(Q33179028)

English

Synthesis and biological evaluation of coumarincarboxylic acids as inhibitors of gyrase B. L-rhamnose as an effective substitute for L-noviose

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scholarly article

1 reference

Europe PubMed Central

23 July 2017

Synthesis and biological evaluation of coumarincarboxylic acids as inhibitors of gyrase B. L-rhamnose as an effective substitute for L-noviose (English)

1 reference

Europe PubMed Central

23 July 2017

author name string

Ferroud D

1

1 reference

Europe PubMed Central

23 July 2017

Collard J

2

1 reference

Europe PubMed Central

23 July 2017

Klich M

3

1 reference

Europe PubMed Central

23 July 2017

Dupuis-Hamelin C

4

1 reference

Europe PubMed Central

23 July 2017

Mauvais P

5

1 reference

Europe PubMed Central

23 July 2017

Lassaigne P

6

1 reference

Europe PubMed Central

23 July 2017

Bonnefoy A

7

1 reference

Europe PubMed Central

23 July 2017

Musicki B

8

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Europe PubMed Central

23 July 2017

language of work or name

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publication date

1 October 1999

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Europe PubMed Central

23 July 2017

number of pages

6

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Bioorganic & Medicinal Chemistry Letters

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Europe PubMed Central

23 July 2017

9

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Europe PubMed Central

23 July 2017

2881-2886

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Europe PubMed Central

23 July 2017

19

1 reference

Europe PubMed Central

23 July 2017

Synthesis and in vitro evaluation of novel highly potent coumarin inhibitors of gyrase B.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

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Structure-activity relationship in two series of aminoalkyl substituted coumarin inhibitors of gyrase B.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

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Biological characterization of cyclothialidine, a new DNA gyrase inhibitor

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

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Cyclothialidine and its congeners: a new class of DNA gyrase inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

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Cyclothialidine, a novel DNA gyrase inhibitor. I. Screening, taxonomy, fermentation and biological activity.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

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Cyclothialidine, a novel DNA gyrase inhibitor. II. Isolation, characterization and structure elucidation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanism of inhibition of DNA gyrase by cyclothialidine, a novel DNA gyrase inhibitor

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cyclothialidine analogs, novel DNA gyrase inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure-activity relationships in coumermycins

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Crystal structure of an N-terminal fragment of the DNA gyrase B protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

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Crystallization of Inhibitor Complexes of an N-Terminal 24 kDa Fragment of the DNA Gyrase B Protein

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

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The high-resolution crystal structure of a 24-kDa gyrase B fragment from E. coli complexed with one of the most potent coumarin inhibitors, clorobiocin

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900493-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0960-894X(99)00493-X

1 reference

Europe PubMed Central

23 July 2017

1 reference

Europe PubMed Central

23 July 2017

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