Idalopirdine-rivastigmine

butyrylcholinesterase inhibitor and 5-HT6 receptor antagonist. BuChE (IC50 = 0.97 microM). After hydrolysis a potent 5-HT6 receptors antagonist (Ki = 11.4 nM) related to idalopirdine is released

General

Type : Drug,Pro-Drug,Carbamate,Derivative of Rivastigmine,Multitarget,5-HT-receptor-ligand

Chemical_Nomenclature :

Canonical SMILES : C1(=C[N]C2=CC(=CC=C12)F)CCNCC3=CC(=CC=C3)OC(=O)N(C)CC

InChI : InChI=1S\/C21H24FN3O2\/c1-3-25(2)21(26)27-18-6-4-5-15(11-18)13-23-10-9-16-14-24-20-12-17(22)7-8-19(16)20\/h4-8,11-12,14,23-24H,3,9-10,13H2,1-2H3

InChIKey : QZGAFMLTVWNDEJ-UHFFFAOYSA-N

Other name(s) : CHEMBL4744490,BDBM50562650,PD168472


MW : 369.43 || 369.4

Formula : C21H24FN3O2

CAS_number :

PubChem : 162648336

UniChem : QZGAFMLTVWNDEJ-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : Idalopirdine-rivastigmine ligand of proteins in family: BCHE

Stucture :

Protein : human-BCHE

References (1)

Title : Pleiotropic prodrugs: Design of a dual butyrylcholinesterase inhibitor and 5-HT(6) receptor antagonist with therapeutic interest in Alzheimer's disease - Toublet_2020_Eur.J.Med.Chem_210_113059
Author(s) : Toublet FX , Lalut J , Hatat B , Lecoutey C , Davis A , Since M , Corvaisier S , Freret T , Sopkova-de Oliveira Santos J , Claeysen S , Boulouard M , Dallemagne P , Rochais C
Ref : Eur Journal of Medicinal Chemistry , 210 :113059 , 2020
Abstract : Toublet_2020_Eur.J.Med.Chem_210_113059
ESTHER : Toublet_2020_Eur.J.Med.Chem_210_113059
PubMedSearch : Toublet_2020_Eur.J.Med.Chem_210_113059
PubMedID: 33310288