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1-(4-chlorophenyl)-5-(2,6-difluorophenyl)-1H-imidazole | 1193511-83-9

中文名称
——
中文别名
——
英文名称
1-(4-chlorophenyl)-5-(2,6-difluorophenyl)-1H-imidazole
英文别名
5-(2,6-difluorophenyl)-1-(4-chlorophenyl)-1H-imidazole;1-(4-chlorophenyl)-5-(2,6-difluorophenyl)imidazole
1-(4-chlorophenyl)-5-(2,6-difluorophenyl)-1H-imidazole化学式
CAS
1193511-83-9
化学式
C15H9ClF2N2
mdl
——
分子量
290.7
InChiKey
WIRXGPBZMAEWDU-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):
    4.2
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • [EN] MULTI-TARGETED HETEROCYCLIC COMPOUNDS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES MULTI-CIBLE POUR LE TRAITEMENT DE MALADIES NEURODÉGÉNÉRATIVES
    申请人:UNIV PENNSYLVANIA
    公开号:WO2018048969A1
    公开(公告)日:2018-03-15
    The present disclosure provides methods of treating neurodegenerative diseases, peripheral inflammatory conditions, cancers, or parasitic diseases in a subject, comprising administering to the subject a compound of Formula (I), (II), (III), and/or (IV):(I), (II), (III), (IV) or a pharmaceutically acceptable salt thereof, wherein X. R1-R8, R21-R28. R31-R38, and R41-R48 are as defined herein.
    本公开提供了治疗受试者的神经退行性疾病、外周炎症性疾病、癌症或寄生虫病的方法,包括向受试者施用式(I)、(II)、(III)和/或(IV)的化合物:(I)、(II)、(III)、(IV)或其药学上可接受的盐,其中X、R1-R8、R21-R28、R31-R38和R41-R48如本文所定义。
  • Multitargeted Imidazoles: Potential Therapeutic Leads for Alzheimer’s and Other Neurodegenerative Diseases
    作者:Anne-Sophie Cornec、Ludovica Monti、Jane Kovalevich、Vishruti Makani、Michael J. James、Krishna G. Vijayendran、Killian Oukoloff、Yuemang Yao、Virginia M.-Y. Lee、John Q. Trojanowski、Amos B. Smith、Kurt R. Brunden、Carlo Ballatore
    DOI:10.1021/acs.jmedchem.7b00475
    日期:2017.6.22
    Alzheimer's disease (AD) is a complex, multifactorial disease in which different neuropathological mechanisms are likely involved, including those associated with pathological tau and A beta species as well as neuroinflammation. In this context, the development of single multitargeted therapeutics directed against two or more disease mechanisms could be advantageous. Starting from a series of 1,5-diarylimidazoles with microtubule (MT)-stabilizing activity and structural similarities with known NSALDs, we conducted structure-activity relationship studies that led to the identification of multitargeted prototypes with activities as MT-stabilizing agents and/or inhibitors of the cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) pathways. Several examples are brain-penetrant and exhibit balanced multitargeted in vitro activity in the low mu M range. As brain-penetrant MT-stabilizing agents have proven effective against tau-mediated neurodegeneration in animal models, and because COX- and 5-LOX-derived eicosanoids are thought to contribute to A beta plaque deposition, these 1,5-diarylimidazoles provide tools to explore novel multitargeted strategies for AD and other neurodegenerative diseases.
  • [EN] FUNGICIDAL SUBSTITUTED AZOLES<br/>[FR] AZOLES SUBSTITUÉS FONGICIDES
    申请人:DU PONT
    公开号:WO2009137538A3
    公开(公告)日:2012-04-19
  • [EN] FUNGICIDAL MIXTURES<br/>[FR] MÉLANGES FONGICIDES
    申请人:DU PONT
    公开号:WO2011056463A4
    公开(公告)日:2011-11-17
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