Cat. No. 1355
Chemical Name: N-cyano-N'-(1,1-dimethylpropyl)-N''-3-
Biological ActivityPotent Kir6 (KATP) channel opener (EC50 for relaxation of rat aorta = 7.5 nM). Binds to SUR2A and SUR2B with high affinity (Kd values are 17 and 3 nM respectively).
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Certificate of Analysis / Safety Data Sheet
Higdon et al (1997) Tissue and species variation in the vascular receptor binding of 3H-P1075, a potent KATP opener vasodilator. J.Pharmacol.Exp.Ther. 280 255. PMID: 8996204.
Gross et al (1999) Stoichiometry of potassium channel opener action. Mol.Pharmacol. 56 1370. PMID: 10570067.
Ashcroft and Gribble (2000) New windows on the mechanism of action of KATP channel openers. TiPS 21 439. PMID: 11121575.
Buckner et al (2000) Pharmacological and molecular analysis of ATP-sensitive K+ channels in the pig and human detrusor. Eur.J.Pharmacol. 400 287. PMID: 10988346.
If you know of a relevant citation for this product please let us know.
Keywords: P1075, supplier, Potent, KATP, channel, openers, Potassium, KIR, Channels, Inward, Rectifier, K+, Kir6
Find multiple products by catalog number
New Products in this Area
Potent TASK-3 channel blockerML 297
Selective Kir3.1/3.2 (GIRK1/2) channel activatorML 365
Potent and selective TASK-1 channel blockerHMR 1556
Potent and selective Iks channel blockerNS 19504
Activator of BKCa (KCa1.1) channels
May 19 - 22, 2015