Coprostane

Coprostane is a lipid of Sterol Lipids (ST) class.

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There are no associated biomedical information in the current reference collection.

Current reference collection contains 34 references associated with Coprostane in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

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All references with Coprostane

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Authors Title Published Journal PubMed Link
Shefer S et al. Biosynthesis of chenodeoxycholic acid in man: stereospecific side-chain hydroxylations of 5beta-cholestane-3alpha,7alpha-diol. 1978 J. Clin. Invest. pmid:690184
Salen G et al. Bile alcohol metabolism in man. Conversion of 5beta-cholestane-3alpha, 7alpha,12alpha, 25-tetrol to cholic acid. 1975 J. Clin. Invest. pmid:1141434
Salen G et al. Cholic acid biosynthesis: the enzymatic defect in cerebrotendinous xanthomatosis. 1979 J. Clin. Invest. pmid:762246
Dayal B et al. Synthesis of 5beta-cholestane-3alpha, 7alpha, 12alpha, 25-tetrol and 5beta-cholestane-3alpha, 7alpha, 245, 25-pentol. 1976 J. Lipid Res. pmid:1255022
Shefer S et al. Identification of pentahydroxy bile alcohols in cerebrotendinous xanthomatosis: characterization of 5beta-cholestane-3alpha, 7alpha, 12alpha, 24xi, 25-pentol and 5beta-cholestane-3alpha, 7alpha, 12alpha, 23xi, 25-pentol. 1975 J. Lipid Res. pmid:1141769
Cheng FW et al. Cholic acid biosynthesis: conversion of 5beta-cholestane-3alpha,7alpha,12alpha,25-tetrol into 5beta-cholestane-3alpha,7alpha, 12alpha,24beta,25-pentol by human and rat liver microsomes. 1977 J. Lipid Res. pmid:13134
Nicolau G et al. Studies on the 12alpha and 26-hydroxylation of bile alcohols by rabbit liver microsomes. 1976 Lipids pmid:814378
Iborra RT et al. Advanced glycation in macrophages induces intracellular accumulation of 7-ketocholesterol and total sterols by decreasing the expression of ABCA-1 and ABCG-1. 2011 Lipids Health Dis pmid:21957962
King FW et al. Timosaponin AIII is preferentially cytotoxic to tumor cells through inhibition of mTOR and induction of ER stress. 2009 PLoS ONE pmid:19789631
Cohen BI et al. New bile alcohols--synthesis of 5beta-cholestane-3alpha, 7alpha, 25-triol and 5beta-cholestane-3alpha, 7alpha, 25-24 (14C)-triol. 1975 Steroids pmid:1145673