T16158 |
PF-02575799
|
863491-70-7
|
98%
|
|
PF-02575799 is an inhibitor of microsomal triglyceride transfer protein (MTP) (IC50: 0.77±0.29 nM).
|
TQ0136 |
GR79236
|
124555-18-6
|
98%
|
|
GR79236 is an effective and selective adenosine A1 receptor agonist (Ki: 3.1 nM) that has analgesic and anti-inflammatory actions.
|
T16281 |
Nelonicline
|
1026134-63-3
|
98%
|
|
Nelonicline is a selective agonist of neuronal nicotinic receptors.
|
T13008 |
ST3932
|
1246018-21-2
|
98%
|
|
ST3932 is a ST1535 metabolite, is a adenosine A2A receptor antagonist(Kis of 8 nM and 33 nM for A2A and A1 receptors, respectively).
|
T11762 |
Kira8 Hydrochloride
|
2250019-92-0
|
98%
|
|
Kira8 Hydrochloride is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity with an IC50 of 5.9 nM.
|
T21620 |
2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine
|
133240-06-9
|
98%
|
|
2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine is an adenosine receptor antagonist.
|
T8613 |
1-Ethyl-6-aminouracil
|
41862-09-3
|
98%
|
|
1-Ethyl-6-aminouracil is an intermediate in the synthesis of a series of new substituted Xanthines which have high affinity and selectivity for the human adenosi...
|
T10248 |
Adenosine antagonist-1
|
431040-19-6
|
98%
|
|
Adenosine antagonist-1 acts as an adenosine A3 receptor (AA3R) antagonist.
|
T9180 |
LUF6096
|
1116652-18-6
|
98%
|
|
LUF6096 is a potent allosteric enhancer of the adenosine A3 receptor. LUF6096 is able to allosterically enhance agonist binding. LUF6096 shows low orthosteric af...
|
T0665 |
Xanthine
|
69-89-6
|
98%
|
|
Xanthine is a product on the pathway of purine degradation. Xanthine is subsequently converted to uric acid by the action of the Xanthine oxidase enzyme. Xanthin...
|
T27076 |
8-Cyclopentyl-1,3-dimethylxanthine
|
35873-49-5
|
98%
|
|
8-Cyclopentyl-1,3-dimethylxanthine is a potent antagonist of adenosine A1 receptor.
|
T14127 |
Adenosine A1 receptor activator T62
|
40312-34-3
|
98%
|
|
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 r...
|
T23016 |
MRS1220
|
183721-15-5
|
98%
|
|
MRS1220, a highly potent and selective human A3 adenosine receptor (hA3AR) antagonist with a Ki of 0.59 nM, has therapeutic potential for the research of disease...
|
T27629 |
ISAM-140
|
932191-62-3
|
98%
|
|
ISAM-140 is a potent and highly selective antagonist of A2B adenosine receptor.
|
T16140 |
MRS 1754
|
264622-58-4
|
98%
|
|
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.
|
T5081 |
Adenine monohydrochloride hemihydrate
|
6055-72-7
|
98%
|
|
Adenine is a high affinity adenine receptor agonist (Ki = 18 nM at rat adenine receptor). It inhibits forskolin-stimulated cAMP formation in CHO cells transfecte...
|
T23518 |
VUF 5574
|
280570-45-8
|
98%
|
|
VUF 5574 is a selective antagonist of adenosine A3 receptor with a Ki of 4.03 nM for the recombinant human receptor.
|
T23535L |
Xanthine amine congener trihydrochloride
|
2459963-12-1
|
98%
|
|
Xanthine amine congener trihydrochloride is a potent adenosine antagonist that reverses the reduction in urine flow, sodium excretion and heart rate produced by ...
|
T16136 |
MRS-1706
|
264622-53-9
|
98%
|
|
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 ...
|
T7320 |
Tozadenant
|
870070-55-6
|
98%
|
|
Tozadenant is an adenosine A2A receptor antagonist(Ki of 11.5 nM and 6 nM on human and rhesus,respectively)
|