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2-Chloro-1-methyl-4-(4-methylphenyl)benzene | 92189-88-3

中文名称
——
中文别名
——
英文名称
2-Chloro-1-methyl-4-(4-methylphenyl)benzene
英文别名
——
2-Chloro-1-methyl-4-(4-methylphenyl)benzene化学式
CAS
92189-88-3
化学式
C14H13Cl
mdl
——
分子量
216.7
InChiKey
SJDZUSHAMYHPNB-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):
    4.9
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

文献信息

  • HEPATITIS C VIRUS INHIBITORS AND USES THEREOF IN PREPARATION OF DRUGS
    申请人:CHANGZHOU YINSHENG PHARMACEUTICAL CO., LTD.
    公开号:US20170253614A1
    公开(公告)日:2017-09-07
    A series of hepatitis C virus (HCV) inhibitors and compositions and applications thereof in the preparation of drugs for treating chronic HCV infection. Especially, a series of compounds that are used as NS5A inhibitors, and compositions and uses thereof in the preparations of drugs.
    一系列丙型肝炎病毒(HCV)抑制剂及其组合物,以及在制备用于治疗慢性HCV感染的药物时的应用。特别是一系列用作NS5A抑制剂的化合物,以及在药物制剂中的组合物和用途。
  • [EN] SMALL MOLECULE INDUCERS OF REACTIVE OXYGEN SPECIES AND INHIBITORS OF MITOCHONDRIAL ACTIVITY<br/>[FR] INDUCTEURS DE PETITES MOLÉCULES DE DÉRIVES RÉACTIFS DE L'OXYGÈNE ET INHIBITEURS DE L'ACTIVITÉ MITOCHONDRIALE
    申请人:UNIV MICHIGAN REGENTS
    公开号:WO2017155991A1
    公开(公告)日:2017-09-14
    This invention is in the field of medicinal chemistry. In particular, the invention relates to a new class of small-molecules having a quinazolinedione structure which function as reactive oxygen species (ROS) inducers and inhibitors of mitochondrial activity within cancer cells (e.g., pancreatic cancer cells), and their use as therapeutics for the treatment of cancer (e.g., pancreatic cancer) and other diseases.
    这项发明属于药物化学领域。具体来说,该发明涉及一类具有喹唑啉二酮结构的小分子,其作为活性氧(ROS)诱导剂和对癌细胞(例如胰腺癌细胞)内线粒体活性的抑制剂,并将它们用作治疗癌症(例如胰腺癌)和其他疾病的药物。
  • [EN] GLUCAGON ANTAGONISTS<br/>[FR] ANTAGONISTES DE GLUCAGON
    申请人:METABASIS THERAPEUTICS INC
    公开号:WO2010019830A1
    公开(公告)日:2010-02-18
    Provided herein are compounds, including enantiomerically pure forms thereof, and pharmaceutically acceptable salts or co-crystals and prodrugs thereof which have glucagon receptor antagonist or inverse agonist activity. Further, provided herein are pharmaceutical compositions comprising the same as well as methods of treating, preventing, delaying the time to onset or reducing the risk for the development or progression of a disease or condition for which one or more glucagon receptor antagonist is indicated, including Type I and II diabetes, insulin resistance and hyperglycemia. Moreover, provided herein are methods of making or manufacturing compounds disclosed herein, including enantiomerically pure forms thereof, and pharmaceutically acceptable salts or Co- crystals and prodrugs thereof. Formula I
    本文提供了化合物,包括其对映体纯形式,以及具有胰高血糖素受体拮抗剂或逆向激动剂活性的药用盐或共晶体和前药。此外,本文提供了包括这些化合物的药物组合物,以及治疗、预防、延缓发病时间或减少一种或多种胰高血糖素受体拮抗剂适用的疾病或病情的发展或进展风险的方法,包括I型和II型糖尿病、胰岛素抵抗和高血糖。此外,本文提供了制备或生产本文披露的化合物的方法,包括其对映体纯形式,以及药用盐或共晶体和前药。公式I
  • [EN] GLUCAGON ANTAGONISTS<br/>[FR] ANTAGONISTES DU GLUCAGON
    申请人:LIGAND PHARM INC
    公开号:WO2015191900A1
    公开(公告)日:2015-12-17
    Provided herein are compounds, including enantiomerically pure forms thereof, and pharmaceutically acceptable salts or co-crystals and prodrugs thereof which have glucagon receptor antagonist or inverse agonist activity. Further, provided herein are pharmaceutical compositions comprising the same as well as methods of treating, preventing, delaying the time to onset or reducing the risk for the development or progression of a disease or condition for which one or more glucagon receptor antagonist is indicated, including Type I and II diabetes, insulin resistance and hyperglycemia. Moreover, provided herein are methods of making or manufacturing compounds disclosed herein, including enantiomerically pure forms thereof, and pharmaceutically acceptable salts or co-crystals and prodrugs thereof.
    本文提供了化合物,包括其对映体纯形式,以及具有胰高血糖素受体拮抗剂或逆向激动剂活性的药用盐或共晶体及前药。此外,本文提供了包括这些化合物的药物组合物,以及治疗、预防、延缓发病时间或减少一种或多种胰高血糖素受体拮抗剂适用的疾病或症状的发展或进展风险的方法,包括I型和II型糖尿病、胰岛素抵抗和高血糖。此外,本文提供了制备或生产本文披露的化合物的方法,包括其对映体纯形式,以及药用盐或共晶体及前药。
  • Glucagon antagonists
    申请人:Metabasis Therapeutics, Inc.
    公开号:EP2799428A2
    公开(公告)日:2014-11-05
    Provided herein are compounds, including enantiomerically pure forms thereof, and pharmaceutically acceptable salts or co-crystals and prodrugs thereof which have glucagon receptor antagonist or inverse agonist activity. Further, provided herein are pharmaceutical compositions comprising the same as well as methods of treating, preventing, delaying the time to onset or reducing the risk for the development or progression of a disease or condition for which one or more glucagon receptor antagonist is indicated, including Type I and II diabetes, insulin resistance and hyperglycemia. Moreover, provided herein are methods of making or manufacturing compounds disclosed herein, including enantiomerically pure forms thereof, and pharmaceutically acceptable salts or co-crystals and prodrugs thereof.
    本文提供了具有胰高血糖素受体拮抗剂或反向激动剂活性的化合物(包括其对映体纯形式)及其药学上可接受的盐或共晶体和原药。此外,本文还提供了包含上述成分的药物组合物,以及治疗、预防、延缓发病时间或降低疾病或病情发展风险的方法,这些疾病或病情适用于一种或多种胰高血糖素受体拮抗剂,包括I型和II型糖尿病、胰岛素抵抗和高血糖症。此外,本文还提供了制造或生产本文公开的化合物的方法,包括其对映体纯形式,以及其药学上可接受的盐或共晶体和原药。
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