N'-(1-([1,1'-biphenyl]-4-yl)ethylidene)-2-cyanoacetohydrazide as scaffold for the synthesis of diverse heterocyclic compounds as prospective antitumor and antimicrobial activities

Hamed, Nancy A.; Marzouk, Magda I.; Hekal, Mohamed H.; Ismail, Mahmoud;

Abstract


In this article, the main target was to study the antitumor and antimicrobial efficacy of new heterocycles conjugated with biphenyl moiety in-vitro. This was implemented by utilizing N'-(1-([1,1'-biphenyl]-4-yl)ethylidene)-2-cyanoacetohydrazide 3 as a material for the synthesis of various heterocyclic compounds. Among of them, some compounds were selected and assayed against two antitumor cell lines as (HepG2) and (HCT-116). Conspicuously, the achieved results showed that compounds 6, 13, and 23 possess significant potency against both cancer cell lines. Particularly, compound 13 exhibited a remarkable efficacy, similar to the standard anticancer drug (doxorubicin), against both cancer cell lines. Noteworthy, compound 13 may serve as a potential anticancer therapeutic drug in the future. On the other hand, In-vitro antifungal and antibacterial activities of selected compounds were assayed and the results indicated that the compound 6 exhibited significant potency against Candida albicans, while compounds 6 and 8 displayed spectacular results for the antibacterial study.


Other data

Title N'-(1-([1,1'-biphenyl]-4-yl)ethylidene)-2-cyanoacetohydrazide as scaffold for the synthesis of diverse heterocyclic compounds as prospective antitumor and antimicrobial activities
Authors Hamed, Nancy A.; Marzouk, Magda I.; Hekal, Mohamed H. ; Ismail, Mahmoud 
Keywords 4-acetyl biphenyl;antimicrobial activity;antitumor activity;cyanoacetamide derivative;cyanoacetohydrazide;POLYBROMINATED DIPHENYL ETHERS;RAPID COLORIMETRIC ASSAY;ORGANOCHLORINE PESTICIDES;POLYCHLORINATED-BIPHENYLS;DERIVATIVES;ANTIOXIDANT;SURVIVAL;GROWTH
Issue Date 2019
Publisher TAYLOR & FRANCIS INC
Journal Synthetic Communications 
Volume 49
Issue 21
Start page 3017
End page 3029
ISSN 0039-7911
1532-2432
DOI 10.1080/00397911.2019.1655578
Scopus ID 2-s2.0-85071309786
Web of science ID WOS:000484036000001

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