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TargetMatrilysin
LigandBDBM50137281
Substrate/Competitorn/a
Meas. Tech.ChEBML_105059
IC50 10690±n/a nM
Citation Ma, DWu, WYang, GLi, JLi, JYe, Q Tetrahydroisoquinoline based sulfonamide hydroxamates as potent matrix metalloproteinase inhibitors. Bioorg Med Chem Lett14:47-50 (2003) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Matrilysin
Name:Matrilysin
Synonyms:MMP7 | MMP7_HUMAN | MPSL1 | Matrix metalloproteinase 7 | Matrix metalloproteinase-7 (MMP-7) | Matrix metalloproteinase-7 (MMP7) | PUMP1
Type:Enzyme
Mol. Mass.:29681.54
Organism:Homo sapiens (Human)
Description:P09237
Residue:267
Sequence:
MRLTVLCAVCLLPGSLALPLPQEAGGMSELQWEQAQDYLKRFYLYDSETKNANSLEAKLK
EMQKFFGLPITGMLNSRVIEIMQKPRCGVPDVAEYSLFPNSPKWTSKVVTYRIVSYTRDL
PHITVDRLVSKALNMWGKEIPLHFRKVVWGTADIMIGFARGAHGDSYPFDGPGNTLAHAF
APGTGLGGDAHFDEDERWTDGSSLGINFLYAATHELGHSLGMGHSSDPNAVMYPTYGNGD
PQNFKLSQDDIKGIQKLYGKRSNSRKK
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  Blast E-value cutoff:
BDBM50137281
n/a
NameBDBM50137281
Synonyms:2-Benzenesulfonyl-6-hydroxy-7-methoxy-1,2,3,4-tetrahydro-isoquinoline-1-carboxylic acid hydroxyamide | CHEMBL148171 | N,6-dihydroxy-7-methoxy-2-(phenylsulfonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxamide
TypeSmall organic molecule
Emp. Form.C17H18N2O6S
Mol. Mass.378.4
SMILESCOc1cc2C(N(CCc2cc1O)S(=O)(=O)c1ccccc1)C(=O)NO
Structure
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