Novel huprine derivatives with inhibitory activity toward β-amyloid aggregation and formation as disease-modifying anti-Alzheimer drug candidates

Article

Abstract: A new family of dual binding site acetylcholinesterase (AChE) inhibitors has been designed, synthesi

Palabras claves:

Acetylcholinesterase, drug design, Inhibitors, β-amyloid peptides, β-secretase

Autores:

Andrisano V., Antoni Camins, Arce M.P., Badia A., Bartolini M., Bidon-Chanal A., Camps P., Clos M.V., Galdeano C., Gómez T., Junyent F., Luque F.J., Mancini F., Muñoz-Torrero D., Pallás M., Ramírez L., Ratia M., Rodríguez-Franco M.I., Verdaguer E., Viayna E.

Fuentes:

scopus