Products for Adenosine Receptor
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BCC6649
DPCPX
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BCC7599
PSB 0788
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BCC7716
(±)-5'-Chloro-5'-deoxy-ENBA
Highly selective A<sub>1</sub> agonist
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BCC7157
CGS 15943
CGS 15943 is an orally bioavailable non-xanthine Adenosine Receptor antagonist. Its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM in transfected CHO cells, respectively. .
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BCC6165
TC-G 1004
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BCC7598
PSB 603
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BCC7338
CGH 2466 dihydrochloride
Anti-inflammatory agent. Inhibitor of PDE4 and p38 MAPK, also adenosine receptor antagonist
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BCC1475
CGS 21680
CGS 21680 is a selective adenosine A2A receptor agonist, with a Ki of 27 nM.
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BCC4316
CGS 21680 HCl
CGS 21680 Hydrochloride is a selective adenosine A2A receptor agonist with a Ki of 27 nM.
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BCC7215
GR 79236
GR79236 is a highly potent and selective adenosine A1 receptor agonist (Ki = 3.1 nM) that has analgesic and anti-inflammatory actions in humans and animals.
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BCC7374
SDZ WAG 994
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BCC7032
PD 81723
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BCC6124
KW 3902
Rolofylline (KW-3902) is a potent, selective adenosine A1 receptor antagonist that is under development for the treatment of patients with acute congestive heart failure and renal impairment. Rolofylline is metabolized primarily to the pharmacologically active M1-trans and M1-cis metabolites by cytochrome P450 (CYP450). Rolofylline is alleviating the presynaptic dysfunction and restores neuronal activity as well as dendritic spine levels in vitro, is an interesting candidate to combat the hypometabolism and neuronal dysfunction associated with Tau-induced neurodegenerative diseases.
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BCC5017
Valsartan
Valsartan (CGP-48933) is an angiotensin II receptor antagonist for the treatment of high blood pressure and heart failure.
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BCC6902
ZM 241385
ZM241385 is a potent, high affinity and selective adenosine A2a receptor (A2AR) antagonist with a Ki value of 1.4 nM.
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BCC7575
2-Chloroadenosine
2-Chloroadenosine, a stable adenosine analogue, protects against long term development of ischaemic cell loss in the rat hippocampus. 2-Chloroadenosine is an apparent competitive inhibitor of uridine influx (apparent Ki=33 μM) and high-affinity nitrobenzylthioinosine binding (apparent Ki=0.18 mM). 2-Chloroadenosine is a transported permeant for the nucleoside transporter in human erythrocytes.
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BCC7640
8-(3-Chlorostyryl)caffeine
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BCC7237
PSB 1115
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BCC3798
Istradefylline (KW-6002)
Istradefylline is a very potent, selective and orally active adenosine A2A receptor antagonist with Ki of 2.2 nM in experimental models of Parkinson's disease.
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BCC7306
SCH 58261
SCH 58261 is a potent, selective and competitive antagonist of adenosine A2A receptor with an IC50 of 15 nM, and displays 323-, 53- and 100-fold more selective for A2A receptor than A1, A2B, and A3 receptors, respectively.
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BCC6938
2-Cl-IB-MECA
2-Cl-IB-MECA is a selective A3 adenosine receptor agonist (Ki = 0.33 nM). Displays 2500- and 1400-fold selectivity over A1 and A2A receptors respectively.
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BCC6972
MRS 1220
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BCC5753
MRS 1334
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BCC7311
2'-MeCCPA
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BCC7656
SLV 320
Derenofylline (SLV 320) is a potent, selective and orally active adenosine A1 receptor antagonist, with Ki values of 1 nM, 200 nM and 398 nM for human A1, A3 and A2A receptors respectively. Derenofylline suppresses cardiac fibrosis and attenuates albuminuria without affecting blood pressure in rats.
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BCC6106
MRE 3008F20
MRE3008F20 is a highly potent and selective antagonist of adenosine A3 receptor (AA3R), inhibits agonist-induced cAMP elevation in resting T lymphocytes with an IC50 of 5 nM.
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BCC7120
MRS 1706
MRS-1706 is a potent and selective adenosine A2B receptor inverse agonist. MRS-1706 has Ki values of 1.39, 112, 157, and 230 nM for human A2B, A2A, A1 and A3 receptors respectively.
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BCC7473
MRS 1754
MRS 1754 is a selective antagonist radioligand for A2B adenosine receptor with very low affinity for A1 and A3 receptors of both humans and rats.
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BCC5214
Nicergoline
Nicergoline is an ergot derivative used to treat senile dementia and other disorders with vascular origins.
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BCC7030
VUF 5574
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BCC6108
8-Aminoadenine
Adenine receptor agonist
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BCC6438
Regadenoson
Regadenoson is an A2A adenosine receptor agonist that is a coronary vasodilator that is commonly used in pharmacologic stress testing.
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BCC7372
SCH 442416
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BCC6237
LUF 5834
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BCC5804
NECA
5'-N-Ethylcarboxamidoadenosine (NECA) is a nonselective adenosine receptor agonist.
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BCC7161
2-Chloro-N6-cyclopentyladenosine
Potent, selective A<sub>1</sub> agonist
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BCC1868
Preladenant
Preladenant is a potent and competitive antagonist of the human adenosine A2A receptor with a Ki of 1.1 nM and has over 1000-fold selectivity over other adenosine receptors.
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BCC7118
HEMADO
HEMADO is a potent and selective adenosine A3 receptor agonist with a Ki of 1.1 nM at the human A3 subtype.
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BCC7160
N6-Cyclopentyladenosine
N6-Cyclopentyladenosine (CPA) is a selective Adenosine A1 receptor agonist, with Ki values of 2.3 nM, 790 nM and 43 nM for human A1, A2A and A3 receptors, respectively.
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BCC7239
PSB 11 hydrochloride
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BCC7240
PSB 36
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BCC7163
CV 1808
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BCC4973
Ticlopidine HCl
Ticlopidine hydrochloride is an adenosine diphosphate (ADP) receptor inhibitor against platelet aggregation with IC50 of ~2 μM.
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BCC1845
Pentostatin
Pentostatin (CI-825; Deoxycoformycin) is an irreversible inhibitor of adenosine deaminase with Ki of 2.5 pM.
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BCC7238
PSB 10 hydrochloride
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BCC5226
UK 14,304
Brimonidine (UK 14304) is a full α2-adrenergic receptor (α2-AR) agonist.
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BCC7815
ANR 94
Adenosine A<sub>2A </sub>antagonist
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BCC6664
1,3-Dipropyl-8-phenylxanthine
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BCC2011
Tozadenant
Tozadenant is an adenosine A2A receptor antagonist, with Ki of 11.5 nM on human A2A and 6 nM on rhesus A2A.
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BCC1710
LUF6000
LUF6000 is an allosteric modulator of the human A3 adenosine receptor (AR).
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BCC6197
BAY 60-6583
BAY 60-6583 is a potent and high-affinity agonist of adenosine A2B receptor (EC50 = 3 nM) over A1, A2A, and A3 receptors. BAY 60-6583 binds to mouse, rabbit, and dog A2BAR with Ki values of 750 nM, 340 nM and 330 nM, respectively. BAY 60-6583 has a cardioprotective effect in a myocardial ischemia model.
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BCC7977
Lu AA 47070
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BCC7890
XCC
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BCC7600
XAC