Title compound reportedin this patent were prepd. as allosteric enhancers of the A1 adenosine receptor. These compounds were provided in a multi-step synthesis starting from 3-(4-chlorophenyl)-3-oxopropionitrile. Certain invention compds., showed increasing the A1 specific binding of the agonist [3H]CCPA to human CHO-A1 membranes up to 5.5-fold at 10 μM concn., and exhibited about 6.3-fold increase in the Bmax value of the agonist [3H]CCPA at 10 μM. Thus, I and their pharmaceutical compns. are useful for the treatment of pain, in particular, chronic pain such as neuropathic pain, and inflammatory pain, cardiac disease or disorder such as cardiac disarrhythmias, e.g., paroxysmal supraventricular tachycardia, angina, myocardial infarction and stroke, neurol. disease or injury, sleep disorders, epilepsy and depression.

Preparation of 3-aroylthiophene-2-amines as allosteric enhancers of the A1 adenosine receptor

BARALDI, Pier Giovanni;ROMAGNOLI, Romeo
2009

Abstract

Title compound reportedin this patent were prepd. as allosteric enhancers of the A1 adenosine receptor. These compounds were provided in a multi-step synthesis starting from 3-(4-chlorophenyl)-3-oxopropionitrile. Certain invention compds., showed increasing the A1 specific binding of the agonist [3H]CCPA to human CHO-A1 membranes up to 5.5-fold at 10 μM concn., and exhibited about 6.3-fold increase in the Bmax value of the agonist [3H]CCPA at 10 μM. Thus, I and their pharmaceutical compns. are useful for the treatment of pain, in particular, chronic pain such as neuropathic pain, and inflammatory pain, cardiac disease or disorder such as cardiac disarrhythmias, e.g., paroxysmal supraventricular tachycardia, angina, myocardial infarction and stroke, neurol. disease or injury, sleep disorders, epilepsy and depression.
2009
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1693104
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