Literature DB >> 4402522

Hydrogen exchange and double bond formation in cholesterol biosynthesis.

A Fiecchi, M GAlli Kienle, A Scala, G Galli, E Grossi Paoletti, F Cattabeni, R Paoletti.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1972        PMID: 4402522     DOI: 10.1098/rspb.1972.0011

Source DB:  PubMed          Journal:  Proc R Soc Lond B Biol Sci        ISSN: 0950-1193


× No keyword cloud information.
  6 in total

Review 1.  Sterol 14alpha-demethylase cytochrome P450 (CYP51), a P450 in all biological kingdoms.

Authors:  Galina I Lepesheva; Michael R Waterman
Journal:  Biochim Biophys Acta       Date:  2006-08-02

2.  Chemical and enzymic studies on the characterization of intermediates during the removal of the 14alpha-methyl group in cholesterol biosynthesis. The use of 32-functionalized lanostane derivatives.

Authors:  M Akhtar; K Alexander; R B Boar; J F McGhie; D H Barton
Journal:  Biochem J       Date:  1978-03-01       Impact factor: 3.857

3.  Studies on the mechanism of lanosterol 14 alpha-demethylation. A requirement for two distinct types of mixed-function-oxidase systems.

Authors:  F G Gibbons; C R Pullinger; K A Mitropoulos
Journal:  Biochem J       Date:  1979-11-01       Impact factor: 3.857

4.  The metabolic sequence by which some 4,4-dimethyl sterols are converted into cholesterol.

Authors:  G F Gibbons
Journal:  Biochem J       Date:  1974-10       Impact factor: 3.857

5.  The effect of carbon monoxide on the nature of the accumulated 4,4-dimethyl sterol precursors of cholesterol during its biosynthesis from (2-14C)mevalonic acid in vitro.

Authors:  G F Gibbons; K A Mitropoulos
Journal:  Biochem J       Date:  1973-03       Impact factor: 3.857

Review 6.  Biosynthesis of cholesterol and other sterols.

Authors:  W David Nes
Journal:  Chem Rev       Date:  2011-09-08       Impact factor: 60.622

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.