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| 189949-98-2

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
189949-98-2
化学式
C15H17ClFNO
mdl
——
分子量
281.757
InChiKey
ZSQRYASUKBGQLV-DGAVXFQQSA-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):
    3.16
  • 重原子数:
    19.0
  • 可旋转键数:
    2.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    20.31
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

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
  • 下游产品
    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:
    吡啶 作用下, 以 四氢呋喃乙醚二氯甲烷 为溶剂, 反应 5.0h, 生成 3β-(p-fluorophenyl)-8-methyl-2β-propanoyl-8-azabicyclo<3.2.1>octane
    参考文献:
    名称:
    A Second-Generation 99mTechnetium Single Photon Emission Computed Tomography Agent That Provides in Vivo Images of the Dopamine Transporter in Primate Brain
    摘要:
    The dopamine transporter (DAT), located presynaptically on dopamine neurons, provides a marker for Parkinson's disease (Pd) and attention deficit hyperactivity disorder (ADHD). In ADHD, DAT density levels are elevated, while in Pd these levels are depleted. The depletion of DAT levels also corresponds with the loss of dopamine. We now describe the design, synthesis, biology, and SPECT imaging in nonhuman primates of second-generation (99m)technetium-based tropane ligands that bind potently and selectively to the DAT. We demonstrate that improved selectivity and biological stability allows sufficient agent to enter the brain and label the DAT in vivo to provide a quantitative measure of DAT density in nonhuman primates. We introduce FLUORATEC (N-[(2-((3'-N-propyl-(1"R)-3"alpha-(4-fluorophenyl)tropane-2"beta-1-propanoyl)(2-mercaptoethyl)amino)acetyl)-2-aminoethanethiolato]technetium(V) oxide), a DAT imaging agent that has emerged from these studies and is now in phase 1 clinical trials in the U.S.
    DOI:
    10.1021/jm0301484
  • 作为产物:
    描述:
    脱水芽子碱甲基酯甲磺酸盐草酰氯 作用下, 以 1,4-二氧六环乙醚二氯甲烷 为溶剂, 反应 7.0h, 生成
    参考文献:
    名称:
    Synthesis and binding affinities of 2β-(3-iodoallyloxycarbonyl)-3β-(4-substituted-aryl)tropane analogues as ligands for the dopamine transporter studies
    摘要:
    Tropane analogues from cocaine, which is known to be one of the most reinforcing and addictive compounds, were designed, synthesized, and characterized for inhibition of presynaptic uptake of dopamine (DA) in brain. Eight new derivatives of 3 beta -aryl-2 beta-(3-iodoallyloxycarbonyl)tropanes were synthesized and tested for their potential abilities to displace [H-3]2 beta -carbomethoxy-3 beta-(4-fluorophenyl)tropane (WIN 35,428) binding to the rat striatal membranes. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(01)00625-4
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文献信息

  • Synthesis and Characterization of Technetium-99m-Labeled Tropanes as Dopamine Transporter-Imaging Agents
    作者:Sanath K. Meegalla、Karl Plössl、Mei-Ping Kung、Sumalee Chumpradit、D. Andrew Stevenson、Steven A. Kushner、William T. McElgin、P. David Mozley、Hank F. Kung
    DOI:10.1021/jm960532j
    日期:1997.1.1
    striatal/cerebellar (ST/ CB) ratio reached 2.8 at 60 min after an iv injection. The specific uptake in rat brain can be blocked by pretreating rats with a competing dopamine transporter binding agent, beta-CIT (RTI-55, 2 beta-carbomethoxy-3 beta-(4-iodophenyl)tropane; iv, 1 mg/kg), which reduced the regional brain uptake ratio (ST/CB) to 1.2. In contrast, the specific striatal uptake was not affected by pretreating
    在开发新型Tc-99m标记的托烷衍生物作为多巴胺转运蛋白(再摄取位点)成像剂时,一系列含有中性和亲脂性的复合物,其中双-(乙硫醇)作为[99mTc] TcO3 +中心核的中性复合部分。准备成功。据报道,Tc-99m标记的复合物13-16作为中枢神经系统(CNS)多巴胺转运蛋白成像剂的生物学评估。通过添加两个乙硫醇单元的逐步反应,可以合成托烷衍生物。通过用Hg(OAc)2使4-甲氧基苄基保护基解封以获得三氟乙酸盐,从而获得最终的游离配体。除16种化合物外,所有Tc-99m复合物在多巴胺转运蛋白集中的纹状体区域均表现出良好的初始大脑摄取和选择性摄取。化合物之一,[2-[[2-[[[3-(4-氯苯基)-8-甲基-8-氮杂双环[3.2.1]辛-2-基]甲基](2-巯基乙基)基] [etheth] amino] ethanethiolato-(3-)-N2,N2',S2,S2'] oxo-
  • Intermediates for the synthesis of radiolabelled tropanes
    申请人:PRESIDENT AND FELLOWS OF HARVARD COLLEGE
    公开号:EP1238978A3
    公开(公告)日:2005-03-02
    The compounds of the present invention comprise a tropane compound or ligand that selectively binds to tropane recognition sites, e.g., neuron transporters such as the DAT. The tropane ligand is radiolabeled with a radioactive technetium or rhenium by a chelating ligand which is attached to the tropane ligand by a linker.Tropane compounds or ligands useful in the pratice of the present invention can generally be represented by formula II where R1 and R2 are defined as above and where R1 can also be substituted at the C4 position of the tropane ring:Any tropane compound of the general formula II is useful in the present invention so long as it binds to DAT.Useful tropane analogs have a 3α-group, i.e., are of the boat configuration.Intermediates for the synthesis of the radiolabeled tropanes are claimed.
    本发明的化合物包括一种特定结合到特罗班识别位点的特罗班化合物或配体,例如神经元转运体如DAT。特罗班配体通过连接剂连接到特罗班配体的螯合配体上,用放射性进行放射标记。本发明实施中有用的特罗班化合物或配体通常可用以下公式表示,其中R1和R2如上定义,且R1也可取代于特罗班环的C4位置:只要结合到DAT,任何符合上述一般公式II的特罗班化合物在本发明中均有用。有用的特罗班类似物具有3α-基团,即处于船状构型。本发明要求合成放射标记特罗班的中间体。
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