Reaction Details Report a problem with these data
Target
Histidine-rich protein PFHRP-II
Ligand
BDBM50202615
Substrate
n/a
Meas. Tech.
ChEMBL_423821 (CHEMBL910656)
IC50
460±n/a nM
Citation
Solomon, VR; Haq, W; Srivastava, K; Puri, SK; Katti, SB Synthesis and antimalarial activity of side chain modified 4-aminoquinoline derivatives. J Med Chem 50:394-8 (2007) [PubMed] Article
More Info.:
Target
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:
MVSFSKNKVLSAAVFASVLLLDNNNSAFNNNLCSKNAKGLNLNKRLLHETQAHVDDAHHAHHVADAHHAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAAYAHHAHHASDAHHAADAHHAAYAHHAHHAADAHHAADAHHAAYAHHAHHAADAHHAADAHHATDAHHAHHAADAHHATDAHHAADAHHAADAHHATDAHHAADAHHATDAHHAADAHHAADAHHATDSHHAHHAADAHHAAAHHATDAHHAAAHHATDAHHAAAHHEAATHCLRH
Inhibitor
Name:
BDBM50202615
Synonyms:
3-(2-(7-chloroquinolin-4-ylamino)ethyl)-2-(2,6-dichlorophenyl)thiazolidin-4-one | 3-[2-(7-chloroquinolin-4-ylamino)-ethyl]-2-(2,6-dichloro-phenyl)-thiazolidin-4-one | CHEMBL219967
Type:
Small organic molecule
Emp. Form.:
C20H16Cl3N3OS
Mol. Mass.:
452.785
SMILES:
Clc1ccc2c(NCCN3C(SCC3=O)c3c(Cl)cccc3Cl)ccnc2c1