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Propylaminopropylacetat | 38825-84-2

中文名称
——
中文别名
——
英文名称
Propylaminopropylacetat
英文别名
3-(Propylamino)propyl acetate;3-(propylamino)propyl acetate
Propylaminopropylacetat化学式
CAS
38825-84-2
化学式
C8H17NO2
mdl
——
分子量
159.228
InChiKey
FVTQUNJIJOUJRR-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):
    0.9
  • 重原子数:
    11
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    38.3
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

点击查看最新优质反应信息

文献信息

  • PROBENECID FOR TREATING CORONAVIRUS INFECTIONS
    申请人:University of Georgia Research Foundation, Inc.
    公开号:EP3892269A1
    公开(公告)日:2021-10-13
    Compositions and methods of treating a subject for a coronavirus infection are provided. The methods typically include administering the subject an effective amount of probenecid, a metabolite or analog thereof, or a pharmaceutically acceptable salt thereof. The methods can by therapeutic and/or prophylactic. The amount of probenecid or a pharmaceutically acceptable salt thereof can be effective to, for example, reduce viral replication, reduce one or more symptoms of disease, disorder, or illness associated with virus, or a combination thereof. In preferred embodiments, the virus is a Severe acute respiratory syndrome-related coronavirus such as SARS-CoV-2 or SARS-CoV, a Middle East respiratory syndrome-related coronavirus such as MERS-CoV, or a coronavirus that causes the common cold.
    提供了治疗冠状病毒感染受试者的组合物和方法。这些方法通常包括向受试者施用有效量的丙磺舒、其代谢物或类似物或其药学上可接受的盐。这些方法可用于治疗和/或预防。丙磺舒或其药学上可接受的盐的用量可以有效地减少病毒复制,减少与病毒有关的一种或多种疾病、紊乱或病症的症状,或其组合。在优选的实施方案中,病毒是严重急性呼吸系统综合征相关冠状病毒,如SARS-CoV-2或SARS-CoV,中东呼吸系统综合征相关冠状病毒,如MERS-CoV,或引起普通感冒的冠状病毒。
  • Methods of using probenecid for treatment of coronavirus infections
    申请人:University of Georgia Research Foundation, Inc.
    公开号:US11116737B1
    公开(公告)日:2021-09-14
    Compositions and methods of treating a subject for a coronavirus infection are provided. The methods typically include administering the subject an effective amount of probenecid, a metabolite or analog thereof, or a pharmaceutically acceptable salt thereof. The methods can by therapeutic and/or prophylactic. The amount of probenecid or a pharmaceutically acceptable salt thereof can be effective to, for example, reduce viral replication, reduce one or more symptoms of disease, disorder, or illness associated with virus, or a combination thereof. In preferred embodiments, the virus is a Severe acute respiratory syndrome-related coronavirus such as SARS-CoV-2 or SARS-CoV, a Middle East respiratory syndrome-related coronavirus such as MERS-CoV, or a coronavirus that causes the common cold.
    提供了治疗冠状病毒感染受试者的组合物和方法。这些方法通常包括向受试者施用有效量的丙磺舒、其代谢物或类似物或其药学上可接受的盐。这些方法可用于治疗和/或预防。丙磺舒或其药学上可接受的盐的用量可以有效地减少病毒复制,减少与病毒有关的一种或多种疾病、紊乱或病症的症状,或其组合。在优选的实施方案中,病毒是严重急性呼吸系统综合征相关冠状病毒,如SARS-CoV-2或SARS-CoV,中东呼吸系统综合征相关冠状病毒,如MERS-CoV,或引起普通感冒的冠状病毒。
  • METHODS OF USING PROBENECID FOR TREATMENT OF CORONAVIRUS INFECTIONS
    申请人:University of Georgia Research Foundation, Inc.
    公开号:US20210393564A1
    公开(公告)日:2021-12-23
    Compositions and methods of treating a subject for a coronavirus infection are provided. The methods typically include administering the subject an effective amount of probenecid, a metabolite or analog thereof, or a pharmaceutically acceptable salt thereof. The methods can by therapeutic and/or prophylactic. The amount of probenecid or a pharmaceutically acceptable salt thereof can be effective to, for example, reduce viral replication, reduce one or more symptoms of disease, disorder, or illness associated with virus, or a combination thereof. In preferred embodiments, the virus is a Severe acute respiratory syndrome-related coronavirus such as SARS-CoV-2 or SARS-CoV, a Middle East respiratory syndrome-related coronavirus such as MERS-CoV, or a coronavirus that causes the common cold.
  • Metabolites of probenecid. Chemical, physical, and pharmacological studies
    作者:Z. H. Israili、J. M. Perel、R. F. Cunningham、P. G. Dayton、T. F. Yu、A. B. Gutman、K. R. Long、R. C. Long、J. H. Goldstein
    DOI:10.1021/jm00277a004
    日期:1972.7
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