Evaluation of 2-thioxo-2,3,5,6,7,8-hexahydropyrimido[4,5-d]pyrimidin-4(1H)-one analogues as GAA activators-Reference-Cited by-同舟云学术

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Evaluation of 2-thioxo-2,3,5,6,7,8-hexahydropyrimido[4,5-d]pyrimidin-4(1H)-one analogues as GAA activators

Published:2010-05 Issue:5 Volume:45 Page:1880-1897
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Marugan Juan J.,Zheng Wei,Motabar Omid,Southall Noel,Goldin Ehud,Sidransky Ellen,Aungst Ronald A.,Liu Ke,Sadhukhan Subir Kumar,Austin Christopher P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference26 articles.

1. Glycogen storage disease type II: acid α- glucosidase (acid maltase) deficiency;Hirschhorn,2001

2. Carrier frequency for glycogen storage disease type II in New York and estimates of affected individuals born with the disease

3. Acid a-Glucosidase Deficiency (Glycogenosis Type II, Pompe Disease)

4. Glycogenosis type II: identification and expression of three novel mutations in the acid α-glucosidase gene causing the infantile form of the disease

5. Twenty-two novel mutations in the lysosomal ?-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II

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1. Molecular Construction Using Formamide as a C1 Feedstock;European Journal of Organic Chemistry;2024-01-15

2. 1,6-epi-Cyclophellitol Cyclosulfamidate Is a Bona Fide Lysosomal α-Glucosidase Stabilizer for the Treatment of Pompe Disease;Journal of the American Chemical Society;2022-08-02

3. Pharmacological Chaperone Therapy for Pompe Disease;Molecules;2021-11-29

4. Carnitine is a pharmacological allosteric chaperone of the human lysosomal α-glucosidase;Journal of Enzyme Inhibition and Medicinal Chemistry;2021-01-01

5. Second-Generation Pharmacological Chaperones: Beyond Inhibitors;Molecules;2020-07-09

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