N-Methyl-acridinium

Tricyclic amine-containing compound

General

Type : Acridine

Chemical_Nomenclature : N-Methyl-acridinium

Canonical SMILES : C[N+]1=C2C=CC=CC2=CC3=CC=CC=C31

InChI : InChI=1S\/C14H12N\/c1-15-13-8-4-2-6-11(13)10-12-7-3-5-9-14(12)15\/h2-10H,1H3\/q+1

InChIKey : GXYLXFITCXXCQV-UHFFFAOYSA-N

Other name(s) : N-Methyl-acridine


MW : 194.26

Formula : C13H11N

CAS_number : 13367-81-2

PubChem : 22000

UniChem : GXYLXFITCXXCQV-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : N-Methyl-acridinium ligand of proteins in family: ACHE

Stucture :

Protein :

References (2)

Title : Binding of the neurotoxin fasciculin 2 to the acetylcholinesterase peripheral site drastically reduces the association and dissociation rate constants for N-methylacridinium binding to the active site - Rosenberry_1996_Biochemistry_35_685
Author(s) : Rosenberry TL , Rabl CR , Neumann E
Ref : Biochemistry , 35 :685 , 1996
Abstract : Rosenberry_1996_Biochemistry_35_685
ESTHER : Rosenberry_1996_Biochemistry_35_685
PubMedSearch : Rosenberry_1996_Biochemistry_35_685
PubMedID: 8547248

Title : Three distinct domains in the cholinesterase molecule confer selectivity for acetyl- and butyrylcholinesterase inhibitors - Radic_1993_Biochemistry_32_12074
Author(s) : Radic Z , Pickering NA , Vellom DC , Camp S , Taylor P
Ref : Biochemistry , 32 :12074 , 1993
Abstract : Radic_1993_Biochemistry_32_12074
ESTHER : Radic_1993_Biochemistry_32_12074
PubMedSearch : Radic_1993_Biochemistry_32_12074
PubMedID: 8218285