9-Amino-6-chloro-2-methoxyacridine

General

Type : Acridine,Derivative of Tacrine

Chemical_Nomenclature : 6-chloro-2-methoxyacridin-9-amine

Canonical SMILES : CC(=O)NC1=C(C2=CC3=CC=CC=C3C4=C2C5=C(C=CC=C51)C=C4)O

InChI : InChI=1S\/C22H15NO2\/c1-12(24)23-21-17-8-4-6-13-9-10-16-15-7-3-2-5-14(15)11-18(22(21)25)20(16)19(13)17\/h2-11,25H,1H3,(H,23,24)

InChIKey : CGVDLHRSVYTJKP-UHFFFAOYSA-N

Other name(s) : ACMA,G 185,6-Chloro-2-methoxy-9-acridinamine,NSC 15300


MW : 258.70

Formula : C14H11ClN2O

CAS_number : 3548-09-2

PubChem : 190803

UniChem : CGVDLHRSVYTJKP-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : 9-Amino-6-chloro-2-methoxyacridine ligand of proteins in family: Carboxylesterase || Carb_B_Chordata

Stucture :

Protein :

References (2)

Title : Inhibition of human carboxylesterases hCE1 and hiCE by cholinesterase inhibitors - Tsurkan_2013_Chem.Biol.Interact_203_226
Author(s) : Tsurkan LG , Hatfield MJ , Edwards CC , Hyatt JL , Potter PM
Ref : Chemico-Biological Interactions , 203 :226 , 2013
Abstract : Tsurkan_2013_Chem.Biol.Interact_203_226
ESTHER : Tsurkan_2013_Chem.Biol.Interact_203_226
PubMedSearch : Tsurkan_2013_Chem.Biol.Interact_203_226
PubMedID: 23123248

Title : Mammalian carboxylesterases: from drug targets to protein therapeutics - Redinbo_2005_Drug.Discov.Today_10_313
Author(s) : Redinbo MR , Potter PM
Ref : Drug Discov Today , 10 :313 , 2005
Abstract : Redinbo_2005_Drug.Discov.Today_10_313
ESTHER : Redinbo_2005_Drug.Discov.Today_10_313
PubMedSearch : Redinbo_2005_Drug.Discov.Today_10_313
PubMedID: 15749280