CAS: 112137-89-0; 7-((1R,2R,3R)-3-Hydroxy-2-((E)-4-Hydroxy-4-Methyloct-1-En-1-yl)-5-Oxocyclopentyl)Heptanoic Acid

该化合物是一种合成的蛋白酸E1类,具有重要的药理应用,其主要优势包括高度稳定性和生物利用率,使其适合各种治疗用途.该化合物展示出强力的子宫和气态细胞保护特性,使其在产科和肠胃环境中具有价值.其行动机制涉及对丙烯菊酯受体的约束,诱发肌肉平稳收缩和减少胃酸分泌.Misoprostol酸常常用于需要精确剂量的配方中,因为其可预见药性很强.该化合物的多功能性和有据可查的功效凸显了其在临床和研究环境中的重要性.适当的处理和储存对于保持其化学完整性至关重要.

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4-methyl-4-trimethylsilyloxyl-1-°Ctyne 4-(Trimethylsilyloxy)-2-(6-carbotrimethylsiloxyhexyl)-cyclopent-2-en-1-on

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    专利信息


    专利号:US-7772278-B2
    优先权日:1999-03-01
    标 题:Nitrosated and nitrosylated prostaglandins, compositions and methods of use
    发明人:GARVEY DAVID S; GASTON RICKY D; LETTS L GORDON; DE TEJADA INIGO SAENZ; TAM SANG WILLIAM; WORCEL MANUEL
    权利人:NITROMED INC
    摘要:The invention describes novel nitrosated and/or nitrosylated prostaglandins, and novel compositions comprising at least one nitrosated and/or nitrosylated prostaglandin, and, optionally, at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase, and/or at least one vasoactive agent. The invention also provides novel compositions comprising at least one prostaglandin and at least one S-nitrosothiol compound, and, optionally, at least one vasoactive agent. The prostaglandin is preferably a prostaglandin E 1 compound, more preferably alprostadil, and the S-nitrosothiol compound is preferably S-nitrosoglutathione. The invention also provides methods for treating or preventing sexual dysfunctions in males and females, for enhancing sexual responses in males and females, and for treating or preventing cerebrovascular disorders, cardiovascular disorders, benign prostatic hyperplasia (BPH), glaucoma, peptic ulcers or for inducing abortions.

    专利号:US-2022281797-A1
    优先权日:2020-09-16
    标 题:Key intermediate for synthesis of prostaglandin compound and preparation method thereof

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1093/humrep/dem098
    摘要:Aronsson A, Fiala C, Stephansson O, Granath F, Watzer B, Schweer H, Gemzell-Danielsson K. Pharmacokinetic profiles up to 12 h after administration of vaginal, sublingual and slow-release oral misoprostol. Hum Reprod. 2007 Jul;22(7):1912–8. doi: 10.1093/humrep/dem098.
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