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Synthesis and Bioactivity of Hydrazide-Hydrazones with the 1-Adamantyl-Carbonyl Moiety

Reaction of 1-adamantyl carbohydrazide (1) with various substituted benzaldehydes and acetophenones yielded the corresponding hydrazide-hydrazones with a 1-adamantane carbonyl moiety. The new synthesized compounds were tested for activities against some Gram-negative and Gram-positive bacteria, and...

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Autores principales: Pham, Van Hien, Phan, Thi Phuong Dung, Phan, Dinh Chau, Vu, Binh Duong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864450/
https://www.ncbi.nlm.nih.gov/pubmed/31694218
http://dx.doi.org/10.3390/molecules24214000
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author Pham, Van Hien
Phan, Thi Phuong Dung
Phan, Dinh Chau
Vu, Binh Duong
author_facet Pham, Van Hien
Phan, Thi Phuong Dung
Phan, Dinh Chau
Vu, Binh Duong
author_sort Pham, Van Hien
collection PubMed
description Reaction of 1-adamantyl carbohydrazide (1) with various substituted benzaldehydes and acetophenones yielded the corresponding hydrazide-hydrazones with a 1-adamantane carbonyl moiety. The new synthesized compounds were tested for activities against some Gram-negative and Gram-positive bacteria, and the fungus Candida albicans. Compounds 4a, 4b, 5a, and 5c displayed potential antibacterial activity against tested Gram-positive bacteria and C. albicans, while compounds 4e and 5e possessed cytotoxicity against tested human cancer cell lines.
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spelling pubmed-68644502019-12-23 Synthesis and Bioactivity of Hydrazide-Hydrazones with the 1-Adamantyl-Carbonyl Moiety Pham, Van Hien Phan, Thi Phuong Dung Phan, Dinh Chau Vu, Binh Duong Molecules Article Reaction of 1-adamantyl carbohydrazide (1) with various substituted benzaldehydes and acetophenones yielded the corresponding hydrazide-hydrazones with a 1-adamantane carbonyl moiety. The new synthesized compounds were tested for activities against some Gram-negative and Gram-positive bacteria, and the fungus Candida albicans. Compounds 4a, 4b, 5a, and 5c displayed potential antibacterial activity against tested Gram-positive bacteria and C. albicans, while compounds 4e and 5e possessed cytotoxicity against tested human cancer cell lines. MDPI 2019-11-05 /pmc/articles/PMC6864450/ /pubmed/31694218 http://dx.doi.org/10.3390/molecules24214000 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pham, Van Hien
Phan, Thi Phuong Dung
Phan, Dinh Chau
Vu, Binh Duong
Synthesis and Bioactivity of Hydrazide-Hydrazones with the 1-Adamantyl-Carbonyl Moiety
title Synthesis and Bioactivity of Hydrazide-Hydrazones with the 1-Adamantyl-Carbonyl Moiety
title_full Synthesis and Bioactivity of Hydrazide-Hydrazones with the 1-Adamantyl-Carbonyl Moiety
title_fullStr Synthesis and Bioactivity of Hydrazide-Hydrazones with the 1-Adamantyl-Carbonyl Moiety
title_full_unstemmed Synthesis and Bioactivity of Hydrazide-Hydrazones with the 1-Adamantyl-Carbonyl Moiety
title_short Synthesis and Bioactivity of Hydrazide-Hydrazones with the 1-Adamantyl-Carbonyl Moiety
title_sort synthesis and bioactivity of hydrazide-hydrazones with the 1-adamantyl-carbonyl moiety
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864450/
https://www.ncbi.nlm.nih.gov/pubmed/31694218
http://dx.doi.org/10.3390/molecules24214000
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