Cargando…
Novel N-Arylsulfonylindoles Targeted as Ligands of the 5-HT(6) Receptor. Insights on the Influence of C-5 Substitution on Ligand Affinity
A new series of twenty-two C-5 substituted N-arylsulfonylindoles was prepared with the aim of exploring the influence of C-5 substitution on 5-HT(6) receptor affinity. Eleven compounds showed moderate to high affinity at the receptor (K(i) = 58–403 nM), with compound 4d being identified as the most...
Autores principales: | Arrieta-Rodríguez, Loreto, Espinoza-Rosales, Daniela, Vera, Gonzalo, Cho, Young Hwa, Cabezas, David, Vásquez-Velásquez, David, Mella-Raipán, Jaime, Lagos, Carlos F., Recabarren-Gajardo, Gonzalo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227400/ https://www.ncbi.nlm.nih.gov/pubmed/34206083 http://dx.doi.org/10.3390/ph14060528 |
Ejemplares similares
-
Extended N-Arylsulfonylindoles as 5-HT(6) Receptor Antagonists: Design, Synthesis & Biological Evaluation
por: Vera, Gonzalo, et al.
Publicado: (2016) -
Design, Synthesis, Binding and Docking-Based 3D-QSAR Studies of 2-Pyridylbenzimidazoles—A New Family of High Affinity CB1 Cannabinoid Ligands
por: Mella-Raipán, Jaime A., et al.
Publicado: (2013) -
High-affinity fluorescent ligands for the 5-HT(3) receptor
por: Simonin, Jonathan, et al.
Publicado: (2012) -
Structure-Activity Relationships Based on 3D-QSAR CoMFA/CoMSIA and Design of Aryloxypropanol-Amine Agonists with Selectivity for the Human β3-Adrenergic Receptor and Anti-Obesity and Anti-Diabetic Profiles
por: Lorca, Marcos, et al.
Publicado: (2018) -
Classification of 5-HT(1A) Receptor Ligands on the Basis of Their Binding Affinities by Using PSO-Adaboost-SVM
por: Cheng, Zhengjun, et al.
Publicado: (2009)