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3-Methyl-5--1.2.4-oxadiazol | 1455-85-2

中文名称
——
中文别名
——
英文名称
3-Methyl-5--1.2.4-oxadiazol
英文别名
3-(3-methyl-[1,2,4]oxadiazol-5-yl)-pyridine;3-(3-Methyl-1,2,4-oxadiazol-5-yl)pyridine;3-methyl-5-pyridin-3-yl-1,2,4-oxadiazole
3-Methyl-5-<pyridyl-(3)>-1.2.4-oxadiazol化学式
CAS
1455-85-2
化学式
C8H7N3O
mdl
MFCD21091823
分子量
161.163
InChiKey
POEMSJAQQSVHGC-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):
    1.1
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.125
  • 拓扑面积:
    51.8
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • Pyrimidine-2,4-dione derivatives as matrix metalloproteinase inhibitors
    申请人:——
    公开号:US20040053952A1
    公开(公告)日:2004-03-18
    This invention provides compounds defined by Formula I 1 or a pharmaceutically acceptable salt thereof, wherein R 1 , Q, R 2 , R 3 , and R 4 are as defined in the specification. The invention also provides pharmaceutical compositions comprising a compound of Formula I, or a pharmaceutically acceptable salt thereof, as defined in the specification, together with a pharmaceutically acceptable carrier, diluent, or excipient. The invention also provides methods of inhibiting an MMP-13 enzyme in an animal, comprising administering to the animal a compound of Formula I, or a pharmaceutically acceptable salt thereof. The invention also provides methods of treating a disease mediated by an MMP-13 enzyme in a patient, comprising administering to the patient a compound of Formula I, or a pharmaceutically acceptable salt thereof, either alone or in a pharmaceutical composition. The invention also provides methods of treating diseases such as heart disease, multiple sclerosis, osteo- and rheumatoid arthritis, arthritis other than osteo- or rheumatoid arthritis, cardiac insufficiency, inflammatory bowel disease, heart failure, age-related macular degeneration, chronic obstructive pulmonary disease, asthma, periodontal diseases, psoriasis, atherosclerosis, and osteoporosis in a patient, comprising administering to the patient a compound of Formula I, or a pharmaceutically acceptable salt thereof, either alone or in a pharmaceutical composition. The invention also provides combinations, comprising a compound of Formula I, or a pharmaceutically acceptable salt thereof, together with another pharmaceutically active component as described in the specification.
    本发明提供了由公式I1定义的化合物或其药学上可接受的盐,其中R1、Q、R2、R3和R4如规范中所定义。本发明还提供了制剂,包括由规范中定义的公式I的化合物或其药学上可接受的盐,以及药学上可接受的载体、稀释剂或赋形剂。本发明还提供了在动物中抑制MMP-13酶的方法,包括向动物施用公式I的化合物或其药学上可接受的盐。本发明还提供了治疗由MMP-13酶介导的疾病的方法,包括向患者施用公式I的化合物或其药学上可接受的盐,单独或与制剂一起。本发明还提供了治疗心脏病、多发性硬化症、骨关节炎和类风湿性关节炎、非骨关节炎和非类风湿性关节炎性关节炎、心力衰竭、炎症性肠病、老年性黄斑变性、慢性阻塞性肺病、哮喘、牙周疾病、屑病、动脉粥样硬化和骨质疏松症的方法,包括向患者施用公式I的化合物或其药学上可接受的盐,单独或与制剂一起。本发明还提供了组合物,包括公式I的化合物或其药学上可接受的盐,以及规范中描述的另一种药学活性成分。
  • Potassium Channel Inhibitors
    申请人:Trotter B. Wesley
    公开号:US20090233897A1
    公开(公告)日:2009-09-17
    The present invention relates to compounds having the structure useful as potassium channel inhibitors to treat cardiac arrhythmias, and the like.
    本发明涉及具有结构的化合物,可用作通道抑制剂以治疗心律失常等。
  • Phosphodiesterase Inhibitors
    申请人:Palle P. Venkata
    公开号:US20070259874A1
    公开(公告)日:2007-11-08
    The present invention relates to isoxazoline derivatives and their analogues, which can be used as phosphodiesterase (PDE) type IV selective inhibitors. Compounds disclosed herein can be useful in the treatment of AIDS, asthma, arthritis, bronchitis, chronic obstructive pulmonary disease (COPD), psoriasis, allergic rhinitis, shock, atopic dermatitis, Crohn's disease, adult respiratory distress syndrome (ARDS), eosinophilic granuloma, allergic conjunctivitis, osteoarthritis, ulcerative colitis and other inflammatory diseases, especially in humans. Processes for the preparation of disclosed compounds, pharmaceutical compositions containing the disclosed compounds, and their use as PDE type IV selective inhibitors, are provided.
    本发明涉及异噁唑啉生物及其类似物,可用作磷酸二酯酶(PDE)IV型选择性抑制剂。本文所披露的化合物可用于治疗艾滋病、哮喘、关节炎、支气管炎、慢性阻塞性肺疾病(COPD)、屑病、过敏性鼻炎、休克、特应性皮炎、克罗恩病、成人呼吸窘迫综合症(ARDS)、嗜酸性肉芽肿、过敏性结膜炎、骨关节炎、溃疡性结肠炎和其他炎症性疾病,尤其是在人类中。本文提供了所披露的化合物的制备方法、含有所披露的化合物的药物组合物以及它们作为PDE IV型选择性抑制剂的用途。
  • PYRIDO [4,3-B] INDOLE AND PYRIDO [3,4-B] INDOLE DERIVATIVES AND METHODS OF USE
    申请人:Medivation Technologies, Inc.
    公开号:US20150335654A1
    公开(公告)日:2015-11-26
    This disclosure is directed to pyrido[4,3-b]indole and pyrido[3,4-b]indole derivatives. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及吡啶并[4,3-b]吲哚吡啶并[3,4-b]吲哚生物。提供了包含这些化合物的制药组合物,以及使用这些化合物治疗各种治疗应用的方法,包括治疗认知障碍、精神障碍、神经递质介导的障碍和/或神经元障碍。
  • PYRIMIDINE-2,4-DIONE DERIVATIVES AS MATRIX METALLOPROTEINASE INHIBITORS
    申请人:Warner-Lambert Company LLC
    公开号:EP1553949B1
    公开(公告)日:2007-04-18
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