Hydroxyl-Substituted sulfonylureas as potent inhibitors of specific [3H]Glyburide binding to rat brain synaptosomes-Reference-Cited by-同舟云学术

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Hydroxyl-Substituted sulfonylureas as potent inhibitors of specific [3H]Glyburide binding to rat brain synaptosomes

Published:2003-05 Issue:9 Volume:11 Page:2099-2113
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Hill Ronald A.,Rudra Sonali,Peng Bo,Roane David S.,Bounds Jeffrey K.,Zhang Yang,Adloo Ahmad,Lu Tiansheng

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference109 articles.

1. Specific receptors for sulfonylureas in brain and in a B-cell tumor of the rat

2. A binding site for [3H]glipizide in the rat cerebral cortex

3. Adenosine-5′-triphosphate-sensitive ion channels in neonatal rat cultured central neurones

4. Characterization, purification, and affinity labeling of the brain [3H]glibenclamide-binding protein, a putative neuronal ATP-regulated K+ channel.

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