正电子发射断层摄影术
左乙拉西坦
药效团
体内
药理学
放射性配体
效力
医学
化学
神经科学
核医学
生物
生物化学
癫痫
体外
遗传学
作者
Joël Mercier,Laurence Archen,Véronique Bollu,Stéphane Carré,Yves Evrard,Eric Jnoff,Benoît Kenda,Bénédicte Lallemand,Philippe Maury,Florian Montel,Florence Moureau,Nathalie Price,Yannick Quesnel,Xavier Sauvage,Anne Valade,Laurent Provins
出处
期刊:ChemMedChem
[Wiley]
日期:2014-01-20
卷期号:9 (4): 693-698
被引量:55
标识
DOI:10.1002/cmdc.201300482
摘要
Abstract The role of the synaptic vesicle protein 2A (SV2A) protein, target of the antiepileptic drug levetiracetam, is still mostly unknown. Considering its potential to provide in vivo functional insights into the role of SV2A in epileptic patients, the development of an SV2A positron emission tomography (PET) tracer has been undertaken. Using a 3D pharmacophore model based on close analogues of levetiracetam, we report the rationale design of three heterocyclic non‐acetamide lead compounds, UCB‐A, UCB‐H and UCB‐J, the first single‐digit nanomolar SV2A ligands with suitable properties for development as PET tracers.
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