Conantokins Derived from the Asprella Clade Impart conRl-B, an N-Methyl d-Aspartate Receptor Antagonist with a Unique Selectivity Profile for NR2B Subunits-Reference-Cited by-同舟云学术

Conantokins Derived from the Asprella Clade Impart conRl-B, an N-Methyl d-Aspartate Receptor Antagonist with a Unique Selectivity Profile for NR2B Subunits

Published:2012-05-30 Issue:23 Volume:51 Page:4685-4692
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Gowd Konkallu Hanumae¹,Han Tiffany S.,Twede Vernon,Gajewiak Joanna,Smith Misty D.,Watkins Maren,Platt Randall J.,Toledo Gabriela,White H. Steve,Olivera Baldomero M.,Bulaj Grzegorz

Affiliation:

1. Molecular Biophysics Unit, Indian Institute of Science, Bangalore 560012, India

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi300055n

Reference55 articles.

1. NMDA receptor antagonists as analgesics: focus on the NR2B subtype

2. Pharmacological Characterization of Ro 63-1908 (1-[2-(4-Hydroxy-phenoxy)-ethyl]-4-(4-methyl-benzyl)-piperidin-4-ol), a Novel Subtype-SelectiveN-Methyl-d-Aspartate Antagonist

3. Quinazolin-4-one Derivatives: A Novel Class of Noncompetitive NR2C/D Subunit-Selective N-Methyl-d-aspartate Receptor Antagonists

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