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Molecular docking analysis of calcium channel blockers with ALR2 and RAGE
Samreen Kazmi1, Surekha Challa2, Malini Devi Alaparthi3
1Department of Biotechnology, Mahatma Gandhi University, Narketpally Mandal, Telangana, India, 508003.
Abstract:
A metabolic condition called diabetes mellitus is linked to a number of substantial challenges. Advanced Glycation End Products (AGEs) and Aldose reductase (ALR2) are crucial in the slow development of several secondary complications. Selected calcium channel blockers (CCB's-1, 4-dihydropyridines) were docked against ALR2 (PDB code: 1Z3N) and RAGE (PDB code: 3CJJ) in the current study. We report that 1, 4-dihydropyridine compounds, particularly Benidipine, bind to the active sites with good efficiency. Thus, 1,4 dihydropyridine derivatives can be considered for further confirmation in drug discovery.
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