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TargetHistidine-rich protein PFHRP-II
LigandBDBM50123587
Substrate/Competitorn/a
Meas. Tech.ChEMBL_215891 (CHEMBL820823)
IC50 23.3±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
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  Blast E-value cutoff:
BDBM50123587
n/a
NameBDBM50123587
Synonyms:(7-Chloro-quinolin-4-yl)-(3-{4-[3-(cyclopropylmethyl-amino)-propyl]-piperazin-1-yl}-propyl)-amine | 7-chloro-N-(3-(4-(3-(cyclopropylmethylamino)propyl)piperazin-1-yl)propyl)quinolin-4-amine | CHEMBL357948
TypeSmall organic molecule
Emp. Form.C23H34ClN5
Mol. Mass.416.003
SMILESClc1ccc2c(NCCCN3CCN(CCCNCC4CC4)CC3)ccnc2c1
Structure
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