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3-amino-N-cyclopropyl-2-hydroxyhept-6-ynamide | 928063-36-9

中文名称
——
中文别名
——
英文名称
3-amino-N-cyclopropyl-2-hydroxyhept-6-ynamide
英文别名
——
3-amino-N-cyclopropyl-2-hydroxyhept-6-ynamide化学式
CAS
928063-36-9
化学式
C10H16N2O2
mdl
——
分子量
196.249
InChiKey
NTEXOGAHKQMETE-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):
    0.1
  • 重原子数:
    14
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    75.4
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (1R,2S,5S)-3-((S)-2-tert-butoxycarbonylamino-3,3-dimethylbutyryl)-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxylic acid3-amino-N-cyclopropyl-2-hydroxyhept-6-ynamideN,N-二异丙基乙胺 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成
    参考文献:
    名称:
    Toward the Back-Up of Boceprevir (SCH 503034): Discovery of New Extended P4-Capped Ketoamide Inhibitors of Hepatitis C Virus NS3 Serine Protease with Improved Potency and Pharmacokinetic Profiles
    摘要:
    Hepatitis C is the most prevalent liver disease. Viral hepatitis C (HCV), a small (+)-RNA virus, infects chronically an estimated 300 million people worldwide. Results of Phase I clinical studies with our first generation HCV inhibitor Boceprevir, SCH 503034 (1), presented at the 56th Annual Meeting of the American Association for the Study of Liver Diseases (AASLD) were encouraging, and thus, additional human clinical studies are underway. In view of the positive data from our first generation compound, further work aimed at optimizing its overall profile was undertaken. Herein, we report that extension of our earlier inhibitor to the P-4 pocket and optimization of the P-1' capping led to the discovery of new ketoamide inhibitors of the HCV NS3 serine protease with improved in vitro potency. In addition to being potent inhibitors of HCV subgenomic RNA replication, some of the new P-4-capped inhibitors were also found to have improved PK profile.
    DOI:
    10.1021/jm801632a
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文献信息

  • Inhibitors of Serine Proteases
    申请人:Farmer Luc
    公开号:US20100272681A1
    公开(公告)日:2010-10-28
    The present invention relates to compounds that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The invention further relates to compositions comprising these compounds either for ex vivo use or for administration to a patient suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a patient by administering a composition comprising a compound of this invention.
    本发明涉及抑制丝氨酸蛋白酶活性的化合物,特别是针对丙型肝炎病毒NS3-NS4A蛋白酶的活性。这些化合物通过干扰丙型肝炎病毒的生命周期来发挥作用,并且也可用作抗病毒剂。本发明还涉及包含这些化合物的组合物,无论是用于体外使用还是用于治疗患有HCV感染的患者。本发明还涉及通过给患者注射包含本发明化合物的组合物来治疗HCV感染的方法。
  • Inhibitors of serine proteases
    申请人:Cottrell M. Kevin
    公开号:US20070179167A1
    公开(公告)日:2007-08-02
    The present invention relates to compounds of formula I: or a pharmaceutically acceptable salt or mixtures thereof that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease.
    本发明涉及式I的化合物:或其药物可接受的盐或混合物,其抑制丝氨酸蛋白酶活性,特别是乙型肝炎病毒NS3-NS4A蛋白酶的活性。
  • INHIBITORS OF SERINE PROTEASES
    申请人:Cottrell Kevin M.
    公开号:US20110165120A1
    公开(公告)日:2011-07-07
    The present invention relates to compounds of formula I: or a pharmaceutically acceptable salt or mixtures thereof that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease.
    本发明涉及式I的化合物:或其药学上可接受的盐或混合物,其抑制丝氨酸蛋白酶活性,特别是乙型肝炎病毒NS3-NS4A蛋白酶的活性。
  • Spirocyclic inhibitors of serine proteases for the treatment of hcv infections
    申请人:VERTEX PHARMACEUTICALS INCORPORATED
    公开号:EP2631238A1
    公开(公告)日:2013-08-28
    The present invention relates to compounds of formula (I): or a pharmaceutically acceptable salt thereof. These compounds inhibit serine protease, particularly the hepatitis C virus NS3-NS4A protease.
    本发明涉及式(I)化合物或其药学上可接受的盐。这些化合物可抑制丝氨酸蛋白酶,特别是丙型肝炎病毒 NS3-NS4A 蛋白酶。
  • INHIBITORS OF SERINE PROTEASES FOR THE TREATMENT OF HCV INFECTIONS
    申请人:Vertex Pharmceuticals Incorporated
    公开号:EP2114958A1
    公开(公告)日:2009-11-11
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