Tomassoli_2011_Eur.J.Med.Chem_46_1

Reference

Title : Synthesis, biological assessment and molecular modeling of new dihydroquinoline-3-carboxamides and dihydroquinoline-3-carbohydrazide derivatives as cholinesterase inhibitors, and Ca channel antagonists - Tomassoli_2011_Eur.J.Med.Chem_46_1
Author(s) : Tomassoli I , Ismaili L , Pudlo M , de los Rios C , Soriano E , Colmena I , Gandia L , Rivas L , Samadi A , Marco-Contelles J , Refouvelet B
Ref : Eur Journal of Medicinal Chemistry , 46 :1 , 2011
Abstract :

The synthesis, biological evaluation, and molecular modeling of new 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxamides(4), 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carbohydrazide (6), and some hexahydropyrimido[5,4-c]quinoline-2,5-diones (9) produced earlier by our laboratory, as AChE/BuChE inhibitors, is described. From these analyses compound 4c resulted equipotent regarding the inhibition of cholinesterases'; inhibitors 6k, 9a, 9b were selective for AChE, whereas product 4d proved selective for BuChE. Docking analysis has been carry out in order to identify the binding mode in the active site, and to explain the observed selectivities. Only compound 9a has been shown to decrease K(+)-induced calcium signals in bovine chromaffin cells.

PubMedSearch : Tomassoli_2011_Eur.J.Med.Chem_46_1
PubMedID: 21111515

Related information

Citations formats

Tomassoli I, Ismaili L, Pudlo M, de los Rios C, Soriano E, Colmena I, Gandia L, Rivas L, Samadi A, Marco-Contelles J, Refouvelet B (2011)
Synthesis, biological assessment and molecular modeling of new dihydroquinoline-3-carboxamides and dihydroquinoline-3-carbohydrazide derivatives as cholinesterase inhibitors, and Ca channel antagonists
Eur Journal of Medicinal Chemistry 46 :1

Tomassoli I, Ismaili L, Pudlo M, de los Rios C, Soriano E, Colmena I, Gandia L, Rivas L, Samadi A, Marco-Contelles J, Refouvelet B (2011)
Eur Journal of Medicinal Chemistry 46 :1