Date published: 2025-9-14

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Homo Sildenafil-d5

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备用名:
5-[2-Ethoxy-5-[(4-(ethyl-d5)-1-piperazinyl)sulfonyl]phenyl]-1,6-dihydro-1-methyl-3-propyl-7H-pyrazolo[4,3-d]pyrimidin -7-one
应用:
Homo Sildenafil-d5 是一种氘标记的西地那非类似物和潜在的 PDE5 抑制剂
分子量:
493.63
分子式:
C23H27D5N6O4S
仅供科研使用。不可用于诊断或治疗。
* 参考分析证明 大量特定数据 (包括水 含量).

快捷链接

Homo Sildenafil-d5 is a deuterium-labelled analog of Sildenafil (sc-338584). Sildenafil is a selective inhibitor of the type 5 cGMP phosphodiesterase (PDE5 inhibitor) which catalyzes the hydrolysis of 3′,5′-cyclic guanosine monophosphate (cGMP). As a PDE5 inhibitor, Sildenafil has been reported to enhance neuro-, synapto- and angiogenesis in rat models of stroke and also is reported to be a mild vasodilator. Sildenafil has also been shown to prevent indomethacin-induced small intestinal ulceration formation through an NO/cGMP- dependent mechanism.

Homo Sildenafil-d5 参考文献

  1. 新加坡的中成药:有毒重金属和未申报药物的监管控制。  |  Koh, HL. and Woo, SO. 2000. Drug Saf. 23: 351-62. PMID: 11085343
  2. 根据选择性, 药代动力学和疗效特征区分 5 型磷酸二酯酶抑制剂。  |  Seftel, AD. 2004. Clin Cardiol. 27: I14-19. PMID: 15115191
  3. 西地那非在中风治疗中的作用。  |  Bednar, MM. 2008. Curr Opin Investig Drugs. 9: 754-9. PMID: 18600581
  4. 5型磷酸二酯酶抑制剂西地那非可通过NO/cGMP依赖机制预防吲哚美辛诱发的大鼠小肠溃疡。  |  Kato, N., et al. 2009. Dig Dis Sci. 54: 2346-56. PMID: 19101800

订购信息

产品名称产品编号规格价格数量收藏夹

Homo Sildenafil-d5, 1 mg

sc-280778
1 mg
RMB4062.00