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Assay Detail

CHEMBL820823

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Functional
In vitro inhibition of beta-hematin formation
19
Total Activities
19
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Confidence 8 — Homologous single protein target
Curated By Expert

Target

Histidine-rich protein PFHRP-II (CHEMBL1923)
Type SINGLE PROTEIN
Organism Plasmodium falciparum

Publication

Synthesis and in vitro and in vivo antimalarial activity of N1-(7-chloro-4-quinolyl)-1,4-bis(3-aminopropyl)piperazine derivatives.
Ryckebusch A, Deprez-Poulain R, Maes L, Debreu-Fontaine MA, Mouray E, Grellier P, Sergheraert C.
J Med Chem (2003) 46 : 542 -557
PubMed 12570376 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 7.45 8.17

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL356811 1 8.17
CHEMBL345958 1 7.82
CHEMBL357948 1 7.63
CHEMBL2111198 1 7.63
CHEMBL153507 1 7.57
CHEMBL149751 1 7.47
CHEMBL152862 1 7.47
CHEMBL357111 1 7.45
CHEMBL356005 1 7.43
CHEMBL152635 1 7.40
CHEMBL151514 1 7.40
CHEMBL152392 1 7.37
CHEMBL152052 1 7.36
CHEMBL152886 1 7.32
CHEMBL422682 1 7.30
CHEMBL356249 1 7.29
CHEMBL152286 1 7.21
CHEMBL346177 1 7.13
CHEMBL152266 1 7.10

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL356811 IC50 = 6.7 nM 8.17
CHEMBL345958 IC50 = 15.0 nM 7.82
CHEMBL357948 IC50 = 23.3 nM 7.63
CHEMBL2111198 IC50 = 23.5 nM 7.63
CHEMBL153507 IC50 = 27.1 nM 7.57
CHEMBL149751 IC50 = 34.2 nM 7.47
CHEMBL152862 IC50 = 34.0 nM 7.47
CHEMBL357111 IC50 = 35.6 nM 7.45
CHEMBL356005 IC50 = 37.5 nM 7.43
CHEMBL152635 IC50 = 40.2 nM 7.40
CHEMBL151514 IC50 = 40.0 nM 7.40
CHEMBL152392 IC50 = 42.5 nM 7.37
CHEMBL152052 IC50 = 43.4 nM 7.36
CHEMBL152886 IC50 = 47.8 nM 7.32
CHEMBL422682 IC50 = 50.6 nM 7.30
CHEMBL356249 IC50 = 50.9 nM 7.29
CHEMBL152286 IC50 = 61.4 nM 7.21
CHEMBL346177 IC50 = 74.9 nM 7.13
CHEMBL152266 IC50 = 79.0 nM 7.10