Phenamil

Pricing Availability   Qty
说明: Inhibits TRPP3-mediated currents; also inhibits epithelial Na+ channels
化学名: 3,5-Diamino-6-chloro-N-[imino(phenylamino)methyl]pyrazinecarboxamide methanesulfonate salt
纯度: ≥99% (HPLC)
说明书
引用文献
评论

生物活性 for Phenamil

Phenamil is a TRPP3 channel inhibitor (IC50 = 0.14 μM). Also inhibits epithelial Na+ channels (Kd = 0.4 nM for a high affinity site on the epithelial Na+ channel). Derivative of amiloride (Cat. No. 0890).

化合物库 for Phenamil

Phenamil is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for Phenamil

分子量 401.83
公式 C12H12ClN7O.CH3SO3H
储存 Store at +4°C
纯度 ≥99% (HPLC)
CAS Number 1161-94-0
PubChem ID 9604979
InChI Key MHPIZTURFVSLTJ-UHFFFAOYSA-N
Smiles NC1=C(Cl)N=C(C(NC(NC2=CC=CC=C2)=N)=O)C(N)=N1.CS(=O)(O)=O

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 Phenamil

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 40.18 100

制备储备液 for Phenamil

以下数据基于产品分子量 401.83。 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
1 mM 2.49 mL 12.44 mL 24.89 mL
5 mM 0.5 mL 2.49 mL 4.98 mL
10 mM 0.25 mL 1.24 mL 2.49 mL
50 mM 0.05 mL 0.25 mL 0.5 mL

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Reconstitution Calculator

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Dilution Calculator

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参考文献 for Phenamil

参考文献是支持产品生物活性的出版物。

Barbry et al (1989) Biochemical identification of two types of phenamil binding sites associated with amiloride-sensitive Na+ channels. Biochemistry. 28 3744 PMID: 2546581

Dai et al (2007) Inhibition of TRPP3 channel by amil. and analogs. Mol.Pharmacol. 72 1576 PMID: 17804601


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关键词: Phenamil, Phenamil supplier, TRPP3, TRP, antagonists, sodium, channels, blocker, amiloride, Na, epithelial, Epithelial, Sodium, Channels, TRPP, 3379, Tocris Bioscience

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