.85% 93.99%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.42% 93.04%
CHEMBL2535 P11166 Glucose transporter 81.57% 98.75%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.38% 100.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.01% 96.67%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 72822813
LOTUS LTS0022814
wikiData Q105351702