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2,6-Dimethyl-4-((E)-2-nitro-vinyl)-phenol | 210057-08-2

中文名称
——
中文别名
——
英文名称
2,6-Dimethyl-4-((E)-2-nitro-vinyl)-phenol
英文别名
2,6-Dimethyl-4-(2-nitroethenyl)phenol;2,6-dimethyl-4-[(E)-2-nitroethenyl]phenol
2,6-Dimethyl-4-((E)-2-nitro-vinyl)-phenol化学式
CAS
210057-08-2
化学式
C10H11NO3
mdl
——
分子量
193.202
InChiKey
ULOPZCZOKDOQOX-ONEGZZNKSA-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):
    2.6
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    66
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • Antitumor Agent
    申请人:Arai Hitoshi
    公开号:US20090012060A1
    公开(公告)日:2009-01-08
    The present invention provides an antitumor agent and the like, which comprises as an active ingredient, a pyrimidine derivative represented by Formula (I): [wherein —X—Y-Z- represents —O—CR 3 ═N— (wherein R 3 represents a hydrogen atom, a substituted or unsubstituted aromatic heterocyclic group and the like) and the like, R 1 represents —NR 10 R 11 (wherein R 10 and R 11 may be the same or different, and each represents a hydrogen atom, substituted or unsubstituted lower alkyl and the like) and the like, R 2 represents —NR 13 R 14 (wherein R 13 and R 14 may be the same or different, and each represents a hydrogen atom, substituted or unsubstituted lower alkyl and the like)] or a pharmaceutically acceptable salt thereof.
    本发明提供了一种抗肿瘤剂及类似物,其包括一种以嘧啶生物为活性成分,其表示为式(I):[其中- X-Y-Z-表示-O-CR3═N-(其中R3表示氢原子,取代或未取代的芳香族杂环基等),R1表示-NR10R11(其中R10和R11可以相同或不同,且每个表示氢原子,取代或未取代的较低烷基等),R2表示-NR13R14(其中R13和R14可以相同或不同,且每个表示氢原子,取代或未取代的较低烷基等)]或其药学上可接受的盐。
  • ANTI-TUMOR AGENT
    申请人:KYOWA HAKKO KOGYO CO., LTD.
    公开号:EP1749827A1
    公开(公告)日:2007-02-07
    The present invention provides an antitumor agent and the like, which comprises as an active ingredient, a pyrimidine derivative represented by Formula (I): [wherein -X-Y-Z- represents -O-CR3=N- (wherein R3 represents a hydrogen atom, a substituted or unsubstituted aromatic heterocyclic group and the like) and the like, R1 represents -NR10R11 (wherein R10 and R11 may be the same or different, and each represents a hydrogen atom, substituted or unsubstituted lower alkyl and the like) and the like, R2 represents -NR13R14 (wherein R13 and R14 may be the same or different, and each represents a hydrogen atom, substituted or unsubstituted lower alkyl and the like)] or a pharmaceutically acceptable salt thereof.
    本发明提供了一种抗肿瘤剂等,其活性成分包括由式(I)表示的嘧啶生物: [其中-X-Y-Z-代表-O-CR3=N-(其中 R3 代表氢原子、取代或未取代的芳香杂环基等)等,R1 代表-NR10R11(其中 R10 和 R11 可以相同或不同,各自代表氢原子、R2代表-NR13R14(其中R13和R14可以相同或不同,且各自代表氢原子、取代或未取代的低级烷基等)]或其药学上可接受的盐。
  • NOVEL EZRIN INHIBITORS AND METHODS OF MAKING AND USING
    申请人:GEORGETOWN UNIVERSITY
    公开号:US20140135325A1
    公开(公告)日:2014-05-15
    The invention encompasses compound and pharmaceutical composition comprising the compound of the following Formula (I): or pharmaceutically acceptable salts or prodrugs thereof, that are useful for inhibiting ezrin protein in a cell or for inhibiting the growth of a cancer cell.
  • US7956060B2
    申请人:——
    公开号:US7956060B2
    公开(公告)日:2011-06-07
  • US9522908B2
    申请人:——
    公开号:US9522908B2
    公开(公告)日:2016-12-20
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