Design, Synthesis, and Preliminary Pharmacological Evaluation of a Set of Small Molecules That Directly Activate Gi Proteins

• Published in: Journal of medicinal chemistry 2005-10, Vol.48 (20), p.6491-6503
• Main Authors: Manetti, Dina, Di Cesare Mannelli, Lorenzo, Dei, Silvia, Galeotti, Nicoletta, Ghelardini, Carla, Romanelli, Maria Novella, Scapecchi, Serena, Teodori, Elisabetta, Pacini, Alessandra, Bartolini, Alessandro, Gualtieri, Fulvio
• Format: Article
• Language: English
• Subjects: Adenylyl Cyclases - metabolism; Analgesics - chemical synthesis; Analgesics - chemistry; Analgesics - pharmacology; Biological and medical sciences; Drug Design; GTP-Binding Protein alpha Subunits, Gi-Go - agonists; GTP-Binding Protein alpha Subunits, Gi-Go - chemistry; GTP-Binding Protein alpha Subunits, Gi-Go - metabolism; Guanosine 5'-O-(3-Thiotriphosphate) - metabolism; Humans; Hydrogen-Ion Concentration; In Vitro Techniques; Lymphocytes - drug effects; Lymphocytes - metabolism; Medical sciences; Miscellaneous; Pharmacology. Drug treatments; Piperidines - chemical synthesis; Piperidines - chemistry; Piperidines - pharmacology; Protein Binding; Recombinant Proteins - chemistry; Structure-Activity Relationship
• ISSN: 0022-2623; 1520-4804
• DOI: 10.1021/jm050498l

Heterotrimeric G proteins play a pivotal role in the communication of cells with the environment. G proteins are stimulated by cell surface receptors (GPCR) that catalyze the exchange of GDP, bound to Gα subunit, with GTP and can per se be the target of drugs. Based on the structure of two nonpeptidic modulators of Gi proteins, a series of new molecules characterized by a long hydrophobic chain and at least two nitrogen atoms protonated at physiological pH was designed. The compounds were tested for their ability to stimulate binding of GTPγS to recombinant Gi proteins. Gi activation properties were also evaluated by inhibition of adenylyl cyclase activity in intact lymphocytes. Most compounds were able to stimulate GTPγS binding and to inhibit cAMP production at micromolar doses. Among the active compounds, 34 showed good efficacy and was the most potent compound studied, particularly on αo subtype; its regioisomer, 36, was the most efficacious one. Compound 7 showed also an interesting profile as it showed selectivity toward the αo subtype, in both efficacy and potency. Some of the compounds synthesized and found to be active may be useful leads to develop more potent and selective Gi protein modulators.