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IUPAC name Cholest-5-ene-3β,7α-diol | |
Systematic IUPAC name (1R,3aS,3bS,4S,7S,9aR,9bS,11aR)-9a,11a-Dimethyl-1--2,3,3a,3b,4,6,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-cyclopentaphenanthrene-4,7-diol | |
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3D model (JSmol) | |
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ChemSpider | |
IUPHAR/BPS | |
MeSH | 7+alpha-hydroxycholesterol |
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CompTox Dashboard (EPA) | |
InChI
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Properties | |
Chemical formula | C27H46O2 |
Molar mass | 402.653 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
7α-Hydroxycholesterol is a precursor of bile acids, created by cholesterol 7α-hydroxylase (CYP7A1). Its formation is the rate-determining step in bile acid synthesis.
References
- Chiang JY, Ferrell JM (March 2020). "Bile acid receptors FXR and TGR5 signaling in fatty liver diseases and therapy". American Journal of Physiology. Gastrointestinal and Liver Physiology. 318 (3): G554 – G573. doi:10.1152/ajpgi.00223.2019. PMC 7099488. PMID 31984784.
Cholesterol and steroid metabolic intermediates | |||||||||||
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Mevalonate pathway |
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From Cholesterol to Steroid hormones |
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Nonhuman |
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