(Q32068308)

English

Synthesis of analogues of the O-beta-D-ribofuranosyl nucleoside moiety of liposidomycins. Part 2: role of the hydroxyl groups upon the inhibition of MraY.

scientific article published in February 2001

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Synthesis of analogues of the O-beta-D-ribofuranosyl nucleoside moiety of liposidomycins. Part 2: role of the hydroxyl groups upon the inhibition of MraY. (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

author name string

Dini C

1

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Drochon N

2

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Guillot JC

3

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Mauvais P

4

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Walter P

5

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Aszodi J

6

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

language of work or name

0 references

publication date

1 February 2001

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Bioorganic & Medicinal Chemistry Letters

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

533-536

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

On the Initial Stage in Peptidoglycan Synthesis. Phospho-N-acetylmuramyl-pentapeptide Translocase (Uridine Monophosphate)*

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2900714-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Synthesis of the nucleoside moiety of liposidomycins: elucidation of the pharmacophore of this family of MraY inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2900714-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Selective inhibition of the bacterial peptidoglycan biosynthesis by the new types of liposidomycins.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2900714-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Synthesis of analogues of the O-beta-D-ribofuranosyl nucleoside moiety of liposidomycins. Part 1: contribution of the amino group and the uracil moiety upon the inhibition of MraY.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2900714-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A general synthesis of N-glycosides. IV. Synthesis of nucleosides of hydroxy and mercapto N-heterocycles

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2900714-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural elucidation of tunicamycin. II. The structure of tunicamycin.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1271/BBB1961.41.2307

Identifiers

10.1016/S0960-894X(00)00714-9

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 July 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=Q32068308&oldid=2129771805"