99828-55-4

MMP-2/MMP-9 Substrate Chemical Structure
99828-55-4

Chemical Structure

MMP-2/MMP-9 Substrate

Synonym(s): Ac-Pro-Leu-Gly-[(S)-2-mercapto-4-methyl-pentanoyl]-Leu-Gly-OEt

  • CAS No.: 99828-55-4
  • Formula:C31H53N5O8S
  • Molecular Weight:655.85

InChIKey: OJIFMDRLHMGYGK-QORCZRPOSA-N

SMILES: CCOC(CNC([C@H](CC(C)C)NC([C@H](CC(C)C)SC(CNC([C@H](CC(C)C)NC([C@H]1N(CCC1)C(C)=O)=O)=O)=O)=O)=O)=O

Biological Activity: MMP-2/MMP-9 Substrate (Ac-Pro-Leu-Gly-[(S)-2-mercapto-4-methyl-pentanoyl]-Leu-Gly-OEt) is a synthetic chromogenic polypeptide substrate whose core structure mimics the cleavage sites of MMP-2 and MMP-9 (gelatinase A and B) in collagen. After being hydrolyzed by collagenase, MMP-2/MMP-9 Substrate reacts with 4,4'-dithiodipyridine or Ellman's Reagent via its thiol fragment to produce a product with ultraviolet absorption properties[1][2].

Cat. No. Product Name Purity Description Pricing
HY-P10143
MMP-2/MMP-9 Substrate 98.48% MMP-2/MMP-9 Substrate (Ac-Pro-Leu-Gly-[(S)-2-mercapto-4-methyl-pentanoyl]-Leu-Gly-OEt) is a synthetic chromogenic polypeptide substrate whose core structure mimics the cleavage sites of MMP-2 and MMP-9 (gelatinase A and B) in collagen. After being hydrolyzed by collagenase, MMP-2/MMP-9 Substrate reacts with 4,4'-dithiodipyridine or Ellman's Reagent via its thiol fragment to produce a product with ultraviolet absorption properties.
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