Ganoderiol G

Details

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Internal ID f6927033-7aa4-4629-89b4-39264e9313d9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 7-methoxy-4,4,10,13,14-pentamethyl-17-(5,6,7-trihydroxy-6-methylheptan-2-yl)-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
SMILES (Canonical) CC(CCC(C(C)(CO)O)O)C1CCC2(C1(CCC3=C2C(CC4C3(CCC(=O)C4(C)C)C)OC)C)C
SMILES (Isomeric) CC(CCC(C(C)(CO)O)O)C1CCC2(C1(CCC3=C2C(CC4C3(CCC(=O)C4(C)C)C)OC)C)C
InChI InChI=1S/C31H52O5/c1-19(9-10-25(34)31(7,35)18-32)20-11-16-30(6)26-21(12-15-29(20,30)5)28(4)14-13-24(33)27(2,3)23(28)17-22(26)36-8/h19-20,22-23,25,32,34-35H,9-18H2,1-8H3
InChI Key YOMOWVJLKFVSNZ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C31H52O5
Molecular Weight 504.70 g/mol
Exact Mass 504.38147475 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 4.30

Synonyms

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CHEBI:171995
DTXSID301201202
24,25,26-Trihydroxy-7a-methoxy-8-lanosten-3-one
Lanost-8-en-3-one, 24,25,26-trihydroxy-7-methoxy-, (7alpha)-
114567-48-5
7-methoxy-4,4,10,13,14-pentamethyl-17-(5,6,7-trihydroxy-6-methylheptan-2-yl)-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one

2D Structure

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2D Structure of Ganoderiol G

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 98.45% 97.25%
CHEMBL2581 P07339 Cathepsin D 96.40% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.11% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 94.91% 93.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.43% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.02% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 91.83% 97.79%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.22% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.25% 97.09%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.39% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.36% 97.14%
CHEMBL4040 P28482 MAP kinase ERK2 85.77% 83.82%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 84.28% 94.78%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.83% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 83.22% 94.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.05% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.51% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.11% 99.23%
CHEMBL1902 P62942 FK506-binding protein 1A 81.99% 97.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.55% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.05% 93.04%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.89% 82.69%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.87% 100.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 80.48% 92.88%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.43% 96.90%

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 15602268
LOTUS LTS0136254
wikiData Q75067109