12 Modeling of Stromelysins Inhibitors

SK Baidya, S Banerjee, N Adhikari… - Modeling Inhibitors of …, 2023 - books.google.com
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 …

Modeling Inhibitors of Stromelysins

SK Baidya, S Banerjee, N Adhikari… - Modeling Inhibitors of …, 2023 - taylorfrancis.com
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) …

Stromelysins and Their Inhibitors

SK Baidya, S Banerjee, N Adhikari… - Modeling Inhibitors of …, 2023 - taylorfrancis.com
Stromelysins are a matrix metalloproteinase (MMP) family member—a zinc-dependent
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 …

[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 …

Potent, selective pyrone-based inhibitors of stromelysin-1

DT Puerta, J Mongan, BL Tran… - Journal of the …, 2005 - ACS Publications
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 …

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 …

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 …

[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 …

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 …