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Enantiomers of 2'-Fluoralky1-6-nitroquipazine as serotonin transporter positron emission tomography imaging agents and antidepressant therapeutics

机译:2'-Fluoralky1-6-nitroquipazine对映体作为5-羟色胺转运体正电子发射断层显像剂和抗抑郁药

摘要

Racemic mixtures and individual enantiomers of fluorine-18 or carbon-11 radiolabelled 2′-alkyl-6-nitroquipazine ligands are serotonin transporter (SERT) tracers for positron emission tomography (PET) imaging. The non-radioactive ligand forms possess therapeutic antidepressant in vitro and in vivo pharmacological binding profiles in rodent brain and cells expressing human serotonin transporter (hSERT). Twelve 2′-alkyl-6-nitroquipazine ligands potently bind in sub-nanomolar concentrations to the pre-synaptic SERT binding site where established antidepressant drugs bind and inhibit the re-uptake of the neurotransmitter serotonin (5-HT). In vivo tracer studies in rats as well as monkey PET scan trial have demonstrated the fluorine-18 and carbon-11 positron radionuclide labeled tracers perform as quantitative tracers of specific binding the SERT protein in live brain.
机译:氟18或碳11放射性标记的2'-烷基-6-硝基喹嗪配体的外消旋混合物和单个对映体是用于正​​电子发射断层扫描(PET)成像的血清素转运蛋白(SERT)示踪剂。非放射性配体形式在啮齿动物的大脑和表达人类血清素转运蛋白(hSERT)的细胞中具有治疗性抗抑郁药的体外和体内药理学结合特征。十二个2'-烷基-6-硝基喹嗪配体有效地以亚纳摩尔浓度结合到突触前SERT结合位点,在那里已建立的抗抑郁药结合并抑制神经递质5-羟色胺(5-HT)的再摄取。在大鼠中进行的体内示踪剂研究以及猴子PET扫描试验已证明,氟18和碳11正电子放射性核素标记的示踪剂可作为定量结合示踪剂的定量示踪剂,在活脑中发挥作用。

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