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Assay Detail

CHEMBL681894

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Binding
Inhibition of Trypanosoma cruzi farnesyl pyrophosphate synthase
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Trypanosoma cruzi
Confidence 8 — Homologous single protein target
Curated By Expert

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 12 5.17 5.71

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL299988 1 5.71
CHEMBL55264 1 5.62
CHEMBL111695 1 5.37
CHEMBL322081 1 5.34
CHEMBL280463 1 5.25
CHEMBL322551 1 5.24
CHEMBL110971 1 5.07
CHEMBL298547 1 5.03
CHEMBL324003 1 4.71
CHEMBL52761 1 4.37
CHEMBL111593 1 -
CHEMBL112840 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL299988 IC50 = 1940.0 nM 5.71
CHEMBL55264 IC50 = 2370.0 nM 5.62
CHEMBL111695 IC50 = 4250.0 nM 5.37
CHEMBL322081 IC50 = 4540.0 nM 5.34
CHEMBL280463 IC50 = 5670.0 nM 5.25
CHEMBL322551 IC50 = 5710.0 nM 5.24
CHEMBL110971 IC50 = 8450.0 nM 5.07
CHEMBL298547 IC50 = 9360.0 nM 5.03
CHEMBL324003 IC50 = 19730.0 nM 4.71
CHEMBL52761 IC50 = 42830.0 nM 4.37
CHEMBL111593 IC50 > 100000.0 nM -
CHEMBL112840 IC50 = 150360.0 nM -