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Assay Detail

CHEMBL998582

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Binding
Inhibition of human FPPS
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

Bisphosphonate inhibitors of ATP-mediated HIV-1 reverse transcriptase catalyzed excision of chain-terminating 3'-azido, 3'-deoxythymidine: a QSAR investigation.
Song Y, Chan JM, Tovian Z, Secrest A, Nagy E, Krysiak K, Bergan K, Parniak MA, Oldfield E.
Bioorg Med Chem (2008) 16 : 8959 -8967
PubMed 18789701 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 4.72 5.07

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL55371 1 5.07
CHEMBL34249 1 4.36

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL55371 IC50 = 8500.0 nM 5.07
CHEMBL34249 IC50 = 44000.0 nM 4.36