Design, synthesis and pharmacological evaluation of novel polycyclic heteroarene ethers as PDE10A inhibitors: Part II
| Autor: | Vijayshree B. Avhad, Rajendra L. Harde, Ashwini A. Joshi, Megha Marathe, Malini Bajpai, Satyawan Jadhav, Mahamad Yunnus A. Mahat, Praveen Kumar Gupta, Sanjib Das, Neelima Khairatkar-Joshi, Maulik Nitinkumar Gandhi, Girish S. Gudi, Deepak K. Bhateja, Srinivas Gullapalli, Shelke Dnyaneshwar Eknath, A. P. Thomas |
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| Rok vydání: | 2014 |
| Předmět: |
Male
Phosphodiesterase Inhibitors Pyridines Stereochemistry Clinical Biochemistry Pharmaceutical Science Ether Biochemistry Rats Sprague-Dawley Mice Structure-Activity Relationship chemistry.chemical_compound Dogs Drug Discovery Animals Humans Potency Structure–activity relationship Molecular Biology chemistry.chemical_classification Dose-Response Relationship Drug Molecular Structure Phosphoric Diester Hydrolases Organic Chemistry Rational design Haplorhini Rats Enzyme chemistry Drug Design Pyrazines Microsome Molecular Medicine PDE10A Linker Ethers |
| Zdroj: | Bioorganic & Medicinal Chemistry Letters. 24:3238-3242 |
| ISSN: | 0960-894X |
| Popis: | We report analogue-based rational design and synthesis of two novel series of polycyclic heteroarenes, pyrrolo[3,2-b]quinolines and pyrido[2,3-b]indoles, tethered to a biaryl system by a methyl-, ethyl- or propyl ether as PDE10A inhibitors. A number of analogues were prepared with variable chain length and evaluated for their ability to block PDE10A enzyme using a radiometric assay. Detailed SAR analyses revealed that compounds with an ethyl ether linker are superior in potency compared to compounds with methyl or propyl ether linkers. These compounds, in general, showed poor metabolic stability in rat and human liver microsomes. The metabolic profile of one of the potent compounds was studied in detail to identify metabolic liabilities of these compounds. Structural modifications were carried out that resulted in improved metabolic stability without significant loss of potency. |
| Databáze: | OpenAIRE |
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