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N-[(3S)-pyrrolidin-3-yl]methanesulfonamide hydrochloride | 1312686-83-1

中文名称
——
中文别名
——
英文名称
N-[(3S)-pyrrolidin-3-yl]methanesulfonamide hydrochloride
英文别名
N-[(3S)-pyrrolidin-3-yl]methanesulfonamide;hydrochloride
N-[(3S)-pyrrolidin-3-yl]methanesulfonamide hydrochloride化学式
CAS
1312686-83-1
化学式
C5H12N2O2S*ClH
mdl
——
分子量
200.689
InChiKey
XGRUMZMLFKHAFW-JEDNCBNOSA-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):
    -0.68
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    66.6
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

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文献信息

  • [EN] SUBSTITUTED FUSED ARYL AND HETEROARYL DERIVATIVES AS PI3K INHIBITORS<br/>[FR] DÉRIVÉS SUBSTITUÉS D'ARYLES ET D'HÉTÉROARYLES FUSIONNÉS AU TITRE D'INHIBITEURS DE PI3K
    申请人:INCYTE CORP
    公开号:WO2011075630A1
    公开(公告)日:2011-06-23
    The present invention provides fused aryl and heteroaryl derivatives of Formula I that modulate the activity of phosphoinositide 3-kinases (PI3Ks) and are useful in the treatment of diseases related to the activity of PI3Ks including, for example, inflammatory disorders, immune-based disorders, cancer, and other diseases.
    本发明提供了式I的融合芳基和杂芳基衍生物,可以调节磷脂酰肌醇3-激酶(PI3Ks)的活性,并且在治疗与PI3Ks活性相关的疾病方面具有用处,例如炎症性疾病、免疫相关疾病、癌症和其他疾病。
  • SUBSTITUTED FUSED ARYL AND HETEROARYL DERIVATIVES AS PI3K INHIBITORS
    申请人:Li Yun-Long
    公开号:US20110183985A1
    公开(公告)日:2011-07-28
    The present invention provides fused aryl and heteroaryl derivatives of Formula I: wherein X, V, Y, U, W, Z, R 1 , R 2 , Cy, and Ar are defined herein, that modulate the activity of phosphoinositide 3-kinases (PI3Ks) and are useful in the treatment of diseases related to the activity of PI3Ks including, for example, inflammatory disorders, immune-based disorders, cancer, and other diseases.
    本发明提供了式I的融合芳基和杂芳基衍生物,其中X,V,Y,U,W,Z,R1,R2,Cy和Ar在此定义,可调节磷脂酰肌醇3-激酶(PI3Ks)的活性,并且在治疗与PI3Ks活性相关的疾病方面具有用处,包括但不限于炎症性疾病、免疫性疾病、癌症和其他疾病。
  • Substituted fused aryl and heteroaryl derivatives as PI3K inhibitors
    申请人:Li Yun-Long
    公开号:US08680108B2
    公开(公告)日:2014-03-25
    The present invention provides fused aryl and heteroaryl derivatives of Formula I: wherein X, V, Y, U, W, Z, R1, R2, Cy, and Ar are defined herein, that modulate the activity of phosphoinositide 3-kinases (PI3Ks) and are useful in the treatment of diseases related to the activity of PI3Ks including, for example, inflammatory disorders, immune-based disorders, cancer, and other diseases.
    本发明提供了公式I的融合芳基和杂芳基衍生物,其中X,V,Y,U,W,Z,R1,R2,Cy和Ar在此定义,可以调节磷脂酰肌醇3-激酶(PI3K)的活性,并且可用于治疗与PI3K活性相关的疾病,例如炎症性疾病,免疫性疾病,癌症和其他疾病。
  • Pyrazolopyrimidines having activity against the respiratory syncytial virus (RSV)
    申请人:Janssen Sciences Ireland Unlimited Company
    公开号:US11339165B2
    公开(公告)日:2022-05-24
    The invention concerns compounds having antiviral activity, in particular, having an inhibitory activity on the replication of the respiratory syncytial virus (RSV). The invention further concerns pharmaceutical compositions comprising these compounds and the compounds for use in the treatment of respiratory syncytial virus infection. Formula (Ia).
    本发明涉及具有抗病毒活性的化合物,尤其是对呼吸道合胞病毒(RSV)的复制具有抑制活性的化合物。本发明还涉及包含这些化合物的药物组合物以及用于治疗呼吸道合胞病毒感染的化合物。式 (Ia).
  • PYRAZOLOPYRIMIDINES HAVING ACTIVITY AGAINST THE RESPIRATORY SYNCYTIAL VIRUS (RSV)
    申请人:Janssen Sciences Ireland Unlimited Company
    公开号:US20200361942A1
    公开(公告)日:2020-11-19
    The invention concerns compounds having antiviral activity, in particular, having an inhibitory activity on the replication of the respiratory syncytial virus (RSV). The invention further concerns pharmaceutical compositions comprising these compounds and the compounds for use in the treatment of respiratory syncytial virus infection. Formula (Ia).
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