Adenosine Receptors
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Pentostatin
Catalog No. A11534 Adenosine deaminase 抑制剂Pentostatin是腺苷脱氨酶的不可逆抑制剂(Ki = 2.5 pM)。 了解更多 -
MT-DADMe-ImmA
Catalog No. A13651 human 5'-methylthioadenosine phosphorylase inhibitorMT-DADMe-ImmA is an inhibitor of human 5'-methylthioadenosine phosphorylase (MTAP) with a Ki of 90 pM. 了解更多 -
A2A receptor antagonist 1
Catalog No. A12567 adenosine A2A/A1 receptor antagonistA2A 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. 了解更多 -
Tonapofylline
Catalog No. A21328 adenosine A1 receptor antagonistTonapofylline (BG 9928) is an orally active and selective adenosine A1 receptor antagonist with a Ki of 7.4 nM for human adenosine A1 receptor (hA1), which displays 915-fold selectivity versus human adenosine A2A receptor and 12-fold selectivity versus human adenosine A2B receptor and is used in development for the treatment of heart failure. 了解更多 -
EHNA hydrochloride
Catalog No. A21585 Adenosine deaminase inhibitorEHNA hydrochloride is a specific inhibitor of adenosine deaminase, prevents dAdo degradation and increases mitochondrial dATP levels in fibroblasts. 了解更多 -
Rolofylline
Catalog No. A21649 adenosine A1 receptor antagonistRolofylline (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. 了解更多 -
Derenofylline
Catalog No. A21990 adenosine A1 receptor antagonistDerenofylline (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. 了解更多 -
N6-Cyclohexyladenosine
Catalog No. A21008 A1 receptor agonistN6-Cyclohexyladenosine is a selective A1 receptor agonist (EC50 = 8.2 nM). 了解更多 -
MRS1177
Catalog No. A16871 -
MRS1186
Catalog No. A16870 -
AZD-4635 (HTL1071)
Catalog No. A16820 -
Proxyphylline
Catalog No. A16821 A1 adenosine receptors 拮抗剂Proxyphylline是茶碱的衍生物,由于其心血管特性而被用作支气管扩张剂。它与A2腺苷受体(对于血小板,Ki = 850μM)选择性拮抗A1腺苷受体(对于牛脑,Ki = 82 nM)。 了解更多 -
Tecadenoson
Catalog No. A13302 A1 adenosine receptor agonistTecadenoson (CVT-510) is a selective A1 adenosine receptor agonist. 了解更多 -
Istradefylline (KW-6002)
Catalog No. A11451 -
SYN-115 (Tozadenant)
Catalog No. A11560 A2a receptor 拮抗剂SYN115是口服,有效和选择性的腺苷2a(A2a)受体抑制剂,作用于人类和恒河猴的 adenosine A2A 受体,Ki 值分别为 11.5 nM 和 6 nM。 了解更多 -
CGS 21680 HCl Hydrate
Catalog No. A11619 -
Aminophylline
Catalog No. A10066 Adenosine receptor 拮抗剂Aminophylline是一种非选择性的腺苷受体拮抗剂和磷酸二酯酶抑制剂,能够逆转局部缺血引起的bradyasystole。 了解更多 -
Dyphylline
Catalog No. A10339 Adenosine receptor 拮抗剂Dyphylline是黄嘌呤衍生物,具有支气管扩张药和血管扩张药的作用。 它充当腺苷受体拮抗剂和磷酸二酯酶抑制剂。 了解更多 -
SCH 442416
Catalog No. A12695 A2A Receptor 拮抗剂SCH 442416是一种选择性的腺苷A2A受体拮抗剂。以高亲和力结合人和大鼠A2A受体(Ki值分别为0.048和0.5 nM)。在体外对hA2A的选择性比hA1高> 23000倍,并且对hA2B和hA3受体的亲和力最小(IC50> 10μM)。 了解更多 -
Tamsulosin hydrochloride
Catalog No. A12846 Tamsulosin hydrochloride是前列腺素α1A肾上腺素受体的拮抗剂。 了解更多 -
CVT 6883
Catalog No. A13745 -
5-Iodotubercidin
Catalog No. A13948 Adenosine kinase 抑制剂5-Iodotubercidin是一种有效的腺苷激酶抑制剂,IC50为26 nM。 了解更多 -
CF-102
Catalog No. A14402 -
CGS-15943
Catalog No. A14327 -
Preladenant
Catalog No. A13504 -
DPCPX
Catalog No. A16104 -
2-Chloroadenosine (CADO)
Catalog No. A16105 Adenosine A Receptor 激动剂2-Chloroadenosine (CADO)是腺苷的代谢稳定的类似物,其表现为腺苷A受体激动剂(腺苷A1-R,腺苷A2A-R和腺苷A3-R的Ki值分别为300、80和1900 nM)。 了解更多 -
CGS 21680 HCl
Catalog No. A16441 -
Regadenoson
Catalog No. A12541 A2A adenosine 激动剂Regadenoson是A2A腺苷受体相对于A1,A2B和A3受体的选择性激动剂。还发现Regadenoson是引起冠状动脉血管扩张的完全而有效的激动剂,这种反应具有非常大的A2A受体储备。 了解更多 -
Vipadenant (BIIB-014)
Catalog No. A13963 A2A receptor 拮抗剂Vipadenant,也称为BIIB014,CEB-4520,是针对帕金森氏症的有效,选择性和口服腺苷A2A受体拮抗剂。Vipadenant在帕金森氏病的常用模型中显示出强大的口服活性。 了解更多 -
Theophylline-7-acetic acid
Catalog No. A16822