Synthesis and biological evaluation of combretastatin-amidobenzothiazole conjugates as potential anticancer agents

• Published in: European journal of medicinal chemistry Vol. 56; pp. 166 - 178
• Main Authors: Kamal, Ahmed, Mallareddy, Adla, Janaki Ramaiah, M., Pushpavalli, S.N.C.V.L., Suresh, Paidakula, Kishor, Chandan, Murty, J.N.S.R.C., Rao, N. Sankara, Ghosh, Sowjanya, Addlagatta, Anthony, Pal-Bhadra, Manika
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier Masson SAS 01-10-2012; Elsevier
• Subjects: Anticancer activity; Antimitotic Agents - chemical synthesis; Antimitotic Agents - chemistry; Antimitotic Agents - pharmacology; Benzothiazoles - chemistry; Benzothiazoles - pharmacology; Bibenzyls - chemistry; Bibenzyls - pharmacology; Biological and medical sciences; CA-4; Cell cycle; Cell Cycle - drug effects; Cell Proliferation - drug effects; Cell Survival - drug effects; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; ERK; Humans; MCF-7 Cells; Medical sciences; Miscellaneous; Models, Molecular; Molecular Dynamics Simulation; Molecular modeling; Molecular Structure; Pharmacology. Drug treatments; Polymerization; Structure-Activity Relationship; Tubulin; Tubulin - metabolism; Tumor Cells, Cultured; CA-4; Tubulin; Molecular modeling; Cell cycle; Anticancer activity; ERK
• ISSN: 0223-5234; 1768-3254
• DOI: 10.1016/j.ejmech.2012.08.021

A series of combretastatin-amidobenzothiazole conjugates have been synthesized and evaluated for their anticancer activity. All these compounds exhibited significant anticancer activity and the most potent compound (11a) showed GI50 values ranging 0.019–11 μM. Biological studies such as cell cycle distribution, effect on tubulin polymerization and effect on ERK signalling pathway have been examined in MCF-7 cell line. FACS analysis revealed that these compounds induced cell cycle arrest at G2/M phase. Compound 11a showed significant effect on tubulin polymerization and affected the ERK signalling pathway that result in the decreased levels of ERK1/2, p-ERK and c-Jun proteins. Docking experiments have shown that the active molecules interact and bind well in the ATP binding pocket of ERK protein.
A series of combretastatin-amidobenzothiazole conjugates have been synthesized and evaluated for their anticancer activity. [Display omitted]
► New series of combretastatin-amidibenzothiazole conjugates have been synthesized. ► These conjugates were evaluated for their anticancer activity. ► These compounds showed cell cycle arrest at G2/M phase. ► The active compounds showed effect on tubulin, c-Jun and ERK protein levels. ► The ERK inhibition exhibited by active compounds rationalized by molecular modeling studies.