Add time:08/29/2019         Source:sciencedirect.com

8-(3,4-Dimethoxystyryl)-1,3-dipropyl-7-methylxanthine exhibited high affinity and selectivity for adenosine A2A receptors in binding assay using rat striatal A2A receptors labeled with [3H2-[p-(2-carboxyethyl)-phenethylamino]-5′-N-ethylcarboxamido- adenosine (CGS21680). The affinity was stereo selective: the E isomer, KF17837, showed a Ki value of 1.0 ±0.057 nM for the A2A receptors, whereas the Z isomer showed much lower affinity. KF17837 had 62-fold selectivity for the A2A receptors versus rat forebrain A1 receptors labeled with [3H]N6-cyclohexyladenosine (CHA). KF17837 was rapidly photoisomerized to form a stable equilibrium mixture (18% E − 82% Z), KF17837S, which showed Ki values of 7.9 ± 0.055 nM and 390 ± 68 nM for the A2A and A1 receptors, respectively. The inhibition type was competitive for [3H]CGS21680 binding. In rat pheochromocytoma PC12 cells KF17837S antagonized cAMP accumulation induced by 1 μM CGS21680 via the A2A receptors, with an IC50 value of 53 ± 10 nM. cAMP accumulation induced by 10 μM 5′-N-ethylcarboxamidoadenosine via the A2B receptors in Jurkat cells (human T-cell line) was inhibited by KF17837S with an IC50 value of 1500 ± 290 nM. These results indicate that KF17837S (and hence KF17837) is a highly potent and selective adenosine A2A receptor antagonist.

We also recommend Trading Suppliers and Manufacturers of 1,3-dipropyl-8-(3-noradamantyl)xanthine (cas 136199-02-5). Pls Click Website Link as below: cas 136199-02-5 suppliers