摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-bromo-9-methylpurine | 1194667-39-4

中文名称
——
中文别名
——
英文名称
6-bromo-9-methylpurine
英文别名
6-bromo-9-methyl-9H-purine
6-bromo-9-methylpurine化学式
CAS
1194667-39-4
化学式
C6H5BrN4
mdl
——
分子量
213.037
InChiKey
JDAHBFHRJASMLL-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

物化性质

  • 熔点:
    157-159 °C(Solv: benzene (71-43-2))
  • 沸点:
    345.3±45.0 °C(Predicted)
  • 密度:
    1.96±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    43.6
  • 氢给体数:
    0
  • 氢受体数:
    3

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

  • 作为产物:
    描述:
    6-溴嘌呤potassium carbonate碘甲烷 作用下, 以 乙腈 为溶剂, 反应 18.0h, 生成 6-bromo-9-methylpurine
    参考文献:
    名称:
    4-Piperidinecarboxamide modulators of vanilloid VR1 receptor
    摘要:
    这项发明涉及辣椒素受体VR1配体。更具体地说,这项发明涉及对VR1具有潜在调节作用的杂环异尼泊酸酰胺,这些化合物对于治疗和预防哺乳动物的疾病状况是有用的。
    公开号:
    US20060116368A1
点击查看最新优质反应信息

文献信息

  • Reactivity of 6-Halopurine Analogs with Glutathione as a Radiotracer for Assessing Function of Multidrug Resistance-Associated Protein 1
    作者:Toshimitsu Okamura、Tatsuya Kikuchi、Kiyoshi Fukushi、Toshiaki Irie
    DOI:10.1021/jm901332c
    日期:2009.11.26
    6-Bromo-7-[C-11]methylpurine is reported to react with glutathione via glutathione S-transferases in the brain and to be converted into a substrate for multidrug resistance-associated protein 1 (MRP1), an efflux pump. The compound with a rapid conversion rate allows quantitative assessment of MRP1 function, but this rate is probably susceptible to interspecies differences. Hence, for application to different species, including humans, it is necessary to adjust the conversion rate by modifying the chemical structure. We therefore designed 6-Halo-9-(or 7)-[C-14]methylpurine (halogen: F, Cl, Br, or I), and evaluated them in vitro with respect to enzymatic reactivity with glutathione using brain homogenates from the mouse, rat, or monkey. There was a marked difference in reactivity between these species. Changes in the position of the methyl group and halogen on N-methyl-6-halopurine provided various compounds possessing wide-ranging reactivity with glutathione. In conclusion, the adjustment of reactivity of 6-bromo-7-[C-11]methylpurine may allow assessment of MRP1 function in the brain in various species.
  • [EN] 4-PIPERIDINECARBOXAMIDE MODULATORS OF VANILLOID VR1 RECEPTOR<br/>[FR] MODULATEURS DE 4-PIPERIDINECARBOXAMIDE DU RECEPTEUR VANILLOIDE VR1
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2006058338A2
    公开(公告)日:2006-06-01
    [EN] This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to hetero isonipecotic amides that are potent modulators of VR1 which are useful for the treatment and prevention of disease conditions in mammals.
    [FR] Cette invention concerne des ligands du récepteur vanilloïde VR1. Plus particulièrement, l'invention concerne des amides isonipecotiques qui sont des modulateurs puissants convenant pour le traitement et la prévention de divers états pathologiques chez les mammifères.
  • 4-Piperidinecarboxamide modulators of vanilloid VR1 receptor
    申请人:Calvo R. Raul
    公开号:US20060116368A1
    公开(公告)日:2006-06-01
    This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to hetero isonipecotic amides that are potent modulators of VR1 which are useful for the treatment and prevention of disease conditions in mammals.
    这项发明涉及辣椒素受体VR1配体。更具体地说,这项发明涉及对VR1具有潜在调节作用的杂环异尼泊酸酰胺,这些化合物对于治疗和预防哺乳动物的疾病状况是有用的。
查看更多