Compound ID | 1498

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Ursolic Acid

Class: Triterpenoid

Spectrum of activity: Gram-negative
Details of activity: Effective against Klebsiella pneumoniae
Year first mentioned: 1920
Highest development stage: Preclinical
Chemical structure(s):
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Molecular weight: 456.7
Iso. SMILES: C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)O)C)C)[C@@H]2[C@H]1C)C)C(=O)O
InChI Key: WCGUUGGRBIKTOS-GPOJBZKASA-N
Can. SMILES: C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@@H](C(C)(C)[C@@H]5CC[C@]43C)O)[C@@H]2[C@H]1C)C(=O)O
InChI: InChI=1S/C30H48O3/c1-18-10-15-30(25(32)33)17-16-28(6)20(24(30)19(18)2)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h8,18-19,21-24,31H,9-17H2,1-7H3,(H,32,33)/t18-,19+,21+,22-,23+,24+,27+,28-,29-,30+/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/64945
Citation: https://www.nature.com/articles/s41429-020-0285-6

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