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Assay Detail

CHEMBL1048804

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

Binding
Inhibition of recombinant Trypanosoma brucei rhodesain after 5 mins by spectrofluorimetric analysis
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Trypanosoma brucei
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Identification and optimization of inhibitors of Trypanosomal cysteine proteases: cruzain, rhodesain, and TbCatB.
Mott BT, Ferreira RS, Simeonov A, Jadhav A, Ang KK, Leister W, Shen M, Silveira JT, Doyle PS, Arkin MR, McKerrow JH, Inglese J, Austin CP, Thomas CJ, Shoichet BK, Maloney DJ.
J Med Chem (2010) 53 : 52 -60
PubMed 19908842 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 7.61 8.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL568171 1 8.30
CHEMBL567785 1 8.22
CHEMBL566924 1 8.22
CHEMBL567783 1 8.10
CHEMBL577121 1 8.00
CHEMBL567784 1 7.70
CHEMBL566273 1 7.52
CHEMBL568172 1 7.52
CHEMBL567147 1 7.40
CHEMBL576648 1 7.30
CHEMBL579273 1 7.16
CHEMBL566903 1 7.00
CHEMBL571295 1 6.52
CHEMBL578162 1 -
CHEMBL567341 1 -
CHEMBL567340 1 -
CHEMBL577764 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL568171 IC50 = 5.0 nM 8.30
CHEMBL567785 IC50 = 6.0 nM 8.22
CHEMBL566924 IC50 = 6.0 nM 8.22
CHEMBL567783 IC50 = 8.0 nM 8.10
CHEMBL577121 IC50 = 10.0 nM 8.00
CHEMBL567784 IC50 = 20.0 nM 7.70
CHEMBL566273 IC50 = 30.0 nM 7.52
CHEMBL568172 IC50 = 30.0 nM 7.52
CHEMBL567147 IC50 = 40.0 nM 7.40
CHEMBL576648 IC50 = 50.0 nM 7.30
CHEMBL579273 IC50 = 70.0 nM 7.16
CHEMBL566903 IC50 = 100.0 nM 7.00
CHEMBL571295 IC50 = 300.0 nM 6.52
CHEMBL578162 IC50 < 6.0 nM -
CHEMBL567341 IC50 < 6.0 nM -
CHEMBL567340 IC50 < 6.0 nM -
CHEMBL577764 IC50 > 10000.0 nM -