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2-[(2R,3S)-3-amino-4-cyclohexyl-2-hydroxybutyl]sulfonyl-N-(2-morpholin-4-ylethyl)acetamide | 769922-26-1

中文名称
——
中文别名
——
英文名称
2-[(2R,3S)-3-amino-4-cyclohexyl-2-hydroxybutyl]sulfonyl-N-(2-morpholin-4-ylethyl)acetamide
英文别名
——
2-[(2R,3S)-3-amino-4-cyclohexyl-2-hydroxybutyl]sulfonyl-N-(2-morpholin-4-ylethyl)acetamide化学式
CAS
769922-26-1
化学式
C18H35N3O5S
mdl
——
分子量
405.559
InChiKey
VQLSUPLQHDLNNY-IRXDYDNUSA-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):
    -0.49
  • 重原子数:
    27.0
  • 可旋转键数:
    10.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    121.96
  • 氢给体数:
    3.0
  • 氢受体数:
    7.0

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:
    2-[(2R,3S)-3-amino-4-cyclohexyl-2-hydroxybutyl]sulfonyl-N-(2-morpholin-4-ylethyl)acetamide 在 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 三乙胺三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 76.0h, 生成 (2S)-2-amino-N-[(2S,3R)-1-cyclohexyl-3-hydroxy-4-[2-(2-morpholin-4-ylethylamino)-2-oxoethyl]sulfonylbutan-2-yl]-3-(1H-imidazol-5-yl)propanamide
    参考文献:
    名称:
    Inhibitors of human renin with C-termini derived from amides and esters of .alpha.-mercaptoalkanoic acids
    摘要:
    New transition-state analogues bearing C-termini derived from alpha-mercaptoalkanoic acids, esters, and amides were prepared and evaluated as inhibitors of human renin. Addition of alpha-mercaptoalkanoate esters to a chiral Boc-amino epoxide intermediate led ultimately to the target [(2R,3S)-3-(BocPheHis-amino)-4-cyclohexyl-2-hydroxy-1-butyl]thio derivatives. The corresponding sulfoxide and sulfone analogues were also investigated. Some of these derivatives, including one with a stable BocPhe replacement, were relatively potent inhibitors of human plasma renin, having IC50 values below 10 nM. When selected compounds were administered intravenously to sodium-deficient rhesus monkeys (Macaca mulatta) at 0.06-1 mg/kg, they reduced plasma renin activity by 87-94%. However, the accompanying drop in blood pressure was of short duration.
    DOI:
    10.1021/jm00093a009
  • 作为产物:
    参考文献:
    名称:
    Inhibitors of human renin with C-termini derived from amides and esters of .alpha.-mercaptoalkanoic acids
    摘要:
    New transition-state analogues bearing C-termini derived from alpha-mercaptoalkanoic acids, esters, and amides were prepared and evaluated as inhibitors of human renin. Addition of alpha-mercaptoalkanoate esters to a chiral Boc-amino epoxide intermediate led ultimately to the target [(2R,3S)-3-(BocPheHis-amino)-4-cyclohexyl-2-hydroxy-1-butyl]thio derivatives. The corresponding sulfoxide and sulfone analogues were also investigated. Some of these derivatives, including one with a stable BocPhe replacement, were relatively potent inhibitors of human plasma renin, having IC50 values below 10 nM. When selected compounds were administered intravenously to sodium-deficient rhesus monkeys (Macaca mulatta) at 0.06-1 mg/kg, they reduced plasma renin activity by 87-94%. However, the accompanying drop in blood pressure was of short duration.
    DOI:
    10.1021/jm00093a009
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