Loratadine and Analogues: Discovery and Preliminary Structure–Activity Relationship of Inhibitors of the Amino Acid Transporter B0AT2-Reference-Cited by-同舟云学术

Loratadine and Analogues: Discovery and Preliminary Structure–Activity Relationship of Inhibitors of the Amino Acid Transporter B0AT2

Published:2014-11-07 Issue:22 Volume:57 Page:9473-9479
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Cuboni Serena¹,Devigny Christian¹,Hoogeland Bastiaan¹,Strasser Andrea²,Pomplun Sebastian¹,Hauger Barbara¹,Höfner Georg³,Wanner Klaus T.³,Eder Matthias¹,Buschauer Armin²,Holsboer Florian¹,Hausch Felix¹

Affiliation:

1. Max Planck Institute of Psychiatry, 80804 Munich, Germany

2. Institute of Pharmacy, University of Regensburg, 93053 Regensburg, Germany

3. Department of Pharmacy, Ludwig-Maximilians-University München, 80539 Munich, Germany

Funder

HolsboerMaschmeyer NeuroChemie GmbH

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm501086v

Reference33 articles.

1. The solute carrier 6 family of transporters

2. SLC6 Neurotransmitter Transporters: Structure, Function, and Regulation

3. The SLC6 transporters: perspectives on structure, functions, regulation, and models for transporter dysfunction

4. The orphan transporter v7-3 (slc6a15) is a Na+-dependent neutral amino acid transporter (B0AT2)

5. Characterization of a branched-chain amino-acid transporter SBAT1 (SLC6A15) that is expressed in human brain

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