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Synthesis of imidazothiadiazole–benzimidazole conjugates as mitochondrial apoptosis inducers

Publication Type : Journal Article

Publisher : MedChemComm

Source : MedChemComm, Vol. 5, pp. 1644-1650, 2014.

Url : https://pubs.rsc.org/en/content/articlelanding/2014/md/c4md00219a

Campus : Kochi

School : School of Pharmacy

Department : Pharmaceutical Chemistry & Analysis

Year : 2014

Abstract : A series of imidazothiadiazole–benzimidazole conjugates (3a–z) were synthesized and evaluated for their cytotoxic activity against a set of four selected human cancer cell lines. Amongst them, compounds 3b and 3y exhibited significant antiproliferative activity in ME-180 (cervical) cell line. Flow cytometric analysis showed that these two compounds arrested the cell cycle in the G0/G1 phase leading to the loss of mitochondrial membrane potential followed by apoptotic cell death. Further, Hoechst 33258 staining, DNA fragmentation assay, Annexin V staining assay and caspase-3 also suggested that 3b and 3y induced cell death by apoptosis. Docking studies revealed that compound 3b binds to the Gly142, Phe101, Asn140 and Arg143 on B-cell lymphoma 2 (Bcl-2) proteins and inhibition of Bcl-2 protein could be the possible mechanism of action for these compounds.

Cite this Research Publication : Kamal, A.; Ponnampalli, S.; Vishnuvardhan, M.; Rao, M. N.; Mullagiri, K.; Nayak, V. L.; Bagul, C;. Synthesis of imidazothiadiazole–benzimidazole conjugates as mitochondrial apoptosis inducers. MedChemComm, Vol. 5, pp. 1644-1650, 2014.

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