Isradipine

Pricing Availability   Qty
说明: CaV1.x blocker
别名: PN 200-110
化学名: 4-(2,1,3-Benzoxadiazol-4-yl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinecarboxylic acid methyl 1-methylethyl ester
纯度: ≥98% (HPLC)
说明书
引用文献 (6)
评论

生物活性 for Isradipine

Isradipine is a potent and selective L-type voltage-gated Ca2+ channel blocker. EC50 and pA2 values are 1.4 nM and 10.3 for relaxation of depolarization- and Ca2+-induced contractions of rabbit aorta respectively; EC25 = 0.45 nM for reduction in rate of spontaneously beating guinea pig right atria. Long-acting antihypertensive agent in vivo, exerting primary effects on vascular tissue with secondary negative chronotropic action.

化合物库 for Isradipine

Isradipine is also offered as part of the Tocriscreen 2.0 Max and Tocriscreen FDA-Approved Drugs. 了解 Tocris 化合物库的更多信息。

技术数据 for Isradipine

分子量 371.39
公式 C19H21N3O5
储存 Store at RT
纯度 ≥98% (HPLC)
CAS Number 75695-93-1
PubChem ID 3784
InChI Key HMJIYCCIJYRONP-UHFFFAOYSA-N
Smiles COC(=O)C1=C(C)NC(C)=C(C1C1=CC=CC2=NON=C12)C(=O)OC(C)C

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.

溶解性数据 for Isradipine

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 18.57 50
ethanol 7.43 20

制备储备液 for Isradipine

以下数据基于产品分子量 371.39。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
0.5 mM 5.39 mL 26.93 mL 53.85 mL
2.5 mM 1.08 mL 5.39 mL 10.77 mL
5 mM 0.54 mL 2.69 mL 5.39 mL
25 mM 0.11 mL 0.54 mL 1.08 mL

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参考文献 for Isradipine

参考文献是支持产品生物活性的出版物。

Hof et al (1984) PN 200-110, a new calcium antagonist: electrophysiological, inotropic, and chronotropic effects on guinea pig myocardial tissue and effects on contraction and calcium uptake of rabbit aorta. J.Cardiovasc.Pharmacol. 6 399 PMID: 6202964

Wada et al (1985) Separation of the coronary vasodilator from the cardiac effects of PN 200-110, a new dihydropyridine calcium antagonist, in the dog heart. J.Cardiovasc.Pharmacol. 7 190 PMID: 2580142

Ruegg and Hof (1990) Pharmacology of the calcium antagonist israd. Drugs 40 3


If you know of a relevant reference for Isradipine, please let us know.

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查看全部 CaV1.x Channel (L-type) Blockers

关键词: Isradipine, Isradipine supplier, Ca2+, channel, blockers, L-type, Calcium, CaV, Channels, voltage-gated, voltage-dependent, PN200110, PN, 200-110, Cav1.x, 2004, Tocris Bioscience

6 篇 Isradipine 的引用文献

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

Pourbadie et al (2015) Preventing effect of L-type calcium channel blockade on electrophysiological alterations in dentate gyrus granule cells induced by entorhinal amyloid pathology. J Neurosci 10 e0117555 PMID: 25689857

McKeithan et al (2017) An Automated Platform for Assessment of Congenital and Drug-Induced Arrhythmia with hiPSC-Derived Cardiomyocytes. Front Physiol 8 766 PMID: 29075196

Dragicevic et al (2014) Cav1.3 channels control D2-autoreceptor responses via NCS-1 in substantia nigra DA neurons. PLoS One 137 2287 PMID: 24934288

Winland et al (2017) Inflammation alters AMPA-stimulated calcium responses in dorsal striatal D2 but not D1 spiny projection neurons. Eur J Neurosci 46 2519 PMID: 28921719


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