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Assay Detail

CHEMBL699574

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

Binding
Inhibitory activity of compound against perine-specific inosine-adenosine-guanosine nucleoside hydrolase (IAG-NH) from Trypanosoma brucei
6
Total Activities
6
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

8-Aza-immucillins as transition-state analogue inhibitors of purine nucleoside phosphorylase and nucleoside hydrolases.
Evans GB, Furneaux RH, Gainsford GJ, Hanson JC, Kicska GA, Sauve AA, Schramm VL, Tyler PC.
J Med Chem (2003) 46 : 155 -160
PubMed 12502369 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 6 6.58 9.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL38245 1 9.05
CHEMBL289941 1 7.64
CHEMBL218291 FORODESINE 4.0 1 7.62
CHEMBL41949 1 5.43
CHEMBL2311112 1 4.86
CHEMBL289848 1 4.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL38245 Ki = 0.9 nM 9.05
CHEMBL289941 Ki = 23.0 nM 7.64
CHEMBL218291 FORODESINE Ki = 24.0 nM 7.62
CHEMBL41949 Ki = 3700.0 nM 5.43
CHEMBL2311112 Ki = 13900.0 nM 4.86
CHEMBL289848 Ki = 14000.0 nM 4.85