N-10-Phenothiazine-3-(dimethylamino)phenyl-carbamate

(Compound 24 Darvesh et al. 2008) Ki BCHE 1.91 micro M (for comparison Donepezil 2.21 for BCHE and 0.024 for ACHE), Ka ACHE 19200 M-1min-1 (for comparison rivastigmine 1130 M-1min-1)

General

Type : Phenothiazine,Carbamate,Sulfur Compound

Chemical_Nomenclature : [3-(dimethylamino)phenyl] phenothiazine-10-carboxylate

Canonical SMILES : CN(C)C1=CC(=CC=C1)OC(=O)N2C3=CC=CC=C3SC4=CC=CC=C42

InChI : InChI=1S\/C21H18N2O2S\/c1-22(2)15-8-7-9-16(14-15)25-21(24)23-17-10-3-5-12-19(17)26-20-13-6-4-11-18(20)23\/h3-14H,1-2H3

InChIKey : UCJSIBVJIPKASB-UHFFFAOYSA-N

Other name(s) : CHEMBL481908,BDBM50292624,3-(dimethylamino)phenyl 10H-phenothiazine-10-carboxylate


MW : 362.4

Formula : C21H18N2O2S

CAS_number :

PubChem : 24905654

UniChem : UCJSIBVJIPKASB-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : N-10-Phenothiazine-3-(dimethylamino)phenyl-carbamate ligand of proteins in family: BCHE

Stucture :

Protein :

References (2)

Title : Selectivity of phenothiazine cholinesterase inhibitors for neurotransmitter systems - Darvesh_2013_Bioorg.Med.Chem.Lett_23_3822
Author(s) : Darvesh S , Macdonald IR , Martin E
Ref : Bioorganic & Medicinal Chemistry Lett , 23 :3822 , 2013
Abstract : Darvesh_2013_Bioorg.Med.Chem.Lett_23_3822
ESTHER : Darvesh_2013_Bioorg.Med.Chem.Lett_23_3822
PubMedSearch : Darvesh_2013_Bioorg.Med.Chem.Lett_23_3822
PubMedID: 23707254

Title : Carbamates with differential mechanism of inhibition toward acetylcholinesterase and butyrylcholinesterase - Darvesh_2008_J.Med.Chem_51_4200
Author(s) : Darvesh S , Darvesh KV , McDonald RS , Mataija D , Walsh R , Mothana S , Lockridge O , Martin E
Ref : Journal of Medicinal Chemistry , 51 :4200 , 2008
Abstract : Darvesh_2008_J.Med.Chem_51_4200
ESTHER : Darvesh_2008_J.Med.Chem_51_4200
PubMedSearch : Darvesh_2008_J.Med.Chem_51_4200
PubMedID: 18570368