Cromakalim

Discontinued Product

1377 has been discontinued.

View all Inward Rectifier Potassium (K<sub>ir</sub>) Channels products.
说明: Kir6 (KATP) channel opener
别名: BRL 34915
化学名: trans-3,4-dihydro-3-hydroxy-2,2-dimethyl-4-(2-oxo-1-pyrrolidinyl)-2H-1-benzopyran-6-carbonitrile
纯度: ≥99% (HPLC)
说明书
引用文献 (7)
评论 (1)

生物活性 for Cromakalim

Cromakalim is a prototypical Kir6 (KATP) channel opener. Relaxes rabbit isolated portal vein with an IC50 value of 21 nM. Potent, orally active and hypotensive in vivo.

Active Enantiomer also available.

许可信息

Sold under license

技术数据 for Cromakalim

分子量 286.33
公式 C16H18N2O3
储存 Store at RT
纯度 ≥99% (HPLC)
CAS Number 94470-67-4
PubChem ID 76968376
InChI Key BVMDRSUIADWFLV-PNSAJKJISA-N
Smiles O=C1CCCN1[C@H]2[C@H](O)C(C)(C)OC3=C2C=C(C#N)C=C3.O=C4CCCN4[C@@H]5[C@@H](O)C(C)(C)OC6=C5C=C(C#N)C=C6

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

参考文献 for Cromakalim

参考文献是支持产品生物活性的出版物。

Escande et al (1988) The potassium channel opener cromakalim (BRL 34915) activates ATP-dependent K+ channels in isolated cardiac myocytes. Biochem.Biophys.Res.Commun. 154 620 PMID: 2456760

Longman et al (1988) Cromakalim, a potassium channel activator: a comparison of its cardiovascular haemodynamic profile and tissue specificity with those of pinacidil and nicorandil. J.Cardiovasc.Pharmacol. 12 535 PMID: 2468052

Wilson et al (1988) Comparative effects of K+ channel blockade on the vasorelaxant activity of cromakalim, pinacidil and nicorandil. Eur.J.Pharmacol. 152 331 PMID: 2851450

关键词: Cromakalim, Cromakalim supplier, KATP, channel, openers, Potassium, KIR, Kir6, Channels, Inward, Rectifier, K+, BRL34915, BRL, 34915, rectifier, 1377, Tocris Bioscience

7 篇 Cromakalim 的引用文献

引用文献是使用了 Tocris 产品的出版物。 Cromakalim 的部分引用包括:

Mathias and Weid (2013) Involvement of the NO-cGMP-K(ATP) channel pathway in the mesenteric lymphatic pump dysfunction observed in the guinea pig model of TNBS-induced ileitis. Am J Physiol Gastrointest Liver Physiol 304 G623 PMID: 23275612

Mehmood et al (2015) Antidiarrhoeal, antisecretory and antispasmodic activities of Matricaria chamomilla are mediated predominantly through K(+)-channels activation. PLoS One 15 75 PMID: 25886126

Institóris et al (2011) Impaired vascular responses of Ins-resistant rats after mild subarachnoid hemorrhage. PLoS One 300 H2080 PMID: 21421821

Seto et al (2013) Acute SimV. inhibits K ATP channels of porcine coronary artery myocytes. Am J Physiol Heart Circ Physiol 8 e66404 PMID: 23799098

Lasker et al (2013) The sGC activator BAY 60-2770 has potent erectile activity in the rat. Am J Physiol Heart Circ Physiol 304 H1670 PMID: 23585129

Erdos et al (2002) Alterations in KATP and KCa channel function in cerebral arteries of Ins-resistant rats. Am J Physiol Heart Circ Physiol 283 H2472 PMID: 12388242

Whidden et al (2016) Altered potassium ATP channel signaling in mesenteric arteries of old high salt-fed rats. J Exerc Nutrition Biochem 20 58 PMID: 27508155


Cromakalim 的评论

平均评分: 5 (Based on 1 Review.)

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Cromakalim used to study BK channel modulation.
By Sadequl Islam on 11/27/2018
分析类型: In Vitro
种属: Human

Cromakalim was used to assess the channel opening properties when used on cell line that express BK channels. Gives consistent result that is reproducible.

review image