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

18F-Fpcit

中文名称
——
中文别名
——
英文名称
18F-Fpcit
英文别名
methyl 8-(3-(18F)fluoranylpropyl)-3-(4-iodophenyl)-8-azabicyclo[3.2.1]octane-2-carboxylate
18F-Fpcit化学式
CAS
——
化学式
C18H23FINO2
mdl
——
分子量
430.3
InChiKey
HXWLAJVUJSVENX-AWDFDDCISA-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
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    29.5
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • METHOD FOR THE SYNTHESIS OF 18F-LABELLED BIOMOLECULES
    申请人:GE HEALTHCARE LIMITED
    公开号:US20140235861A1
    公开(公告)日:2014-08-21
    The present invention provides a method for the synthesis of 18 F-labelled biomolecules, which is amenable to automation. The present invention also provides a cassette for automating the method of the invention. The method of the present invention provides numerous advantages over the prior art methods. One less purification step is required as compared with known methods. Also, one less reagent is required as a particular reagent is employed in two different steps. The chemistry process is thereby simplified, the cost of goods is reduced and the burden of validation and documentation of reagents required for GMP clinical production is minimised.
  • METHOD FOR THE SYNTHESIS OF 18F-LABELLED MOLECULES
    申请人:GE HEALTHCARE LIMITED
    公开号:US20140243555A1
    公开(公告)日:2014-08-28
    The present invention provides a method for the synthesis of 18F-labelled biomolecules, which is amenable to automation. The present invention also provides a cassette for automating the method of the invention. The method of the present invention provides numerous advantages over the prior art methods. One less purification step is required as compared with known methods. Also, in a preferred embodiment, one less reagent is required as a particular reagent is employed in two different steps. The chemistry process is thereby simplified, the cost of goods is reduced and the burden of validation and documentation of reagents required for GMP clinical production is minimised.
  • METHOD FOR SYNTHESIZING RADIOPHARMACEUTICALS USING A CARTRIDGE
    申请人:Futurechem Co., LTD.
    公开号:US20150232392A1
    公开(公告)日:2015-08-20
    The present invention relates to a method for synthesizing a radiopharmaceutical using a cartridge, which makes it possible to carry out several steps of reaction required for synthesizing a radiopharmaceutical in the cartridge filled with a polymer. A method for synthesizing a radiopharmaceutical according to the present invention enables each step's reaction to be carried out with the solution confined in the cartridge so as not to flow out, thus being simplified compared to the conventional methods for synthesizing radiopharmaceuticals, and expediting the synthesis thereof.
  • US9085518B2
    申请人:——
    公开号:US9085518B2
    公开(公告)日:2015-07-21
  • US9125954B2
    申请人:——
    公开号:US9125954B2
    公开(公告)日:2015-09-08
查看更多

同类化合物

马拉维若 降莨菪鹼 阿托美品 阿托品硫酸盐 阿托品杂质6 阿托品EP杂质E 辛托溴铵 西克托溴铵 莨菪鹼鹽酸鹽 莨菪碱 莨菪烷 苯酰胺,2-乙氧基-N-[[(8-甲基-8-氮杂二环[3.2.1]辛-3-基)氨基]羰基]-,内- 苯酰胺,2-丁氧基-N-[[(8-甲基-8-氮杂二环[3.2.1]辛-3-基)氨基]羰基]-,内- 苯甲胺,3,5-二氯-N-甲基- 苯甲基2-乙酰氨基-3,6-DI-O-苯甲酰-2-脱氧-α-D-吡喃半乳糖苷 苯基(1R)-3-(4-碘苯基)-8-甲基-8-氮杂双环[3.2.1]辛烷-2-羧酸酯 芽子碱盐酸盐 芽子碱甲酯 芽子碱甲基酯盐酸盐 芽子碱 碘氟潘 硫酸莨菪碱水合物 硫酸茛菪素 盐酸去甲托品 白曼陀罗碱 甲硫托铵 甲基8-甲基-3-苯基-8-氮杂双环[3.2.1]辛烷-2-羧酸酯 甲基(1R,2S,3S,5S)-3-(4-氯苯基)-8-[(Z)-3-碘丙-2-烯基]-8-氮杂双环[3.2.1]辛烷-2-羧酸酯 甲基(1R,2S,3S,5S)-3-(4-氟苯基)-8-甲基-8-氮杂双环[3.2.1]辛烷-2-甲酸酯 甲基(1R,2S,3S,5S)-3-(4-氟苯基)-8-丙-2-烯基-8-氮杂双环[3.2.1]辛烷-2-羧酸酯 甲基(1R)-3-(4-氯苯基)-8-甲基-8-氮杂双环[3.2.1]辛烷-2-羧酸酯 甲基(1R)-3-(4-氟苯基)-8-丙基-8-氮杂双环[3.2.1]辛烷-2-羧酸酯 瑞他莫林杂质7 瑞他莫林中间体 环戊烯,1,5-二甲基-3,4-二(亚甲基)-2-(1-甲基乙基)-(9CI) 环己醇并,2-[(4-乙基苯基)氨基]-,(1R,2R)-rel- 特索芬辛 泽泊思定 氢溴酸天仙子胺 氢溴酸天仙子胺 暂无 斯泰因N1 托品醇异丁酸酯 托品醇壬酸酯 托品醇-3-黄酸酯 托品醇 托品酮 托品巴酯 托品-3-硫醇 打碗花精A5