Bis-Thiazolidinone-Based-20

ACHE IC50 = 0.070 +/-0.050 microM, BCHE IC50 = 0.10+/-0.050 microM

General

Type : Thiazolidine,Sulfur Compound

Chemical_Nomenclature : 2-((4-oxo-5-((E)-2,3,4-trihydroxybenzylidene)thiazolidin-2-ylidene)hydrazono)-5-((E)-3,4,5-trihydroxybenzylidene)thiazolidin-4-one

Canonical SMILES : C3(=NN=C1NC(C(S1)=CC2=CC=C(C(=C2O)O)O)=O)SC(C(N3)=O)=CC4=C(C(=C(C=C4)O)O)O

InChI : InChI=1S\/C20H14N4O8S2\/c25-9-3-1-7(13(27)15(9)29)5-11-17(31)21-19(33-11)23-24-20-22-18(32)12(34-20)6-8-2-4-10(26)16(30)14(8)28\/h1-6,25-30H,(H,21,23,31)(H,22,24,32)\/b11-5-,12-6+

InChIKey : MSQZMILSECVAJQ-JTAXDKCCSA-N

Other name(s) :


MW : 502.47

Formula : C20H14N4O8S2

CAS_number :

PubChem :

UniChem : MSQZMILSECVAJQ-JTAXDKCCSA-N

IUPHAR :

Wikipedia :

Target

Families : Bis-Thiazolidinone-Based-20 ligand of proteins in family: ACHE || BCHE

Stucture :

Protein :

References (1)

Title : New bis-thiazolidinone based chalcone analogues as effective inhibitors of Alzheimer's disease: Synthesis, molecular docking, acetylcholinesterase and butyrylcholinesterase study - Hussain_2022_Chem.Biodivers__
Author(s) : Hussain R , Rahim F , Rehman W , Taha M , Khan S , Zaman K , Ali Shah SA , Wadood A , Imran S , Abdellatif M
Ref : Chem Biodivers , : , 2022
Abstract : Hussain_2022_Chem.Biodivers__
ESTHER : Hussain_2022_Chem.Biodivers__
PubMedSearch : Hussain_2022_Chem.Biodivers__
PubMedID: 35997224