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5-[2-(2-chlorophenyl)acetylamino]-3-(2-naphthyl)-4-(4-pyridyl)isoxazole | 1000188-50-0

中文名称
——
中文别名
——
英文名称
5-[2-(2-chlorophenyl)acetylamino]-3-(2-naphthyl)-4-(4-pyridyl)isoxazole
英文别名
2-(2-chlorophenyl)-N-(3-naphthalen-2-yl-4-pyridin-4-yl-1,2-oxazol-5-yl)acetamide
5-[2-(2-chlorophenyl)acetylamino]-3-(2-naphthyl)-4-(4-pyridyl)isoxazole化学式
CAS
1000188-50-0
化学式
C26H18ClN3O2
mdl
——
分子量
439.901
InChiKey
XJAWFNXINNHMOQ-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):
    5.6
  • 重原子数:
    32
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    68
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • Pyridylisoxazole Derivatives
    申请人:Hasumi Koichi
    公开号:US20090306145A1
    公开(公告)日:2009-12-10
    This invention offers isoxazole derivatives represented by the following formula (I) in which R 1 and R 2 each stands for hydrogen, lower alkyl, amino and the like; R 3 stands for substituted or unsubstituted aryl or hetero aryl; R 4 stands for hydrogen or lower alkyl; R 5 stands for substituted or unsubstituted phenyl, furyl and the like; and Y stands for —CH 2 —, —CO—, —O—, —NH— and the like, or pharmaceutically acceptable salts thereof which exhibit excellent p38MAPkinase-inhibiting action with reduced side-effects, and are useful for treating such diseases as chronic rheumatoid arthritis, ulcerative colitis and the like.
    该发明提供了以下式(I)所表示的异唑啉衍生物,其中R1和R2分别代表氢,低碳基,基等; R3代表取代或未取代的芳基或杂环芳基; R4代表氢或低碳基; R5代表取代或未取代的苯基,呋喃基等; Y代表-CH2-,-CO-,-O-,-NH-等,或其药学上可接受的盐,具有出色的p38MAPkinase抑制作用,副作用减少,并且用于治疗慢性类风湿性关节炎,溃疡性结肠炎等疾病。
  • PYRIDYLISOXAZOLE DERIVATIVE
    申请人:ASKA Pharmaceutical Co., Ltd.
    公开号:EP2036905A1
    公开(公告)日:2009-03-18
    This invention offers isoxazole derivatives represented by the following formula (I) in which R1 and R2 each stands for hydrogen, lower alkyl, amino and the like; R3 stands for substituted or unsubstituted aryl or hetero aryl; R4 stands for hydrogen or lower alkyl; R5 stands for substituted or unsubstituted phenyl, furyl and the like; and Y stands for -CH2-, -CO-, -O-, -NH- and the like, or pharmaceutically acceptable salts thereof which exhibit excellent p38MAPkinase-inhibiting action with reduced side-effects, and are useful for treating such diseases as chronic rheumatoid arthritis, ulcerative colitis and the like.
    本发明提供了由下式(I)表示的异噁唑生物 其中 R1 和 R2 分别代表氢、低级烷基、基等;R3 代表取代或未取代的芳基或杂芳基;R4 代表氢或低级烷基;R5 代表取代或未取代的苯基、呋喃基等;Y 代表-CH2-、-CO-、-O-、-NH-等、 或其药学上可接受的盐类,它们具有优异的 p38MAPkinase 抑制作用,且副作用较小,可用于治疗慢性类风湿性关节炎、溃疡性结肠炎等疾病。
  • US8207203B2
    申请人:——
    公开号:US8207203B2
    公开(公告)日:2012-06-26
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