Veratridine

Pricing Availability   Qty
说明: Voltage-gated Na+ channel opener
化学名: 4α,9-Epoxy-3β-veratroyloxy-5β-cevan-4β,12,14,16β,17,20-hexaol
纯度: ≥98% (HPLC)
说明书
引用文献 (6)
评论 (2)

生物活性 for Veratridine

Veratridine is a voltage-gated Na+ channel opener; increases intracellular Ca2+ with no effect on the Na+/Ca2+ exchanger. Steroid-derived alkaloid neurotoxin. Increases membrane Na+ permeability and depolarizes excitable tissues.

技术数据 for Veratridine

分子量 673.79
公式 C36H51NO11
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 71-62-5
PubChem ID 6280
InChI Key FVECELJHCSPHKY-YFUMOZOISA-N
Smiles O=C(C8=CC=C(OC)C(OC)=C8)O[C@H]1CC[C@@]2(C)[C@@]3([H])[C@@](O)1O[C@@]42[C@@]([C@@](C[C@H](O)[C@@]6(O)[C@]([H])5CN7[C@](CC[C@H](C)C7)([H])[C@@](O)6C)(O)[C@@]5(O)C4)([H])CC3

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 Veratridine

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 33.69 50

制备储备液 for Veratridine

以下数据基于产品分子量 673.79。 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 2.97 mL 14.84 mL 29.68 mL
2.5 mM 0.59 mL 2.97 mL 5.94 mL
5 mM 0.3 mL 1.48 mL 2.97 mL
25 mM 0.06 mL 0.3 mL 0.59 mL

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产品说明书 for Veratridine

分析证书/产品说明书
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参考文献 for Veratridine

参考文献是支持产品生物活性的出版物。

McKinney et al (1986) Purification, solubility and pKa of veratridine. Anal.Biochem. 153 33 PMID: 3963380

Maroto et al (1994) Effects of Ca2+ channel antagonists on chromaffin cell death and cytosolic Ca2+ oscillations induced by veratridine. Eur.J.Pharmacol. 270 331 PMID: 7805782

Fekete et al (2009) Mechanism of the persistant sodium current activator veratridine-evoked Ca2+ elevation: implication for epilepsy. J.Neurochem. 111 745 PMID: 19719824


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

关键词: Veratridine, Veratridine supplier, Sodium, channel, opener, neutoxin, Na+, Na, voltage-gated, ion, channels, neurotoxins, Voltage-gated, Channels, 2918, Tocris Bioscience

6 篇 Veratridine 的引用文献

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

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

Agarwal et al (2017) Transient Opening of the Mitochondrial Permeability Transition Pore Induces Microdomain Calcium Transients in Astrocyte Processes. Neuron 93 587 PMID: 28132831

Malmersjö et al (2013) Neural progenitors organize in small-world networks to promote cell proliferation. Nat Commun 110 E1524 PMID: 23576737

Bedut et al (2016) High-throughput drug profiling with voltage- and calcium-sensitive fluorescent probes in human iPSC-derived cardiomyocytes. Am J Physiol Heart Circ Physiol 311 H44 PMID: 27199128


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Veratridine 的评论

平均评分: 5 (基于 2 条评论。)

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Voltage sensitive sodium channel opening.
By Anonymous on 11/19/2018
分析类型: Ex Vivo
种属: Mouse

Can be used to activate and open voltage sensitive sodium channels in neurons. Elicits rapid reaction when applied directly to tissue.


Increases intracellular Na+ and tissue swelling.
By Anonymous on 05/02/2018
分析类型: Ex Vivo
种属: Rat

Verstridine is a voltage-gated sodium channel agonist. It increases intracellular Na+ concentration and also induces cellular and tissue swelling. We used at 50 microM to rat brain slices.