A facile and single pot strategy for the synthesis of novel naphthyridine derivatives under microwave irradiation conditions using ZnCl2 as catalyst, evaluation of AChE inhibitory activity, and molecular modeling studies


Autoria(s): Santhosh Kumar, G; Kurumurthy, C; Sambasiva Rao, P; Veeraswamy, B; Shanthan Rao, P; Srigiridhar, Kotamraju; Sathish Babu, Vasamsetti; Chinmayee, Choudhury; Narsaiah, B
Data(s)

21/07/2014

21/07/2014

22/06/2011

Resumo

A series of novel naphthyridine derivatives 3 and 4 was prepared from substituted pyridine 2 and ketones using ZnCl2 as catalyst under microwave irradiation conditions. All the compounds were evaluated for AChE inhibitory activity and promising compounds 3d, 3e, 4b, and 4g was identified. Representative compounds 3d and 3e were found to show insignificant THLE-2 liver cell viability/toxicity. The binding mode between X-ray crystal structure of human AChE and compounds was studied using molecular docking method and fitness scores were found to be in good correlation with the activity data.

Med Chem Res (2012) 21:1785–1795 DOI 10.1007/s00044-011-9695-0

CUSAT

Identificador

http://dyuthi.cusat.ac.in/purl/4162

Idioma(s)

en

Publicador

Springer

Palavras-Chave #Acyclic ketones #Cyclic ketones #Microwave irradiation #Catalyst #Tacrine #Naphthyridine #AChE inhibitory activity #Liver cell viability #Molecular modelling
Tipo

Article