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2-phenylamino-4-(4'-fluorophenylamino)-6-chloro-s-triazine | 753494-70-1

中文名称
——
中文别名
——
英文名称
2-phenylamino-4-(4'-fluorophenylamino)-6-chloro-s-triazine
英文别名
6-chloro-N-(4-fluorophenyl)-N'-phenyl-1,3,5-triazine-2,4-diamine;6-Chloro-N~2~-(4-fluorophenyl)-N~4~-phenyl-1,3,5-triazine-2,4-diamine;6-chloro-2-N-(4-fluorophenyl)-4-N-phenyl-1,3,5-triazine-2,4-diamine
2-phenylamino-4-(4'-fluorophenylamino)-6-chloro-s-triazine化学式
CAS
753494-70-1
化学式
C15H11ClFN5
mdl
——
分子量
315.737
InChiKey
AUEOSOVBMOMURL-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):
    4.8
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    62.7
  • 氢给体数:
    2
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-phenylamino-4-(4'-fluorophenylamino)-6-chloro-s-triazine氢氧化钾 、 sodium carbonate 作用下, 以 N,N-二甲基甲酰胺丙酮 为溶剂, 反应 6.0h, 生成 (E)-1-{4-[4-(4-Fluoro-phenylamino)-6-phenylamino-[1,3,5]triazin-2-ylamino]-phenyl}-3-(3-methoxy-phenyl)-propenone
    参考文献:
    名称:
    Solankee, Anjani; Thakor, Indrajit, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2006, vol. 45, # 2, p. 517 - 522
    摘要:
    DOI:
  • 作为产物:
    描述:
    苯胺 、 alkaline earth salt of/the/ methylsulfuric acid 在 sodium carbonate 作用下, 以 丙酮 为溶剂, 生成 2-phenylamino-4-(4'-fluorophenylamino)-6-chloro-s-triazine
    参考文献:
    名称:
    Solankee, Anjani; Thakor, Indrajit, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2006, vol. 45, # 2, p. 517 - 522
    摘要:
    DOI:
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文献信息

  • 2,4,6-Triamino-1,3,5-triazine derivative
    申请人:Kubota Hideki
    公开号:US20060194803A1
    公开(公告)日:2006-08-31
    This invention relates to an anti-dementia agent which uses a BEC 1 potassium channel inhibitor as the active ingredient. It was proved that the BEC 1 potassium channel inhibitor has an action to improve learning disorder and is useful as a preventive or therapeutic agent for diseases, preferably dementia, in which the BEC 1 potassium channel is considered to be concerned. Illustratively, it was confirmed by an in vivo test that the BEC 1 potassium channel inhibitor has an action to improve learning disorder. Also, it was found that a compound having 2,4,6-triamino-1,3,5-triazine has a BEC 1 potassium channel inhibitory action.
    本发明涉及一种使用BEC 1钾通道抑制剂作为活性成分的抗痴呆剂。证明了BEC 1钾通道抑制剂具有改善学习障碍的作用,并且作为预防或治疗剂,特别是在BEC 1钾通道被认为与疾病,尤其是痴呆症有关的情况下具有用处。例如,通过体内试验证实了BEC 1钾通道抑制剂具有改善学习障碍的作用。此外,还发现一种具有2,4,6-三氨基-1,3,5-三嗪的化合物具有BEC 1钾通道抑制作用。
  • 2,4,6-TRIAMINO-1,3,5-TRIAZINE DERIVATIVE
    申请人:Astellas Pharma Inc.
    公开号:EP1479397B1
    公开(公告)日:2011-06-08
  • US7375222B2
    申请人:——
    公开号:US7375222B2
    公开(公告)日:2008-05-20
  • Synthesis and antitumor evaluation of a novel series of triaminotriazine derivatives
    作者:Mingfang Zheng、Chenghui Xu、Jianwei Ma、Yan Sun、Feifei Du、Hong Liu、Liping Lin、Chuan Li、Jian Ding、Kaixian Chen、Hualiang Jiang
    DOI:10.1016/j.bmc.2006.11.028
    日期:2007.2
    A series of triaminotriazine derivatives (compounds 5a-f, 6a-x, and 7a-g) was designed, synthesized, and evaluated for their inhibition activities to colorectal cancer (CRC) cell lines (HCT-116 and HT-29). Most of the synthesized compounds demonstrated moderate anti-proliferatory effects on both HCT-116 and HT-29 cell lines at the concentration of 10 mu M. The inhibitory activities against HCT-116 and HT-29 cell lines were discussed to develop the structure-activity relationships of this new series. Compounds 61 and 6o exhibited prominent inhibition activities toward HCT-116, with IC50S of 0.76 and 0.92 mu M, respectively. The in vivo antitumor studies and pharmacokinctics of compound 61 showed that it might be a promising new hit for further development of antitumor agents. (c) 2006 Elsevier Ltd. All rights reserved.
  • Solankee, Anjani; Thakor, Indrajit, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2006, vol. 45, # 2, p. 517 - 522
    作者:Solankee, Anjani、Thakor, Indrajit
    DOI:——
    日期:——
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