Drug Information
Drug General Information | Top | |||
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Drug ID |
D00ASL
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Former ID |
DNC014296
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Drug Name |
N-Butyl 2beta-hydroxyolean-12-en-28-oate
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Synonyms |
CHEMBL1077758; n-Butyl 2beta-hydroxyolean-12-en-28-oate
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C34H56O3
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Canonical SMILES |
CCCCOC(=O)C12CCC(CC1C3=CCC4C(C3(CC2)C)(CCC5C4(CC(CC5(C)C)O)C)C)(C)C
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InChI |
1S/C34H56O3/c1-9-10-19-37-28(36)34-17-15-29(2,3)22-25(34)24-11-12-27-31(6)21-23(35)20-30(4,5)26(31)13-14-33(27,8)32(24,7)16-18-34/h11,23,25-27,35H,9-10,12-22H2,1-8H3/t23-,25+,26+,27-,31+,32-,33-,34+/m1/s1
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InChIKey |
UZTYAEIRVQJQQC-XXJJMGNBSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Glycogen phosphorylase muscle form (GP) | Target Info | Inhibitor | [1] |
BioCyc | Glycogenolysis | |||
KEGG Pathway | Starch and sucrose metabolism | |||
Metabolic pathways | ||||
Insulin signaling pathway | ||||
Glucagon signaling pathway | ||||
Panther Pathway | Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway | |||
WikiPathways | Glycogen Metabolism | |||
Metabolism of carbohydrates |
References | Top | |||
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REF 1 | Synthesis of 3-deoxypentacyclic triterpene derivatives as inhibitors of glycogen phosphorylase. J Nat Prod. 2009 Aug;72(8):1414-8. |
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