- Vías de señalización
- GPCR/G Protein
- Adenosine Receptor
Adenosine Receptor
P1 receptor
Adenosine Receptor Isoform Specific Products
All Product Categories
-
Adenosine Receptor Inhibitors
(40)
View all products
-
Adenosine Receptor Agonists
(118)
View all products
-
Adenosine Receptor Antagonists
(199)
View all products
-
Adenosine Receptor Activators
(8)
View all products
-
Adenosine Receptor Modulators
(11)
View all products
-
Adenosine Receptor Degrader
(1)
View all products
-
Adenosine Receptor Ligands
(13)
View all products
-
=Productos relacionados con Adenosine Receptor (421)
-
Antibodies (2)
-
Adenosine Receptor Isoform Comparison
-
Adenosine receptor inhibitor 1
0 ImagesAdenosine receptor inhibitor 1 is a potent and selective adenosine receptor (AR) inhibitor with Ki values of >1000, 68.5, >1000, >1000 nM for A1AR, A2AAR, A2BAR, A3AR, respectively. Adenosine receptor inhibitor 1 shows antinociceptive activity, anti-inflammatory effect and peripheral analgesic effect. Adenosine receptor inhibitor 1 has the potential for the research of cancer or neurodegenerative diseases. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
TAT-GluA2 3Y
0 ImagesTAT-GluA2 3Y is a blood-brain barrier-permeable AMPA receptor inhibitory peptide that crosses cell membranes via the HIV-1 TAT protein domain. TAT-GluA2 3Y blocks the endocytosis of AMPA receptors, including the internalization of GluA1/GluA2 subunits, by disrupting interactions with the AP2, Brag2 and Syt3-GluA2 complexes, while also inhibiting long-term depression. TAT-GluA2 3Y blocks hypoxia-mediated AMPAR internalization, alleviates A1R-induced persistent synaptic inhibition, and reduces cerebral ischemic volume, neurological deficits and spatial memory deficits. TAT-GluA2 3Y blocks the effect of NLRP3 deficiency on fear generalization, inhibits amphetamine-induced behavioral/neurochemical sensitization, weakens the unconditioned stimulus-conditioned stimulus association of morphine, and promotes the extinction of morphine CPP. TAT-GluA2 3Y can be used in studies related to fear generalization, ischemic stroke, hypoxia, drug addiction and opioid addiction. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
CV1808
0 ImagesSynonyms: 2-PhenylaminoadenosineCV1808 (2-Phenylaminoadenosine) is a non-selective A2 adenosine receptor (A2 AR) agonist with Kis of 76 and 1450 nM for A2A and A3 adenosine receptor subtypes, respectively. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
2'-MeCCPA
0 ImagesSynonyms: 2-Chloro-N-cyclopentyl-2′-C-methyladenosine2'-MeCCPA is a potent and selective A1 adenosine receptors (A1AR) agonist. 2'-MeCCPA efficiently inhibits cAMP modulation in both direct pathway medium spiny neurons (dMSNs) and indirect pathway medium spiny neurons (iMSNs). -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
9-Ethyladenine
0 Images9-Ethyladenine is a precursor of competitive antagonists of adenosine receptors (A1, A2, A3), with no significant inhibitory effect on adenine phosphoribosyltransferase (APRT). 9-Ethyladenine derivatives have high affinity and selectivity for A1 (Ki=27 nM), A2A (Ki=46 nM), and A3 (Ki=86 nM) receptors. 9-Ethyladenine does not inhibit brain APRT activity, can be used in the study of adenosine receptor-related diseases (such as nervous system diseases) models. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
Evodenoson
0 ImagesSynonyms: ATL 313; DE 112Evodenoson is a selective agonist of the A2A adenosine receptor. Evodenoson’s primary actions include reducing inflammatory responses, decreasing intestinal fluid secretion, edema, tissue damage, and neutrophil infiltration induced by Clostridium difficile toxin A. Evodenoson’s protective effect is achieved by reducing myeloperoxidase (MPO) and adenosine deaminase (ADA) activities, and by lowering the production of tumor necrosis factor-alpha (TNF-α). -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
- Draflazine
-
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
Norisoboldine hydrochloride
0 ImagesSynonyms: (+)-Laurelliptine hydrochlorideNorisoboldine hydrochloride is an orally active natural aryl hydrocarbon receptor (AhR) agonist. Norisoboldine hydrochloride, as a major isoquinoline alkaloid present in Radix Linderae, can be used for the research of Rheumatoid arthritis and Ulcerative colitis. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
ANR94
0 ImagesANR94 is a potent and selective adenosine A2A receptor (AA2AR) antagonist with an Ki of 46 nM for hAA2AR. ANR94 has the potential for the research of Parkinson's disease. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
Apadenoson
0 ImagesSynonyms: BMS 068645; DWH 146eApadenoson is an adenosine analog with selective agonist activity for the adenosine A2a receptor and induces coronary vasodilatation. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
GS-9667
0 ImagesSynonyms: CVT 3619GS-9667 (CVT 3619), a novel N6-5'-substituted adenosine analog, is a selective, partial agonist of the A1 adenosine receptor (A1AdoR). GS-9667 binds to adipocyte membranes with high (KH=14 nM) and low (KL=5.4 μM) affinities. GS-9667 reduces cyclic AMP content and release of nonesterified fatty acids from epididymal adipocytes with IC50 values of 6 nM and 44 nM, respectively. GS-9667 inhibits lipolysis and has the potential for Type 2 diabetes (T2DM) and dyslipidemia via lowering of free fatty acids (FFA). -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
N6,N6-Dimethyladenosine (Standard)
0 ImagesN6,N6-Dimethyladenosine (Standard) is the analytical standard of N6,N6-Dimethyladenosine (HY-101984). This product is intended for research and analytical applications. N6,N6-Dimethyladenosine, a modified ribonucleoside, is an endogenous A3 adenosine receptor ligand. N6,N6-Dimethyladenosine is an AKT inhibitor with antitumor effects. N6, N6-Dimethyladenosine targets SARS-CoV-2 entry protein ADAM17. N6, N6-Dimethyladenosine robustly inhibits AKT signaling in a variety of non-small cell lung cancer cell lines. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
Enprofylline
0 ImagesEnprofylline acts as a selective and competitive A2B receptor antagonist with the Ki of 7 μM. Enprofylline also acts as a phosphodiesterase inhibitor. Enprofylline can be used for the research of asthma, chronic obstructive pulmonary disease. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
Adenosine monophosphate-13C10,15N5 dilithium
0 ImagesReferencia número: HY-A0181SSynonyms: AMP-13C10,15N5 dilithiumAdenosine monophosphate-13C10,15N5(AMP-13C10,15N5) is the 13C-labeled and 15N-labeled Adenosine monophosphate (HY-A0181). Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
Adenosine amine congener
0 ImagesSynonyms: ADACAdenosine amine congener (ADAC) is a selective A1 adenosine receptor agonist, can ameliorate noise- and Cisplatin-induced cochlear injury. Adenosine amine congener also has neuroprotective effects. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
Inosine-2,8-d2
0 ImagesInosine-2,8-d2 is the deuterium labeled Inosine. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
Vipadenant
0 ImagesSynonyms: BIIB-014; CEB-4520Vipadenant (BIIB-014; CEB-4520) is an adenosine receptor antagonist, with Kis of 1.3 nM and 68 nM for A2A and A1, respectively. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
MRS-3777 hemioxalate
0 ImagesReferencia número: HY-110037No. CAS: 1186195-57-2MRS-3777 hemioxalate is a selective adenosine A3 receptor antagonist. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
AB-MECA
0 ImagesAB-MECA is a high affinity A3 adenosine receptor agonist with a binding Ki of 430.5 nM for human A3 receptors in CHO cells. AB-MECA can enhance plasma histamine level. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
-
Sulcatone
0 ImagesSynonyms: 6-Methyl-5-hepten-2-oneSulcatone (6-Methyl-5-hepten-2-one) is a plant-derived volatile organic compound with activities such as insecticidal, antifungal, and blood pressure-lowering effects. Sulcatone also serves as an insect pheromone and an endogenous metabolite, which can be found in feces. Changes in Sulcatone levels can be used for the auxiliary diagnosis of ulcerative colitis. -
loading...Please select quantityObtener un presupuesto
August 31
-
Please select quantity
August 31
Obtener un presupuesto
loading... -
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
Your Search Returned No Results.
Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.