Cargando…
One Pot Single Step Synthesis and Biological Evaluation of Some Novel Bis(1,3,4-thiadiazole) Derivatives as Potential Cytotoxic Agents
A novel series of bis(1,3,4-thiadiazole) derivatives were synthesized in one step methodology with good yields by condensation reaction between bis-hydrazonoyl chloride 1 and various reagents. The structures of the prepared compounds were confirmed by spectral data (IR, NMR, and MS), and elemental a...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274530/ https://www.ncbi.nlm.nih.gov/pubmed/27854300 http://dx.doi.org/10.3390/molecules21111532 |
_version_ | 1783377639856144384 |
---|---|
author | Gomha, Sobhi M. Kheder, Nabila A. Abdelhamid, Abdou O. Mabkhot, Yahia N. |
author_facet | Gomha, Sobhi M. Kheder, Nabila A. Abdelhamid, Abdou O. Mabkhot, Yahia N. |
author_sort | Gomha, Sobhi M. |
collection | PubMed |
description | A novel series of bis(1,3,4-thiadiazole) derivatives were synthesized in one step methodology with good yields by condensation reaction between bis-hydrazonoyl chloride 1 and various reagents. The structures of the prepared compounds were confirmed by spectral data (IR, NMR, and MS), and elemental analysis. The anticancer activity against human breast carcinoma (MCF-7) cancer cell lines was evaluated in MTT assay. The results revealed that the bis-thiadiazole derivatives 5c,d, 7b,c and 9c had higher antitumor activity than the standard drug Imatinib. |
format | Online Article Text |
id | pubmed-6274530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62745302018-12-28 One Pot Single Step Synthesis and Biological Evaluation of Some Novel Bis(1,3,4-thiadiazole) Derivatives as Potential Cytotoxic Agents Gomha, Sobhi M. Kheder, Nabila A. Abdelhamid, Abdou O. Mabkhot, Yahia N. Molecules Article A novel series of bis(1,3,4-thiadiazole) derivatives were synthesized in one step methodology with good yields by condensation reaction between bis-hydrazonoyl chloride 1 and various reagents. The structures of the prepared compounds were confirmed by spectral data (IR, NMR, and MS), and elemental analysis. The anticancer activity against human breast carcinoma (MCF-7) cancer cell lines was evaluated in MTT assay. The results revealed that the bis-thiadiazole derivatives 5c,d, 7b,c and 9c had higher antitumor activity than the standard drug Imatinib. MDPI 2016-11-15 /pmc/articles/PMC6274530/ /pubmed/27854300 http://dx.doi.org/10.3390/molecules21111532 Text en © 2016 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 Gomha, Sobhi M. Kheder, Nabila A. Abdelhamid, Abdou O. Mabkhot, Yahia N. One Pot Single Step Synthesis and Biological Evaluation of Some Novel Bis(1,3,4-thiadiazole) Derivatives as Potential Cytotoxic Agents |
title | One Pot Single Step Synthesis and Biological Evaluation of Some Novel Bis(1,3,4-thiadiazole) Derivatives as Potential Cytotoxic Agents |
title_full | One Pot Single Step Synthesis and Biological Evaluation of Some Novel Bis(1,3,4-thiadiazole) Derivatives as Potential Cytotoxic Agents |
title_fullStr | One Pot Single Step Synthesis and Biological Evaluation of Some Novel Bis(1,3,4-thiadiazole) Derivatives as Potential Cytotoxic Agents |
title_full_unstemmed | One Pot Single Step Synthesis and Biological Evaluation of Some Novel Bis(1,3,4-thiadiazole) Derivatives as Potential Cytotoxic Agents |
title_short | One Pot Single Step Synthesis and Biological Evaluation of Some Novel Bis(1,3,4-thiadiazole) Derivatives as Potential Cytotoxic Agents |
title_sort | one pot single step synthesis and biological evaluation of some novel bis(1,3,4-thiadiazole) derivatives as potential cytotoxic agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274530/ https://www.ncbi.nlm.nih.gov/pubmed/27854300 http://dx.doi.org/10.3390/molecules21111532 |
work_keys_str_mv | AT gomhasobhim onepotsinglestepsynthesisandbiologicalevaluationofsomenovelbis134thiadiazolederivativesaspotentialcytotoxicagents AT khedernabilaa onepotsinglestepsynthesisandbiologicalevaluationofsomenovelbis134thiadiazolederivativesaspotentialcytotoxicagents AT abdelhamidabdouo onepotsinglestepsynthesisandbiologicalevaluationofsomenovelbis134thiadiazolederivativesaspotentialcytotoxicagents AT mabkhotyahian onepotsinglestepsynthesisandbiologicalevaluationofsomenovelbis134thiadiazolederivativesaspotentialcytotoxicagents |