Literature DB >> 30736134

Eliglustat tartrate, a prototypic glucosylceramide synthase inhibitor.

James A Shayman1.   

Abstract

Eliglustat tartrate is a highly specific inhibitor of glucosylceramide synthase, developed for the treatment glucosylceramide-based glycosphingolipidoses. Eliglustat is in late clinical development for Gaucher disease type 1. Phase II and III clinical trials have demonstrated clinical efficacy for eliglustat as a stand-alone agent for newly diagnosed patients that are naïve to prior therapy and for patients who have been previously treated with enzyme replacement therapy. Importantly, the reported toxicity of eliglustat has been limited. Eliglustat will be submitted for the US FDA and EMA review in late 2013. Several structurally unrelated glucosylceramide synthase inhibitors have been identified and are in various stages of development, some of which cross the blood-brain barrier. Targeting glucosylceramide synthesis is also a promising approach for the treatment of type 2 diabetes mellitus, autosomal dominant polycystic kidney disease and certain cancers.

Entities:  

Keywords:  Fabry disease; Gaucher disease; glucosylceramide; glycosphingolipid; polycystic kidney disease; type 2 diabetes mellitus

Year:  2013        PMID: 30736134     DOI: 10.1586/17446651.2013.846213

Source DB:  PubMed          Journal:  Expert Rev Endocrinol Metab        ISSN: 1744-6651


  4 in total

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2.  Optimization of Eliglustat-Based Glucosylceramide Synthase Inhibitors as Substrate Reduction Therapy for Gaucher Disease Type 3.

Authors:  Michael W Wilson; Liming Shu; Vania Hinkovska-Galcheva; Yafei Jin; Walajapet Rajeswaran; Akira Abe; Ting Zhao; Ruijuan Luo; Lu Wang; Bo Wen; Benjamin Liou; Venette Fannin; Duxin Sun; Ying Sun; James A Shayman; Scott D Larsen
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3.  Inhibition of P-Glycoprotein Does Not Increase the Efficacy of Proteasome Inhibitors in Multiple Myeloma Cells.

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Journal:  ACS Pharmacol Transl Sci       Date:  2021-02-04

4.  Endocytosis, Cytotoxicity, and Translocation of Shiga Toxin-2 Are Stimulated by Infection of Human Intestinal (HCT-8) Monolayers With an Hypervirulent E. coli O157:H7 Lacking stx2 Gene.

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Journal:  Front Cell Infect Microbiol       Date:  2019-11-21       Impact factor: 5.293

  4 in total

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