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2-(Cyclopropylamino)-1-phenylethanone | 18381-60-7

中文名称
——
中文别名
——
英文名称
2-(Cyclopropylamino)-1-phenylethanone
英文别名
——
2-(Cyclopropylamino)-1-phenylethanone化学式
CAS
18381-60-7
化学式
C11H13NO
mdl
——
分子量
175.23
InChiKey
BWYDQVGGIRXHDE-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

物化性质

  • 沸点:
    300.7±25.0 °C(Predicted)
  • 密度:
    1.10±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • [EN] HUMAN PLASMA KALLIKREIN INHIBITORS<br/>[FR] INHIBITEURS DE LA KALLICRÉINE PLASMATIQUE HUMAINE
    申请人:BIOCRYST PHARM INC
    公开号:WO2015134998A1
    公开(公告)日:2015-09-11
    Disclosed are compounds of formula (I), as described herein, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of plasma kallikrein. Also provided are pharmaceutical compositions comprising at least one compound of the invention, and methods involving use of the compounds and compositions of the invention in the treatment and prevention of diseases and conditions characterized by unwanted plasma kallikrein activity.
    本文披露的是公式(I)的化合物及其药用盐。这些化合物是血浆激肽酶的抑制剂。还提供了包含本发明化合物的药物组合物,以及涉及使用这些化合物和组合物治疗和预防由不需要的血浆激肽酶活性特征的疾病和症状的方法。
  • Combination therapy for dementia, depression and apathy
    申请人:Sheldon James Leslie
    公开号:US20060287299A1
    公开(公告)日:2006-12-21
    The invention provides, in part, methods and compositions for treating psychiatric disorders, for example, apathy, dementia, or depression, using combination therapies such a monoamine oxidase inhibitor or a selective serotonin reuptake inhibitor in combination with an anti-psychotic agent.
    本发明提供了治疗精神障碍的方法和组合物,例如,使用单胺氧化酶抑制剂或选择性血清素再摄取抑制剂与抗精神病药物等组合疗法治疗无动于衷、痴呆或抑郁等精神障碍。
  • SUBSTITUTED PYRAZOLES AS HUMAN PLASMA KALLIKREIN INHIBITORS
    申请人:BioCryst Pharmaceuticals, Inc.
    公开号:EP3828173A1
    公开(公告)日:2021-06-02
    Disclosed are compounds of formula (I), as described herein, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of plasma kallikrein. Also provided are pharmaceutical compositions comprising at least one compound of the invention, and methods involving use of the compounds and compositions of the invention and the treatment and prevention of diseases and conditions characterized by unwanted plasma kallikrein activity.
    公开了本文所述的式 (I) 化合物及其药学上可接受的盐类。这些化合物是血浆卡立克雷因的抑制剂。还提供了包含至少一种本发明化合物的药物组合物,以及涉及使用本发明化合物和组合物、治疗和预防以不需要的血浆卡利克雷因活性为特征的疾病和病症的方法。
  • Human plasma kallikrein inhibitors
    申请人:BioCryst Pharmaceuticals, Inc.
    公开号:US10125102B2
    公开(公告)日:2018-11-13
    Disclosed are compounds of formula I as described herein, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of plasma kallikrein. Also disclosed are pharmaceutical compositions comprising at least one such compound, and methods involving use of the compounds and compositions in the treatment and prevention of diseases and conditions characterized by unwanted plasma kallikrein activity.
    公开了式 I 的化合物 及其药学上可接受的盐类。这些化合物是血浆激肽的抑制剂。此外,还公开了包含至少一种此类化合物的药物组合物,以及涉及使用这些化合物和组合物治疗和预防以不需要的血浆激肽活性为特征的疾病和病症的方法。
  • EP1713486A4
    申请人:——
    公开号:EP1713486A4
    公开(公告)日:2009-04-29
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