(Q42554014)

English

Metabolism of polycyclic compounds. 21. The metabolism of phenanthrene in rabbits and rats: dihydrodihydroxy compounds and related glucosiduronic acids

scientific article published on September 1962

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

2 November 2017

Metabolism of polycyclic compounds. 21. The metabolism of phenanthrene in rabbits and rats: dihydrodihydroxy compounds and related glucosiduronic acids (English)

1 reference

Europe PubMed Central

2 November 2017

author name string

BOYLAND E

1

1 reference

Europe PubMed Central

2 November 2017

SIMS P

2

1 reference

Europe PubMed Central

2 November 2017

language of work or name

0 references

publication date

1 September 1962

1 reference

Europe PubMed Central

2 November 2017

number of pages

12

1 reference

based on heuristic

inferred from page(s)

Biochemical Journal

1 reference

Europe PubMed Central

2 November 2017

84

1 reference

Europe PubMed Central

2 November 2017

571-582

1 reference

Europe PubMed Central

2 November 2017

An enzyme from rat liver catalysing conjugations with glutathione

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 16. The metabolism of 1:2-dihydronaphthalene and 1:2-epoxy-1:2:3:4-tetrahydronaphthalene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 5. Formation of 1:2-dihydroxy-1:2-dihydronaphthalenes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

The metabolic conversion of naphthalene to 1:2-dihydronaphthalene-1:2-diol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 6. Conversion of phenanthrene into dihydroxydihydrophenanthrenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 8 Acid-labile precursors of naphthalene produced as metabolites of naphthalene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 19. The metabolism of phenanthrene in rabbits and rats: phenols and sulphuric esters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 22. The metabolism of trans-9,10-dihydro-9,10-dihydroxyphenanthrene in rats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 20. The metabolism of phenanthrene in rabbits and rats: mercapturic acids and related compounds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 15. The conversion of naphthalene into a derivative of glutathione by rat-liver slices

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

A liver enzyme that conjugates sulfobromophthalein sodium with glutathione

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 13. Enzymic hydroxylation of naphthalene by rat-liver microsomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Biochemical studies of toxic agents. 9. The metabolic conversion of indene into cis- and trans- indane-1: 2-diol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Enzymatic hydroxylation of aromatic compounds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Biochemical studies of toxic agents. VII. The metabolism of naphthalene in animals of different species

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Studies in detoxication. XLIX. The metabolism of benzene containing (14C1) benzene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

28 May 2018

Metabolism of polycyclic compounds. 18. The secretion of metabolites of naphthalene, 1:2-dihydronaphthalene and 1:2-epoxy-1:2:3:4-tetrahydronaphthalene in rat bile

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

16 August 2018

Metabolism of polycyclic compounds. 14. The conversion of naphthalene into compounds related to trans-1:2-dihydro-1:2-dihydroxynaphthalene by rabbits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

16 August 2018

The formation of mercapturic acids. 2. The possible role of glutathionase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

16 August 2018

Biochemical studies of toxic agents. 8. 1:2-Dihydronaphthalene-1:2-diol and its role in the metabolism of naphthalene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1243716

16 August 2018

Electronic structure and carcinogenic activity of aromatic molecules; new developments

1 reference

https://pubmed.ncbi.nlm.nih.gov/13872198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Metabolic formation of diols and phenols of aromatic hydrocarbons]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13872198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymic hydroxylation of aromatic compounds. III. Studies on the mechanism of microsomal hydroxylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/13872198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymic hydroxylation of aromatic compounds. II. Further studies of the properties of the microsomal hydroxylating system

1 reference

https://pubmed.ncbi.nlm.nih.gov/13872198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[On the chemistry of benzene glycol. VI. Metabolism of benzene glycols and muconic dialdehydes]

1 reference

https://pubmed.ncbi.nlm.nih.gov/13872198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1042/BJ0840571

1 reference

Europe PubMed Central

2 November 2017

1 reference

Europe PubMed Central

2 November 2017

1 reference

Europe PubMed Central

2 November 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42554014&oldid=1961483924"