BDBM50215928 4-(4-bromo-1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridin-2-amine::CHEMBL231012
SMILES: Nc1nc2c(nccc2[nH]1)-c1cc(Br)c[nH]1
InChI Key: InChIKey=PZVQODCOQPBJAM-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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Matrix metalloproteinase-12 (MMP12) (Homo sapiens (Human)) | BDBM50215928 (4-(4-bromo-1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridi...) | 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 | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Kyorin Pharmaceutical Co., Ltd Curated by ChEMBL | Assay Description Inhibition of human MMP12 catalytic domain | Bioorg Med Chem Lett 19: 5461-3 (2009) Article DOI: 10.1016/j.bmcl.2009.07.099 BindingDB Entry DOI: 10.7270/Q2HX1CRC | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Matrix metalloproteinase-12 (MMP12) (Homo sapiens (Human)) | BDBM50215928 (4-(4-bromo-1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridi...) | 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 | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Kyorin Pharmaceutical Co. Ltd Curated by ChEMBL | Assay Description Inhibition of MMP12 | Bioorg Med Chem Lett 17: 4495-9 (2007) Article DOI: 10.1016/j.bmcl.2007.06.005 BindingDB Entry DOI: 10.7270/Q2MW2GVX | |||||||||||
More data for this Ligand-Target Pair |