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Adenosine Receptor

The adenosine receptors are a class of purinergic G protein-coupled receptors with adenosine as the endogenous ligand. There are four known types of adenosine receptors in humans: A1, A2A, A2B and A3; each is encoded by a different gene.
Cat. No. Product name CAS No. Purity Chemical Structure
T16158 PF-02575799 863491-70-7 98%
PF-02575799 is an inhibitor of microsomal triglyceride transfer protein (MTP) (IC50: 0.77±0.29 nM).
TQ0136 GR79236 124555-18-6 98%
GR79236 is an effective and selective adenosine A1 receptor agonist (Ki: 3.1 nM) that has analgesic and anti-inflammatory actions.
T16281 Nelonicline 1026134-63-3 98%
Nelonicline is a selective agonist of neuronal nicotinic receptors.
T13008 ST3932 1246018-21-2 98%
ST3932 is a ST1535 metabolite, is a adenosine A2A receptor antagonist(Kis of 8 nM and 33 nM for A2A and A1 receptors, respectively).
T11762 Kira8 Hydrochloride 2250019-92-0 98%
Kira8 Hydrochloride is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity with an IC50 of 5.9 nM.
T21620 2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine 133240-06-9 98%
2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine is an adenosine receptor antagonist.
T8613 1-Ethyl-6-aminouracil 41862-09-3 98%
1-Ethyl-6-aminouracil is an intermediate in the synthesis of a series of new substituted Xanthines which have high affinity and selectivity for the human adenosi...
T10248 Adenosine antagonist-1 431040-19-6 98%
Adenosine antagonist-1 acts as an adenosine A3 receptor (AA3R) antagonist.
T9180 LUF6096 1116652-18-6 98%
LUF6096 is a potent allosteric enhancer of the adenosine A3 receptor. LUF6096 is able to allosterically enhance agonist binding. LUF6096 shows low orthosteric af...
T0665 Xanthine 69-89-6 98%
Xanthine is a product on the pathway of purine degradation. Xanthine is subsequently converted to uric acid by the action of the Xanthine oxidase enzyme. Xanthin...
T27076 8-Cyclopentyl-1,3-dimethylxanthine 35873-49-5 98%
8-Cyclopentyl-1,3-dimethylxanthine is a potent antagonist of adenosine A1 receptor.
T14127 Adenosine A1 receptor activator T62 40312-34-3 98%
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 r...
T23016 MRS1220 183721-15-5 98%
MRS1220, a highly potent and selective human A3 adenosine receptor (hA3AR) antagonist with a Ki of 0.59 nM, has therapeutic potential for the research of disease...
T27629 ISAM-140 932191-62-3 98%
ISAM-140 is a potent and highly selective antagonist of A2B adenosine receptor.
T16140 MRS 1754 264622-58-4 98%
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.
T5081 Adenine monohydrochloride hemihydrate 6055-72-7 98%
Adenine is a high affinity adenine receptor agonist (Ki = 18 nM at rat adenine receptor). It inhibits forskolin-stimulated cAMP formation in CHO cells transfecte...
T23518 VUF 5574 280570-45-8 98%
VUF 5574 is a selective antagonist of adenosine A3 receptor with a Ki of 4.03 nM for the recombinant human receptor.
T23535L Xanthine amine congener trihydrochloride 2459963-12-1 98%
Xanthine amine congener trihydrochloride is a potent adenosine antagonist that reverses the reduction in urine flow, sodium excretion and heart rate produced by ...
T16136 MRS-1706 264622-53-9 98%
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 ...
T7320 Tozadenant 870070-55-6 98%
Tozadenant is an adenosine A2A receptor antagonist(Ki of 11.5 nM and 6 nM on human and rhesus,respectively)
PF-02575799
T16158
PF-02575799 is an inhibitor of microsomal triglyceride transfer protein (MTP) (IC50: 0.77±0.29 nM).
GR79236
TQ0136
GR79236 is an effective and selective adenosine A1 receptor agonist (Ki: 3.1 nM) that has analgesic and anti-inflammatory actions.
Nelonicline
T16281
Nelonicline is a selective agonist of neuronal nicotinic receptors.
ST3932
T13008
ST3932 is a ST1535 metabolite, is a adenosine A2A receptor antagonist(Kis of 8 nM and 33 nM for A2A and A1 receptors, respectively).
Kira8 Hydrochloride
T11762
Kira8 Hydrochloride is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity with an IC50 of 5.9 nM.
2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine
T21620
2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine is an adenosine receptor antagonist.
1-Ethyl-6-aminouracil
T8613
1-Ethyl-6-aminouracil is an intermediate in the synthesis of a series of new substituted Xanthines which have high affinity and selectivity for the human adenosi...
Adenosine antagonist-1
T10248
Adenosine antagonist-1 acts as an adenosine A3 receptor (AA3R) antagonist.
LUF6096
T9180
LUF6096 is a potent allosteric enhancer of the adenosine A3 receptor. LUF6096 is able to allosterically enhance agonist binding. LUF6096 shows low orthosteric af...
Xanthine
T0665
Xanthine is a product on the pathway of purine degradation. Xanthine is subsequently converted to uric acid by the action of the Xanthine oxidase enzyme. Xanthin...
8-Cyclopentyl-1,3-dimethylxanthine
T27076
8-Cyclopentyl-1,3-dimethylxanthine is a potent antagonist of adenosine A1 receptor.
Adenosine A1 receptor activator T62
T14127
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 r...
MRS1220
T23016
MRS1220, a highly potent and selective human A3 adenosine receptor (hA3AR) antagonist with a Ki of 0.59 nM, has therapeutic potential for the research of disease...
ISAM-140
T27629
ISAM-140 is a potent and highly selective antagonist of A2B adenosine receptor.
MRS 1754
T16140
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.
Adenine monohydrochloride hemihydrate
T5081
Adenine is a high affinity adenine receptor agonist (Ki = 18 nM at rat adenine receptor). It inhibits forskolin-stimulated cAMP formation in CHO cells transfecte...
VUF 5574
T23518
VUF 5574 is a selective antagonist of adenosine A3 receptor with a Ki of 4.03 nM for the recombinant human receptor.
Xanthine amine congener trihydrochloride
T23535L
Xanthine amine congener trihydrochloride is a potent adenosine antagonist that reverses the reduction in urine flow, sodium excretion and heart rate produced by ...
MRS-1706
T16136
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 ...
Tozadenant
T7320
Tozadenant is an adenosine A2A receptor antagonist(Ki of 11.5 nM and 6 nM on human and rhesus,respectively)
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