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(2S)-N-甲基-5-氧代四氢-2-呋喃甲酰胺 | 166765-05-5

中文名称
(2S)-N-甲基-5-氧代四氢-2-呋喃甲酰胺
中文别名
N-(三氟乙酰基)缬氨酰-O'-(2,3-环氧丙基)酪氨酰-缬氨酸甲基酯
英文名称
(S)-(-)-2-Oxo-4,5-dihydro-3H-furan-2-carbonsaeure-N-methylamid
英文别名
(S)-N-methyl-5-oxotetrahydrofuran-2-carboxamide;(2S)-N-methyl-5-oxooxolane-2-carboxamide
(2S)-N-甲基-5-氧代四氢-2-呋喃甲酰胺化学式
CAS
166765-05-5
化学式
C6H9NO3
mdl
——
分子量
143.142
InChiKey
BUXQGDNKRZCGCI-BYPYZUCNSA-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

物化性质

  • 沸点:
    441.3±34.0 °C(Predicted)
  • 密度:
    1.230±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.4
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    55.4
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:9821ca6ad8ca58ef5d7c81ec2220030d
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反应信息

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文献信息

  • [EN] HOST TARGETED INHIBITORS OF DENGUE VIRUS AND OTHER VIRUSES<br/>[FR] INHIBITEURS CIBLANT L'HÔTE DU VIRUS DE LA DENGUE ET D'AUTRES VIRUS
    申请人:DANA FARBER CANCER INST INC
    公开号:WO2013154778A1
    公开(公告)日:2013-10-17
    Novel antiviral compounds of Formulae (I)-(III) are provided: (I) (II) (III) The inventive compounds, pharmaceutical compositions thereof, and kits including the inventive compounds are useful for the prevention and treatment of infectious diseases caused by viruses, for example, by Flaviviridae virus (e.g., Dengue virus (DENY)), Kunjin virus, Japanese encephalitis virus, vesicular stomatitis virus (VSV), herpes simplex virus 1 (HSV-1), human cytomegalovirus (HCMV), poliovirus, Junin virus, Ebola virus, Marburg virus (MARV), Lassa fever virus (LASV), Venezuelan equine encephalitis virus (VEEV), or Rift Valley Fever virus (RVFV).
    提供了化合物式(I)-(III)的新型抗病毒化合物:(I)(II)(III)。这些创新化合物,其药物组合物和包括这些创新化合物的工具包可用于预防和治疗由病毒引起的传染病,例如黄热病毒科病毒(例如登革热病毒(DENY),昆明病毒,日本脑炎病毒,口疮病毒(VSV),单纯疱疹病毒1型(HSV-1),人类巨细胞病毒(HCMV),脊髓灰质炎病毒,胡尼恩病毒,埃博拉病毒,马尔堡病毒(MARV),拉沙热病毒(LASV),委内瑞拉马蹄热病毒(VEEV)或裂谷热病毒(RVFV)。
  • RAS INHIBITORS AND USES THEREOF
    申请人:DANA-FARBER CANCER INSTITUTE, INC.
    公开号:US20160046661A1
    公开(公告)日:2016-02-18
    Described herein are compounds of Formulae (I)-(II), and pharmaceutically acceptable salts, and pharmaceutical compositions thereof. Also provided are methods and kits involving the inventive compounds or compositions for treating or preventing proliferative diseases such as cancers (e.g., lung cancer, large bowel cancer, pancreas cancer, biliary tract cancer, or endometrial cancer), benign neoplasms, angiogenesis, inflammatory diseases, autoinflammatory diseases, and autoimmune diseases in a subject.
    本文描述了式(I)-(II)的化合物,以及其药学上可接受的盐和制药组合物。还提供了涉及创新化合物或组合物的方法和工具包,用于治疗或预防受试者的增殖性疾病,如癌症(例如肺癌,大肠癌,胰腺癌,胆道癌或子宫内膜癌),良性肿瘤,血管生成,炎症性疾病,自身炎症性疾病和自身免疫性疾病。
  • HOST TARGETED INHIBITORS OF DENGUE VIRUS AND OTHER VIRUSES
    申请人:President and Fellows of Harvard College
    公开号:US20150166532A1
    公开(公告)日:2015-06-18
    Novel antiviral compounds of Formulae (I)-(III) are provided: (I) (II) (III) The inventive compounds, pharmaceutical compositions thereof, and kits including the inventive compounds are useful for the prevention and treatment of infectious diseases caused by viruses, for example, by Flaviviridae virus (e.g., Dengue virus (DENY)), Kunjin virus, Japanese encephalitis virus, vesicular stomatitis virus (VSV), herpes simplex virus 1 (HSV-1), human cytomegalovirus (HCMV), poliovirus, Junin virus, Ebola virus, Marburg virus (MARV), Lassa fever virus (LASV), Venezuelan equine encephalitis virus (VEEV), or Rift Valley Fever virus (RVFV).
  • Ligand-Directed Covalent Modification of Protein
    申请人:Celgene CAR LLC
    公开号:US20170218353A1
    公开(公告)日:2017-08-03
    The present invention relates to enzyme inhibitors. More specifically, the present invention relates to ligand-directed covalent modification of proteins; method of designing same; pharmaceutical formulation of same; and method of use.
  • Pieper; Trankle; Nieger, Pharmazie, 1995, vol. 50, # 1, p. 15 - 21
    作者:Pieper、Trankle、Nieger、Mohr、Lehmann
    DOI:——
    日期:——
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