9-Amino-6-chloro-2-methoxyacridine

General

Type : Acridine, Derivative of Tacrine, Organochlorine

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

Canonical SMILES : COC1=CC2=C(C3=C(C=C(C=C3)Cl)N=C2C=C1)N

InChI : InChI=1S\/C14H11ClN2O\/c1-18-9-3-5-12-11(7-9)14(16)10-4-2-8(15)6-13(10)17-12\/h2-7H,1H3,(H2,16,17)

InChIKey : IHHSSHCBRVYGJX-UHFFFAOYSA-N

Other name(s) : ACMA  ||  G 185  ||  6-Chloro-2-methoxy-9-acridinamine  ||  NSC 15300  ||  2-methoxy-6-chloro-9-aminoacridine  ||  CHEMBL76954  ||  SCHEMBL106725  ||  SCHEMBL9641759  ||  SCHEMBL29365544  ||  SCHEMBL29445571


MW : 258.70

Formula : C14H11ClN2O

CAS_number : 3548-09-2

PubChem : 19080

UniChem : IHHSSHCBRVYGJX-UHFFFAOYSA-N

Target

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

References (3)

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 :
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 :
PubMedSearch : Redinbo_2005_Drug.Discov.Today_10_313
PubMedID: 15749280

Title : Crystal structure of human carboxylesterase 1 complexed with the Alzheimer's drug tacrine: from binding promiscuity to selective inhibition - Bencharit_2003_Chem.Biol_10_341
Author(s) : Bencharit S , Morton CL , Hyatt JL , Kuhn P , Danks MK , Potter PM , Redinbo MR
Ref : Chemical Biology , 10 :341 , 2003
Abstract :
PubMedSearch : Bencharit_2003_Chem.Biol_10_341
PubMedID: 12725862
Gene_locus related to this paper: human-CES1