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TargetHistidine-rich protein PFHRP-II
LigandBDBM50123613
Substrate/Competitorn/a
Meas. Tech.ChEMBL_215891 (CHEMBL820823)
IC50 47.8±n/a nM
Citation Ryckebusch, ADeprez-Poulain, RMaes, LDebreu-Fontaine, MAMouray, EGrellier, PSergheraert, C Synthesis and in vitro and in vivo antimalarial activity of N1-(7-chloro-4-quinolyl)-1,4-bis(3-aminopropyl)piperazine derivatives. J Med Chem46:542-57 (2003) [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:
BDBM50123613
n/a
NameBDBM50123613
Synonyms:CHEMBL152886 | [3-(4-{3-[Bis-(4-methoxy-benzyl)-amino]-propyl}-piperazin-1-yl)-propyl]-(7-chloro-quinolin-4-yl)-amine
TypeSmall organic molecule
Emp. Form.C35H44ClN5O2
Mol. Mass.602.209
SMILESCOc1ccc(CN(CCCN2CCN(CCCNc3ccnc4cc(Cl)ccc34)CC2)Cc2ccc(OC)cc2)cc1
Structure
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