BDBM50095570 4-(3-Methyl-2,5-dioxo-imidazolidin-1-yl)-1-[4-(pyridin-4-yloxy)-benzenesulfonyl]-pyrrolidine-2-carboxylic acid hydroxyamide::CHEMBL343414
SMILES: Cn1cc(O)n([C@H]2C[C@@H](N(C2)S(=O)(=O)c2ccc(Oc3ccncc3)cc2)C(=O)NO)c1=O
InChI Key: InChIKey=LUCWASGSJPPQEE-SUMWQHHRSA-N
Data: 5 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Collagenase 3 (Homo sapiens (Human)) | BDBM50095570 (4-(3-Methyl-2,5-dioxo-imidazolidin-1-yl)-1-[4-(pyr...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 0.700 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals Curated by ChEMBL | Assay Description In vitro inhibitory activity against human recombinant matrix metalloproteinase-13 (collagenase-3) | J Med Chem 43: 4948-63 (2001) BindingDB Entry DOI: 10.7270/Q21N80DW | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Interstitial collagenase (Homo sapiens (Human)) | BDBM50095570 (4-(3-Methyl-2,5-dioxo-imidazolidin-1-yl)-1-[4-(pyr...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 600 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals Curated by ChEMBL | Assay Description In vitro inhibitory activity against matrix metalloproteinase -1 (collagenase-1) | J Med Chem 43: 4948-63 (2001) BindingDB Entry DOI: 10.7270/Q21N80DW | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Matrilysin (Homo sapiens (Human)) | BDBM50095570 (4-(3-Methyl-2,5-dioxo-imidazolidin-1-yl)-1-[4-(pyr...) | 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 | 7.41E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pomona College Curated by ChEMBL | Assay Description Inhibition of MMP7 | Bioorg Med Chem 15: 2223-68 (2007) Article DOI: 10.1016/j.bmc.2007.01.011 BindingDB Entry DOI: 10.7270/Q2571DBD | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Stromelysin-1 (Homo sapiens (Human)) | BDBM50095570 (4-(3-Methyl-2,5-dioxo-imidazolidin-1-yl)-1-[4-(pyr...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals Curated by ChEMBL | Assay Description In vitro inhibitory activity against matrix metalloproteinase -3 (stromelysin) | J Med Chem 43: 4948-63 (2001) BindingDB Entry DOI: 10.7270/Q21N80DW | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Matrilysin (Homo sapiens (Human)) | BDBM50095570 (4-(3-Methyl-2,5-dioxo-imidazolidin-1-yl)-1-[4-(pyr...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 7.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals Curated by ChEMBL | Assay Description In vitro inhibitory activity against matrix metalloproteinase-7 (matrilysin, MMP-7) | J Med Chem 43: 4948-63 (2001) BindingDB Entry DOI: 10.7270/Q21N80DW | |||||||||||
More data for this Ligand-Target Pair |