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Design, synthesis, and biological evaluation of arylmethylpiperidines as Kv1.5 potassium channel inhibitors.
- Source :
-
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2022 Dec; Vol. 37 (1), pp. 462-471. - Publication Year :
- 2022
-
Abstract
- Kv1.5 potassium channel, encoded by KCNA5, is a promising target for the treatment of atrial fibrillation, one of the common arrhythmia. A new series of arylmethylpiperidines derivatives based on DDO-02001 were synthesised and evaluated for their ability to inhibit Kv1.5 channel. Among them, compound DDO-02005 showed good inhibitory activity (IC <subscript>50</subscript> = 0.72 μM), preferable anti-arrhythmic effects and favoured safety. These results indicate that DDO-02005 can be a promising Kv1.5 inhibitor for further studies.
- Subjects :
- Dose-Response Relationship, Drug
Humans
Kv1.5 Potassium Channel metabolism
Molecular Structure
Piperidines chemical synthesis
Piperidines chemistry
Potassium Channel Blockers chemical synthesis
Potassium Channel Blockers chemistry
Structure-Activity Relationship
Drug Design
Kv1.5 Potassium Channel antagonists & inhibitors
Piperidines pharmacology
Potassium Channel Blockers pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1475-6374
- Volume :
- 37
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of enzyme inhibition and medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 35012386
- Full Text :
- https://doi.org/10.1080/14756366.2021.2018683