4-thiazolidinone-cpd18

Compound 18 of Vidal-Albalat et al. Specific inhibition of mosquitoe AChE IC50 (microM) AgAChE1 0.86 (0.62-1.2); AaAChE1 0.56 (0.41-0.76); hAChE >200 G122SAgACHE1 >200

General

Type : Thiazolidine,Sulfur Compound

Chemical_Nomenclature : 2-(4-chlorophenyl)-3-[3-(dimethylamino)propyl]-1,3-thiazolidin-4-one

Canonical SMILES : CN(C)CCCN1C(SCC1=O)C2=CC=C(C=C2)Cl

InChI : InChI=1S\/C14H19ClN2OS\/c1-16(2)8-3-9-17-13(18)10-19-14(17)11-4-6-12(15)7-5-11\/h4-7,14H,3,8-10H2,1-2H3

InChIKey : UHOAIESFARWLTF-UHFFFAOYSA-N

Other name(s) : CHEMBL100486,CBMicro_028133,Oprea1_185679,Oprea1_682598,BDBM50002118


MW : 298.8

Formula : C14H19ClN2OS

CAS_number :

PubChem : 2861271

UniChem : UHOAIESFARWLTF-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : 4-thiazolidinone-cpd18 ligand of proteins in family: ACHE

Stucture :

Protein :

References (1)

Title : Structure-Activity Relationships Reveal Beneficial Selectivity Profiles of Inhibitors Targeting Acetylcholinesterase of Disease-Transmitting Mosquitoes - Vidal-Albalat_2023_J.Med.Chem__
Author(s) : Vidal-Albalat A , Kindahl T , Rajeshwari R , Lindgren C , Forsgren N , Kitur S , Tengo LS , Ekstrom F , Kamau L , Linusson A
Ref : Journal of Medicinal Chemistry , : , 2023
Abstract : Vidal-Albalat_2023_J.Med.Chem__
ESTHER : Vidal-Albalat_2023_J.Med.Chem__
PubMedSearch : Vidal-Albalat_2023_J.Med.Chem__
PubMedID: 37094110