CHEMBL3104293

IC50 ACHE 45.5 +/- 4.4 microM BCHE 0.903 +/- 0.003 micro M This is the most active compound against BCHE in Kratky et al. 2014. Many more compounds of this class were tested by the same group but were not more active compounds (Imramovsky et al. 2012) and Phosphorothioates analogues were tested also for antimycobacterial activity Vinsova et al. 2014

General

Type : Organophosphate,Carboxamide

Chemical_Nomenclature : [5-chloro-2-[(3,4-dichlorophenyl)carbamoyl]phenyl] diethyl phosphate

Canonical SMILES : CCOP(=O)(OCC)OC1=C(C=CC(=C1)Cl)C(=O)NC2=CC(=C(C=C2)Cl)Cl

InChI : InChI=1S\/C17H17Cl3NO5P\/c1-3-24-27(23,25-4-2)26-16-9-11(18)5-7-13(16)17(22)21-12-6-8-14(19)15(20)10-12\/h5-10H,3-4H2,1-2H3,(H,21,22)

InChIKey : VAVYJVCTFBRYSO-UHFFFAOYSA-N

Other name(s) : Compound 25,BDBM150745,[5-chloro-2-[(3,4-dichlorophenyl)carbamoyl]phenyl] diethyl phosphate,5-chloro-2-[(3,4-dichlorophenyl)carbamoyl]phenyl diethyl phosphate (25)


MW : 452.6

Formula : C17H17Cl3NO5P

CAS_number :

PubChem : 73334558

UniChem : VAVYJVCTFBRYSO-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : CHEMBL3104293 ligand of proteins in family: BCHE

Stucture :

Protein :

References (3)

Title : Salicylanilide diethyl phosphates as cholinesterases inhibitors - Kratky_2014_Bioorg.Chem_58C_48
Author(s) : Kratky M , Stepankova S , Vorcakova K , Vinsova J
Ref : Bioorg Chem , 58C :48 , 2014
Abstract : Kratky_2014_Bioorg.Chem_58C_48
ESTHER : Kratky_2014_Bioorg.Chem_58C_48
PubMedSearch : Kratky_2014_Bioorg.Chem_58C_48
PubMedID: 25462625

Title : Diethyl 2-(Phenylcarbamoyl)phenyl Phosphorothioates: Synthesis, Antimycobacterial Activity and Cholinesterase Inhibition - Vinsova_2014_Molecules_19_7152
Author(s) : Vinsova J , Kratky M , Komloova M , Dadapeer E , Stepankova S , Vorcakova K , Stolarikova J
Ref : Molecules , 19 :7152 , 2014
Abstract : Vinsova_2014_Molecules_19_7152
ESTHER : Vinsova_2014_Molecules_19_7152
PubMedSearch : Vinsova_2014_Molecules_19_7152
PubMedID: 24886941

Title : Acetylcholinesterase-inhibiting activity of salicylanilide N-alkylcarbamates and their molecular docking - Imramovsky_2012_Molecules_17_10142
Author(s) : Imramovsky A , Stepankova S , Vanco J , Pauk K , Monreal-Ferriz J , Vinsova J , Jampilek J
Ref : Molecules , 17 :10142 , 2012
Abstract : Imramovsky_2012_Molecules_17_10142
ESTHER : Imramovsky_2012_Molecules_17_10142
PubMedSearch : Imramovsky_2012_Molecules_17_10142
PubMedID: 22922284