|M9774||Namodenoson||Namodenoson (also known as 2-Cl-IB-MECA and CF-102) is an orally bioavailable, synthetic, highly selective adenosine A3 receptor (A3AR) agonist (Ki=0.33 nM) with potential antineoplastic activity.|
|M9674||MRS-3777 hemioxalate||MRS-3777 hemioxalate is a selective adenosine A3 receptor antagonist.|
|M9569||AB928||AB928 is an orally bioavailable, dual antagonist of the A2aR and A2bR adenosine receptors, leads to greater immunomodulatory activity and reduced tumor growth.|
|M7531||AZD4635||AZD4635 is a novel adenosine 2A receptor (A2AR) inhibitor with a Ki of 1.7 nM.|
|M6126||CPI-444||CPI-444 is a potent and selective inhibitor of A2A receptor (A2AR) induces antitumor responses.|
|M5924||Regadenoson||Regadenoson is an A2A adenosine receptor agonist that is a coronary vasodilator that is commonly used in pharmacologic stress testing.|
|M5211||ZM241385||ZM-241385 is a high affinity antagonist ligand selective for the adenosine A2A receptor.|
|M4497||Norisoboldine||Norisoboldine is an isoquinoline alkaloid which acts as an AhR agonist.|
|M3749||Pentostatin||Pentostatin (Deoxycoformycin) is an irreversible inhibitor of adenosine deaminase (Ki = 2.5 pM).|
|M3228||CGS 21680||CGS 21680 is a selective adenosine receptor agonist for A2A and A3 with Ki of 15 ng/mL and 37 ng/mL, respectively.|
|M3188||Istradefylline||Istradefylline is a selective adenosine A2A receptor (A2AR) antagonist with Ki of 2.2 nM.|
|M2282||CGS 21680 hydrochloride||CGS 21680 hydrochloride is an A2A adenosine receptor agonist with an Ki of 27 nM.|
|M1864||SYN115||SYN115 is a novel, selective adenosine A(2A) receptor antagonist.|
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2020 AbMole BioScience. All Rights Reserved.