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1-Bromobicyclo[3.2.1]octane | 35589-15-2

中文名称
——
中文别名
——
英文名称
1-Bromobicyclo[3.2.1]octane
英文别名
——
1-Bromobicyclo[3.2.1]octane化学式
CAS
35589-15-2
化学式
C8H13Br
mdl
——
分子量
189.095
InChiKey
AMGNUIPDCBVJPO-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):
    3
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

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文献信息

  • [EN] BENZPYRAZOL DERIVATIVES AS INHIBITORS OF PI3 KINASES<br/>[FR] DÉRIVÉS DE BENZPYRAZOLE EN TANT QU'INHIBITEURS DE P13 KINASES
    申请人:GLAXO GROUP LTD
    公开号:WO2009147188A1
    公开(公告)日:2009-12-10
    The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.
    这项发明涉及某些新颖化合物。具体来说,该发明涉及式(I)的化合物及其盐。该发明的化合物是PI3-激酶活性的抑制剂。
  • [EN] NOVEL COMPOUNDS<br/>[FR] NOUVEAUX COMPOSÉS
    申请人:GLAXO GROUP LTD
    公开号:WO2009147190A1
    公开(公告)日:2009-12-10
    The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.
    这项发明涉及某些新颖的化合物。具体来说,该发明涉及式(I)的化合物及其盐。该发明的化合物是PI3-激酶活性的抑制剂。
  • [EN] INDAZOLE DERIVATIVES AS PI 3 - KINASE INHIBITORS<br/>[FR] DÉRIVÉS D'INDAZOLE COMME INHIBITEURS DES PI3-KINASES
    申请人:GLAXO GROUP LTD
    公开号:WO2011067366A1
    公开(公告)日:2011-06-09
    The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.
    这项发明涉及某些新颖化合物。具体而言,该发明涉及具有化学式(I)及其盐的化合物。该发明的化合物是PI3-激酶活性的抑制剂。
  • [EN] 4-CARBOXAMIDE INDAZOLE DERIVATIVES USEFUL AS INHIBITORS OF P13-KINASES<br/>[FR] DÉRIVÉS DE 4-CARBOXAMIDE INDAZOLE UTILES EN TANT QU'INHIBITEURS DE P13 KINASES
    申请人:GLAXO GROUP LTD
    公开号:WO2009147187A1
    公开(公告)日:2009-12-10
    The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of P13-kinase activity.
    这项发明涉及某些新颖的化合物。具体来说,该发明涉及具有式(I)的化合物及其盐。该发明的化合物是P13-激酶活性的抑制剂。
  • [EN] OXAZOLE SUBSTITUTED INDAZOLES AS PI3-KINASE INHIBITORS<br/>[FR] INDAZOLES SUBSTITUÉS PAR OXAZOLE COMME INHIBITEURS DE PI3-KINASE
    申请人:GLAXO GROUP LTD
    公开号:WO2010125082A1
    公开(公告)日:2010-11-04
    The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I): and salts thereof. The compounds of the invention are inhibitors of kinase activity, in particular PI3-kinase activity.
    这项发明涉及某些新颖化合物。具体来说,该发明涉及公式(I)的化合物及其盐。该发明的化合物是激酶活性抑制剂,特别是PI3-激酶活性抑制剂。
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