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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6864450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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