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Products for Adenosine Receptor

  1. Cat.No. Product Name Information
  2. BCC6649 DPCPX DPCPX
  3. BCC7599 PSB 0788 PSB 0788
  4. BCC7716 (±)-5'-Chloro-5'-deoxy-ENBA Highly selective A<sub>1</sub> agonist (±)-5'-Chloro-5'-deoxy-ENBA
  5. BCC7157 CGS 15943 CGS 15943 is an orally bioavailable non-xanthine Adenosine Receptor antagonist. Its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM in transfected CHO cells, respectively. . CGS 15943
  6. BCC6165 TC-G 1004 TC-G 1004
  7. BCC7598 PSB 603 PSB 603
  8. BCC7338 CGH 2466 dihydrochloride Anti-inflammatory agent. Inhibitor of PDE4 and p38 MAPK, also adenosine receptor antagonist CGH 2466 dihydrochloride
  9. BCC1475 CGS 21680 CGS 21680 is a selective adenosine A2A receptor agonist, with a Ki of 27 nM. CGS 21680
  10. BCC4316 CGS 21680 HCl CGS 21680 Hydrochloride is a selective adenosine A2A receptor agonist with a Ki of 27 nM. CGS 21680 HCl
  11. BCC7215 GR 79236 GR79236 is a highly potent and selective adenosine A1 receptor agonist (Ki = 3.1 nM) that has analgesic and anti-inflammatory actions in humans and animals. GR 79236
  12. BCC7374 SDZ WAG 994 SDZ WAG 994
  13. BCC7032 PD 81723 PD 81723
  14. BCC6124 KW 3902 Rolofylline (KW-3902) is a potent, selective adenosine A1 receptor antagonist that is under development for the treatment of patients with acute congestive heart failure and renal impairment. Rolofylline is metabolized primarily to the pharmacologically active M1-trans and M1-cis metabolites by cytochrome P450 (CYP450). Rolofylline is alleviating the presynaptic dysfunction and restores neuronal activity as well as dendritic spine levels in vitro, is an interesting candidate to combat the hypometabolism and neuronal dysfunction associated with Tau-induced neurodegenerative diseases. KW 3902
  15. BCC5017 Valsartan Valsartan (CGP-48933) is an angiotensin II receptor antagonist for the treatment of high blood pressure and heart failure. Valsartan
  16. BCC6902 ZM 241385 ZM241385 is a potent, high affinity and selective adenosine A2a receptor (A2AR) antagonist with a Ki value of 1.4 nM. ZM 241385
  17. BCC7575 2-Chloroadenosine 2-Chloroadenosine, a stable adenosine analogue, protects against long term development of ischaemic cell loss in the rat hippocampus. 2-Chloroadenosine is an apparent competitive inhibitor of uridine influx (apparent Ki=33 μM) and high-affinity nitrobenzylthioinosine binding (apparent Ki=0.18 mM). 2-Chloroadenosine is a transported permeant for the nucleoside transporter in human erythrocytes. 2-Chloroadenosine
  18. BCC7640 8-(3-Chlorostyryl)caffeine 8-(3-Chlorostyryl)caffeine
  19. BCC7237 PSB 1115 PSB 1115
  20. BCC3798 Istradefylline (KW-6002) Istradefylline is a very potent, selective and orally active adenosine A2A receptor antagonist with Ki of 2.2 nM in experimental models of Parkinson's disease. Istradefylline (KW-6002)
  21. BCC7306 SCH 58261 SCH 58261 is a potent, selective and competitive antagonist of adenosine A2A receptor with an IC50 of 15 nM, and displays 323-, 53- and 100-fold more selective for A2A receptor than A1, A2B, and A3 receptors, respectively. SCH 58261
  22. BCC6938 2-Cl-IB-MECA 2-Cl-IB-MECA is a selective A3 adenosine receptor agonist (Ki = 0.33 nM). Displays 2500- and 1400-fold selectivity over A1 and A2A receptors respectively. 2-Cl-IB-MECA
  23. BCC6972 MRS 1220 MRS 1220
  24. BCC5753 MRS 1334 MRS 1334
  25. BCC7311 2'-MeCCPA 2'-MeCCPA
  26. BCC7656 SLV 320 Derenofylline (SLV 320) is a potent, selective and orally active adenosine A1 receptor antagonist, with Ki values of 1 nM, 200 nM and 398 nM for human A1, A3 and A2A receptors respectively. Derenofylline suppresses cardiac fibrosis and attenuates albuminuria without affecting blood pressure in rats. SLV 320
  27. BCC6106 MRE 3008F20 MRE3008F20 is a highly potent and selective antagonist of adenosine A3 receptor (AA3R), inhibits agonist-induced cAMP elevation in resting T lymphocytes with an IC50 of 5 nM. MRE 3008F20
  28. BCC7120 MRS 1706 MRS-1706 is a potent and selective adenosine A2B receptor inverse agonist. MRS-1706 has Ki values of 1.39, 112, 157, and 230 nM for human A2B, A2A, A1 and A3 receptors respectively. MRS 1706
  29. BCC7473 MRS 1754 MRS 1754 is a selective antagonist radioligand for A2B adenosine receptor with very low affinity for A1 and A3 receptors of both humans and rats. MRS 1754
  30. BCC5214 Nicergoline Nicergoline is an ergot derivative used to treat senile dementia and other disorders with vascular origins. Nicergoline
  31. BCC7030 VUF 5574 VUF 5574
  32. BCC6108 8-Aminoadenine Adenine receptor agonist 8-Aminoadenine
  33. BCC6438 Regadenoson Regadenoson is an A2A adenosine receptor agonist that is a coronary vasodilator that is commonly used in pharmacologic stress testing. Regadenoson
  34. BCC7372 SCH 442416 SCH 442416
  35. BCC6237 LUF 5834 LUF 5834
  36. BCC5804 NECA 5'-N-Ethylcarboxamidoadenosine (NECA) is a nonselective adenosine receptor agonist. NECA
  37. BCC7161 2-Chloro-N6-cyclopentyladenosine Potent, selective A<sub>1</sub> agonist 2-Chloro-N6-cyclopentyladenosine
  38. BCC1868 Preladenant Preladenant is a potent and competitive antagonist of the human adenosine A2A receptor with a Ki of 1.1 nM and has over 1000-fold selectivity over other adenosine receptors. Preladenant
  39. BCC7118 HEMADO HEMADO is a potent and selective adenosine A3 receptor agonist with a Ki of 1.1 nM at the human A3 subtype. HEMADO
  40. BCC7160 N6-Cyclopentyladenosine N6-Cyclopentyladenosine (CPA) is a selective Adenosine A1 receptor agonist, with Ki values of 2.3 nM, 790 nM and 43 nM for human A1, A2A and A3 receptors, respectively. N6-Cyclopentyladenosine
  41. BCC7239 PSB 11 hydrochloride PSB 11 hydrochloride
  42. BCC7240 PSB 36 PSB 36
  43. BCC7163 CV 1808 CV 1808
  44. BCC4973 Ticlopidine HCl Ticlopidine hydrochloride is an adenosine diphosphate (ADP) receptor inhibitor against platelet aggregation with IC50 of ~2 μM. Ticlopidine HCl
  45. BCC1845 Pentostatin Pentostatin (CI-825; Deoxycoformycin) is an irreversible inhibitor of adenosine deaminase with Ki of 2.5 pM. Pentostatin
  46. BCC7238 PSB 10 hydrochloride PSB 10 hydrochloride
  47. BCC5226 UK 14,304 Brimonidine (UK 14304) is a full α2-adrenergic receptor (α2-AR) agonist. UK 14,304
  48. BCC7815 ANR 94 Adenosine A<sub>2A </sub>antagonist ANR 94
  49. BCC6664 1,3-Dipropyl-8-phenylxanthine 1,3-Dipropyl-8-phenylxanthine
  50. BCC2011 Tozadenant Tozadenant is an adenosine A2A receptor antagonist, with Ki of 11.5 nM on human A2A and 6 nM on rhesus A2A. Tozadenant
  51. BCC1710 LUF6000 LUF6000 is an allosteric modulator of the human A3 adenosine receptor (AR). LUF6000
  52. BCC6197 BAY 60-6583 BAY 60-6583 is a potent and high-affinity agonist of adenosine A2B receptor (EC50 = 3 nM) over A1, A2A, and A3 receptors. BAY 60-6583 binds to mouse, rabbit, and dog A2BAR with Ki values of 750 nM, 340 nM and 330 nM, respectively. BAY 60-6583 has a cardioprotective effect in a myocardial ischemia model. BAY 60-6583
  53. BCC7977 Lu AA 47070 Lu AA 47070
  54. BCC7890 XCC XCC
  55. BCC7600 XAC XAC

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