(Q43690301)

English

Methanethiol as a catabolite of methionine provides methylthio- group for chemical formation of 19-S-methylgeldanamycin and 17,19-dimethylthioherbimycin A.

scientific article published on 17 April 2013

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Methanethiol as a catabolite of methionine provides methylthio- group for chemical formation of 19-S-methylgeldanamycin and 17,19-dimethylthioherbimycin A. (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

author name string

Shufen Li

1

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Jing Cui

2

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Xinhua Lu

3

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Zhihui Zheng

4

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Xin Liu

5

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Siyang Ni

6

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Yiguang Wang

7

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Linzhuan Wu

8

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

publication date

17 April 2013

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

The Journal of Antibiotics

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

66

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

499-503

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

https://scigraph.springernature.com/pub.10.1038/ja.2013.31

0 references

Inactivation of the carbamoyltransferase gene refines post-polyketide synthase modification steps in the biosynthesis of the antitumor agent geldanamycin.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

Cloning and characterization of a gene cluster for geldanamycin production in Streptomyces hygroscopicus NRRL 3602.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

The methylthiolation reaction mediated by the Radical-SAM enzymes

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

Trierixin, a novel Inhibitor of ER stress-induced XBP1 activation from Streptomyces sp. II. structure elucidation

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

Herbimycin, a new antibiotic produced by a strain of Streptomyces

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

SAR study of a novel triene-ansamycin group compound, quinotrierixin, and related compounds, as inhibitors of ER stress-induced XBP1 activation.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

The biosynthetic gene cluster of the maytansinoid antitumor agent ansamitocin from Actinosynnema pretiosum

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

Microbial L-methioninase: production, molecular characterization, and therapeutic applications

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

Naphthomycins L-N, ansamycin antibiotics from Streptomyces sp. CS.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

3-amino-5-hydroxybenzoic acid in antibiotic biosynthesis. XI. Biological origins and semisynthesis of thionaphthomycins, and the structures of naphthomycins I and J.

2 references

https://api.crossref.org/works/10.1038%2FJA.2013.31

21 January 2018

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

A pair of sulfur-containing geldanamycin analogs, 19-S-methylgeldanamycin and 4,5-dihydro- 19-S-methylgeldanamycin, from Streptomyces hygroscopicus 17997

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure of awamycin, a novel antitumor ansamycin antibiotic

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

New ansamycin antibiotics, naphthoquinomycins A and B, inhibitors of fatty acid synthesis in Escherichia coli

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

Biosynthetic formation of the S-methyl group of the angucycline antibiotic urdamycin E

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

Interaction of naphthomycin A with sulfhydryl compounds

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure of herbimycin A new ansamycin antibiotic

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

1H-nmr analysis of herbimycins and dihydro-herbimycins

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

Studies on mycotrienin antibiotics, a novel class of ansamycins. II. Structure elucidation and biosynthesis of mycotrienins I and II

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

Reaction of geldanamycin and C17-substituted analogues with glutathione: product identifications and pharmacological implications

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

Chemical modification and antitumor activity of herbimycin A. 8,9-Epoxide, 7,9-cyclic carbamate, and 17 or 19-amino derivatives

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

Chemical modification of herbimycin A. Synthesis and in vivo antitumor activities of halogenated and other related derivatives of herbimycin A

1 reference

https://api.crossref.org/works/10.1038%2FJA.2013.31

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/JA.2013.31

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

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=Q43690301&oldid=2102603229"