Direct Activation of β-Cell KATP Channels with a Novel Xanthine Derivative-Reference-Cited by-同舟云学术

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Direct Activation of β-Cell KATP Channels with a Novel Xanthine Derivative

Published:2014-03-19 Issue:6 Volume:85 Page:858-865
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Raphemot Rene,Swale Daniel R.,Dadi Prasanna K.,Jacobson David A.,Cooper Paige,Wojtovich Andrew P.,Banerjee Sreedatta,Nichols Colin G.,Denton Jerod S.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference48 articles.

1. Sulfonylurea Receptor-Dependent and -Independent Pathways Mediate Vasodilation Induced by ATP-Sensitive K+ Channel Openers

2. 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

3. Adenosine 5'-Triphosphate-Sensitive Potassium Channels

4. ATP-sensitive K+ channels and disease: from molecule to malady

5. NN414, a SUR1/Kir6.2-Selective Potassium Channel Opener, Reduces Blood Glucose and Improves Glucose Tolerance in the VDF Zucker Rat

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2. Discovery and Characterization of VU0542270, the First Selective Inhibitor of Vascular Kir6.1/SUR2B K_ATPChannels;Molecular Pharmacology;2024-02-01

3. Non-radioactive Rb+ Efflux Assay for Screening KATP Channel Modulators;Methods in Molecular Biology;2024

4. Therapeutic Targeting of Potassium Channels;Ion Channels as Targets in Drug Discovery;2024

5. Pulmonary hypertension associated with diazoxide: the SUR1 paradox;ERJ Open Research;2023-10-12

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