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Cat No. | Product Name | Synonyms | Targets |
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T14127 | Adenosine A1 receptor activator T62 | Adenosine Receptor | |
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 reduces hypersensitivity in models of inflammatory and nerve... | |||
T22466 | Adenosine receptor A1 antagonist 5 | cAMP | |
Adenosine receptor A1 antagonist 5 acts as an adenosine antagonist, is an oxypurine, acts as an insecticide and pest control agent, and has an inhibitory effect on elevated blood pressure. | |||
T7683 | Adenosine amine congener | ADAC | Adenosine Receptor |
Adenosine amine congener (ADAC) (ADAC) is an agonist of selective A1 adenosine receptor,. | |||
T27076 | 8-Cyclopentyl-1,3-dimethylxanthine | CPT | Adenosine Receptor |
8-Cyclopentyl-1,3-dimethylxanthine (CPT) is a potent antagonist of adenosine A1 receptor. | |||
T12160 | N6-Cyclohexyladenosine | CHA | Adenosine Receptor |
N6-Cyclohexyladenosine (CHA) is a selective agonist of A1 receptor with EC50 of 8.2 Nm. N6-Cyclohexyladenosine exerts anticonvulsant effects and protects against neuronal death. CHA was also found to inhibit the pressor ... | |||
T17023 | Tecadenoson | CVT-510 | Adenosine Receptor |
Tecadenoson (CVT-510) is a selective agonist of A1 adenosine receptor. | |||
T70722 | N 0861 | Adenosine Receptor | |
N 0861 is a selective adenosine A1 receptor antagonist that attenuates renal insufficiency during adenosine-controlled hypotension in rats. | |||
TQ0125 | Capadenoson | BAY 68-4986 | Adenosine Receptor |
Capadenoson (BAY 68-4986) is a selective adenosine-A1 receptor agonist. | |||
T15655 | KFM19 | Adenosine Receptor | |
KFM19 is a potent and selective adenosine receptor (A1-receptor) antagonist (IC50 : 50 nM) for the study of neurological disorders. | |||
T29112 | VPC171 | VPC 171,VPC-171 | Adenosine Receptor |
VPC171 is a novel adenosine A1 receptor positive allosteric modulator (PAM). | |||
T22744 | DPCPX | PD 116948 | Adenosine Receptor |
DPCPX (PD 116948) is an A1 adenosine receptor antagonist | |||
T34914 | Trabodenoson | INNO-8875,INO-8875,PJ875,PJ-875,INNO 8875,INNO8875,PJ 875 | Adenosine Receptor |
Trabodenoson (INO-8875) is a selective and potent adenosine A1 receptor agonist, an adenosine analog, for the study of primary open-angle glaucoma. | |||
T27323 | FK-453 | FK453,FK 453 | Adenosine Receptor |
FK-453 is a potent antagonist of non-xanthine adenosine A1 receptor with diuretic and renal vasodilatory activity. | |||
T21519 | CCPA | 2-chloro-N(6)cyclopentyladenosine,2-CHLORO-N-CYCLOPENTYLADENOSINE | Adenosine Receptor |
CCPA (2-chloro-N(6)cyclopentyladenosine) is a potent and selective agonist of adenosine A1 receptor | |||
T23347 | SDZ WAG 994 | Adenosine Receptor | |
SDZ WAG 994 is an A1 adenosine receptor agonist. | |||
T16263 | N6-Cyclopentyladenosine | UK-80882,CPA | Adenosine Receptor |
N6-Cyclopentyladenosine (CPA) is a selective agonist of the adenosine A1 receptor and can be used to mimic the action of the adenosine A1 receptor, with Ki's of 2.3 nM, 790 nM, and 43 nM for human A1, A2A, and A3 recepto... | |||
T37792 | A2A receptor antagonist 1 | CPI-444 analog,A2A receptor antagonist 1 | Adenosine Receptor |
A2A receptor antagonist 1 (CPI-444 analog) is an antagonist of both adenosine A2A receptor and A1 receptor with Kis of 4 and 264 nM, respectively. | |||
T16140 | MRS 1754 | Adenosine Receptor | |
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. | |||
T28748 | Selodenoson | RG14202,DTI0009,DTI-0009,RG-14202,DT-009,DT009 | Adenosine Receptor |
Selodenoson (RG-14202) is a selective adenosine A1 receptor agonist used to slow the heart rate in patients with atrial fibrillation and to treat arrhythmias. | |||
T39039 | FSCPX | Adenosine Receptor | |
FSCPX is a potent and selective irreversible antagonist of the A1 adenosine receptor (A1AR), exhibiting low nanomolar binding potency. Additionally, FSCPX can effectively decrease the interstitial adenosine level in the ... | |||
T17117 | Tonapofylline | BG 9928 | Adenosine Receptor |
Tonapofylline is an orally active and selective antagonist of the A1 adenosine receptor (Ki: 7.4 nM for human A1). Tonapofylline can be used in studies about heart failure. | |||
T67972L | Amp579 TFA | Amp579 TFA(213453-89-5 Free base) | Adenosine Receptor |
Amp579 TFA is a novel adenosine A1/A2a receptor agonist that induces acute and delayed preconditioning against myocardial shock in vivo. | |||
T14944 | CGS 15943 | PI3K , Adenosine Receptor | |
CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively. | |||
T6441 | CGS 21680 Hydrochloride | CGS 21680 HCl | Adenosine Receptor |
CGS 21680 Hydrochloride (CGS 21680 HCl)(IC50=22 nM), an adenosine receptor agonist, exhibits 140-fold potency in A2 receptor over A1 receptor. | |||
T16782 | Rolofylline | KW-3902,MK-7418,KF-15372 | Adenosine Receptor |
Rolofylline (KW-3902) is a selective adenosine A1 receptor antagonist used in the study of acute congestive heart failure and renal dysfunction, and in the study of neurodegenerative disorders. | |||
T16136 | MRS-1706 | Adenosine Receptor | |
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 receptor inverse agonist. | |||
T16808 | Runcaciguat | Others , Guanylate cyclase | |
Runcaciguat is a soluble guanylate cyclase stimulator. Runcaciguat combines with selective partial adenosine A1 receptor agonists and can be used in studies about cardiovascular and renal diseases. | |||
T2671 | Regadenoson | CVT-3146,Lexiscan | Adenosine Receptor |
Regadenoson (CVT-3146) is an adenosine derivative and selective A2A adenosine receptor agonist with coronary vasodilating activity. Upon administration, regadenoson selectively binds to and activates the A2A adenosine re... | |||
T6884 | Namodenoson | 2-Cl-IB-MECA,CF-102 | Adenosine Receptor |
Namodenoson (2-Cl-IB-MECA) is an adenosine A3 receptor agonist. | |||
T22489 | 2'-MeCCPA | 2-Chloro-N-cyclopentyl-2′-C-methyladenosine | HCV Protease , Adenosine Receptor |
2'-MeCCPA is a potent and highly selective A1 adenosine receptor (A1AR) agonist with a K-value of 1.8 nM for AR.2'-MeCCPA inhibits trichostatin-stimulated adenylate cyclase activity with an IC value of 13.1 nM.2'-MeCCPA ... | |||
T6979 | SCH 58261 | SCH58261 | Adenosine Receptor |
SCH 58261 is a potent and selective A2a adenosine receptor antagonist.The Ki =2.3 nM for rat A2a and 2 nM is for bovine A2a. | |||
T14506 | BAY 60-6583 | Others , Adenosine Receptor | |
BAY 60-6583 is a potent, high-affinity adenosine A2B receptor agonist (EC50 = 3 nM) with affinity for A2B receptors that exceeds that for A1, A2A, and A3 receptors.BAY 60-6583 is cardioprotective in a model of myocardial... | |||
T23202 | PSB 36 | Others | |
A1 adenosine receptor antagonist | |||
T23130 | PD 81723 | Others | |
Allosteric potentiator at the adenosine A1 receptor | |||
T27861 | LUF5831 | LUF 5831,LUF-5831 | |
LUF5831 is an agonist of adenosine A1 receptor. | |||
T70067 | IRFI-165 | ||
IRFI-165 is an adenosine A1 receptor inhibitor | |||
T27862 | LUF5981 | LUF-5981,LUF 5981 | |
LUF5981 is a selective agonist of human adenosine A1 receptor. | |||
T69450 | DU172 | ||
DU172 is the tyrosine-targeted covalent adenosine A1 receptor antagonist. | |||
T24384 | L-97-1 | L97-1,L 97-1 | |
L-97-1 is an antagonist of the adenosine A1 receptor. | |||
T23964 | Dansyl-NECA | DansylNECA | |
Dansyl-NECA is a selective agonist of fluorescent adenosine A1 receptor. | |||
T31086 | CPFPX | [18F]CPFPX | |
CPFPX is a highly selective radioactive ligand for the A1 adenosine receptor (A1AR). | |||
T28446 | PQ-69 | PQ69,PQ 69 | |
PQ-69 is a selective adenosine A1 receptor antagonist with inverse agonist activity. | |||
T70827 | MDL-102234 | ||
MDL-102234 is an adenosine A1 receptor antagonist. | |||
T26565 | Adentri | BG-9719,BG9719,BG 9719,CVT124,CVT-124,CVT 124 | |
Adentri is a novel antagonist of adenosine A1 receptor with unique diuretic activity. | |||
T70667 | KF 20274 | ||
KF 20274 is an adenosine A1 antagonist; purinergic receptor antagonist. | |||
T24526 | Neladenoson dalanate HCl | Neladenoson dalanate hydrochloride | |
Neladenoson dalanate HCl is a potent, selective, orally active partial agonist of adenosine A1 receptor (EC50: 0.1 nM). | |||
T26621 | AMP-579 | RPR100579,RPR 100579,AMP 579,RPR-100579 | |
AMP-579 is an adenosine A1 receptor agonist. AMP-579 also acts as a A2b-adenosine receptor agonist in human 293 cells and rabbit hearts. | |||
T14015 | ST4206 | Others | |
ST4206 is an antagonist of adenosine A2A. For adenosine A2A receptor and adenosine A1 receptor, the Kis values are 12 nM and 197 nM , respectively. | |||
T26737 | Bamifylline Hydrochloride | BAX-2793Z,AC 3810,AC-3810,BAX2793Z,BAX 2793Z | |
Bamifylline Hydrochloride, an adenosine A1 receptor antagonist, is uesd to treat bronchiectasis and chronic obstructive pulmonary disease. | |||
T31068 | CP-608039 | UNII-A1LB8I4247 | |
CP-608039 is a selective adenosine A3 receptor agonist for both human A3 and human A1 receptors. |
Cat No. | Product Name | Synonyms | Targets |
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TN2247 | Swertisin | Adenosine Receptor | |
Swertisin, a novel herbal biomolecule, shows a strong antihyperglycemic action. Swertisin is an adenosine A1 receptor antagonist, is known to have antidiabetic, anti-inflammatory and antioxidant effects. | |||
T2133 | Adenosine monophosphate | 5'-Adenylic acid,AMP,Adenosine 5'-monophosphate | Endogenous Metabolite , AMPK |
Adenosine monophosphate (AMP) is a purine ribonucleoside 5'-monophosphates and a key cellular metabolite in signal transduction and regulation of energy homeostasis.It has a role as an EC 3.1.3.11 (fructose-bisphosphatas... | |||
T10822 | Cirsimarin | Cirsitakaoside | Adenosine Receptor |
Cirsimarin (Cirsitakaoside) is a flavonoid isolated from Microtea debilis. It shows a potent antilipogenic effect and decreases adipose tissue deposition in mice. Cirsimarin has antagonist activity on the adenosine A1 re... | |||
T5940 | Proxyphylline | 7-(2-Hydroxypropyl)theophylline | PDE , Adenosine Receptor |
Proxyphylline (7-(2-Hydroxypropyl)theophylline) is a dual of adenosine A1/A2a receptor inhibitor and phosphodiesterase (PDE) inhibitor. Proxyphylline acts as a cardiac stimulant, vasodilator and bronchodilator. |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00892 | A1AR Protein, Human, Recombinant (His) | Human | in vitro E. coli expression system |
Receptor for adenosine. The activity of this receptor is mediated by G proteins which inhibit adenylyl cyclase. | |||
TMPK-00861 | A2AR Protein-VLP, Human, Recombinant | Human | HEK293 |
Adenosine is a neuromodulator in the adult central nervous system. Membrane-bound receptors for adenosine have been identified and cDNAs for A1, A2a, A2b, and A3 adenosine receptor subtypes have been cloned recently.Expr... |