Abstract
On the basis of i.r. and chromatographic evidence 5α-cholestane-3α,7α,12α,24ξ,26-pentol(I) and 24ξ,26-oxido-5α-cholestane-3α,7α,12α-triol (IV) structures have been proposed for the principal cleavage and alkaline-hydrolysis products of the bile salts from Catostomus commersoni (Anderson & Haslewood, 1969). N.m.r.- and mass-spectral analyses of these substances and the tetra- (II) and penta-acetate (III) derivatives of (I) provided supporting evidence for the structural assignments.
Full text
PDF
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Anderson I. G., Briggs T., Haslewood G. A. Comparative studies of 'bile salts'. 18. The chemistry of cyprinol. Biochem J. 1964 Feb;90(2):303–308. doi: 10.1042/bj0900303. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anderson I. G., Haslewood G. A. Comparative studies of bile salts. 5 alpha-Chimaerol, a new bile alcohol from the white sucker Catostomus commersoni Lacépède. Biochem J. 1970 Feb;116(4):581–585. doi: 10.1042/bj1160581. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cross A. D. A nuclear magnetic resonance spectral study of cyprinol. Biochem J. 1964 Feb;90(2):308–309. doi: 10.1042/bj0900308. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cross A. D. Nuclear-magnetic-resonance and mass-spectral analysis of ranol tetra-acetate. Biochem J. 1964 Feb;90(2):314–315. doi: 10.1042/bj0900314. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haslewood G. A., Tökés L. Comparative studies of bile salts. Bile salts of the lamprey Petromyzon marinus L. Biochem J. 1969 Sep;114(2):179–184. doi: 10.1042/bj1140179. [DOI] [PMC free article] [PubMed] [Google Scholar]