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2-(5-piperidin-4-yl-2H-[1,2,4]triazol-3-yl)-4-trifluoromethyl-pyridine hydrochloride | 1240108-73-9

中文名称
——
中文别名
——
英文名称
2-(5-piperidin-4-yl-2H-[1,2,4]triazol-3-yl)-4-trifluoromethyl-pyridine hydrochloride
英文别名
2-(5-piperidin-4-yl-1H-1,2,4-triazol-3-yl)-4-(trifluoromethyl)pyridine;hydrochloride
2-(5-piperidin-4-yl-2H-[1,2,4]triazol-3-yl)-4-trifluoromethyl-pyridine hydrochloride化学式
CAS
1240108-73-9
化学式
C13H14F3N5*ClH
mdl
——
分子量
333.744
InChiKey
XSTJEJCZZJLXCI-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):
    2.77
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    66.5
  • 氢给体数:
    3
  • 氢受体数:
    7

文献信息

  • [EN] FUSED PYRIMIDINES AS AKT INHIBITORS<br/>[FR] PYRIMIDINES CONDENSÉES EN TANT QU'INHIBITEURS D'AKT
    申请人:BAYER SCHERING PHARMA AG
    公开号:WO2010091824A1
    公开(公告)日:2010-08-19
    The present invention relates to compounds of formula (I), a N-oxide or tautomer or stereoisomer thereof, or a salt thereof, wherein ring B and the imidazole to which it is fused, R4, R6, R7, R10, m and n have the meanings as given in the description and the claims, which are effective inhibitors of the Pi3K/Akt pathway, processes for their production and their use as pharmaceuticals.
    本发明涉及式(I)的化合物,其N-氧化物或互变异构体或立体异构体,或其盐,其中环B和与其融合的咪唑,R4、R6、R7、R10、m和n的含义如描述和权利要求中所给出,这些化合物是Pi3K/Akt途径的有效抑制剂,其生产过程及其作为药物的用途。
  • FUSED PYRIMIDINES
    申请人:Beckers Barbara
    公开号:US20130317002A1
    公开(公告)日:2013-11-28
    Compounds of formula (I) or an N-oxide, a salt, a tautomer or a stereoisomer of said compound, or a salt of said N-oxide, tautomer or stereoisomer, wherein ring B and the pyrimidine to which it is fused, R4, R5, R6, R7, m and n have the meanings as given in the description and the claims, which are effective inhibitors of the Pi3K/Akt pathway, processes for their production and their use as pharmaceuticals.
    式(I)的化合物或其N-氧化物、盐、互变异构体或立体异构体的盐或N-氧化物、互变异构体或立体异构体,其中环B和与其融合的嘧啶基团R4、R5、R6、R7、m和n的含义如说明书和权利要求所述,它们是有效的Pi3K/Akt途径抑制剂,其制备方法及其作为药物的用途。
  • FUSED PYRIMIDINES AS AKT INHIBITORS
    申请人:Bayer Intellectual Property GmbH
    公开号:EP2396331B1
    公开(公告)日:2013-10-16
  • US8957064B2
    申请人:——
    公开号:US8957064B2
    公开(公告)日:2015-02-17
  • [EN] FUSED PYRIMIDINES<br/>[FR] PYRIMIDINES CONDENSÉES
    申请人:BAYER SCHERING PHARMA AG
    公开号:WO2010091808A1
    公开(公告)日:2010-08-19
    Compounds of formula (I), or an N-oxide, a salt, a tautomer or a stereoisomer of said compound, or a salt of said N-oxide, tautomer or stereoisomer, wherein ring B and the pyrimidine to which it is fused, R4, R5, R6, R7, m and n have the meanings as given in the description and the claims, which are effective inhibitors of the Pi3K/Akt pathway, processes for their production and their use as pharmaceuticals.
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