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Assay Detail

CHEMBL901651

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Binding
Inhibition of Plasmodium falciparum recombinant M17 LAP
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Plasmodium falciparum
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Identification of phosphinate dipeptide analog inhibitors directed against the Plasmodium falciparum M17 leucine aminopeptidase as lead antimalarial compounds.
Skinner-Adams TS, Lowther J, Teuscher F, Stack CM, Grembecka J, Mucha A, Kafarski P, Trenholme KR, Dalton JP, Gardiner DL.
J Med Chem (2007) 50 : 6024 -6031
PubMed 17960925 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 5 7.35 7.98

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL393950 1 7.98
CHEMBL393949 1 7.88
CHEMBL538595 BESTATIN HYDROCHLORIDE 1 7.60
CHEMBL238227 1 7.01
CHEMBL395125 1 6.28

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL393950 Ki = 10.4 nM 7.98
CHEMBL393949 Ki = 13.2 nM 7.88
CHEMBL538595 BESTATIN HYDROCHLORIDE Ki = 25.0 nM 7.60
CHEMBL238227 Ki = 97.3 nM 7.01
CHEMBL395125 Ki = 524.8 nM 6.28