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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
TN2247 | Swertisin | Adenosine Receptor | |
Swertisin, a novel herbal biomolecule, shows a strong antihyperglycemic action. Swertisin is an adenosine A1 receptor antagonist, is known to have antidiabetic, anti-inflammatory and antioxidant effects. | |||
T22234 | Alloxazine | Adenosine Receptor | |
Alloxazine (Isoalloxazine) is an A2 receptor antagonist, which is approximately 10-fold more selective for the A2B receptor than for the A2A receptor. | |||
T7021 | ZM241385 | Adenosine Receptor | |
ZM-241385 is a high-affinity antagonist ligand selective for the adenosine A2A receptor. | |||
T1681 | Aminophylline | Phyllocontin | PDE , Adenosine Receptor |
Aminophylline (Phyllocontin) is a competitive nonselective phosphodiesterase inhibitor giving a bronchodilatory effect. | |||
T16140 | MRS 1754 | Adenosine Receptor | |
MRS 1754 is a selective antagonist radioligand for the A2B adenosine receptor. It has a very low affinity for A1 and A3 receptors of both humans and rats. | |||
T8512 | BAY-545 | Adenosine Receptor | |
BAY-545 is an antagonist of A2B adenosine receptor(IC50 : 59 nM). | |||
T14078 | AB928 | Adenosine Receptor | |
AB928 is an orally bioavailable, selective dual adenosine receptor (A2aR/A2bR) antagonist. It has immunomodulatory activity[1]. | |||
T12161 | N6-Ethyladenosine | Adenosine Receptor | |
N6-Ethyladenosine is an adenosine derivative, acts as an agonist of Adenosine receptor(hA1AR and hA3AR with Kis of 4.9 and 4.7 nM , respectively). | |||
T6979 | SCH 58261 | SCH58261 | Adenosine Receptor |
SCH 58261 is a potent and selective A2a adenosine receptor antagonist.The Ki =2.3 nM for rat A2a and 2 nM is for bovine A2a. | |||
T8312 | Derenofylline | Adenosine Receptor | |
Derenofylline is a selective and potent adenosine A(1) antagonist in vitro (Ki=1 nM) | |||
T17023 | Tecadenoson | CVT-510 | Adenosine Receptor |
Tecadenoson (CVT-510) is a selective agonist of A1 adenosine receptor. | |||
T14944 | CGS 15943 | PI3K , Adenosine Receptor | |
CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively. | |||
T0892 | Diphylline | Dyphylline,Diprophylline | PDE , Adenosine Receptor |
Diphylline (Diprophylline) is a xanthine derivative. Diphylline exerts bronchodilator effects and to a lesser extent vasodilator and diuretic properties. Diphylline probably acts as a competitive inhibitor of phosphodies... | |||
TQ0125 | Capadenoson | BAY 68-4986 | Adenosine Receptor |
Capadenoson (BAY 68-4986) is a selective adenosine-A1 receptor agonist. | |||
T14127 | Adenosine A1 receptor activator T62 | Adenosine Receptor | |
Adenosine A1 receptor activator T62 is an allosteric enhancer of adenosine A1 receptor, and it produces antinociception in animal models of acute pain and also reduces hypersensitivity in models of inflammatory and nerve... | |||
T16136 | MRS-1706 | Adenosine Receptor | |
MRS-1706 has Ki values of 1.39, 112, 157, and 230 nM for human A2B, A2A, A1, and A3 receptors respectively. MRS-1706 is an effective and selective adenosine A2B receptor inverse agonist. | |||
T4290 | Preladenant | SCH-420814 | Adenosine Receptor |
Preladenant (SCH-420814) is an orally bioavailable antagonist of the adenosine A2A receptor (Ki: 1.1 nM) and has >1000-fold selectivity over all other adenosine receptors. | |||
T6552 | Istradefylline | KW-6002 | Adenosine Receptor |
Istradefylline (KW-6002)(Ki of 2.2 nM) is a selective adenosine A2A receptor (A2AR) antagonist, which is under development in Phase 3 trails. It has been used in trials studying the treatment and basic science of Drug Ab... | |||
T5940 | Proxyphylline | 7-(2-Hydroxypropyl)theophylline | PDE , Adenosine Receptor |
Proxyphylline (7-(2-Hydroxypropyl)theophylline) is a dual of adenosine A1/A2a receptor inhibitor and phosphodiesterase (PDE) inhibitor. Proxyphylline acts as a cardiac stimulant, vasodilator and bronchodilator. | |||
T9238 | KI-7 | Adenosine Receptor | |
KI-7 is an adenosine A2B receptor positive allosteric modulator. |