N-Benzylpyridinium

General

Type : Pyridine

Chemical_Nomenclature : 1-benzylpyridin-1-ium chloride

Canonical SMILES : C1=CC=C(C=C1)C[N+]2=CC=CC=C2.[Cl-]

InChI : InChI=1S\/C12H12N.ClH\/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13\;\/h1-10H,11H2\;1H\/q+1\;\/p-1

InChIKey : GNPSDJOWGWWXSS-UHFFFAOYSA-M

Other name(s) : 1-Benzylpyridinium chloride, Pyridinium, 1-(phenylmethyl)-, chloride, 2876-13-3, 1-benzylpyridin-1-ium chloride, Pyridinium, 1-(phenylmethyl)-, chloride (1:1), benzylpyridinium chloride


MW : 205.68

Formula : C12H12ClN

CAS_number : 2876-13-3

PubChem : 76135

UniChem : GNPSDJOWGWWXSS-UHFFFAOYSA-M

Target

Families : N-Benzylpyridinium ligand of proteins in family
ACHE

References (3)

Title : Benzofuran-derived benzylpyridinium bromides as potent acetylcholinesterase inhibitors - Baharloo_2015_Eur.J.Med.Chem_93C_196
Author(s) : Baharloo F , Moslemin MH , Nadri H , Asadipour A , Mahdavi M , Emami S , Firoozpour L , Mohebat R , Shafiee A , Foroumadi A
Ref : Eur Journal of Medicinal Chemistry , 93C :196 , 2015
PubMedID: 25681712

Title : Indolinone-based acetylcholinesterase inhibitors: Synthesis, biological activity and molecular modeling - Akrami_2014_Eur.J.Med.Chem_84C_375
Author(s) : Akrami H , Mirjalili BF , Khoobi M , Nadri H , Moradi A , Sakhteman A , Emami S , Foroumadi A , Shafiee A
Ref : Eur Journal of Medicinal Chemistry , 84C :375 , 2014
PubMedID: 25036795

Title : Design, synthesis, biological evaluation and docking study of 5-oxo-4,5-dihydropyrano[3,2-c]chromene derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors - Khoobi_2013_Eur.J.Med.Chem_68C_260
Author(s) : Khoobi M , Alipour M , Sakhteman A , Nadri H , Moradi A , Ghandi M , Emami S , Foroumadi A , Shafiee A
Ref : Eur Journal of Medicinal Chemistry , 68C :260 , 2013
PubMedID: 23988409