BDBM50144337 3-(6-Amino-pyridin-3-yl)-2-[1-(4-methyl-pentyl)-1H-imidazol-4-yl]-propionic acid::CHEMBL70177
SMILES: CC(C)CCCn1cnc(c1)C(Cc1ccc(N)nc1)C(O)=O
InChI Key: InChIKey=UFHFBHSKTSVCMN-UHFFFAOYSA-N
Data: 2 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Thrombin-activatable fibrinolysis (TAFI) (Homo sapiens (Human)) | BDBM50144337 (3-(6-Amino-pyridin-3-yl)-2-[1-(4-methyl-pentyl)-1H...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human carboxypeptidase B (CPB) | Bioorg Med Chem Lett 14: 2141-5 (2004) Article DOI: 10.1016/j.bmcl.2004.02.033 BindingDB Entry DOI: 10.7270/Q2N8797S | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Carboxypeptidase B2 isoform A (Homo sapiens (Human)) | BDBM50144337 (3-(6-Amino-pyridin-3-yl)-2-[1-(4-methyl-pentyl)-1H...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibitory potency against human TAFIa (thrombin-activatable fibrinolysis inhibitor) | Bioorg Med Chem Lett 14: 2141-5 (2004) Article DOI: 10.1016/j.bmcl.2004.02.033 BindingDB Entry DOI: 10.7270/Q2N8797S | |||||||||||
More data for this Ligand-Target Pair |