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Submit ReviewValsartan is a high affinity AT1 receptor antagonist (Ki = 2.38 nM). Displays 30,000-fold selectivity over AT2 receptors. Inhibits angiotensin II-induced release of aldosterone in vitro. Orally active.
Valsartan is also offered as part of the Tocriscreen 2.0 Max, Tocriscreen Antiviral Library and Tocriscreen FDA-Approved Drugs. 了解 Tocris 化合物库的更多信息。
分子量 | 435.52 |
公式 | C24H29N5O3 |
储存 | Store at RT |
纯度 | ≥99% (HPLC) |
CAS Number | 137862-53-4 |
PubChem ID | 60846 |
InChI Key | ACWBQPMHZXGDFX-QFIPXVFZSA-N |
Smiles | CC(C)[C@@H]([C@@](O)=O)N(C(CCCC)=O)CC(C=C3)=CC=C3C1=CC=CC=C1C2=NN=NN2 |
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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 43.55 | 100 |
以下数据基于产品分子量 435.52。 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.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.3 mL | 11.48 mL | 22.96 mL |
5 mM | 0.46 mL | 2.3 mL | 4.59 mL |
10 mM | 0.23 mL | 1.15 mL | 2.3 mL |
50 mM | 0.05 mL | 0.23 mL | 0.46 mL |
参考文献是支持产品生物活性的出版物。
Criscione et al (1993) Pharmacological profile of valsartan: a potent, orally active, nonpeptide antagonist of the angiotensin II AT1-receptor subtype. Br.J.Pharmacol. 110 761 PMID: 8242249
Wexler et al (1996) Nonpeptide angiotensin II receptor antagonists: the next generation in antihypertensive therapy. J.Med.Chem. 39 625 PMID: 8576904
Hanafy et al (2008) Effects of angiotensin II blockade on inflammation-induced alterations of pharmacokinetics and pharmacodynamics of calcium channel blockers. Br.J.Pharmacol. 153 90 PMID: 17965735
If you know of a relevant reference for Valsartan, please let us know.
关键词: Valsartan, Valsartan supplier, Valsartan, CGP48933, atII, receptors, atI, angiotensin1, angiotensinI, antagonists, selective, CGP, 48933, Angiotensin, AT1, Receptors, 4216, Tocris Bioscience
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