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4-(naphth-2-yl)benzyl bromide | 344797-47-3

中文名称
——
中文别名
——
英文名称
4-(naphth-2-yl)benzyl bromide
英文别名
2-[4-(Bromomethyl)phenyl]naphthalene
4-(naphth-2-yl)benzyl bromide化学式
CAS
344797-47-3
化学式
C17H13Br
mdl
——
分子量
297.194
InChiKey
HZZCLRZKVBUUNO-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):
    5.3
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Evaluation of NovelN-(piperidine-4-yl)benzamide Derivatives as Potential Cell Cycle Inhibitors in HepG2 Cells
    摘要:
    In this study, a series of novel N‐(piperidine‐4‐yl)benzamide derivatives was designed, synthesized, and evaluated for antitumor activity. Some compounds were found to have potent antitumor activity. In particular, compound 47 showed the most potent biological activity against HepG2 cells, with an IC50 value of 0.25 μm. Western blot analysis demonstrated that compound 47 inhibited the expression of cyclin B1 and p‐Rb and enhanced the expression of p21, p53, Rb, and phospho‐adenosine monophosphate‐activated protein kinase (p‐AMPK). Further, cell cycle arrest was observed by flow cytometry (FCM). In summary, compound 47 was screened to have potential activity for the treatment of hepatocarcinoma via the induction of cell cycle arrest by a p53/p21‐dependent pathway.
    DOI:
    10.1111/cbdd.12484
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文献信息

  • US5385912A
    申请人:——
    公开号:US5385912A
    公开(公告)日:1995-01-31
  • US5494918A
    申请人:——
    公开号:US5494918A
    公开(公告)日:1996-02-27
  • [EN] MULTICYCLIC TERTIARY AMINE POLYAROMATIC SQUALENE SYNTHETASE INHIBITORS
    申请人:RHONE-POULENC RORER INTERNATIONAL (HOLDINGS) INC.
    公开号:WO1992015579A1
    公开(公告)日:1992-09-17
    (EN) This invention relates to polycyclic compounds containing two mono and/or bicyclic rings and a basic tertiary amino group capable of forming an ammonium ion at biological pH and which reduces levels of serum cholesterol in the body without significantly reducing mevalonic metabolite synthesis. This invention relates also to pharmacological compositions and method of treatment for lowering serum cholesterol levels using the compounds of this invention.(FR) L'invention se rapporte à des composés polycycliques contenant deux chaînes monocycliques et/ou bicycliques et un groupe aminé tertiaire basique qui est capable de former an ion ammonium à un pH biologique et qui réduit les niveaux de cholestérol séral dans l'organisme sans réduire de façon sensible la synthèse des métabolites mévaloniques. L'invention se rapporte également à des compositions pharmacologiques et à des procédés de traitement pour abaisser les niveaux de cholestérol séral au moyen desdits composés.
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