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Assay Detail

CHEMBL681892

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Binding
Inhibitory concentration against Trypanosoma brucei farnesyl pyrophosphate synthase activity
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Trypanosoma brucei
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Farnesyl pyrophosphate synthase (CHEMBL1782)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase.
Szajnman SH, Montalvetti A, Wang Y, Docampo R, Rodriguez JB.
Bioorg Med Chem Lett (2003) 13 : 3231 -3235
PubMed 12951099 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 5.62 6.18

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL55264 1 6.18
CHEMBL299988 1 5.51
CHEMBL298547 1 5.45
CHEMBL110971 1 5.34

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL55264 IC50 = 660.0 nM 6.18
CHEMBL299988 IC50 = 3120.0 nM 5.51
CHEMBL298547 IC50 = 3570.0 nM 5.45
CHEMBL110971 IC50 = 4540.0 nM 5.34