7-<1-(4-Hydroxynonyl)-ureido>-heptansaeure | 61042-46-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 7-<1-(4-Hydroxynonyl)-ureido>-heptansaeure
• 英文别名: 7-[1-(4-hydroxynonyl)ureido]heptanoic acid；7-[Carbamoyl(4-hydroxynonyl)amino]heptanoic acid
• CAS: 61042-46-4
• 化学式: C₁₇H₃₄N₂O₄
• 分子量: 330.468
• InChiKey: JPSRIGGGCROFSO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  23
• 可旋转键数：
  15
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.88
• 拓扑面积：
  104
• 氢给体数：
  3
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  7-<1-(4-Hydroxynonyl)-ureido>-heptansaeure 、 乙酸酐 在 ice 、 乙醚 、 水 、 Sodium sulfate-III 、 silica gel 、 氯仿 作用下， 以 乙醚 为溶剂， 反应 18.0h， 以Thus there is obtained 7-[1-(4-acetoxynonyl)ureido] heptanoic acid as a yellow oil的产率得到7-{[4-(Acetyloxy)nonyl](carbamoyl)amino}heptanoic acid
  参考文献：
  名称：

  11,12-Secoprostaglandins

  摘要：

  本发明涉及8,10-二氮杂-9-氧（和硫）-11,12-丙环前列腺素及其制备方法。这些化合物具有类似前列腺素的生物活性，特别适用于肾脏血管扩张剂，并用于预防血栓形成。

  公开号：

  US03989749A1
• 作为产物：
  描述：

  7-氨基庚酸 在 对甲苯磺酸 作用下， 生成 7-<1-(4-Hydroxynonyl)-ureido>-heptansaeure
  参考文献：
  名称：

  11,12-Secoprostaglandins. 2. N-Acyl-N-alkyl-7-aminoheptanoic acids

  摘要：

  A series of N-acyl-N-alkyl-7-aminoheptanoic acids has been prepared and evaluated for their ability to mimic the natural prostaglandins in certain biological systems. These compounds can be regarded as 8-aza-11,12-secoprostaglandins and, indeed, most of them stimulate cAMP formation in the mouse ovary assay, just as is observed with the natural prostaglandins. Selected compounds from this series also have been studied and shown to have prostaglandin-like effects in vivo.

  DOI：

  10.1021/jm00211a008

文献信息

• US3989749A
  申请人：——

  公开号：US3989749A

  公开（公告）日：1976-11-02
• 11,12-Secoprostaglandins. 2. N-Acyl-N-alkyl-7-aminoheptanoic acids
  作者：James H. Jones、Wilbur J. Holtz、John B. Bicking、Edward J. Cragoe、Lewis R. Mandel、Frederick A. Kuehle

  DOI：10.1021/jm00211a008

  日期：1977.1

  A series of N-acyl-N-alkyl-7-aminoheptanoic acids has been prepared and evaluated for their ability to mimic the natural prostaglandins in certain biological systems. These compounds can be regarded as 8-aza-11,12-secoprostaglandins and, indeed, most of them stimulate cAMP formation in the mouse ovary assay, just as is observed with the natural prostaglandins. Selected compounds from this series also have been studied and shown to have prostaglandin-like effects in vivo.
• 11,12-Secoprostaglandins
  申请人：Merck & Co., Inc.

  公开号：US03989749A1

  公开（公告）日：1976-11-02

  This invention relates to 8,10-diaza-9-oxo(and thioxo)-11,12-secoprostaglandins and processes for their manufacture. These compounds have prostaglandin-like biological activity and are particularly useful as renal vasodilators, and for the prevention of thrombus formation.

  本发明涉及8,10-二氮杂-9-酮（和硫代氧）-11,12-赛可前列腺素及其制造方法。这些化合物具有类似前列腺素的生物活性，特别适用于作为肾脏血管扩张剂，并用于预防血栓形成。