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Discovery of Heterocyclic Nonacetamide Synaptic Vesicle Protein 2A (SV2A) Ligands with Single‐Digit Nanomolar Potency: Opening Avenues towards the First SV2A Positron Emission Tomography (PET) Ligands
Authors:Joël Mercier  Laurence Archen  Véronique Bollu  Stéphane Carré  Yves Evrard  Dr. Eric Jnoff  Dr. Benoît Kenda  Bénédicte Lallemand  Dr. Philippe Michel  Dr. Florian Montel  Dr. Florence Moureau  Nathalie Price  Dr. Yannick Quesnel  Dr. Xavier Sauvage  Dr. Anne Valade  Dr. Laurent Provins
Affiliation:1. Global Chemistry, UCB NewMedicines, UCB Pharma, Chemin du Foriest, B‐1420 Braine‐L'Alleud (Belgium);2. Cyclotron Research Center, University of Liège, Allée du 6 Ao?t, Bldg. B30, Sart Tilman, 4000 Liège (Belgium);3. StemCell Sciences UK, Babraham Research Campus, Cambridge, CB22 3AT (UK)
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.
Keywords:epilepsy  imaging agents  levetiracetam  positron emission tomography (PET)  synaptic vesicle proteins  tracers
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