BDBM50072569 (2R,3S)-2-Allyl-N*4*-((S)-1-benzyl-2-oxazol-2-yl-2-oxo-ethyl)-N*1*-hydroxy-3-isobutyl-succinamide::(2S,3R)-2-allyl-N1-hydroxy-3-isobutyl-N4-((S)-1-(oxazol-2-yl)-1-oxo-3-phenylpropan-2-yl)succinamide::CHEMBL430524
SMILES CC(C)C[C@H]([C@H](CC=C)C(=O)NO)C(=O)N[C@@H](Cc1ccccc1)C(=O)c1ncco1
InChI Key InChIKey=BZTWELLPCHJZLB-OTWHNJEPSA-N
Data 8 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 8 hits for monomerid = 50072569
Affinity DataIC50: 4.20nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloproteinase 7More data for this Ligand-Target Pair
Affinity DataIC50: 2.70nMAssay Description:In vitro inhibitory activity against matrix metalloproteinase 1 isolated from the culture medium of human skin fibroblasts induced with PMAMore data for this Ligand-Target Pair
Affinity DataIC50: 1.80nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloproteinase 3More data for this Ligand-Target Pair
Target72 kDa type IV collagenase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development
Curated by ChEMBL
Johnson & Johnson Pharmaceutical Research & Development
Curated by ChEMBL
Target72 kDa type IV collagenase(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development
Curated by ChEMBL
Johnson & Johnson Pharmaceutical Research & Development
Curated by ChEMBL
Affinity DataIC50: 7.20nMAssay Description:In vitro inhibitory activity against matrix metalloproteinase 2 isolated from human HT-1080 fibrosarcoma cells induced with TNFMore data for this Ligand-Target Pair