Use the link below to share a full-text version of this article with your friends and colleagues. Learn more. The matrix metalloproteinases MMPs are a family of tightly regulated proteases that are involved in the catabolic aspect of remodeling and maintenance of normal tissue, and more than 20 human MMPs have been identified thus far. The MMPs collectively degrade a broad range of protein components of the extracellular matrix. While some substrate overlap exists, individual MMPs have been shown to process certain substrates more efficiently than others.
This suggests the need to assess the inhibition potency of test compounds across a range of MMP family members. Described in this unit is a method for the in vitro characterization of MMP inhibitors.
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The is used to determine the potency of test compounds as inhibitors of 8 representative MMPs through the measurement of their inhibition of cleavage of a fluorogenic substrate. Since this substrate is efficiently hydrolyzed by all MMPs in the screening assays presented here, the method is convenient for assessing the selectivity of inhibitors against multiple enzymes.
A describes the activation of MMP zymogens. Volume 13 , Issue 1. If you do not receive an email within 10 minutes, your email address may not be registered, and you may need to create a new Wiley Online Library account. If the address matches an existing account you will receive an email with instructions to retrieve your username. Webinars Videos.
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Patrick A. Steven K. Read the full text. Tools Request permission Export citation Add to favorites Track citation. A study of a d -proline peptidomimetic inhibitor of melanoma and endothelial cell invasion through activity towards MMP-2 and MMP MedChemComm , 6 2 , Sukesh Kalva, D. Vinod, Lilly M. Combined structure- and ligand-based pharmacophore modeling and molecular dynamics simulation studies to identify selective inhibitors of MMP Search for novel histone deacetylase inhibitors.
Part II: Design and synthesis of novel isoferulic acid derivatives. Development of novel ferulic acid derivatives as potent histone deacetylase inhibitors. European Journal of Medicinal Chemistry , 56 , Synthesis and biological evaluation in U87MG glioma cells of ethynylthiophene sulfonamido-based hydroxamates as matrix metalloproteinase inhibitors. European Journal of Medicinal Chemistry , 46 7 , Barchi, Christopher Michejda. European Journal of Organic Chemistry , 1 , Synthesis of 3-azabicyclo[4.
Matrix Metalloproteinases (MMPs)
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Purification of matrix metalloproteinases by column chromatography
Proteins: Structure, Function, and Bioinformatics , 69 1 , Stephen Hanessian. ChemMedChem , 1 12 , Design, synthesis and molecular modeling study of iminodiacetyl monohydroxamic acid derivatives as MMP inhibitors. Linear and nonlinear QSAR study of N-hydroxy[ phenylsulfonyl amino]acetamide derivatives as matrix metalloproteinase inhibitors. ChemBioChem , 6 8 , Rajeshwar P. Verma, Alka Kurup, Corwin Hansch.
On the role of polarizability in QSAR. Svab, D. Binding affinities for sulfonamide inhibitors with matrix metalloproteinase-2 using a linear response method. Journal of Cellular and Molecular Medicine , 8 4 , Journal of Inorganic Biochemistry , 98 5 , Calvo, Stefan Balaz.
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