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3-dipropylsulfamoyl-propionic acid | 388072-50-2

中文名称
——
中文别名
——
英文名称
3-dipropylsulfamoyl-propionic acid
英文别名
3-(Dipropylsulfamoyl)propanoic acid
3-dipropylsulfamoyl-propionic acid化学式
CAS
388072-50-2
化学式
C9H19NO4S
mdl
——
分子量
237.32
InChiKey
PZQROWIVWDYHEM-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):
    0.8
  • 重原子数:
    15
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    83.1
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    3-dipropylsulfamoyl-propionic acid盐酸1-羟基苯并三唑1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 作用下, 以 1,4-二氧六环 为溶剂, 生成 N-[(1S,2R)-1-benzyl-2-hydroxy-3-(3-methoxy-benzylamino)-propyl]-3-dipropylsulfamoyl-propionamide
    参考文献:
    名称:
    Design of potent inhibitors of human β-secretase. Part 1
    摘要:
    We describe a novel series of potent inhibitors of human beta-secretase. These compounds possess the hydroxyethyl amine transition state isostere. A 2.5A crystal structure of inhibitor 32 bound to BACE is provided.
    DOI:
    10.1016/j.bmcl.2006.09.092
  • 作为产物:
    描述:
    二正丙胺sodium hydroxide 作用下, 以 乙醇二氯甲烷 为溶剂, 生成 3-dipropylsulfamoyl-propionic acid
    参考文献:
    名称:
    Design of potent inhibitors of human β-secretase. Part 1
    摘要:
    We describe a novel series of potent inhibitors of human beta-secretase. These compounds possess the hydroxyethyl amine transition state isostere. A 2.5A crystal structure of inhibitor 32 bound to BACE is provided.
    DOI:
    10.1016/j.bmcl.2006.09.092
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文献信息

  • Substituted ureas and carbamates
    申请人:ELAN PHARMACEUTICALS, INC.
    公开号:US20040209925A1
    公开(公告)日:2004-10-21
    The invention provides compounds of formula I: 1 useful in treating Alzheimer's disease and other similar diseases. These compounds include inhibitors of the beta-secretase enzyme that are useful in the treatment of Alzheimer's disease and other diseases characterized by deposition of A beta peptide in a mammal. The compounds of the invention are useful in pharmaceutical compositions and methods of treatment to reduce A beta peptide formation.
    本发明提供了公式I:1的化合物,用于治疗阿尔茨海默病和其他类似疾病。这些化合物包括β-分泌酶酶抑制剂,对于治疗阿尔茨海默病和其他在哺乳动物中表现为A beta肽沉积的疾病非常有用。本发明的化合物在制药组合物和治疗方法中非常有用,以减少A beta肽的形成。
  • 1, 3, Diamino-2-Hydroxypropane Pro-Drug Derivatives
    申请人:Fobian Yvette M.
    公开号:US20080161325A1
    公开(公告)日:2008-07-03
    The present invention relates to compounds of formula (AA) (I) and (X): useful in treating Alzheimer's disease and other similar diseases. These compounds include inhibitors of the beta-secretase enzyme that are useful in the treatment of Alzheimer's disease and other diseases characterized by deposition of A beta peptide in a mammal. The compounds of the invention are useful in pharmaceutical compositions and methods of treatment to reduce A beta peptide formation.
    本发明涉及公式(AA)(I)和(X)的化合物,用于治疗阿尔茨海默病和其他类似疾病。这些化合物包括β-分泌酶酶的抑制剂,对治疗阿尔茨海默病和其他哺乳动物中A beta肽沉积的疾病具有用处。本发明的化合物适用于制备药物组合物和治疗方法,以减少A beta肽的形成。
  • Substituted Ureas and Carbamates
    申请人:Pulley Shon R.
    公开号:US20080306136A1
    公开(公告)日:2008-12-11
    The invention provides compounds of formula I: useful in treating Alzheimer's disease and other similar diseases. These compounds include inhibitors of the beta-secretase enzyme that are useful in the treatment of Alzheimer's disease and other diseases characterized by deposition of A beta peptide in a mammal. The compounds of the invention are useful in pharmaceutical compositions and methods of treatment to reduce A beta peptide formation.
    本发明提供了式I的化合物:用于治疗阿尔茨海默病和其他类似疾病。这些化合物包括β-分泌酶酶的抑制剂,对于治疗阿尔茨海默病和其他以A beta肽在哺乳动物中沉积为特征的疾病非常有用。本发明的化合物在制药组合物和治疗方法中用于减少A beta肽的形成。
  • 1, 3-DIAMINO-2-HYDROXYPROPANE PRODRUG DERIVATIVES
    申请人:Elan Pharmaceuticals, Inc.
    公开号:EP1534693A2
    公开(公告)日:2005-06-01
  • US7294642B2
    申请人:——
    公开号:US7294642B2
    公开(公告)日:2007-11-13
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