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Submit ReviewWIN 64338 hydrochloride is a the first potent, non-peptide, competitive bradykinin B2 receptor antagonist. In organ bath studies, WIN 64338 inhibits [3H]-bradykinin binding on guinea pig trachea with nanomolar affinity but is not active in the rabbit aorta (the classical bradykinin B1 preparation).
分子量 | 783.95 |
公式 | C45H68ClN4OP.HCl |
储存 | Desiccate at +4°C |
CAS Number | 163727-74-0 |
PubChem ID | 9832172 |
InChI Key | YYJGBEZPVOUBMJ-KRFCICRISA-N |
Smiles | CCCC[P+](CCCC)(CC1=CC=C(C=C1)NC([C@@H](/N=C(NC2CCCCC2)/NC3CCCCC3)CC4=CC5=CC=CC=C5C=C4)=O)CCCC.Cl.[Cl-] |
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 | 58.8 | 75 |
以下数据基于产品分子量 783.95。 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 |
---|---|---|---|
0.75 mM | 1.7 mL | 8.5 mL | 17.01 mL |
3.75 mM | 0.34 mL | 1.7 mL | 3.4 mL |
7.5 mM | 0.17 mL | 0.85 mL | 1.7 mL |
37.5 mM | 0.03 mL | 0.17 mL | 0.34 mL |
参考文献是支持产品生物活性的出版物。
Hu et al (2004) Action of bradykinin in the submucosal plexus of guinea pig small intestine. J.Pharmacol.Exp.Ther. 309 320 PMID: 14718600
Marceau et al (1994) Effects of peptide and nonpeptide antagonists of bradykinin B2 receptors on the venoconstrictor action of bradykinin. J.Pharmacol.Exp.Ther. 269 1136 PMID: 8014858
Scherrer et al (1995) Effects of WIN 64338, a nonpeptide bradykinin B2 receptor antagonist, on guinea-pig trachea. Br.J.Pharmacol. 115 1127 PMID: 7582533
If you know of a relevant reference for WIN 64338 hydrochloride, please let us know.
关键词: WIN 64338 hydrochloride, WIN 64338 hydrochloride supplier, Bradykinin, B2, antagonists, Receptors, WIN64338, hydrochloride, 1057, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 WIN 64338 hydrochloride 的部分引用包括:
Gross et al (2013) Factors mediating remote preconditioning of trauma in the rat heart: central role of the cytochrome p450 epoxygenase pathway in mediating infarct size reduction. J Cardiovasc Pharmacol Ther 18 38 PMID: 22407888
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