BDBM50216838 (3R)-6-cyclohexyl-N-hydroxy-3-{3-[1-(methylsulfonyl)-4-piperidinyl]-1,2,4-oxadiazol-5-yl}hexanamide::CHEMBL226840
SMILES: CS(=O)(=O)N1CCC(CC1)NCc1noc(n1)[C@H](CCCC1CCCCC1)CC(=O)NO
InChI Key: InChIKey=QDRXDXOBHKCANX-QGZVFWFLSA-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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
72 kDa type IV collagenase (Homo sapiens (Human)) | BDBM50216838 ((3R)-6-cyclohexyl-N-hydroxy-3-{3-[1-(methylsulfony...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL 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 |
Pfizer Global Research and Development Curated by ChEMBL | Assay Description Inhibition of MMP2 | J Med Chem 50: 3442-56 (2007) Article DOI: 10.1021/jm061010z BindingDB Entry DOI: 10.7270/Q2W66KGB | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Bone morphogenetic protein 1 (Homo sapiens (Human)) | BDBM50216838 ((3R)-6-cyclohexyl-N-hydroxy-3-{3-[1-(methylsulfony...) | 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 | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Global Research and Development Curated by ChEMBL | Assay Description Inhibition of human procollagen C-proteinase expressed in CHO cells | J Med Chem 50: 3442-56 (2007) Article DOI: 10.1021/jm061010z BindingDB Entry DOI: 10.7270/Q2W66KGB | |||||||||||
More data for this Ligand-Target Pair |