Cholane
Names | |
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IUPAC name
(5S,8R,9S,10S,13R,14S,17R)-10,13-Dimethyl-17-[(1R)-1-methylbutyl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene | |
Identifiers | |
80373-86-0 | |
ChEBI | CHEBI:35519 |
ChemSpider | 5256866 |
Jmol interactive 3D | Image Image |
PubChem | 6857530 |
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Properties | |
C24H42 | |
Molar mass | 330.59 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Cholane is a steroid with a molecular weight of 330.59. It can exist as either of two stereoisomers, 5α-cholane and 5β-cholane.
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5α-Cholane
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5β-Cholane
See also
External links
- Cholanes at the US National Library of Medicine Medical Subject Headings (MeSH)
- Bellini A, Mencini E, Quaglio M, Guarneri M, Fini A (1991). "Antimicrobial activity of basic cholane derivatives. X. Synthesis of 3 alpha- and 3 beta-amino-5 beta-cholan-24-oic acids". Steroids 56 (7): 395–398. doi:10.1016/0039-128X(91)90073-5. PMID 1780957.
- Fini A, Fazio G, Roda A, Bellini A, Mencini E, Guarneri M (1992). "Basic cholane derivatives. XI: Comparison between acid and basic derivatives". J Pharm Sci 81 (7): 726–730. doi:10.1002/jps.2600810728. PMID 1403713.
- Roda A, Bellini A, Mencini E, Minutello A, Fini A, Guarneri M (1992). "Effect of basic cholane derivatives on intestinal cholic acid metabolism: in vitro and in vivo activity". J Pharm Sci 81 (3): 237–240. doi:10.1002/jps.2600810310. PMID 1640360.
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