Rapid preparation of (3R,4S,5R) polyhydroxylated pyrrolidine-based libraries to discover a pharmacological chaperone for treatment of Fabry disease-Reference-Cited by-同舟云学术

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Rapid preparation of (3R,4S,5R) polyhydroxylated pyrrolidine-based libraries to discover a pharmacological chaperone for treatment of Fabry disease

Published:2017-01 Issue: Volume:126 Page:1-6
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Cheng Wei-Chieh,Wang Jen-Hon,Yun Wen-Yi,Li Huang-Yi,Hu Jia-Ming

Funder

Ministry of Science and Technology

Academia Sinica

Taiwan Foundation For Rare Disorders

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference28 articles.

1. Fabry disease – current treatment and new drug development;Motabar;Curr. Chem. Genom.,2010

2. Molecular basis of 1-deoxygalactonojirimycin arylthiourea binding to human α-galactosidase A: pharmacological chaperoning efficacy on Fabry disease mutants;Yu;ACS Chem. Biol.,2014

3. Newborn screening for Fabry disease by measuring GLA activity using tandem mass spectrometry;Dajnoki;Clin. Chim. Acta,2010

4. Safety and efficacy of recombinant human α-galactosidase A replacement therapy in Fabry's disease;Eng;N. Engl. J. Med.,2001

5. Enzyme replacement therapy in Fabry disease: a randomized controlled trial;Schiffmann;JAMA,2001

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