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TargetHistidine-rich protein PFHRP-II
LigandBDBM50202591
Substrate/Competitorn/a
Meas. Tech.ChEMBL_423821 (CHEMBL910656)
IC50 560±n/a nM
Citation Solomon, VRHaq, WSrivastava, KPuri, SKKatti, SB Synthesis and antimalarial activity of side chain modified 4-aminoquinoline derivatives. J Med Chem50:394-8 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Histidine-rich protein PFHRP-II
Name:Histidine-rich protein PFHRP-II
Synonyms:HRP1_PLAFA | Histidine-rich protein | Histidine-rich protein PFHRP-II
Type:PROTEIN
Mol. Mass.:35156.49
Organism:Plasmodium falciparum
Description:ChEMBL_500704
Residue:332
Sequence:
MVSFSKNKVLSAAVFASVLLLDNNNSAFNNNLCSKNAKGLNLNKRLLHETQAHVDDAHHA
HHVADAHHAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHA
ADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAAYAHHAHHASDAHHAADAHHAAYA
HHAHHAADAHHAADAHHAAYAHHAHHAADAHHAADAHHATDAHHAHHAADAHHATDAHHA
ADAHHAADAHHATDAHHAADAHHATDAHHAADAHHAADAHHATDSHHAHHAADAHHAAAH
HATDAHHAAAHHATDAHHAAAHHEAATHCLRH
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50202591
n/a
NameBDBM50202591
Synonyms:2-(4-chloro-phenyl)-3-[3-(7-chloroquinolin-4-ylamino)-propyl]-thiazolidin-4-one | CHEMBL376916
TypeSmall organic molecule
Emp. Form.C21H19Cl2N3OS
Mol. Mass.432.366
SMILESClc1ccc(cc1)C1SCC(=O)N1CCCNc1ccnc2cc(Cl)ccc12
Structure
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