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Assay Detail

CHEMBL870817

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of Trypanosoma brucei rhodesiense rhodesain in presence of 31.6 uM substrate Cbz-Phe-Arg-AMC
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Trypanosoma brucei rhodesiense
Confidence 9 — Direct single protein target
Curated By Expert

Target

Rhodesain (CHEMBL4188)
Type SINGLE PROTEIN
Organism Trypanosoma brucei rhodesiense

Publication

Aziridine-2,3-dicarboxylate inhibitors targeting the major cysteine protease of Trypanosoma brucei as lead trypanocidal agents.
Vicik R, Hoerr V, Glaser M, Schultheis M, Hansell E, McKerrow JH, Holzgrabe U, Caffrey CR, Ponte-Sucre A, Moll H, Stich A, Schirmeister T.
Bioorg Med Chem Lett (2006) 16 : 2753 -2757
PubMed 16516467 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 1 6.44 6.44

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL208156 1 6.44

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL208156 Ki = 360.0 nM 6.44