α-Substituted hydroxamic acids as novel bacterial deformylase inhibitor-based antibacterial agents (Q44658900)

5 December 2017

title

Alpha-substituted hydroxamic acids as novel bacterial deformylase inhibitor-based antibacterial agents (English)

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5 December 2017

α-Substituted hydroxamic acids as novel bacterial deformylase inhibitor-based antibacterial agents (English)

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https://api.crossref.org/works/10.1016/J.BMCL.2003.07.020

3 April 2024

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https://api.crossref.org/works/10.1016/J.BMCL.2003.07.020

3 April 2024

pharmaceutical science

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https://api.crossref.org/works/10.1016/J.BMCL.2003.07.020

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https://api.crossref.org/works/10.1016/J.BMCL.2003.07.020

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https://api.crossref.org/works/10.1016/J.BMCL.2003.07.020

3 April 2024

author name string

R. Jain

1

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3 April 2024

A. Sundram

2

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3 April 2024

S. Lopez

3

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G. Neckermann

4

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C. Wu

5

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3 April 2024

C. Hackbarth

6

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D. Chen

7

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W. Wang

8

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3 April 2024

N. S. Ryder

9

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B. Weidmann

10

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D. Patel

11

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J. Trias

12

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R. White

13

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Z. Yuan

14

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3 April 2024

language of work or name

English

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publication date

1 December 2003

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full work available at URL

5 December 2017

https://api.elsevier.com/content/article/PII:S0960894X03008801?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/J.BMCL.2003.07.020

https://api.elsevier.com/content/article/PII:S0960894X03008801?httpAccept=text/plain

3 April 2024

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https://api.crossref.org/works/10.1016/J.BMCL.2003.07.020

Bioorganic & Medicinal Chemistry Letters

3 April 2024

published in

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5 December 2017

volume

13

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5 December 2017

issue

23

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5 December 2017

page(s)

4223-4228

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A novel gene, algK, from the alginate biosynthesis cluster of Pseudomonas aeruginosa

5 December 2017

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Solution structure of nickel-peptide deformylase

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The crystal structures of four peptide deformylases bound to the antibiotic actinonin reveal two distinct types: a platform for the structure-based design of antibacterial agents

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N-alkyl urea hydroxamic acids as a new class of peptide deformylase inhibitors with antibacterial activity

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Hydroxamic acid derivatives as potent peptide deformylase inhibitors and antibacterial agents

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Crystal structure of type II peptide deformylase from Staphylococcus aureus

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Protease inhibitors: current status and future prospects

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Peptide deformylase as a target for new generation, broad spectrum antimicrobial agents

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Deformylase as a novel antibacterial target.

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Preparation of disaccharides having a beta-D-mannopyranosyl group from N-phthaloyllactosamine derivatives by double or triple SN2 substitution

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Identifiers

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5 December 2017

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