T21519 |
CCPA
|
37739-05-2
|
99.91%
|
|
CCPA (2-chloro-N(6)cyclopentyladenosine) is a potent and selective agonist of adenosine A1 receptor
|
T23347 |
SDZ WAG 994
|
130714-47-5
|
99.90%
|
|
SDZ WAG 994 is an A1 adenosine receptor agonist.
|
T9330 |
MIPS521
|
1146188-19-3
|
99.88%
|
|
MIPS521 ({2-Amino-4-[3,5-bis(trifluoromethyl)phenyl]thiophen-3-yl}(4-chlorophenyl)methanone) is a positive allosteric modulator of the A1R.
|
T8312 |
Derenofylline
|
251945-92-3
|
99.84%
|
|
Derenofylline is a selective and potent adenosine A(1) antagonist in vitro (Ki=1 nM)
|
T9516 |
Binodenoson
|
144348-08-3
|
99.84%
|
|
Binodenoson (WRC 0470) is a potent and selective A2A adenosine receptor agonist (KD=270 nM). Binodenoson is being developed as a short-acting coronary vasodilato...
|
T0362 |
Ticlopidine hydrochloride
|
53885-35-1
|
99.82%
|
|
Ticlopidine hydrochloride (Ticlodix) is an effective inhibitor of platelet aggregation commonly used in the placement of STENTS in CORONARY ARTERIES.
|
T0625 |
Theobromine
|
83-67-0
|
99.82%
|
|
Theobromine (3,7-Dimethylxanthine), a xanthine alkaloid, is used as a bronchodilator and as a vasodilator.
|
T10212 |
A2AR-agonist-1
|
41552-95-8
|
99.82%
|
|
A2AR-agonist-1 (N-(2-(1H-Indol-3-yl)ethyl)adenosine) is a potent A2AR and ENT1 agonist (Ki: 4.39 and 3.47 for A2AR and ENT1. It targets the Adenosine A2A Recepto...
|
T1083L |
Theophylline monohydrate
|
5967-84-0
|
99.79%
|
|
Theophylline monohydrate (Quibron) appears to inhibit phosphodiesterase and prostaglandin production, regulate calcium flux and intracellular calcium distributio...
|
T5940 |
Proxyphylline
|
603-00-9
|
99.79%
|
|
Proxyphylline (7-(2-Hydroxypropyl)theophylline) is a dual of adenosine A1/A2a receptor inhibitor and phosphodiesterase (PDE) inhibitor. Proxyphylline acts as a c...
|
T0437 |
Inosine
|
58-63-9
|
99.78%
|
|
Inosine (NSC-20262) is a purine nucleoside that has hypoxanthine linked by the N9 nitrogen to the C1 carbon of ribose. It has immunomodulatory, neuroprotective, ...
|
T27439 |
GS-9667
|
618380-90-8
|
99.76%
|
|
GS-9667, a selective and partial agonist of the A(1) adenosine receptor (AR), represents an effective therapy for Type 2 diabetes (T2DM) and dyslipidemia via low...
|
T27509 |
GW-493838
|
253124-46-8
|
99.76%
|
|
GW-493838 is a potent adenosine A1A receptor agonist for the treatment of dyslipidemia and neuropathic pain, with analgesic effects on post-herpetic neuralgia or...
|
T17023 |
Tecadenoson
|
204512-90-3
|
99.76%
|
|
Tecadenoson (CVT-510) is a selective agonist of A1 adenosine receptor.
|
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).
|
T31731 |
Evodenoson
|
844873-47-8
|
99.74%
|
|
Evodenoson (ATL313) is a potent and selective adenosine A2a receptor (A2aR) agonist for the treatment of eye diseases, tumors, and immune system disorders, and m...
|
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...
|