Structure activity relationship exploration of 5-hydroxy-2-(3-phenylpropyl)chromones as a unique 5-HT2B receptor antagonist scaffold
| Autor: | Yan Zhang, Martha A. Essandoh, Minsoo Kim, Dwight A. Williams, Piyusha P. Pagare, Myles Truss |
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| Rok vydání: | 2020 |
| Předmět: |
010405 organic chemistry
Stereochemistry Organic Chemistry Clinical Biochemistry Pharmaceutical Science Ligand (biochemistry) 01 natural sciences Biochemistry 5-HT2B receptor 0104 chemical sciences 010404 medicinal & biomolecular chemistry chemistry.chemical_compound chemistry Drug Discovery Chromone Molecular Medicine Structure–activity relationship Receptor Antagonism Molecular Biology 5-HT receptor G protein-coupled receptor |
| Zdroj: | Bioorganic & Medicinal Chemistry Letters. 30:127511 |
| ISSN: | 0960-894X |
| Popis: | Antagonists for the serotonin receptor 2B (5-HT2B) have clinical applications towards migraine, anxiety, irritable bowl syndrome, and MDMA abuse; however, few selective 5-HT2B antagonists have been identified. Previous studies from these labs identified a natural product, 5-hydroxy-2-(2-phenylethyl)chromone (5-HPEC, 2) as the first non-nitrogenous ligand for the 5-HT2B receptor. Studies on 5-HPEC optimization led to the identification of 5-hydroxy-2-(3-phenylpropyl)chromone (5-HPPC, 3), which showed a tenfold improvement in binding affinity over 2 at 5-HT2B. This study aimed to further improve receptor pharmacology of this unique scaffold. Guided by molecular modeling studies modifications at the C-3′ and C-4′ positions of 3 were made to probe their effects on ligand binding affinity and efficacy. Among the derivatives synthesized 5-hydroxy-2-(3-(3-cyanophenyl)propyl)chromone (5-HCPC, 3d) showed the most promise with a multifold improvement in binding affinity (pKi = 7.1 ± 0.07) over 3 with retained antagonism. |
| Databáze: | OpenAIRE |
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