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Green Synthesis and Molecular Docking of Thiazolyl-thiazole Derivatives as Potential Cytotoxic Agents

[ Vol. 17 , Issue. 9 ]

Author(s):

Sobhi M. Gomha*, Mohamad R. Abdelaziz, Hassan M. Abdel-Aziz and Shaimaa A. Hassan   Pages 805 - 815 ( 11 )

Abstract:


Method: A series of novel thiazole derivatives were synthesized in a good yield via reaction of 2-(1-(4-methyl-2-phenylthiazol-5-yl)ethylidene)hydrazine carbothioamide with hydrazonoyl halides. The reaction was performed in the presence of DABCO as an organocatalyst in short reaction times, easy workup, good to excellent yields. The structure of the newly synthesized products was elucidated via elemental analysis, spectral data and alternative routes whenever possible. Ten compounds were evaluated for their anti-cancer activity against the colon carcinoma cell line (HCT-116).

Results & Conclusion: The results revealed that most of the tested compounds showed high or moderate anti-cancer activity. The molecular docking of five novel thiazolyl-thiazole derivatives was performed by the Molecular Operating Environment (MOE) program.

Keywords:

Cytotoxic activity, hydrazonoyl halides, molecular docking, tautomerism, thiazoles, thiosemicarbazone.

Affiliation:

Department of Chemistry, Faculty of Science, Cairo University, Giza, 12613, Department of Pharmaceutical Chemistry, Faculty of Pharmacy, MIU University, Department of Chemistry, Faculty of Science, University of Bani Suef, Department of Chemistry, Faculty of Science, Cairo University, Giza, 12613

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