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6-Chloronaphthalene-2-carbonitrile | 1261626-91-8

中文名称
——
中文别名
——
英文名称
6-Chloronaphthalene-2-carbonitrile
英文别名
——
6-Chloronaphthalene-2-carbonitrile化学式
CAS
1261626-91-8
化学式
C11H6ClN
mdl
——
分子量
187.62
InChiKey
VIJMEUNAVBOWBY-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):
    3.9
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    23.8
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • [EN] BET INHIBITORS FOR MODULATING DUX4 EXPRESSION IN FSHD<br/>[FR] INHIBITEURS DE BET POUR MODULER L'EXPRESSION DE DUX4 DANS LA FSHD
    申请人:UNIV SAINT LOUIS
    公开号:WO2020132004A1
    公开(公告)日:2020-06-25
    The present disclosure provides BET inhibitors of the formula: wherein the variables are defined herein, as well as pharmaceutical compositions thereof. The present disclosure also provides methods of treating a patient comprising administering a bromo- and extra-terminal (BET) domain inhibitor for the treatment of FSHD which modulates DUX4 expression. In some embodiments, the present methods comprise using one or more BET inhibitors as a therapeutic agent for the treatment of FSHD patients including patients who are being treated with one or more palliative treatments such as therapy and/or agents which lead to increased muscle mass.
    本公开提供了以下式的BET抑制剂:其中变量在此处定义,以及其药物组合物。本公开还提供了治疗患者的方法,包括给予和额外端(BET)结构域抑制剂治疗FSHD以调节DUX4表达。在某些实施例中,本方法包括使用一个或多个BET抑制剂作为FSHD患者的治疗剂,包括正在接受一种或多种缓解治疗(如治疗和/或导致肌肉增加的药物)的患者。
  • COMPOUND CAPABLE OF INHIBITING PHOSPHODIESTERASE 4, PREPARATION METHOD, AND MEDICAL USE THEREOF
    申请人:Hefei Industrial Pharmaceutical Institute Co., Ltd
    公开号:EP3708568A1
    公开(公告)日:2020-09-16
    The disclosure relates to the field of medicinal chemistry, in particular, to a class of small molecule compounds for inhibiting phosphodiesterase 4 (I), a preparation method thereof and a pharmaceutical composition comprising the compound. The pharmacodynamic test proves that the compound of the disclosure has the inhibitory activity of PDE-4 enzyme and the efficacy of inflammation treatment.
    本公开涉及药物化学领域,尤其涉及一类抑制磷酸二酯酶4(I)的小分子化合物、其制备方法以及包含该化合物的药物组合物。药效学试验证明,本公开的化合物具有抑制 PDE-4 酶的活性和治疗炎症的疗效。
  • Compound having effects of inhibiting phosphodiesterase 4, preparation method thereof and pharmaceutical use thereof
    申请人:Hefei Industrial Pharmaceutical Institute Co., Ltd.
    公开号:US11161860B2
    公开(公告)日:2021-11-02
    The disclosure relates to the field of medicinal chemistry, in particular, to a class of small molecule compounds for inhibiting phosphodiesterase 4 (I), a preparation method thereof and a pharmaceutical composition comprising the compound. The pharmacodynamic test proves that the compound of the disclosure has the inhibitory activity of PDE-4 enzyme and the efficacy of inflammation treatment.
    本公开涉及药物化学领域,尤其涉及一类抑制磷酸二酯酶4(I)的小分子化合物、其制备方法以及包含该化合物的药物组合物。药效学试验证明,本公开的化合物具有抑制 PDE-4 酶的活性和治疗炎症的疗效。
  • COMPOUND HAVING EFFECTS OF INHIBITING PHOSPHODIESTERASE 4, PREPARATION METHOD THEREOF AND PHARMACEUTICAL USE THEREOF
    申请人:Hefei Industrial Pharmaceutical Institute Co., Ltd.
    公开号:US20210179640A1
    公开(公告)日:2021-06-17
    The disclosure relates to the field of medicinal chemistry, in particular, to a class of small molecule compounds for inhibiting phosphodiesterase 4 (I), a preparation method thereof and a pharmaceutical composition comprising the compound. The pharmacodynamic test proves that the compound of the disclosure has the inhibitory activity of PDE-4 enzyme and the efficacy of inflammation treatment.
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