Design of selective COX-2 inhibitors in the (aza)indazole series. Chemistry, in vitro studies, radiochemistry and evaluations in rats of a [18F] PET tracer

A series of novel derivatives exhibiting high affinity and selectivity towards the COX-2 enzyme in the (aza) indazole series was developed. A short synthetic route involving a bromination/arylation sequence under microwave irradiation and direct C-H activation were established in the indazole and az...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Jonathan Elie (Автор), Johnny Vercouillie (Автор), Nicolas Arlicot (Автор), Lucas Lemaire (Автор), Rudy Bidault (Автор), Sylvie Bodard (Автор), Christel Hosselet (Автор), Jean-Bernard Deloye (Автор), Sylvie Chalon (Автор), Patrick Emond (Автор), Denis Guilloteau (Автор), Frédéric Buron (Автор), Sylvain Routier (Автор)
Формат:
Опубликовано: Taylor & Francis Group, 2019-01-01T00:00:00Z.
Предметы:
Online-ссылка:Connect to this object online.
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!
Описание
Итог:A series of novel derivatives exhibiting high affinity and selectivity towards the COX-2 enzyme in the (aza) indazole series was developed. A short synthetic route involving a bromination/arylation sequence under microwave irradiation and direct C-H activation were established in the indazole and azaindazole series respectively. In vitro assays were conducted and structural modifications were carried out on these scaffolds to furnish compound 16 which exhibited effective COX-2 inhibitory activity, with IC50 values of 0.409 µM and an excellent selectivity versus COX-1. Radiolabeling of this most potent derivative [18F]16 was achieved after boron ester release and the tracer was evaluated in vivo in a rat model of neuroinflammation. All chemistry, radiochemistry and biological experimental data are discussed.
Примечание:1475-6366
1475-6374
10.1080/14756366.2018.1501043