7-acetoxy-N-methylquinolinium

General

Type : Quinoline, Acetate

Chemical_Nomenclature : (1-methylquinolin-1-ium-7-yl) acetate\;iodide

Canonical SMILES : CC(=O)OC1=CC2=C(C=CC=[N+]2C)C=C1.[I-]

InChI : InChI=1S\/C12H12NO2.HI\/c1-9(14)15-11-6-5-10-4-3-7-13(2)12(10)8-11\;\/h3-8H,1-2H3\;1H\/q+1\;\/p-1

InChIKey : IFUAVRXVEJBLFI-UHFFFAOYSA-M

Other name(s) : M7A  ||  7-Acetoxy-1-methylquinolinium iodide  ||  N-methyl-7-acetoxyquinolinium  ||  7-Acetoxy-1-methylquinoliniumiodide  ||  AMQI  ||  7-ACETOXY-1-METHYL-QUINOLINIUM IODID  ||  7-(acetyloxy)-1-methylquinolin-1-ium iodide


MW : 329.13

Formula : C12H12INO2

CAS_number : 7270-83-9

PubChem : 9883921

UniChem : IFUAVRXVEJBLFI-UHFFFAOYSA-M

Target

Families : ACHE

References (2)

Title : Substrate binding to the peripheral site of acetylcholinesterase initiates enzymatic catalysis. Substrate inhibition arises as a secondary effect - Szegletes_1999_Biochemistry_38_122
Author(s) : Szegletes T , Mallender WD , Thomas PJ , Rosenberry TL
Ref : Biochemistry , 38 :122 , 1999
Abstract :
PubMedSearch : Szegletes_1999_Biochemistry_38_122
PubMedID: 9890890

Title : Studies of catalysis by acetylcholinesterase. Synergistic effects of inhibitors during the hydrolysis of acetic acid esters -
Author(s) : Rosenberry TL , Bernhard SA
Ref : Biochemistry , 11 :4308 , 1972
PubMedID: 5079901