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dc.contributor.authorWALSH, JOHNen
dc.date.accessioned2014-12-11T10:42:00Z
dc.date.available2014-12-11T10:42:00Z
dc.date.issued2013en
dc.date.submitted2013en
dc.identifier.citationFinn, D.F., Walsh, J.J., Twenty-first century mast cell stabilizers, British Journal of Pharmacology, 170, 1, 2013, 23-37en
dc.identifier.issn00071188en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractMast cell stabilizing drugs inhibit the release of allergic mediators from mast cells and are used clinically to prevent allergic reactions to common allergens. Despite the relative success of the most commonly prescribed mast cell stabilizer, disodium cromoglycate, in use for the preventative treatment of bronchial asthma, allergic conjunctivitis and vernal keratoconjunctivitis, there still remains an urgent need to design new substances that are less expensive and require less frequent dosing schedules. In this regard, recent developments towards the discovery of the next generation of mast cell stabilizing drugs has included studies on substances isolated from natural sources, biological, newly synthesized compounds and drugs licensed for other indications. The diversity of natural products evaluated range from simple phenols, alkaloids, terpenes to simple amino acids. While in some cases their precise mode of action remains unknown it has nevertheless sparked interest in the development of synthetic derivatives with improved pharmacological properties. Within the purely synthetic class of inhibitors, particular attention has been devoted to the inhibition of important signalling molecules including spleen TK and JAK3. The statin class of cholesterol-lowering drugs as well as nilotinib, a TK inhibitor, are just some examples of clinically used drugs that have been evaluated for their anti-allergic properties. Here, we examine each approach under investigation, summarize the test data generated and offer suggestions for further preclinical evaluation before their therapeutic potential can be realized.en
dc.description.sponsorshipDF is grateful to Enterprise Ireland for financial support CFTD/2004/115. We wish to thank Sheila Ryder for her assist- ance in producing Figure 1en
dc.format.extent23-37en
dc.language.isoenen
dc.relation.ispartofseriesBritish Journal of Pharmacologyen
dc.relation.ispartofseries170en
dc.relation.ispartofseries1en
dc.rightsYen
dc.subjectTK inhibitor,en
dc.subject.lcshTK inhibitor,en
dc.titleTwenty-first century mast cell stabilizersen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/walshj1en
dc.identifier.peoplefinderurlhttp://people.tcd.ie/jjwalshen
dc.identifier.rssinternalid93377en
dc.identifier.doihttp://dx.doi.org/10.1111/bph.12138en
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeImmunology, Inflammation & Infectionen
dc.identifier.urihttp://hdl.handle.net/2262/72416


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