Herapin mimetics

Explorations of the therapeutic potential of heparin mimetics, anionic compounds that are analogues of glycosaminoglycans (GAGs), have gone hand-in-hand with the emergence of understanding as to the role of GAGs in many essential biological processes. A myriad of structurally different heparin mimet...

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Main Authors: Coombe, Deirdre, Kett, Warren
Other Authors: Lever, Rebecca
Format: Book Chapter
Published: Springer 2012
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/43614
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author Coombe, Deirdre
Kett, Warren
author2 Lever, Rebecca
author_facet Lever, Rebecca
Coombe, Deirdre
Kett, Warren
author_sort Coombe, Deirdre
building Curtin Institutional Repository
collection Online Access
description Explorations of the therapeutic potential of heparin mimetics, anionic compounds that are analogues of glycosaminoglycans (GAGs), have gone hand-in-hand with the emergence of understanding as to the role of GAGs in many essential biological processes. A myriad of structurally different heparin mimetics have been prepared and examined in many diverse applications. They range in complexity from heterogeneous polysaccharides that have been chemically sulphated to well-defined compounds, designed in part to mimic the natural ligand, but with binding specificity and potency increased by conjugation to non-carbohydrate pharmacophores. The maturity of the field is illustrated by the seven heparin mimetics that have achieved marketing approval and there are several more in late-stage clinical development. An overview of the structural determinants of heparin mimetics is presented together with an indication of their activities. The challenges in developing heparin mimetics as drugs, specificity and potential toxicity issues, are highlighted. Finally, the development path of three structurally very different mimetics, PI-88®, GMI-1070 and RGTAs, each of which is in clinical trials, is described.
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spelling curtin-20.500.11937-436142023-02-07T08:01:21Z Herapin mimetics Coombe, Deirdre Kett, Warren Lever, Rebecca Mulloy, Barbara Page, Clive P. Heparin-mimetic GMI-1070 Glycosaminoglycan RGTAs PI-88 Heparin Explorations of the therapeutic potential of heparin mimetics, anionic compounds that are analogues of glycosaminoglycans (GAGs), have gone hand-in-hand with the emergence of understanding as to the role of GAGs in many essential biological processes. A myriad of structurally different heparin mimetics have been prepared and examined in many diverse applications. They range in complexity from heterogeneous polysaccharides that have been chemically sulphated to well-defined compounds, designed in part to mimic the natural ligand, but with binding specificity and potency increased by conjugation to non-carbohydrate pharmacophores. The maturity of the field is illustrated by the seven heparin mimetics that have achieved marketing approval and there are several more in late-stage clinical development. An overview of the structural determinants of heparin mimetics is presented together with an indication of their activities. The challenges in developing heparin mimetics as drugs, specificity and potential toxicity issues, are highlighted. Finally, the development path of three structurally very different mimetics, PI-88®, GMI-1070 and RGTAs, each of which is in clinical trials, is described. 2012 Book Chapter http://hdl.handle.net/20.500.11937/43614 Springer restricted
spellingShingle Heparin-mimetic
GMI-1070
Glycosaminoglycan
RGTAs
PI-88
Heparin
Coombe, Deirdre
Kett, Warren
Herapin mimetics
title Herapin mimetics
title_full Herapin mimetics
title_fullStr Herapin mimetics
title_full_unstemmed Herapin mimetics
title_short Herapin mimetics
title_sort herapin mimetics
topic Heparin-mimetic
GMI-1070
Glycosaminoglycan
RGTAs
PI-88
Heparin
url http://hdl.handle.net/20.500.11937/43614