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N-[4-(5,7,7,10,10-Pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diazabenzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)phenyl]-(2-chloro-5-nitrophenyl)carboxamide | 372096-02-1

中文名称
——
中文别名
——
英文名称
N-[4-(5,7,7,10,10-Pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diazabenzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)phenyl]-(2-chloro-5-nitrophenyl)carboxamide
英文别名
2-chloro-5-nitro-N-[4-(5,7,7,10,10-pentamethyl-8,9-dihydronaphtho[2,3-b][1,5]benzodiazepin-12-yl)phenyl]benzamide
N-[4-(5,7,7,10,10-Pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diazabenzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)phenyl]-(2-chloro-5-nitrophenyl)carboxamide化学式
CAS
372096-02-1
化学式
C35H33ClN4O3
mdl
——
分子量
593.125
InChiKey
RYORBWDGPPAXQA-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):
    9.2
  • 重原子数:
    43
  • 可旋转键数:
    3
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    90.5
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

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文献信息

  • PPAR-gamma modulator
    申请人:SANKYO COMPANY, LIMITED
    公开号:US20030134859A1
    公开(公告)日:2003-07-17
    A compound of the following formula or a pharmacologically acceptable salt thereof: 1 wherein A represents a phenyl group or the like, B represents an aryl group or the like, X represents an oxygen atom or the like, and n represents 0 or 1. The compound is a PPAR &ggr; modulator which is a therapeutic agent for retrograde osteoporosis in which excessive differentiation of adipocytes is inhibited and formation and differentiation of osteoblasts from stem cells is facilitated, and for diabetes mellitus without characteristics such as excessive adipogenesis, liver dysfunction, vascular disorders, heart diseases and the like.
    以下化学式的化合物或其药理学上可接受的盐:其中A代表苯基或类似物,B代表芳基或类似物,X代表氧原子或类似物,n代表0或1。该化合物是一种PPAR &ggr; 调节剂,用于治疗逆行性骨质疏松症,通过抑制脂肪细胞的过度分化并促进干细胞向成骨细胞的形成和分化,以及用于糖尿病而不具有过度脂肪生成、肝功能障碍、血管紊乱、心脏疾病等特征。
  • PPAR (GAMMA) MODULATORS
    申请人:Sankyo Company, Limited
    公开号:EP1277729A1
    公开(公告)日:2003-01-22
    [Subject] The present invention has a purpose for providing a PPAR γ modulator which can be a therapeutic agent for retrograde osteoporosis in which excessive differentiation of adipocytes was inhibited and formation and differentiation of osteoblasts from stem cells is facilitated or that for diabetes mellitus without characteristics such as excessive adipogenesis, liver dysfunction, vascular disorders, heart diseases and the like. [Solution] A compound of the following formula or a pharmacologically acceptable salt thereof: wherein A represents a phenyl group or the like, B represents an aryl group or the like, X represents an oxygen atom or the like, and n represents 0 or 1.
    主题 本发明的目的在于提供一种PPAR γ调节剂,该调节剂可作为逆行性骨质疏松症的治疗药物,在逆行性骨质疏松症中,脂肪细胞的过度分化受到抑制,而干细胞的成骨细胞的形成和分化得到促进,或者可作为无过度脂肪生成、肝功能障碍、血管紊乱、心脏病等特征的糖尿病的治疗药物。 [解决方案] 下式化合物或其药理学上可接受的盐: 其中 A 代表苯基或类似物,B 代表芳基或类似物,X 代表氧原子或类似物,n 代表 0 或 1。
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