Design, synthesis, and evaluation of orally active inhibitors of plasminogen activator inhibitor-1 (PAI-1) production
摘要:
A novel series of butadiene-imide 1 (T-686) derivatives having an inhibitory activity against PAI-1 production was synthesized and evaluated their biological activities and DMPK profiles, in which 15k (T-2639) was selected as the best compound based on its strong antithrombotic activity and good bioavailability. (C) 2008 Elsevier Ltd. All rights reserved.
Design, synthesis, and evaluation of orally active inhibitors of plasminogen activator inhibitor-1 (PAI-1) production
摘要:
A novel series of butadiene-imide 1 (T-686) derivatives having an inhibitory activity against PAI-1 production was synthesized and evaluated their biological activities and DMPK profiles, in which 15k (T-2639) was selected as the best compound based on its strong antithrombotic activity and good bioavailability. (C) 2008 Elsevier Ltd. All rights reserved.
Abstract The tricyclic enones 4 and 5 have been synthesised involving acid catalysed intramolecular cyclisation of the diazo-methyl ketones 1 and 2 respectively. The present synthesis constitutes a new route to hydrophenanthrene ring system.
A novel series of butadiene-imide 1 (T-686) derivatives having an inhibitory activity against PAI-1 production was synthesized and evaluated their biological activities and DMPK profiles, in which 15k (T-2639) was selected as the best compound based on its strong antithrombotic activity and good bioavailability. (C) 2008 Elsevier Ltd. All rights reserved.