Structure-Activity Relationships, Pharmacokinetics, and Pharmacodynamics of the Kir6.2/SUR1-Specific Channel Opener VU0071063-Reference-Cited by-同舟云学术

Structure-Activity Relationships, Pharmacokinetics, and Pharmacodynamics of the Kir6.2/SUR1-Specific Channel Opener VU0071063

Published:2019-06-14 Issue:3 Volume:370 Page:350-359
ISSN:0022-3565
Container-title:Journal of Pharmacology and Experimental Therapeutics
language:en
Short-container-title:J Pharmacol Exp Ther

Author:

Kharade Sujay V.,Sanchez-Andres Juan Vicente,Fulton Mark G.,Shelton Elaine L.,Blobaum Anna L.,Engers Darren W.,Hofmann Christopher S.,Dadi Prasanna K.,Lantier Louise,Jacobson David A.,Lindsley Craig W.,Denton Jerod S.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference58 articles.

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2. Cloning of the β Cell High-Affinity Sulfonylurea Receptor: a Regulator of Insulin Secretion

3. Attenuation of hyperinsulinemia by NN414, a SUR1/Kir6.2 selective K+-adenosine triphosphate channel opener, improves glucose tolerance and lipid profile in obese Zucker rats

4. The ATP-Sensitive Potassium Channel Subunit, Kir6.1, in Vascular Smooth Muscle Plays a Major Role in Blood Pressure Control

5. Involvement of hippocampal CA3 KATP channels in contextual memory

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