12 Modeling of Stromelysins Inhibitors
ABSTRACT Stromelysins (namely MMP-3, MMP-10, and MMP-11) are zinc-dependent
endopeptidases that are a subclass of MMPs that help with tissue remodeling and …
endopeptidases that are a subclass of MMPs that help with tissue remodeling and …
Modeling Inhibitors of Stromelysins
Stromelysins (namely MMP-3, MMP-10, and MMP-11) are zinc-dependent endopeptidases
that are a subclass of MMPs that help with tissue remodeling and extracellular matrix (ECM) …
that are a subclass of MMPs that help with tissue remodeling and extracellular matrix (ECM) …
Stromelysins and Their Inhibitors
Stromelysins are a matrix metalloproteinase (MMP) family member—a zinc-dependent
endopeptidase responsible for the breakdown of the extracellular matrix (ECM). However …
endopeptidase responsible for the breakdown of the extracellular matrix (ECM). However …
X-ray structure of human stromelysin catalytic domain complexed with nonpeptide inhibitors: implications for inhibitor selectivity
AG Pavlovsky, MG Williams, QZ Ye, DF Ortwine… - Protein …, 1999 - cambridge.org
Effective inhibitors of matrix metalloproteinases (MMPs), a family of connective tissue-
degrading enzymes, could be useful for the treatment of diseases such as cancer, multiple …
degrading enzymes, could be useful for the treatment of diseases such as cancer, multiple …
[PDF][PDF] SS LL GGLGG LLLLLLGGG GGGGGGGG GGLL kTT
S Toba - academia.edu
Matrix metalloproteinases (MMPs) is an important new class of therapeutic targets for the
treatment of diseases characterized by excessive extracellular matrix degradation and/or …
treatment of diseases characterized by excessive extracellular matrix degradation and/or …
Potent, selective pyrone-based inhibitors of stromelysin-1
In an effort to develop alternatives to hydroxamate-based matrix metalloproteinase inhibitors
(MPIs), we have utilized the drug discovery program LUDI enhanced with the structural …
(MPIs), we have utilized the drug discovery program LUDI enhanced with the structural …
Three-dimensional quantitative structure− activity relationship (3D-QSAR) models for a novel class of piperazine-based stromelysin-1 (MMP-3) inhibitors: Applying a “ …
EA Amin, WJ Welsh - Journal of medicinal chemistry, 2001 - ACS Publications
Three-dimensional quantitative structure− activity relationship (3D-QSAR) models have
been obtained using comparative molecular field analysis (CoMFA) for a novel series of …
been obtained using comparative molecular field analysis (CoMFA) for a novel series of …
Structural characterizations of nonpeptidic thiadiazole inhibitors of matrix metalloproteinases reveal the basis for stromelysin selectivity
BC Finzel, ET Baldwin, GL Bryant Jr, GF Hess… - Protein …, 1998 - Wiley Online Library
The binding of two 5‐substituted‐l, 3, 4‐thiadiazole‐2‐thione inhibitors to the matrix
metalloproteinase stromelysin (MMP‐3) have been characterized by protein crystallography …
metalloproteinase stromelysin (MMP‐3) have been characterized by protein crystallography …
[PDF][PDF] X-ray structure of a hydroxamate inhibitor complex of stromelysin catalytic domain and its comparison with members of the zinc metalloproteinase superfamily
V Dhanaraj, QZ Ye, LL Johnson, DJ Hupe, DF Ortwine… - Structure, 1996 - cell.com
Background: Stromelysin belongs to a family of zinc-dependent endopeptidases referred to
as matrix metalloproteinases (MMPs, matrixins) because of their capacity for selective …
as matrix metalloproteinases (MMPs, matrixins) because of their capacity for selective …
Structure–activity relationships by mass spectrometry: identification of novel MMP-3 inhibitors
DA Ockey, JL Dotson, ME Struble, JT Stults… - Bioorganic & medicinal …, 2004 - Elsevier
A novel class of nonpeptide inhibitors of stromelysin (MMP-3) has been discovered with the
use of mass spectrometry. The method relies on the development of structure–activity …
use of mass spectrometry. The method relies on the development of structure–activity …