T37792 |
A2A receptor antagonist 1
|
443103-97-7
|
99.76%
|
|
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.
|
T6979 |
SCH 58261
|
160098-96-4
|
99.75%
|
|
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.
|
T1825 |
Reversine
|
656820-32-5
|
99.75%
|
|
Reversine, a small synthetic purine analogue (2, 6-disubstituted purine), is a potent inhibitior of Aurora A/B/C(IC50s=150-500 nM).
|
TN2247 |
Swertisin
|
6991-10-2
|
99.74%
|
|
Swertisin, a novel herbal biomolecule, shows a strong antihyperglycemic action. Swertisin is an adenosine A1 receptor antagonist, is known to have antidiabetic, ...
|
T16378 |
Ogerin
|
1309198-71-7
|
99.7%
|
|
Ogerin is a selective GPR68 positive allosteric modulator (pEC50: 6.83). Ogerin blocks recall in fear conditioning in mice. Ogerin displays inverse agonist and a...
|
T27323 |
FK-453
|
121524-18-3
|
99.69%
|
|
FK-453 is a potent antagonist of non-xanthine adenosine A1 receptor with diuretic and renal vasodilatory activity.
|
T1083 |
Theophylline
|
58-55-9
|
99.65%
|
|
Theophylline (1,3-Dimethylxanthine) is a methyl xanthine derivative from tea with diuretic, smooth muscle relaxant, bronchial dilation, cardiac and central nervo...
|
T28881 |
Sulmazole
|
73384-60-8
|
99.64%
|
|
Sulmazole (AR-L 115-BS) is a small molecule Sulmazole is a small molecule cGMP-PDE inhibitor.Sulmazole is a competitive inhibitor of A1 adenosine receptors.Sulma...
|
T28861 |
ST-1535
|
496955-42-1
|
99.64%
|
|
ST 1535 is a potent and orally active antagonist of A2A adenosine receptor with antiparkinsonian activity and antitremorigenic effects. ST 1535 exhibits the pote...
|
T14944 |
CGS 15943
|
104615-18-1
|
99.63%
|
|
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 Rec...
|
T4265 |
AZD4635
|
1321514-06-0
|
99.61%
|
|
AZD4635 (HTL1071) is a new-type adenosine 2A receptor (A2AR) inhibitor(Ki=1.7 nM).
|
T12159 |
APNEA
|
89705-21-5
|
99.58%
|
|
APNEA ((2R,3R,4S,5R)-2-[6-[2-(4-aminophenyl)ethylamino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol) is a non-selective agonist of adenosine A3 receptor.
|
T2671 |
Regadenoson
|
313348-27-5
|
99.57%
|
|
Regadenoson (CVT-3146) is an adenosine derivative and selective A2A adenosine receptor agonist with coronary vasodilating activity. Upon administration, regadeno...
|
T10822 |
Cirsimarin
|
13020-19-4
|
99.55%
|
|
Cirsimarin (Cirsitakaoside) is a flavonoid isolated from Microtea debilis. It shows a potent antilipogenic effect and decreases adipose tissue deposition in mice...
|
T17117 |
Tonapofylline
|
340021-17-2
|
99.52%
|
|
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 hea...
|
T4006 |
Pentostatin
|
53910-25-1
|
99.47%
|
|
Pentostatin (CI-825) is an extremely effective and irreversible inhibitor of adenosine deaminase (Ki: 2.5 pM).
|
T6884 |
Namodenoson
|
163042-96-4
|
99.4%
|
|
Namodenoson (2-Cl-IB-MECA) is an adenosine A3 receptor agonist.
|
T10248 |
Adenosine antagonist-1
|
431040-19-6
|
99.37%
|
|
Adenosine antagonist-1 acts as an adenosine A3 receptor (AA3R) antagonist.
|
T28748 |
Selodenoson
|
110299-05-3
|
99.33%
|
|
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.
|
T7736 |
2-Chloroadenosine
|
146-77-0
|
99.24%
|
|
2-Chloroadenosine (CADO) is a metabolically stable analog of adenosine that binds to adenosine A1, A2A, and A3 receptors( Ki:300, 80, and 1,900 nM, respectively)...
|