1452-29-5
1452-29-5
Chemical Structure
4-Cholenic acid-3-one
- CAS No.: 1452-29-5
- Formula:C24H36O3
- Molecular Weight:372.55
IUPAC Name: (R)-4-((8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid
InChIKey: WCFIGQHNBJXROP-IHMUCKAYSA-N
SMILES: C[C@@]12[C@]([C@]3([C@@]([C@]4(C)C(CC3)=CC(=O)CC4)(CC1)[H])[H])(CC[C@@]2([C@@H](CCC(O)=O)C)[H])[H]
Biological Activity: 4-Cholenic acid-3-one is an antifeedant steroid metabolite formed via anaerobic biotransformation of Lithocholic acid (HY-B0172) by Pseudomonas sp. strain NCIB 10590[1][2][3].
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4-Cholenic acid-3-one | 4-Cholenic acid-3-one is an antifeedant steroid metabolite formed via anaerobic biotransformation of Lithocholic acid (HY-B0172) by Pseudomonas sp. strain NCIB 10590. | |||||||||||||||||||||
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References
- [1]. Owen RW, et al. Bioconversion of Lithocholic Acid Under Anaerobic Conditions by Pseudomonas sp. Strain NCIB 10590. Appl Environ Microbiol. 1984;48(3):606-609. [Content Brief]
- [2]. Lievens SC, et al. New 3-oxo-chol-4-en-24-oic acids from the marine soft coral Eleutherobia sp. J Nat Prod. 2004;67(12):2130-2132. [Content Brief]
- [3]. Ayer SW, et al. Steroidal antifeedants from the dorid nudibranch Aldisa sanguinea cooperi. Tetrahedron Lett. 1982;23(10):1039-1042.
