- Signaling Pathways
- GPCR/G Protein
- Adenosine Receptor
Adenosine Receptor
P1 receptor
Adenosine Receptor Isoform Specific Products
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Adenosine Receptor Inhibitors
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Adenosine Receptor Agonists
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Adenosine Receptor Antagonists
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Adenosine Receptor Ligands
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Adenosine Receptor Related Products (432)
Related Products (432)
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Antibodies (2)
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Adenosine Receptor Isoform Comparison
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Aminophylline solution
0 ImagesCat. No.: HY-FLB0140ACAS No.: 56440-60-9Aminophylline solution is mainly composed of Aminophylline dihydrate (HY-B0140A). Aminophylline is a competitive and non-selective phosphodiesterase (PDE) inhibitor. Aminophylline is a competitive adenosine receptor antagonist. Aminophylline has apulmonary vasodilator action as well as a bronchodilator action and has the potential for asthma research. -
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OT-7100
0 ImagesCat. No.: HY-105410CAS No.: 174858-27-6OT-7100 is an orally active analgesic agent. OT-7100 inhibits hyperalgesia possibly by enhancing adenosinergic neurotransmission in the dorsal horn. OT-7100 can be used for the researches of inflammation, neurological and metabolic disease such as diabetes2]. -
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DTI 0009
0 ImagesCat. No.: HY-106180CAS No.: 110299-05-3Synonyms: GR 56072; RG 14202; SelodenosonDTI 0009 is a selective adenosine A1 receptor agonist used to reduce heart rate in patients with atrial fibrillation and to treat arrhythmias. -
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8-Phenyltheophylline
0 Images8-Phenyltheophylline is an adenosine receptor (adenosine receptor) antagonist. 8-Phenyltheophylline blocks adenosine-stimulated cAMP accumulation, inhibits tissue-selective cAMP hydrolysis, and antagonizes the inhibitory effects of adenosine. 8-Phenyltheophylline enhances apomorphine-induced rotational behavior in lesioned rats, reverses the analgesic effect of morphine in the rat hot plate test, and slightly enhances contractile responses of the atrium and ileum. 8-Phenyltheophylline can be used in studies related to unilateral nigrostriatal pathway injury. -
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A3AR antagonist 2
0 ImagesCat. No.: HY-12099CAS No.: 1144161-05-6A3AR antagonist 2 (compound 18) is a potent Human A3 adenosine receptor antagonist with an Ki value of 4.54 nM. -
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- A2AR/A2BR antagonist 1
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Adenosine 5'-monophosphate disodium (Standard)
0 ImagesAdenosine 5'-monophosphate (disodium) (Standard) is the analytical standard of Adenosine 5'-monophosphate (disodium). This product is intended for research and analytical applications. Adenosine 5'-monophosphate disodium is an orally active purine nucleotide, and participates in ATP metabolism. Adenosine 5'-monophosphate disodium is also a ligand for adenosine 2B receptor. Adenosine 5'-monophosphate disodium can activate AMPK in skeletal muscle, and ameliorates insulin resistance and impaired glucose metabolism. Adenosine 5'-monophosphate disodium can be used for research of diabetes. -
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SAR113945 monopotassium
0 ImagesCat. No.: HY-111970BCAS No.: 899418-65-6SAR113945 monopotassium is a highly selective IKK-β inhibitor with an IC50 value of 0.4 nM. SAR113945 monopotassium blocks the canonical NFκB signaling pathway. SAR113945 monopotassium alleviates hyperalgesia to heat and mechanical stimuli, and exerts effects in a zymosan-induced knee joint inflammation model. SAR113945 monopotassium is applicable to research related to symptomatic knee osteoarthritis. -
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Neladenoson dalanate
0 ImagesCat. No.: HY-123353CAS No.: 1239309-58-0Synonyms: Neladenoson bialanate; BAY-1067197Neladenoson dalanate (Neladenoson bialanate; BAY-1067197) is a orally active agonist precursor of partial Adenosine A1 Receptor. Neladenoson dalanate has a good pharmacokinetic and safety profile, can be used for the chronic heart diseases. -
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SDZ-WAG994
0 ImagesCat. No.: HY-103179CAS No.: 130714-47-5Synonyms: WAG-994; N6-Cyclohexy-2'-0-methyladenosineSDZ-WAG994 (WAG-994) is a stable, long-acting, selective and orally active A1-adenosine receptor agonist with a KD of 23 nM. SDZ-WAG994 can be used for the research of atrial fibrillation. -
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- A3AR antagonist 6
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MRS8028
0 ImagesCat. No.: HY-161718CAS No.: 1784714-67-5MRS8028 is an agonist for A3 adenosine receptor (A3AR), which binds hA3AR with Ki of 2.44 nM. MRS8028 is potential for ameliorating ischemia and inflammatory diseases. -
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ADORA2A/PDE4D-IN-1
0 ImagesCat. No.: HY-170397CAS No.: 1321513-73-8ADORA2A/PDE4D-IN-1 (Compound 9) is a dual inhibitor for adenosine A2a receptor (ADORA2A) and phosphodiesterase 4D (PDE4D). ADORA2A/PDE4D-IN-1 can be used in research of bronchial asthma. -
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SYAF080
0 ImagesCat. No.: HY-180424CAS No.: 352692-70-7SYAF080 is a human A₂B adenosine receptor (hA₂B AdoR) antagonist with a Ki of 23.6 nM and a KB of 25.2 nM. SYAF080no relevant inhibition of human CYP450 cytochromes. SYAF080 can be used for the research of inflammation, metabolic and cardiovascular disease. -
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A1AR antagonist 1
0 ImagesCat. No.: HY-144115CAS No.: 2760128-99-0A1AR antagonist 1 (compound 18g) is a potent A1 adenosine receptor (AR) antagonist with Kis of 2.08, 6.91, and 31.2 nM for hA1, hA2A and hA2B, respectively. -
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KT-1
0 ImagesCat. No.: HY-118991CAS No.: 47487-05-8KT-1 is a vasodilator. KT 1 can decrease aortic pressure, renal blood flow, left ventricular enddiastolic pressure and resistances of total peripheral, vertebral, coronary and renal vasculatures and increase aortic blood flow, vertebral blood flow, coronary blood flow, peak positive left ventricular dP/dt and heart rate in anesthetized open-chest dogs. KT-1 can be used for the research of cardiovascular disease. -
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MRS8454
0 ImagesCat. No.: HY-178783MRS8454 is a positive allosteric modulator (PAM) of the A3 adenosine receptor (A3AR). MRS8454 can significantly enhance the maximum effect of the standard agonist Cl-IB-MECA by approximately 286%-300%, and significantly reduce its EC50 value. MRS8454 effectively enhances the ability of A3AR agonists to inhibit the cAMP accumulation induced by Forskolin (HY-15371). MRS8454 can be used for the development of molecular probes. -
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Danshenol B
0 ImagesCat. No.: HY-122963CAS No.: 189308-09-6Danshenol B is a diterpenoid. Danshenol B has strong aldose reductase (AR) inhibitory activity with IC50 value of 0.042μM. Danshenol B can be used for the research of diabetic related complication resulted by metabolic abnormality, such as cataracts, retinopathy, neuropathy, and nephropathy. -
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A2A/A3 agonist-1
0 ImagesCat. No.: HY-179681A2A/A3 agonist-1 is a dual A2A/A3 adenosine receptor agonist. A2A/A3 agonist-1 has a Ki value of 2.9 nM and an EC50 of 0.51 nM for hA2AAR. A2A/A3 agonist-1 has a Ki of 0.8 nM and an EC50 < 0.10 nM for hA3AR. A2A/A3 agonist-1 possesses anti-inflammatory activity and can be used for the research of inflammatory diseases. -
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CGS 24012
0 ImagesCat. No.: HY-118229CAS No.: 120442-40-2Synonyms: DPMA; PD 125944CGS 24012 (DPMA) is a selective adenosine A2 agonist. CGS 24012 produces significant increases in cardiac output. CGS 24012 reduces renal vascular resistance to the greatest extent and produces a concomitant significant increase in renal blood flow. CGS 24012 can be used in the research of hypertension. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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