Journal of Medicinal Chemistry · 2006 · 30 citations · 25 references
MedicineMedicinal ChemistryPharmacologyCell SignalingDrug DiscoveryMolecular PharmacologyChannel StructureEnzyme InhibitionIon Channel PharmacologyIon Channel PhysiologyIon Channel RegulationIon ChannelsGlucose-dependent Insulin SecretionGlucose-responsive ReleaseGlucose-stimulated Insulin SecretionIon Channel Structure-function RelationshipsPotassium Channel FunctionPotassium Channel OpenersPotassium Channel PharmacologyPotassium Channel Physiology
Compound 1a (NN414) is a potent opener of Kir6.2/SUR1 K(ATP) channels. Compound 1a inhibits insulin release in vitro and in vivo and preserves beta cell function in preclinical animal models suggesting that such a compound could find use in treatment or prevention of type 1 and type 2 diabetes. The crystal structure and a convergent synthesis of 1a are presented together with a range of new analogues of 1a. Several compounds, e.g., 6-chloro-3-(1-methyl-1-phenylethyl)amino-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-dioxide (1h), were found to be potent openers of Kir6.2/SUR1 K(ATP) channels and were able to suppress glucose-stimulated insulin release from rat islets in vitro (EC(50) = 0.04 +/- 0.01 muM) and in vivo after intravenous or peroral administration to hyperinsulinemic obese Zucker rats (ED(50) = 4.0 mg/kg). Structural modifications of this series of K(ATP) channel openers have provided compounds with promising pharmacokinetic properties indicating that brief periods of beta cell rest can be achieved.
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Phosphorus in organic synthesis—VII
Kunihiro Ninomiya, Takayuki Shioiri, Susumu Yamada · Tetrahedron · 1974 · 364 citations
Kathrin Maedler, Joachim Størling, Jeppe Sturis et al. · Diabetes · 2004 · 145 citations