Hydrazonoyl chlorides possess promising antitumor properties.


Journal

Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521

Informations de publication

Date de publication:
15 Apr 2022
Historique:
received: 22 09 2021
revised: 01 02 2022
accepted: 02 02 2022
pubmed: 11 2 2022
medline: 12 3 2022
entrez: 10 2 2022
Statut: ppublish

Résumé

the main purpose of this study was to identify new selective antitumor agents. several hydrazonoyl chlorides (HCs) were synthesized and human tumor cell line viability was determined using the MTT assay. Tumor development was assessed using Ehrlich ascites carcinoma (EAC)-bearing mice. our results showed that 2-oxo-N-phenyl-2-(phenylamino)acetohydrazonoyl chloride (compound 4; CPD 4) and 2-oxo-2-(phenylamino)-N-(p-tolyl)acetohydrazonoyl chloride (CPD 5) were the most cytotoxic HCs to human cervical tumor HeLa (IC hydrazonoyl chlorides can be considered as hit compounds for the development of new antitumor agents.

Identifiants

pubmed: 35143825
pii: S0024-3205(22)00080-7
doi: 10.1016/j.lfs.2022.120380
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Chlorides 0
Hydrazones 0
Phosphotransferases (Alcohol Group Acceptor) EC 2.7.1.-
Proto-Oncogene Proteins c-akt EC 2.7.11.1
TOR Serine-Threonine Kinases EC 2.7.11.1
PTEN Phosphohydrolase EC 3.1.3.67
DNA Repair Enzymes EC 6.5.1.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

120380

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Mohamed A M El Gendy (MAM)

Drug Bioassay-Cell Culture Laboratory, Pharmacognosy Department, Pharmaceutical and Drug Industries Research Institute, National Research Centre, Dokki, Giza 12622, Egypt. Electronic address: elgendy@ualberta.ca.

Hamdy Hassanein (H)

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt.

Fatma M Saleh (FM)

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt.

Feridoun Karimi-Busheri (F)

Experimental Oncology, Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, Alberta, Canada.

Mesfin Fanta (M)

Experimental Oncology, Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, Alberta, Canada.

Xiaoyan Yang (X)

Experimental Oncology, Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, Alberta, Canada.

Doaa Tawfik (D)

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt.

Shorouk Morsy (S)

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt.

Merna Fahmy (M)

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt.

Mahmoud Hemid (M)

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt.

Mohamed Abdel Azeiz (M)

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt.

Ahmed Fared (A)

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt.

Michael Weinfeld (M)

Experimental Oncology, Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, Alberta, Canada.

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Classifications MeSH