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TargetHistidine-rich protein PFHRP-II
LigandBDBM50202607
Substrate/Competitorn/a
Meas. Tech.ChEMBL_423821 (CHEMBL910656)
IC50 390±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
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  Blast E-value cutoff:
BDBM50202607
n/a
NameBDBM50202607
Synonyms:3-[3-(7-chloroquinolin-4-ylamino)-propyl]-2-(2,6-dichloro-phenyl)-thiazolidin-4-one | CHEMBL219189
TypeSmall organic molecule
Emp. Form.C21H18Cl3N3OS
Mol. Mass.466.811
SMILESClc1ccc2c(NCCCN3C(SCC3=O)c3c(Cl)cccc3Cl)ccnc2c1
Structure
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