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2-(5-[18F]fluoropentyl)-2-methylmalonic acid diethyl ester | 1443627-00-6

中文名称
——
中文别名
——
英文名称
2-(5-[18F]fluoropentyl)-2-methylmalonic acid diethyl ester
英文别名
[18F]-diethyl 2-(5-fluoropentyl)-2-methylmalonate;diethyl 2-(5-(18F)fluoranylpentyl)-2-methylpropanedioate
2-(5-[<sup>18</sup>F]fluoropentyl)-2-methylmalonic acid diethyl ester化学式
CAS
1443627-00-6
化学式
C13H23FO4
mdl
——
分子量
261.323
InChiKey
VMLKBZCSDKGRCU-UMSOTBISSA-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):
    3.2
  • 重原子数:
    18
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.85
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    5

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:
    2-(5-[18F]fluoropentyl)-2-methylmalonic acid diethyl ester 、 sodium hydroxide 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 0.33h, 生成 [18F]-ML-10
    参考文献:
    名称:
    Microfluidic radiosynthesis and biodistribution of [18F] 2-(5-fluoro-pentyl)-2-methyl malonic acid
    摘要:
    微流体技术已成为正电子发射断层扫描(PET)和单光子发射计算机断层扫描放射性标记化合物放射合成的强大工具。在这项工作中,我们利用连续流动微流体系统(Advion, Inc., USA)对马来酸衍生物[18F] 2-(5-氟戊基)-2-甲基马来酸([18F]-FPMA),即[18F]-ML-10的[18F]氟标记进行了探索,这是一种被提议作为潜在凋亡PET成像剂的放射性示踪剂。放射合成采用了一种新的磷酸酯前体进行开发。通过手动合成初步优化了氟化反应,并作为优化微流体放射合成反应参数的基础。在优化条件下,放射薄层色谱分析显示在水解和纯化之前的[18F]-氟掺入率为79%。水解后,通过C18 Sep-Pak对[18F]-FPMA进行了纯化,最终产品通过放射性高效液相色谱(radio-HPLC)进行了分析,得到了校正后的60%放射化学产率和≥98%的放射化学纯度。生物分布数据显示,注射后60分钟内血液中剩余完整[18F]-FPMA放射性不足2%,表明快速清除。大多数器官对放射性示踪剂的积累较低,放射性主要通过肾脏排除(1小时内清除率为95%)。对血浆和尿液样品的放射性HPLC分析显示,放射性示踪剂在注射后至少稳定存在60分钟。
    DOI:
    10.1002/jlcr.3016
  • 作为产物:
    描述:
    diethyl 2-methyl-2-(5-((tetrahydro-2H-pyran-2-yl)oxy)pentyl)malonate 在 4-二甲氨基吡啶Kryptofix222[18F]钾盐4-甲基苯磺酸吡啶三乙胺 作用下, 以 乙醇二氯甲烷乙腈 为溶剂, 反应 12.5h, 生成 2-(5-[18F]fluoropentyl)-2-methylmalonic acid diethyl ester
    参考文献:
    名称:
    Detection of apoptosis by PET/CT with the diethyl ester of [18F]ML-10 and fluorescence imaging with a dansyl analogue
    摘要:
    The diethyl ester of [F-18]ML-10 is a small molecule apoptotic PET probe for cancer studies. Here we report a novel multi-step synthesis of the diethyl ester of ML-10 in excellent yields via fluorination using Xtal-Fluor-E. In addition, a one-pot radiosynthesis of the diethyl ester of [F-18]ML-10 from nucleophilic [F-18]fluoride was completed in 23% radiochemical yield (decay corrected). The radiochemical purity of the product was >= 99%. The diethyl ester of [F-18]ML-10 was used in vivo to detect apoptosis in the testes of mice. In parallel studies, the dansyl-ML-10 diethyl ester was prepared and used to detect apoptotic cells in an in vitro cell based assay. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.11.019
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文献信息

  • Microfluidic radiosynthesis and biodistribution of [<sup>18</sup>F] 2-(5-fluoro-pentyl)-2-methyl malonic acid
    作者:Gajanan K. Dewkar、Gobalakrishnan Sundaresan、Narottam Lamichhane、Jerry Hirsch、Celina Thadigiri、Thomas Collier、Matthew C. T. Hartman、Ganesan Vaidyanthan、Jamal Zweit
    DOI:10.1002/jlcr.3016
    日期:2013.5.15
    Microfluidics technology has emerged as a powerful tool for the radiosynthesis of positron emission tomography (PET) and single-photon emission computed tomography radiolabeled compounds. In this work, we have exploited a continuous flow microfluidic system (Advion, Inc., USA) for the [18F]-fluorine radiolabeling of the malonic acid derivative, [18F] 2-(5-fluoro-pentyl)-2-methyl malonic acid ([18F]-FPMA), also known as [18F]-ML-10, a radiotracer proposed as a potential apoptosis PET imaging agent. The radiosynthesis was developed using a new tosylated precursor. Radiofluorination was initially optimized by manual synthesis and served as a basis to optimize reaction parameters for the microfluidic radiosynthesis. Under optimized conditions, radio-thin-layer chromatography analysis showed 79% [18F]-fluorine incorporation prior to hydrolysis and purification. Following hydrolysis, the [18F]-FPMA was purified by C18 Sep-Pak, and the final product was analyzed by radio-HPLC (high-performance liquid chromatography). This resulted in a decay-corrected 60% radiochemical yield and ≥98% radiochemical purity. Biodistribution data demonstrated rapid blood clearance with less than 2% of intact [18F]-FPMA radioactivity remaining in the circulation 60 min post-injection. Most organs showed low accumulation of the radiotracer, and radioactivity was predominately cleared through kidneys (95% in 1 h). Radio-HPLC analysis of plasma and urine samples showed a stable radiotracer at least up to 60 min post-injection.
    微流体技术已成为正电子发射断层扫描(PET)和单光子发射计算机断层扫描放射性标记化合物放射合成的强大工具。在这项工作中,我们利用连续流动微流体系统(Advion, Inc., USA)对马来酸衍生物[18F] 2-(5-氟戊基)-2-甲基马来酸([18F]-FPMA),即[18F]-ML-10的[18F]氟标记进行了探索,这是一种被提议作为潜在凋亡PET成像剂的放射性示踪剂。放射合成采用了一种新的磷酸酯前体进行开发。通过手动合成初步优化了氟化反应,并作为优化微流体放射合成反应参数的基础。在优化条件下,放射薄层色谱分析显示在水解和纯化之前的[18F]-氟掺入率为79%。水解后,通过C18 Sep-Pak对[18F]-FPMA进行了纯化,最终产品通过放射性高效液相色谱(radio-HPLC)进行了分析,得到了校正后的60%放射化学产率和≥98%的放射化学纯度。生物分布数据显示,注射后60分钟内血液中剩余完整[18F]-FPMA放射性不足2%,表明快速清除。大多数器官对放射性示踪剂的积累较低,放射性主要通过肾脏排除(1小时内清除率为95%)。对血浆和尿液样品的放射性HPLC分析显示,放射性示踪剂在注射后至少稳定存在60分钟。
  • Detection of apoptosis by PET/CT with the diethyl ester of [18F]ML-10 and fluorescence imaging with a dansyl analogue
    作者:Manikandan Kadirvel、Michael Fairclough、Christopher Cawthorne、Emily J. Rowling、Muhammad Babur、Adam McMahon、Paul Birkket、Alison Smigova、Sally Freeman、Kaye J. Williams、Gavin Brown
    DOI:10.1016/j.bmc.2013.11.019
    日期:2014.1
    The diethyl ester of [F-18]ML-10 is a small molecule apoptotic PET probe for cancer studies. Here we report a novel multi-step synthesis of the diethyl ester of ML-10 in excellent yields via fluorination using Xtal-Fluor-E. In addition, a one-pot radiosynthesis of the diethyl ester of [F-18]ML-10 from nucleophilic [F-18]fluoride was completed in 23% radiochemical yield (decay corrected). The radiochemical purity of the product was >= 99%. The diethyl ester of [F-18]ML-10 was used in vivo to detect apoptosis in the testes of mice. In parallel studies, the dansyl-ML-10 diethyl ester was prepared and used to detect apoptotic cells in an in vitro cell based assay. (C) 2013 Elsevier Ltd. All rights reserved.
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