1620389-76-5

CQPQGLAKC Chemical Structure
1620389-76-5

Chemical Structure

CQPQGLAKC

  • CAS No.: 1620389-76-5
  • Formula:C38H66N12O12S2
  • Molecular Weight:947.13

InChIKey: HUVFHCQPJQNUCK-APGJSSKUSA-N

SMILES: O=C(N[C@@H](CCC(N)=O)C(N1[C@@H](CCC1)C(N[C@@H](CCC(N)=O)C(NCC(N[C@@H](CC(C)C)C(N[C@@H](C)C(N[C@@H](CCCCN)C(N[C@@H](CS)C(O)=O)=O)=O)=O)=O)=O)=O)=O)[C@H](CS)N

Biological Activity: CQPQGLAKC is a peptide crosslinker and hydrogel component that can be cleaved by MMP. The degradation of CQPQGLAKC is primarily mediated by endogenous MMP-13, with a Km value of 1.10 µM. CQPQGLAKC crosslinks hyaluronic acid hydrogels via Michael-type addition, thereby enabling cell-mediated matrix remodeling and promoting cell survival, proliferation, and endothelial differentiation. CQPQGLAKC can be used in research on rotator cuff tears and ischemic injury[1][2][3][4].

Cat. No. Product Name Purity Description Pricing
HY-P12373
CQPQGLAKC CQPQGLAKC is a peptide crosslinker and hydrogel component that can be cleaved by MMP. The degradation of CQPQGLAKC is primarily mediated by endogenous MMP-13, with a Km value of 1.10 µM. CQPQGLAKC crosslinks hyaluronic acid hydrogels via Michael-type addition, thereby enabling cell-mediated matrix remodeling and promoting cell survival, proliferation, and endothelial differentiation. CQPQGLAKC can be used in research on rotator cuff tears and ischemic injury.
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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