A New Class of Conformationally Rigid Analogues of 4-Amino-5-halopentanoic Acids, Potent Inactivators of γ-Aminobutyric Acid Aminotransferase-Reference-Cited by-同舟云学术

A New Class of Conformationally Rigid Analogues of 4-Amino-5-halopentanoic Acids, Potent Inactivators of γ-Aminobutyric Acid Aminotransferase

Published:2000-02-01 Issue:4 Volume:43 Page:706-720
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Qiu Jian¹,Silverman Richard B.¹

Affiliation:

1. Department of Chemistry and Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston, Illinois 60208-3113

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm9904755

Reference34 articles.

1. The γ-Aminobutyric Acid-α-Ketoglutaric Acid Transaminase of Beef Brain

2. Effect of ethanolamine-O-sulphate on regional gaba metabolism in the mouse brain

3. The effects of sodium valproate on γ-aminobutyrate metabolism and behaviour in naive and ethanolamine-O-sulphate pretreated rats and mice

4. GABA in Epilepsy: The Pharmacologic Basis

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