Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Farnesyl pyrophosphate synthase (Homo sapiens (Human)) | BDBM50273714 (CHEMBL446734 | [2-(Imidazol-1-yl)ethyl]-bisphospho...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 9.03 | n/a | n/a | n/a | n/a | n/a | n/a |
Universita di Ferrara Curated by ChEMBL | Assay Description Inhibition of human FPP synthase expressed in Escherichia coli BL21 (DE3) | J Med Chem 51: 6800-7 (2008) Article DOI: 10.1021/jm801003y BindingDB Entry DOI: 10.7270/Q2F76CD8 | |||||||||||
More data for this Ligand-Target Pair |