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Structure-based design, synthesis, and SAR exploration of pyrrole-2-one analogues as inhibitors of the annexin A2-S100A10 protein interaction : Potential anti-angiogenesis therapeutics

dc.contributor.authorReddy, Tummala Rama Krishna
dc.contributor.authorLi, Chan
dc.contributor.authorGuo, Xiaoxia
dc.contributor.authorFischer, Peter
dc.contributor.authorDekker, Lodewijk
dc.date.accessioned2014-07-28T13:00:24Z
dc.date.available2014-07-28T13:00:24Z
dc.date.issued2010
dc.identifier.citationReddy , T R K , Li , C , Guo , X , Fischer , P & Dekker , L 2010 , ' Structure-based design, synthesis, and SAR exploration of pyrrole-2-one analogues as inhibitors of the annexin A2-S100A10 protein interaction : Potential anti-angiogenesis therapeutics ' , Journal of Pharmacy and Pharmacology , vol. 62 , no. 10 , pp. 1373-1374 .
dc.identifier.issn2042-7158
dc.identifier.urihttp://hdl.handle.net/2299/14103
dc.descriptionAbstract from UK-PharmSci Conference 1-3 Sept 2010
dc.language.isoeng
dc.relation.ispartofJournal of Pharmacy and Pharmacology
dc.titleStructure-based design, synthesis, and SAR exploration of pyrrole-2-one analogues as inhibitors of the annexin A2-S100A10 protein interaction : Potential anti-angiogenesis therapeuticsen
dc.contributor.institutionDepartment of Pharmacy
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionMedicinal and Analytical Chemistry
dc.description.statusPeer reviewed
rioxxterms.typeOther
herts.preservation.rarelyaccessedtrue


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