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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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References