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4-(4-Bromophenyl)-3-methyl-2-oxobut-3-enoic acid | 920972-74-3

中文名称
——
中文别名
——
英文名称
4-(4-Bromophenyl)-3-methyl-2-oxobut-3-enoic acid
英文别名
——
4-(4-Bromophenyl)-3-methyl-2-oxobut-3-enoic acid化学式
CAS
920972-74-3
化学式
C11H9BrO3
mdl
——
分子量
269.09
InChiKey
ZBVCIVAMLIRUGF-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):
    2.8
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • [EN] N-SULFONYLATED PYRAZOLO[3,4-B]PYRIDIN-6-CARBOXAMIDES AND METHOD OF USE<br/>[FR] PYRAZOLO[3,4-B]PYRIDIN-6-CARBOXAMIDES N-SULFONYLÉS ET LEUR PROCÉDÉ D'UTILISATION
    申请人:ABBVIE S Á R L
    公开号:WO2017060874A1
    公开(公告)日:2017-04-13
    The present invention provides for compounds of formula (I) wherein R1, R2, R3, R4, R5, and R6 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions mediated and modulated by CFTR, including cystic fibrosis, Sjögren's syndrome, pancreatic insufficiency, chronic obstructive lung disease, and chronic obstructive airway disease. Also provided are pharmaceutical compositions comprised of one or more compounds of formula (I).
    本发明提供了一种具有以下结构的化合物(I),其中R1、R2、R3、R4、R5和R6具有规范中定义的任何值,以及其药学上可接受的盐,这些化合物在治疗由CFTR介导和调节的疾病和症状中是有用的,包括囊性纤维化、Sjögren综合征、胰腺功能不全、慢性阻塞性肺病和慢性阻塞性气道疾病。还提供了由一个或多个具有结构(I)的化合物组成的药物组合物。
  • SUBSTITUTED PYRAZOLO[3,4-b]PYRIDIN-6-CARBOXYLIC ACIDS AND METHOD OF USE
    申请人:AbbVie S.à.r.l.
    公开号:US20170101406A1
    公开(公告)日:2017-04-13
    The present invention provides for compounds of formula (I) wherein R 1 , R 2 , R 3 , and R 4 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions mediated and modulated by CFTR, including cystic fibrosis, Sjögren's syndrome, pancreatic insufficiency, chronic obstructive lung disease, and chronic obstructive airway disease. Also provided are pharmaceutical compositions comprised of one or more compounds of formula (I).
    本发明提供了式(I)的化合物 其中R 1 ,R 2 ,R 3 和R 4 具有规范中定义的任何值,以及其药学上可接受的盐,这些化合物在治疗由CFTR介导和调节的疾病和症状中是有用的,包括囊性纤维化、Sjögren综合征、胰腺功能不全、慢性阻塞性肺病和慢性阻塞性气道疾病。还提供了由一个或多个式(I)的化合物组成的药物组合物。
  • Active substance combination for the treatment of diabetes
    申请人:Laboratorios del Dr. Esteve S.A.
    公开号:EP1946778A1
    公开(公告)日:2008-07-23
    The present invention relates to an active substance combination comprising at least one substituted pyrazoline compound and at least one drug, used to treat diabetes, a medicament comprising said active substance combination, a pharmaceutical formulation comprising said active substance combination and the use of said active substance combination for the manufacture of a medicament.
    本发明涉及一种活性物质组合,包括至少一种取代吡唑啉化合物和至少一种药物,用于治疗糖尿病,包括该活性物质组合的药物、包括该活性物质组合的制药配方以及利用该活性物质组合制造药物的用途。
  • Substituted pyrazoline for preventing weight gain
    申请人:Laboratorios del Dr. Esteve S.A.
    公开号:EP1946777A1
    公开(公告)日:2008-07-23
    The present invention relates to an active substance combination comprising at least one substituted pyrazoline compound and at least one drug, known to produce weight-gain as a side effect, a medicament comprising said active substance combination, a pharmaceutical formulation comprising said active substance combination and the use of said active substance combination for the manufacture of a medicament.
    本发明涉及一种活性物质组合,包括至少一种取代吡唑啉化合物和至少一种药物,该药物以体重增加作为副作用而知名,包括所述活性物质组合的药物、包括所述活性物质组合的药物制剂、以及利用所述活性物质组合制造药物。
  • 4-Substituted Pyrazoline Compounds, their Preparation and Use as Medicaments
    申请人:TORRENS Antoni
    公开号:US20070073056A1
    公开(公告)日:2007-03-29
    The present invention relates to 4-substituted pyrazoline compounds, methods for their preparation, medicaments comprising these compounds as well as their use for the preparation of a medicament for the treatment of humans and animals.
    本发明涉及4-取代吡唑啉化合物,其制备方法,包含这些化合物的药物以及它们用于制备用于治疗人类和动物的药物的用途。
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