T23201 |
PSB 1115
|
152529-79-8
|
99.24%
|
|
human A2B adenosine receptor antagonist
|
T16980 |
Taminadenant
|
1337962-47-6
|
99.2%
|
|
Taminadenant is an adenosine receptor antagonist.
|
T15655 |
KFM19
|
133058-72-7
|
99.18%
|
|
KFM19 is a potent and selective adenosine receptor (A1-receptor) antagonist (IC50 : 50 nM) for the study of neurological disorders.
|
T0892 |
Diphylline
|
479-18-5
|
99.1%
|
|
Diphylline (Diprophylline) is a xanthine derivative. Diphylline exerts bronchodilator effects and to a lesser extent vasodilator and diuretic properties. Diphyll...
|
T14506 |
BAY 60-6583
|
910487-58-0
|
98.87%
|
|
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 recepto...
|
TQ0125 |
Capadenoson
|
544417-40-5
|
98.85%
|
|
Capadenoson (BAY 68-4986) is a selective adenosine-A1 receptor agonist.
|
T10058 |
A2B receptor antagonist 1
|
531506-36-2
|
98.83%
|
|
A2B receptor antagonist 1 (EXAMPLE 9B) is a potent A2B adenosine receptor antagonist.
|
T8551 |
Nitrobenzylthioinosine
|
38048-32-7
|
98.83%
|
|
Nitrobenzylthioinosine (NBMPR) is an inhibitor of ENT1 transporter that binds to ENT1 transporter with high affinity.
|
T6441 |
CGS 21680 Hydrochloride
|
124431-80-7
|
98.81%
|
|
CGS 21680 Hydrochloride (CGS 21680 HCl)(IC50=22 nM), an adenosine receptor agonist, exhibits 140-fold potency in A2 receptor over A1 receptor.
|
T27800 |
LAS38096
|
851371-22-7
|
98.71%
|
|
LAS38096 is an A2B adenosine receptor antagonist (Ki : 17 nM) that is potent, selective and efficient .
|
T22234 |
Alloxazine
|
490-59-5
|
98.68%
|
|
Alloxazine (Isoalloxazine) is an A2 receptor antagonist, which is approximately 10-fold more selective for the A2B receptor than for the A2A receptor.
|
T5S1895 |
Norisoboldine
|
23599-69-1
|
98.64%
|
|
1. Norisoboldine ((+)-Laurelliptine) might be a potential therapeutic agent for rheumatoid arthritis, and it functions through protecting joint destruction as we...
|
T6552 |
Istradefylline
|
155270-99-8
|
98.57%
|
|
Istradefylline (KW-6002)(Ki of 2.2 nM) is a selective adenosine A2A receptor (A2AR) antagonist, which is under development in Phase 3 trails. It has been used in...
|
T26641L |
Apadenoson TFA
|
|
98.40%
|
|
Apadenoson TFA is a potent adenosine A2A receptor (A2AR) agonist that can be used to improve survival in patients infected with SARS.
|
T0853L |
Adenosine 5'-monophosphate monohydrate
|
18422-05-4
|
98.36%
|
|
Adenosine 5'-monophosphate monohydrate (5'-AMP) , also known as 5'-adenylic acid, is a nucleotide that is used as a monomer in RNA. It is an ester of phosphoric ...
|
T12160 |
N6-Cyclohexyladenosine
|
36396-99-3
|
98.31%
|
|
N6-Cyclohexyladenosine (CHA) is a selective agonist of A1 receptor with EC50 of 8.2 Nm. N6-Cyclohexyladenosine exerts anticonvulsant effects and protects against...
|
T7683 |
Adenosine amine congener
|
96760-69-9
|
98.29%
|
|
Adenosine amine congener (ADAC) (ADAC) is an agonist of selective A1 adenosine receptor,.
|
T6115 |
Fostamatinib
|
901119-35-5
|
98.24%
|
|
Fostamatinib (R788)(IC50 of 41 nM), which is a prodrug of the active metabolite R406, is a Syk inhibitor. It does not work on Lyn.
|
T22031 |
ANR 94
|
634924-89-3
|
98.21%
|
|
ANR94 is a potent, selective antagonist of the adenosine A2A receptor (AA2AR), exhibiting a K_i value of 46 nM for the human AA2AR (hAA2AR). This compound shows ...
|
T4290 |
Preladenant
|
377727-87-2
|
98.18%
|
|
Preladenant (SCH-420814) is an orally bioavailable antagonist of the adenosine A2A receptor (Ki: 1.1 nM) and has >1000-fold selectivity over all other adenosine ...
|