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N-[4-methoxy-3-(naphthylmethoxy)phenyl]-2-naphthylethanamide | 444343-25-3

中文名称
——
中文别名
——
英文名称
N-[4-methoxy-3-(naphthylmethoxy)phenyl]-2-naphthylethanamide
英文别名
N-[4-methoxy-3-(naphthalen-1-ylmethoxy)phenyl]-2-naphthalen-1-ylacetamide
N-[4-methoxy-3-(naphthylmethoxy)phenyl]-2-naphthylethanamide化学式
CAS
444343-25-3
化学式
C30H25NO3
mdl
——
分子量
447.533
InChiKey
IGIRCFLGTAOSLW-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):
    6.6
  • 重原子数:
    34
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    47.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • Trisubstituted carbocyclic cyclophilin binding compounds and their use
    申请人:——
    公开号:US20020165275A1
    公开(公告)日:2002-11-07
    The present invention relates to novel, non-peptidic small organic compounds having an affinity for cyclophilin (CyP)-type immunophilin proteins, and to pharmaceutical compositions comprising one or more of the said compounds. The invention further relates to the uses of these compounds and compositions for binding CyP-type proteins, inhibiting their peptidyl-prolyl isomerase activity, and for research, development, and therapeutic applications in a variety of medical disorders.
    本发明涉及一种新型的非肽类小有机化合物,其具有与环肽亚精蛋白(CyP)型免疫蛋白亲和力,并且涉及包含所述化合物中的一个或多个的药物组合物。该发明还涉及这些化合物和组合物用于结合CyP型蛋白,抑制其肽基脯酸异构酶活性,并在各种医学疾病的研究、开发和治疗应用中的用途。
  • TRISUBSTITUTED CARBOCYCLIC CYCLOPHILIN BINDING COMPOUNDS AND THEIR USE
    申请人:GUILFORD PHARMACEUTICALS INC.
    公开号:EP1360173A2
    公开(公告)日:2003-11-12
  • US6656971B2
    申请人:——
    公开号:US6656971B2
    公开(公告)日:2003-12-02
  • [EN] TRISUBSTITUTED CARBOCYCLIC CYCLOPHILIN BINDING COMPOUNDS AND THEIR USE<br/>[FR] COMPOSES DE LIAISON DE LA CYCLOPHILINE CARBOXYLIQUE TRISUBSTITUEE ET LEUR UTILISATION
    申请人:GUILFORD PHARM INC
    公开号:WO2002059080A2
    公开(公告)日:2002-08-01
    The present invention relates to novel, non-peptidic small organic compounds having an affinity for cyclophilin (CyP)-type immunophilin proteins, and to pharmaceutical compositions comprising one or more of the said compounds. The invention further relates to the uses of these compounds and compositions for binding CyP-type proteins, inhibiting their peptidyl-prolyl isomerase activity, and for research, development, and therapeutic applications in a variety of medical disorders.
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