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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
B2 bradykinin receptor (Homo sapiens (Human)) | BDBM50146905 (4-{(E)-2-[({[2,4-Dichloro-3-(4-methoxy-2-methyl-qu...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 0.230 | n/a | n/a | n/a | n/a | n/a | n/a |
Fujisawa Pharmaceutical Co. Ltd. Curated by ChEMBL | Assay Description Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 | J Med Chem 47: 2853-63 (2004) Article DOI: 10.1021/jm030468n BindingDB Entry DOI: 10.7270/Q2JM2BCM | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
B2 bradykinin receptor (Homo sapiens (Human)) | BDBM50146905 (4-{(E)-2-[({[2,4-Dichloro-3-(4-methoxy-2-methyl-qu...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 8.10 | n/a | n/a | n/a | n/a | n/a | n/a |
Fujisawa Pharmaceutical Co. Ltd. Curated by ChEMBL | Assay Description Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells | J Med Chem 47: 2853-63 (2004) Article DOI: 10.1021/jm030468n BindingDB Entry DOI: 10.7270/Q2JM2BCM | |||||||||||
More data for this Ligand-Target Pair |