(Q28316968)

English

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

scientific article (publication date: March 1978)

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scholarly article

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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 (English)

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

1 reference

10.1042/BJ1690449B

https://api.crossref.org/works/10.1042/BJ1690449B

26 March 2022

1 reference

10.1042/BJ1690449B

https://api.crossref.org/works/10.1042/BJ1690449B

26 March 2022

1 reference

10.1042/BJ1690449B

https://api.crossref.org/works/10.1042/BJ1690449B

26 March 2022

author name string

M. Akhtar

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A25646

26 March 2022

K. Alexander

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A25646

26 March 2022

R. B. Boar

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A25646

26 March 2022

J. F. McGhie

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A25646

26 March 2022

D. H. Barton

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A25646

26 March 2022

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publication date

1 March 1978

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full work available at URL

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/25646/?tool=EBI

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A25646

26 March 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/25646/pdf/?tool=EBI

Portable Document Format

online access status

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A25646

26 March 2022

https://europepmc.org/articles/PMC1183817

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A25646

26 March 2022

https://europepmc.org/articles/PMC1183817?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A25646

26 March 2022

https://portlandpress.com/biochemj/article-pdf/169/3/449/569906/bj1690449b.pdf

Portable Document Format

1 reference

10.1042/BJ1690449B

https://api.crossref.org/works/10.1042/BJ1690449B

26 March 2022

Biochemical Journal

0 references

169

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449-63

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3

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Hydrogen exchange and double bond formation in cholesterol biosynthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

29 September 2017

Substrate activation in pyridine nucleotide-linked reactions: illustrations from the steroid field

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

29 September 2017

Recent investigations on the nature of sterol intermediates in the biosynthesis of cholesterol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

29 September 2017

Biosynthesis of carotenoids and plant triterpenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

29 September 2017

The stereospecific removal of a C-19 hydrogen atom in oestrogen biosynthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

2 June 2018

The role of a cholesta-8,14-dien-3-beta-ol system in cholesterol biosynthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

2 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

2 June 2018

The formation and reduction of the 14,15-double bond in cholesterol biosynthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

2 June 2018

Studies on the control of cholesterol biosynthesis: the adenosine 3':5'-cyclic monophosphate-dependent accumulation of a steroid carboxylic acid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

2 June 2018

Enzymatic conversion of 32-oxygenated Δ7-lanosterol derivatives and of Δ8(14)-4,4-dimethyl-cholestenol to cholesterol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183817

27 November 2018

On the demethylation of lanosterol to cholesterol

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of isomeric 4,4-dimethylcholestenols and identification of a lanosterol metabolite

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formaldehyde dehydrogenase, a glutathionedependent enzyme system

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A carboxylic acid intermediate of lanostenol demethylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Investigation of the component reactions of oxidative sterol demethylation. Oxidation of a 4 alpha-methyl sterol to a 4 alpha-carboxylic acid during cholesterol biosynthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Investigation of the component reactions of oxidative sterol demethylation. Oxidation of a 4,4-dimethyl sterol to a 4 beta-methyl-4 alpha-carboxylic acid during cholesterol biosynthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent investigations on the nature of sterol intermediates in the biosynthesis of cholesterol

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The synthesis of some 32-functionalised lanostane derivatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The status of C-6, C-7, C-15 and C-16 hydrogen atoms in cholesterol biosynthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

4,4-di methyl-5α-cholesta-8,14-dien-3β-ol A new precursor of cholesterol in mammalian tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Synthesis of Tritium-labeled 14α-Methyl-5α-cholest-7-en-3β-ol and Its Enzymatic Demethylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1042/BJ1690449B

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