Meltzer Peter C, Blundell Paul, Zona Thomas, Yang Lihua, Huang Hong, Bonab Ali A, Livni Eli, Fischman Alan, Madras Bertha K
Organix Inc., 240 Salem Street, Woburn, MA 01801, USA.
J Med Chem. 2003 Jul 31;46(16):3483-96. doi: 10.1021/jm0301484.
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.
多巴胺转运体(DAT)位于多巴胺神经元的突触前,是帕金森病(Pd)和注意力缺陷多动障碍(ADHD)的一个标志物。在ADHD中,DAT密度水平升高,而在Pd中这些水平则降低。DAT水平的降低也与多巴胺的丧失相对应。我们现在描述了第二代基于(99m)锝的托烷配体在非人类灵长类动物中的设计、合成、生物学特性和单光子发射计算机断层扫描(SPECT)成像,这些配体与DAT有强效且选择性的结合。我们证明,提高的选择性和生物学稳定性使得有足够的药物进入大脑并在体内标记DAT,从而提供非人类灵长类动物中DAT密度的定量测量。我们介绍了氟瑞泰克(N - [(2 - ((3'-N'-丙基 - (1"R) - 3"α - (4 - 氟苯基)托烷 - 2"β - 1 - 丙酰基)(2 - 巯基乙基)氨基)乙酰基] - 2 - 氨基乙硫醇合锝(V)氧化物),一种从这些研究中产生的DAT成像剂,目前正在美国进行1期临床试验。