Publication Type : Journal Article
Publisher : Med. Chem. Res,Vol. 30, pp.
Source : Med. Chem. Res,Vol. 30, pp. 685-701 2021
Campus : Kochi
School : School of Pharmacy
Department : Pharmaceutical Chemistry & Analysis
Year : 2021
Abstract : A Series of new tacrine analogs were designed, synthesized, characterized by respective spectral data and evaluated for cholinesterase inhibitory activity to be useful in Alzheimer’s disease. Most of the synthesized compounds showed good in vitro inhibitory activities toward acetyl cholinesterase (AChE) and butyrylcholinesterase (BuChE) enzymes. Among the compounds, 6i, 6o and 6r with increased saturated carboxylic ring size attached to the pyridine moiety and having 3,4-dihydroxy, 3,4,5-trimethoxy substituents on the aromatic ring attached at the stereogenic center have shown equal potency to that of tacrine with IC50values 0.65 ± 0.06, 1.32 ± 0.02 and 0.85 ± 0.05, 1.65 ± 0.12 and 0.92 ± 0.03, 1.91 ± 0.12 μM against AChE and BuChE, respectively. Standard drug tacrine exhibited IC50 values of 0.47 ± 0.02 and 0.65 ± 0.08, while Donepezil showed IC50 0.71 ± 0.06
Cite this Research Publication : B, Macha,; R, Kulkarni,; C, Bagul,; A, Garige,; R, Akkinepally,; A, Garlapati, Molecular Hybridization Based Design and Synthesis of New benzo[5,6]chromeno[2,3-b]- quinolin-13(14H)-one Analogues as Cholinesterase Inhibitors, Med. Chem. Res,Vol. 30, pp. 685-701 2021