| Cat.No. | Name | Information |
|---|---|---|
| M4497 | Norisoboldine | Norisoboldine is an isoquinoline alkaloid which acts as an AhR agonist. |
| M7531 | AZD4635 | AZD4635 is a novel adenosine 2A receptor (A2AR) inhibitor with a Ki of 1.7 nM. |
| M7282 | SCH 58261 | SCH 58261 is a potent, highly selective A2A antagonist. |
| M2282 | CGS 21680 hydrochloride | CGS 21680 hydrochloride is an A2A adenosine receptor agonist with an Ki of 27 nM. |
| M10132 | Inosine | Inosine (Inosine) is an endogenous purine nucleoside produced by the catabolism of adenosine. It has immunomodulatory, neuroprotective effects. |
| M5211 | ZM241385 | ZM-241385 is a high affinity antagonist ligand selective for the adenosine A2A receptor. |
| 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. |
| M27845 | JNJ-40255293 | JNJ-40255293 is a high-affinity human A 2A receptor antagonist with a KiKi of 7.5 nM. JNJ-40255293 can be used in the research of neurodegenerative diseases such as Parkinson's disease. |
| M27806 | LUF6096 | LUF6096, a potent allosteric enhancer of the adenosine A3 receptor, is able to allosterically enhance agonist binding. LUF6096 shows low orthosteric affinity for any of the adenosine receptors. LUF6096 shows protective effects in myocardial ischemia/reperfusion injury. |
| M27646 | VCP171 | VCP171 is a potent adenosine A1 receptor (A1R) positive allosteric modulator (PAM). VCP171 is effective at decreasing excitatory synaptic currents in Lamina II of neuropathic pain model. VCP171 can be used for researching neuropathic pain. |
| M27586 | ATL-801 | ATL-801, an A2B receptor selective antagonist, ameliorates murine colitis. |
| M25400 | KW-6356 | KW-6356 is a potent and selective adenosine A2A receptor antagonist/inverse agonist and exhibits insurmountable antagonism. |
| M20878 | Alloxazine | Alloxazine is an A2 receptor antagonist, which is approximately 10-fold more selective for the A2B receptor than for the A2A receptor. |
| M20848 | MIPS521 | MIPS521 is a positive allosteric modulator of the A1R that exhibits analgesic efficacy in rats in vivo. |
| M20627 | A2AR antagonist 1 | A2AR antagonist 1 is a potent A2AR (Adenosine A2A Receptor) antagonist with Ki values of 4 nM and 264 nM for A2AR and A1R, respectively. |
| M20421 | Theophylline-7-acetic acid | Theophylline-7-acetic acid (Acefylline), acting as an adenosine receptor antagonist, is a stimulant drug of the xanthine chemical class. |
| M20190 | WAY-603264 | WAY-603264 is a adenosine kinase inhibitor. |
| M14295 | 8-Azaadenosine | 8-Azaadenosine is a potent ADAR1 inhibitor and an A-to-I editing inhibitor. 8-Azaadenosine blocks RNA editing and inhibits proliferation, 3D growth, invasion, and migration in thyroid cancer cells. |
| M13883 | LUF6000 | LUF6000 is an orally active allosteric modulator of the A3 adenosine receptor. LUF6000 has potent anti-inflammatory effect. |
| M9674 | MRS-3777 hemioxalate | MRS-3777 hemioxalate is a selective adenosine A3 receptor antagonist. |
| M8788 | FR194921 | FR194921 is a blood-brain barrier-permeable A1R adenosine receptor antagonist. |
| M7169 | PSB 36 | PSB 36 is a potent and selective A 1 antagonist. |
| M6998 | MRS 1334 | MRS 1334 is a potent, highly selective hA 3 antagonist. |
| M6767 | GS 6201 | GS 6201 is a selective antagonist of adenosine A2B receptors (Ki values are 22, 1070, 1940 and 3280 nM for human A2B, A3, A1 and A2A receptors respectively). |
| M6445 | ANR 94 | ANR 94 is a adenosine A 2A antagonist. |
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