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{1-[hydroxy-(3-phenyl-[1,2,4]oxadiazol-5-yl)-methyl]-propyl}-carbamic acid tert-butyl ester | 530123-66-1

中文名称
——
中文别名
——
英文名称
{1-[hydroxy-(3-phenyl-[1,2,4]oxadiazol-5-yl)-methyl]-propyl}-carbamic acid tert-butyl ester
英文别名
tert-butyl N-[1-hydroxy-1-(3-phenyl-1,2,4-oxadiazol-5-yl)butan-2-yl]carbamate
{1-[hydroxy-(3-phenyl-[1,2,4]oxadiazol-5-yl)-methyl]-propyl}-carbamic acid tert-butyl ester化学式
CAS
530123-66-1
化学式
C17H23N3O4
mdl
——
分子量
333.387
InChiKey
BJVCZTJYACIVNH-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):
    2.6
  • 重原子数:
    24
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    97.5
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    {1-[hydroxy-(3-phenyl-[1,2,4]oxadiazol-5-yl)-methyl]-propyl}-carbamic acid tert-butyl ester三氟乙酸二氯甲烷 为溶剂, 反应 1.0h, 生成 2(S)-amino-1-(3-phenyl-[1,2,4]oxadiazol-5-yl)-butan-1-ol trifluoroacetate
    参考文献:
    名称:
    [EN] CYSTEINE PROTEASE INHIBITORS
    [FR] INHIBITEURS DE LA CYSTEINE PROTEASE
    摘要:
    本发明涉及一种抑制半胱氨酸蛋白酶的化合物,特别是包括B、K、L、F和S型半胱氨酸蛋白酶,在治疗由这些蛋白酶介导的疾病中具有用途。本发明涉及包括这些化合物的药物组合物和其制备方法。
    公开号:
    WO2003097617A1
  • 作为产物:
    参考文献:
    名称:
    [EN] CYSTEINE PROTEASE INHIBITORS
    [FR] INHIBITEURS DE LA CYSTEINE PROTEASE
    摘要:
    本发明涉及一种抑制半胱氨酸蛋白酶的化合物,特别是包括B、K、L、F和S型半胱氨酸蛋白酶,在治疗由这些蛋白酶介导的疾病中具有用途。本发明涉及包括这些化合物的药物组合物和其制备方法。
    公开号:
    WO2003097617A1
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文献信息

  • [EN] PEPTIDIC COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS<br/>[FR] COMPOSES PEPTIDIQUES EN TANT QU'INHIBITEURS DE LA PROTEASE A CYSTEINE
    申请人:AXYS PHARM INC
    公开号:WO2004000838A1
    公开(公告)日:2003-12-31
    The present invention is directed to compounds that are inhibitors of cysteine proteases, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceutical compositions comprising these compounds and processes for preparing them.
    本发明涉及一种抑制半胱蛋白酶的化合物,特别是卡特普辛B、K、L、F和S,因此在治疗由这些蛋白酶介导的疾病方面具有用途。本发明涉及包含这些化合物的药物组合物以及制备它们的方法。
  • [EN] AMIDINO COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS<br/>[FR] COMPOSES AMIDINO SERVANT D'INHIBITEURS DE PROTEASES A CYSTEINE
    申请人:AXYS PHARMACEUTICALS
    公开号:WO2004108661A1
    公开(公告)日:2004-12-16
    The present invention is directed to compounds that are inhibitors of cysteine proteases, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceutical compositions comprising these compounds and processes for preparing them.
    本发明涉及一种抑制半胱蛋白酶的化合物,特别是包括B、K、L、F和S半胱蛋白酶,因此在治疗由这些蛋白酶介导的疾病方面具有用处。本发明涉及包含这些化合物的药物组合物以及其制备方法。
  • Novel compounds and compositions as cathepsin S inhibitors
    申请人:——
    公开号:US20030199506A1
    公开(公告)日:2003-10-23
    The present invention relates to novel selective cathepsin S inhibitors, the pharmaceutically acceptable salts and N-oxides thereof, their uses as therapeutic agents and the methods of their making. 1
    本发明涉及新型选择性卡特普西林S抑制剂,其药学上可接受的盐和N-氧化物,以及它们作为治疗剂的用途和制备方法。
  • Peptidic compounds as cysteine protease inhibitors
    申请人:AXYS PHARMACEUTICALS, INC.
    公开号:US20040127426A1
    公开(公告)日:2004-07-01
    The present invention is directed to compounds that are inhibitors of cysteine proteases, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceutical compositions comprising these compounds and processes for preparing them.
    本发明涉及一种抑制半胱蛋白酶的化合物,特别是抑制B、K、L、F和S型猫蛋白酶,因此可用于治疗由这些蛋白酶介导的疾病。本发明涉及包含这些化合物的制药组合物和其制备方法。
  • Amidino compounds as cysteine protease inhibitors
    申请人:Graupe Michael
    公开号:US20070105892A1
    公开(公告)日:2007-05-10
    The present invention is directed to compounds that are inhibitors of cysteine proteases, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceutical compositions comprising these compounds and processes for preparing them.
    本发明涉及一种抑制半胱蛋白酶的化合物,特别是cathepsins B、K、L、F和S,因此在治疗由这些蛋白酶介导的疾病方面具有用处。本发明涉及包含这些化合物的药物组合物和其制备过程。
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