Target
Matrilysin
Ligand
BDBM50246792
Substrate
n/a
Meas. Tech.
ChEMBL_557955 (CHEMBL963053)
Ki
523±n/a nM
Citation
 Ledour, GMoroy, GRouffet, MBourguet, EGuillaume, DDecarme, MElmourabit, HAugé, FAlix, AJLaronze, JYBellon, GHornebeck, WSapi, J Introduction of the 4-(4-bromophenyl)benzenesulfonyl group to hydrazide analogs of Ilomastat leads to potent gelatinase B (MMP-9) inhibitors with improved selectivity. Bioorg Med Chem 16:8745-59 (2008) [PubMed]  Article
Target
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:
MRLTVLCAVCLLPGSLALPLPQEAGGMSELQWEQAQDYLKRFYLYDSETKNANSLEAKLKEMQKFFGLPITGMLNSRVIEIMQKPRCGVPDVAEYSLFPNSPKWTSKVVTYRIVSYTRDLPHITVDRLVSKALNMWGKEIPLHFRKVVWGTADIMIGFARGAHGDSYPFDGPGNTLAHAFAPGTGLGGDAHFDEDERWTDGSSLGINFLYAATHELGHSLGMGHSSDPNAVMYPTYGNGDPQNFKLSQDDIKGIQKLYGKRSNSRKK
  
Inhibitor
Name:
BDBM50246792
Synonyms:
CHEMBL508335 | N'-{3-(R)-[2-(S)-(1H-Indol-3-yl)-1-(methylcarbamoyl)-ethylcarbamoyl]-(5-methylhexanoyl)}-N-4-(4-bromophenyl)-benzenesulfonylhydrazide
Type:
Small organic molecule
Emp. Form.:
C32H36BrN5O5S
Mol. Mass.:
682.628
SMILES:
CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)CC(=O)NNS(=O)(=O)c1ccc(cc1)-c1ccc(Br)cc1 |r|
Structure:
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