Synthesis and cytotoxicity of novel (thiazol-2-yl)hydrazine derivatives as promising anti-Candida agents-Reference-Cited by-同舟云学术

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Synthesis and cytotoxicity of novel (thiazol-2-yl)hydrazine derivatives as promising anti-Candida agents

Published:2013-07 Issue: Volume:65 Page:102-111
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Carradori Simone,Secci Daniela,Bolasco Adriana,Rivanera Daniela,Mari Emanuela,Zicari Alessandra,Lotti Lavinia Vittoria,Bizzarri Bruna

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference22 articles.

1. Candida albicans, a major human fungal pathogen

2. Mucosal Immunity andCandida albicansInfection

3. Candida albicans versus non-albicans bloodstream infections: The comparison of risk factors and outcome

4. Antifungal use influences Candida species distribution and susceptibility in the intensive care unit

5. Candida glabrata, Candida parapsilosisandCandida tropicalis: biology, epidemiology, pathogenicity and antifungal resistance

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3. Synthesis, Crystal Structure and Hirshfeld Surface Analysis of (E)-2-(4-Methylbenzylidene)-N-Phenylhydrazine-1-Carbothioamide;Journal of Structural Chemistry;2023-06

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