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7-{N-[4-hydroxy-5-(4-fluorophenoxy)-pentyl]methanesulfonamido}heptanoic acid | 59896-44-5

中文名称
——
中文别名
——
英文名称
7-{N-[4-hydroxy-5-(4-fluorophenoxy)-pentyl]methanesulfonamido}heptanoic acid
英文别名
7-[[5-(4-fluorophenoxy)-4-hydroxypentyl]-methylsulfonylamino]heptanoic acid
7-{N-[4-hydroxy-5-(4-fluorophenoxy)-pentyl]methanesulfonamido}heptanoic acid化学式
CAS
59896-44-5
化学式
C19H30FNO6S
mdl
——
分子量
419.515
InChiKey
LIILGFYPUDQVOG-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    28
  • 可旋转键数:
    15
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.63
  • 拓扑面积:
    113
  • 氢给体数:
    2
  • 氢受体数:
    8

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    7-{N-[4-hydroxy-5-(4-fluorophenoxy)-pentyl]methanesulfonamido}heptanoic acid乙酸酐 在 ice 、 crude product 、 乙醚Sodium sulfate-III 、 silica gel 、 氯仿 作用下, 以 乙醚 为溶剂, 反应 18.0h, 以There is obtained 7-{N-[4-acetoxy-5-(4-fluorophenoxy)pentyl]methanesulfonamido}-heptanoic acid as a viscous oil的产率得到7-{N-[4-acetoxy-5-(4-fluorophenoxy)pentyl]methanesulfonamido}-heptanoic acid
    参考文献:
    名称:
    16-Ethers of 8-aza-9-dioxothia-11,12-seco-prostaglandins
    摘要:
    本发明涉及新型的16-芳氧基、16-烷氧基、16-芳硫基和16-烷硫基-8-氮杂-9-二氧硫-11,12-环丙孕酮类化合物及其制备方法。这些新型化合物可作为药物使用,因为它们可用于动物的发情同步和治疗黄体功能持续引起的不育症。
    公开号:
    US03991106A1
  • 作为产物:
    参考文献:
    名称:
    11,12-Secoprostaglandins. 5. 8-Acetyl- or8-(1-hydroxyethyl)-12-hydroxy-13-aryloxytridecanoic acids and sulfonamide isosteres as inhibitors of platelet aggregation
    摘要:
    The synthesis of a series of 8-acetyl- (or 1-hydroxyethyl-) 12-hydroxy-13-aryloxytridecanoic acids and their sulfonamide isosteres is described. These compounds are formally derived from members of earlier reported series of modified secoprostaglandins by replacing the omega-butyl chain termini by substituted aryloxy groups. A number of these compounds are potent inhibitors of collagen-induced blood platelet aggregation in guinea pigs on oral administration.
    DOI:
    10.1021/jm00208a003
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文献信息

  • 11,12-Seco-prostaglandins
    申请人:Merck & Co., Inc.
    公开号:US04055596A1
    公开(公告)日:1977-10-25
    The invention is concerned with novel 16-aryloxy-, 16-alkoxy-, 16-arylthio- and 16-alkylthio-8-aza-9-dioxothia-11,12-seco-prostaglandins and processes for their preparation. These novel compounds are useful as pharmaceuticals since they can be used in animals for estrus synchronization and treatment of infertility due to persistence of luteal function.
    该发明涉及一种新型的16-芳氧基、16-烷氧基、16-芳硫基和16-烷硫基-8-氮杂-9-二氧硫-11,12-去环前列腺素以及它们的制备方法。这些新型化合物可用作药物,因为它们可用于动物的发情同步和治疗黄体功能持续引起的不孕症。
  • US3991106A
    申请人:——
    公开号:US3991106A
    公开(公告)日:1976-11-09
  • US4055596A
    申请人:——
    公开号:US4055596A
    公开(公告)日:1977-10-25
  • 11,12-Secoprostaglandins. 5. 8-Acetyl- or8-(1-hydroxyethyl)-12-hydroxy-13-aryloxytridecanoic acids and sulfonamide isosteres as inhibitors of platelet aggregation
    作者:John B. Bicking、James H. Jones、Wilbur J. Holtz、Charles M. Robb、Frederick A. Kuehl、David H. Minsker、Edward J. Cragoe
    DOI:10.1021/jm00208a003
    日期:1978.10
    The synthesis of a series of 8-acetyl- (or 1-hydroxyethyl-) 12-hydroxy-13-aryloxytridecanoic acids and their sulfonamide isosteres is described. These compounds are formally derived from members of earlier reported series of modified secoprostaglandins by replacing the omega-butyl chain termini by substituted aryloxy groups. A number of these compounds are potent inhibitors of collagen-induced blood platelet aggregation in guinea pigs on oral administration.
  • 16-Ethers of 8-aza-9-dioxothia-11,12-seco-prostaglandins
    申请人:Merck & Co., Inc.
    公开号:US03991106A1
    公开(公告)日:1976-11-09
    The invention is concerned with novel 16-aryloxy-, 16-alkoxy-, 16-arylthio- and 16-alkylthio-8-aza-9-dioxothia-11,12-seco-prostaglandins and processes for their preparation. These novel compounds are useful as pharmaceuticals since they can be used in animals for estrus synchronization and treatment of infertility due to persistence of luteal function.
    本发明涉及新型的16-芳氧基、16-烷氧基、16-芳硫基和16-烷硫基-8-氮杂-9-二氧硫-11,12-环丙孕酮类化合物及其制备方法。这些新型化合物可作为药物使用,因为它们可用于动物的发情同步和治疗黄体功能持续引起的不育症。
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