Abstract
SH2 domains are discrete structural motifs common to a variety of critical intracellular signaling proteins. Inhibitors of specific SH2 domains have become important therapeutic targets in the treatment and/or prevention of restenosis, cancers (including small cell lung), cardiovascular disease, osteoporosis, apoptosis among others. Considering the social and economic impact of these diseases significant attention has been focused on the development of potent and selective inhibitors of specific SH2 domains. In particular, considerable research has been performed on Src, PI 3-kinase, Grb2 and more recently, Lck. In this review, we will focus on progress in the development of inhibitors for these specific SH2 domains and evaluate potential future targets.
Keywords: inhibitors, SH2 Domains, signaling proteins, intracellular, restenosis, cancer, small cell lung, cardiovascular disease, Lck, apoptosis, osteporosis, Src PI3 kinase Grb2, receptor, tyrosine kinases RTK, Fgr, Yrk, Fyn, HcK, Blk, mechansims, platelet derived growth factor PDGF, hepatovyte, fibroblast growth factor FGF, epidermal, focal adhesion kinase, mitogen activated protein kinase, FAK, Cortactin
Current Pharmaceutical Design
Title: Progress in the Development of Inhibitors of SH2 Domains
Volume: 6 Issue: 1
Author(s): Wayne L. Cody, Zhiwu Lin, Robert L. Panek, David W. Rose and John R. Rubin
Affiliation:
Keywords: inhibitors, SH2 Domains, signaling proteins, intracellular, restenosis, cancer, small cell lung, cardiovascular disease, Lck, apoptosis, osteporosis, Src PI3 kinase Grb2, receptor, tyrosine kinases RTK, Fgr, Yrk, Fyn, HcK, Blk, mechansims, platelet derived growth factor PDGF, hepatovyte, fibroblast growth factor FGF, epidermal, focal adhesion kinase, mitogen activated protein kinase, FAK, Cortactin
Abstract: SH2 domains are discrete structural motifs common to a variety of critical intracellular signaling proteins. Inhibitors of specific SH2 domains have become important therapeutic targets in the treatment and/or prevention of restenosis, cancers (including small cell lung), cardiovascular disease, osteoporosis, apoptosis among others. Considering the social and economic impact of these diseases significant attention has been focused on the development of potent and selective inhibitors of specific SH2 domains. In particular, considerable research has been performed on Src, PI 3-kinase, Grb2 and more recently, Lck. In this review, we will focus on progress in the development of inhibitors for these specific SH2 domains and evaluate potential future targets.
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Cite this article as:
Cody L. Wayne, Lin Zhiwu, Panek L. Robert, Rose W. David and Rubin R. John, Progress in the Development of Inhibitors of SH2 Domains, Current Pharmaceutical Design 2000; 6 (1) . https://dx.doi.org/10.2174/1381612003401532
DOI https://dx.doi.org/10.2174/1381612003401532 |
Print ISSN 1381-6128 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-4286 |
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