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2-Chloro-5-(3-(3-methylphenyl)-1,2,4-oxadiazol-5-yl)pyridine

中文名称
——
中文别名
——
英文名称
2-Chloro-5-(3-(3-methylphenyl)-1,2,4-oxadiazol-5-yl)pyridine
英文别名
5-(6-chloropyridin-3-yl)-3-(3-methylphenyl)-1,2,4-oxadiazole
2-Chloro-5-(3-(3-methylphenyl)-1,2,4-oxadiazol-5-yl)pyridine化学式
CAS
——
化学式
C14H10ClN3O
mdl
——
分子量
271.7
InChiKey
SLRNRSJURNBOPB-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):
    3.7
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    51.8
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • 1,2,4-Oxadiazole benzoic acid compositions and their use for nonsense suppression and the treatment of disease
    申请人:Karp Mitchell Gary
    公开号:US20070161687A1
    公开(公告)日:2007-07-12
    Novel 1,2,4-oxadiazole benzoic acid compounds, methods of using and pharmaceutical compositions comprising an 1,2,4-oxadiazole benzoic acid derivative are disclosed. The methods include methods of treating or preventing a disease ameliorated by modulation of premature translation termination or nonsense-mediated mRNA decay, or ameliorating one or more symptoms associated therewith.
    本发明揭示了一种1,2,4-噁二唑苯甲酸生物化合物,使用方法和包含1,2,4-噁二唑苯甲酸生物的制药组合物。该方法包括治疗或预防通过调节过早翻译终止或无义介导的mRNA降解减轻的疾病的方法,或减轻与之相关的一个或多个症状的方法。
  • METHODS FOR THE PRODUCTION OF FUNCTIONAL PROTEIN FROM DNA HAVING A NONSENSE MUTATION AND THE TREATMENT OF DISORDERS ASSOCICATED THEREWITH
    申请人:Almstead Neil G.
    公开号:US20110046136A1
    公开(公告)日:2011-02-24
    The present invention relates to functional proteins encoded by nucleic acid sequences comprising a nonsense mutation. The present invention also relates to methods for the production of functional proteins encoded by nucleic acid sequences comprising a nonsense mutation and the use of such proteins for prevention, management and/or treatment of diseases associated with a nonsense mutation(s) in a gene.
    本发明涉及由核酸序列编码的功能性蛋白质,其中包括一个无意义突变。本发明还涉及用于生产由包含无意义突变的核酸序列编码的功能性蛋白质的方法,以及利用这些蛋白质预防、管理和/或治疗与基因中的无意义突变相关的疾病。
  • METHODS FOR THE SYNTHESIS OF 1,2,4-OXADIAZOLE BENZOIC ACID COMPOUNDS
    申请人:Karp Gary Mitchell
    公开号:US20100121070A1
    公开(公告)日:2010-05-13
    Novel 1,2,4-oxadiazole benzoic acid compounds, methods of using and pharmaceutical compositions comprising an 1,2,4-oxadiazole benzoic acid derivative are disclosed. The methods include methods of treating or preventing a disease ameliorated by modulation of premature translation termination or nonsense-mediated mRNA decay, or ameliorating one or more symptoms associated therewith.
    本发明揭示了1,2,4-噁二唑苯甲酸化合物,其包括小说1,2,4-噁二唑苯甲酸生物的使用方法以及包含该衍生物的制药组合物。该方法包括治疗或预防通过调节过早翻译终止或无意义介导的mRNA降解而改善的疾病的方法,或改善与之相关的一个或多个症状的方法。
  • METHODS FOR THE PRODUCTION OF FUNCTIONAL PROTEIN FROM DNA HAVING A NONSENSE MUTATION AND THE TREATMENT OF DISORDERS ASSOCIATED THEREWITH
    申请人:PTC THERAPEUTICS, INC
    公开号:US20160199357A1
    公开(公告)日:2016-07-14
    The present invention relates to functional proteins encoded by nucleic acid sequences comprising a nonsense mutation. The present invention also relates to methods for the production of functional proteins encoded by nucleic acid sequences comprising a nonsense mutation and the use of such proteins for prevention, management and/or treatment of diseases associated with a nonsense mutation(s) in a gene.
    本发明涉及由包含无意义突变的核酸序列编码的功能蛋白质。本发明还涉及用于生产由包含无意义突变的核酸序列编码的功能蛋白质的方法,并使用这些蛋白质预防、管理和/或治疗与基因中的无意义突变相关的疾病。
  • Methods for the production of functional protein from DNA having a nonsense mutation and the treatment of disorders associated therewith
    申请人:PTC Therapeutics, Inc.
    公开号:EP2387995A1
    公开(公告)日:2011-11-23
    The present invention relates to functional proteins encoded by nucleic acid sequences comprising a nonsense mutation. The present invention also relates to methods for the production of functional proteins encoded by nucleic acid sequences comprising a nonsense mutation and the use of such proteins for prevention, management and/or treatment of diseases associated with a nonsense mutation(s) in a gene.
    本发明涉及由包含无义突变的核酸序列编码的功能性蛋白质。本发明还涉及生产由包含无义突变的核酸序列编码的功能性蛋白质的方法,以及将这种蛋白质用于预防、控制和/或治疗与基因中的无义突变有关的疾病的方法。
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