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Cat. No.	Product Name	Target	Signaling Pathways
T40307	Adenosine receptor antagonist 1
	Adenosine receptor antagonist 1 is a highly selective antagonist for the A2aR adenosine receptor, exhibiting an IC50 value of 0.29 nM. It demonstrates a remarkable 14-fold selectivity towards the A2aR receptor in comparison to the A2bR receptor.
T37792	A2A receptor antagonist 1 CPI-444 analog,A2A receptor antagonist 1	Adenosine Receptor	GPCR/G Protein; Neuroscience
	A2A receptor antagonist 1 (CPI-444 analog)是腺苷 A2A 和 A1受体的拮抗剂，Ki 值分别为4和264 nM。
T22466	Adenosine receptor A1 antagonist 5	cAMP	GPCR/G Protein
	Adenosine receptor A1 antagonist 5 可作为一种腺苷拮抗剂，是一种氧嘌呤，可作为杀虫剂和虫害防治剂，对血压升高有抑制作用。
T10248	Adenosine antagonist-1	Adenosine Receptor	GPCR/G Protein; Neuroscience
	Adenosine antagonist-1 可作为一种腺苷 A3 受体 (AA3R) 拮抗剂。
T10058	A2B receptor antagonist 1	Adenosine Receptor	GPCR/G Protein; Neuroscience
	A2B receptor antagonist 1 是一个有效的 A2B 腺苷受体 (A2B adenosine receptor) 拮抗剂。
T14078	AB928	Adenosine Receptor	GPCR/G Protein; Neuroscience
	AB928 是可口服的选择性腺苷受体(A2aR/A2bR)双拮抗剂，可减轻腺苷介导的免疫抑制，具有免疫调节和抗肿瘤活性。
T15418	GS-6201 CVT-6883	Adenosine Receptor	GPCR/G Protein; Neuroscience
	GS-6201 (CVT-6883) 是选择性腺苷 A2B 受体拮抗剂。它对人腺苷 A2B 受体具有高亲和力和选择性 (Ki=22 nM)。它降低了小鼠急性心肌梗死后心脏中 caspase-1 的活性，并减弱了心脏重塑。它减弱了致敏小鼠 NECA，AMP 或变应原诱导的气道反应性。
T22031	ANR 94	Adenosine Receptor	GPCR/G Protein; Neuroscience
	ANR94 是一种有效的、选择性的腺苷 A2A 受体 (AA2AR) 拮抗剂，对 hAA2AR 的Ki 值为 46 nM。ANR94 具有用于帕金森病的研究潜力。
T70996	FK-838
	FK-838 is an adenosine subtype-1 receptor antagonist.
T60872	Adenosine receptor antagonist 3
	Adenosine receptor antagonist 3 具有用于癌症疾病研究的潜力，它是腺苷受体的有效拮抗剂。
T72000	N 0840
	N 0840 is a selective, orally active A(1) adenosine receptor antagonist.
T24384	L-97-1 L97-1,L 97-1
	L-97-1 is an antagonist of the adenosine A1 receptor.
T62611	Adenosine receptor antagonist 2
	Adenosine receptor antagonist 2 是一种具有口服活性的 A2a (IC50: 1 nM) /A2b (IC50: 3 nM) 腺苷受体拮抗剂。Adenosine receptor antagonist 2 表现出抗肿瘤效果。
T70648	FK-352
	FK-352 is a pyrazolopyridine derivative and adenosine-1 receptor antagonist.
T61850	Adenosine receptor inhibitor 1
	Adenosine receptor inhibitor 1 is a highly potent and selective antagonist of adenosine receptor (AR). It exhibits exceptional affinity for A1 AR, A2A AR, A2B AR, and A3 AR, with respective Ki values of >1000, 68.5, >1000, >1000 nM. This compound demonstrates notable antinociceptive, anti-inflammatory, and peripheral analgesic properties. Therefore, Adenosine receptor inhibitor 1 holds great promise for investigating cancer and neurodegenerative diseases [1].
T60580	A1AR antagonist 2
	A1AR antagonist 2 (compound 18h) 是 A1腺苷受体 (A1 adenosine receptor) 的有效的选择性拮抗剂。A1AR antagonist 2对于 hA1, hA2A，hA2B 的Ki 值分别为 1.49、10.2 和 50.1 nM。
T60687	A1AR antagonist 1
	A1AR antagonist 1 (compound 18g) 是A1腺苷受体的选择性拮抗剂。A1AR antagonist 1对 hA1, hA2A，hA2B 受体的Ki 值分别为 2.08、6.91 和 31.2 nM。
T60615	A1AR antagonist 6
	A1AR antagonist 6 (化合物 15) 是 A1 腺苷受体(A1AR)的有效的选择性拮抗剂，其pKi 值为 7.13，pIC50值为 6.38。
T61536	A1AR antagonist 4
	A1AR antagonist 4 (compound 22) is a highly developed chemical compound that acts as a potent and selective antagonist of the A1 adenosine receptor (A1AR). It possesses a pIC50 value of 5.51 and a pKi value of 6.29 [1].
T60915	A1AR antagonist 5
	A1AR antagonist 5 (化合物 20) 是A1 腺苷受体(A1AR)的有效选择性拮抗剂，其pKi 值为 6.11，pIC50值为 5.83。
T60591	A2AAR antagonist 1
	A2AAR antagonist 1 (compound 21a) 是A2AAR(腺苷A2A 受体) 的拮抗剂，具有高配体效率，Ki 值为 20 nM。A2AAR antagonist 1 可用于神经退行性疾病的相关研究。
T62134	A1/A3 AR antagonist 1
	A1/A3 AR antagonist 1 (compound 10) 是一种有效的、双重腺苷酸 1 (A1)和腺苷酸 3 (A3)受体拮抗剂，能够作用于人 A1 (Ki: 37.6 nM)、人 A3 (Ki: 25.4 nM) 和大鼠 A1 (Ki: 1.47 nM)。A1/A3 AR antagonist 1 能够用于研究肾衰竭、炎症性肺部疾病和阿尔茨海默症。
T26855	BMS-665053 BMS665053
	BMS-665053 is a corticotropin-releasing factor-1 (CRF1) receptor antagonist (IC50 = 1.0 nM). BMS-665053)11 is a potent inhibitor of CRF-stimulated cyclic adenosine monophosphate (cAMP) production in human Y-79 retinoblastoma cells (IC50 = 4.9 nM). In addi
T37014	Inupadenant
	Inupadenant is an orally active, highly selective A2A receptor antagonist. Inupadenant is not brain-penetrant. Inupadenant has potent anti-tumor activity[1]. [1]. Laurence Buisseret, et al. Phase 1 trial of the adenosine A2Areceptor antagonist inupadenant (EOS-850): Update on tolerability, and antitumor activity potentially associated with the expression of the A2A receptor within the tumor. Journal of Clinical Oncology. Volume 39, Issue 15_suppl.
T74606	A2A/A3 AR antagonist-1
	A2A/A3 AR antagonist-1 (化合物 23) 是一种双重 A2A/A3adenosine receptor(AR)荧光配体，对 hA2AAR 和 hA3AR 的 Ki 值分别为 90 nM 和 31.8 nM。
T70770	Cyclazosin Free Base
	Cyclazosin Free Base is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of furoic acid with the secondary amino group of 6,7-dimethoxy-2-[(4aR,8aS)-octahydroquinoxalin-1-yl]quinazolin-4-amine. It has a role as an adenosine A2A receptor antagonist. It is a member of quinazolines, a member of furans, an aromatic ether, a quinoxaline derivative, an aromatic amide and a monocarboxylic acid amide.
T72626	A2AR-antagonist-1	Adenosine Receptor	GPCR/G Protein; Neuroscience
	A2AR-antagonist-1 (compound 38) 为一种口服活性的腺苷 A2A 受体 (A2AR) 拮抗剂，IC50 值为 29 nM。此化合物展示出抗肿瘤作用，并在小鼠肝微粒体中表现出良好的代谢稳定性，半衰期为 86.1 分钟。同时，A2AR-antagonist-1 能够作为 T 细胞激活剂，通过抑制免疫抑制分子 LAG-3 和 TIM-3，以及增强 GZMB、IFNG 和 IL-2 等效应分子的表达。
T63400	hA2A/hCA XII modulator 1
	hA2A/hCA XII modulator 1 是 hA2A 腺苷受体 (hA2AAR) 的有效拮抗剂，是一种三唑并吡嗪，能够作用于hA2AAR (Ki: 6.4 nM)、hA1AR (Ki: 4.819 μM)、hA3AR (Ki>30 μM)。hA2A/hCA XII modulator 1 也人碳酸酐酶 XII (hCA XII) 的有效抑制剂，能够作用于 hCA XII (Ki: 6.2 nM)、hCA II (Ki: 46 nM)、hCA IX (Ki: 466 nM) 和 hCA I (Ki: 8.351 μM)。hA2A/hCA XII modulator 1 表现出研究癌症的潜力。
T60511	Theophylline sodium glycinate
	Theophylline (1,3-Dimethylxanthine) sodium glycinate 是一种有效的磷酸二酯酶 (PDE) 抑制剂，可抑制 PDE3 活性以松弛气道平滑肌。Theophylline sodium glycinate 可用于研究哮喘和慢性阻塞性肺疾病 (COPD) 。Theophylline sodium glycinate 也是一种腺苷受体拮抗剂和组蛋白脱乙酰酶 (HDAC) 激活剂。 Theophylline sodium glycinate 通过增加 IL-10 和抑制 NF-κB 的核输入而具有抗炎活性。Theophyllin sodium glycinate 可诱导细胞凋亡。
T36679	Rp-cAMPS sodium salt
	Rp-cAMPS sodium salt, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 12.5 μM and 4.5 μM, respectively) antagonist. Rp-cAMPS sodium salt is resistant to hydrolysis by phosphodiesterases[1][2][3][4][5][6]. A membrane-permeable competitive cAMP antagonist (Rp-cAMPS) that blocks PKA activation by binding to the regulatory subunits without dissociating the kinase holoenzyme also inhibits synaptic plasticity but has no effect on normal synaptic t...

化合物

Adenosine receptor antagonist 1

Cat.No: T40307

A2A receptor antagonist 1

Cat.No: T37792

Synonym: CPI-444 analog,A2A receptor antagonist 1

Target: Adenosine Receptor

Adenosine receptor A1 antagonist 5

Cat.No: T22466

Target: cAMP

Adenosine antagonist-1

Cat.No: T10248

Target: Adenosine Receptor

A2B receptor antagonist 1

Cat.No: T10058

Target: Adenosine Receptor

Cat.No: T14078

Target: Adenosine Receptor

Cat.No: T15418

Synonym: CVT-6883

Target: Adenosine Receptor

Cat.No: T22031

Target: Adenosine Receptor

Cat.No: T70996

Adenosine receptor antagonist 3

Cat.No: T60872

Cat.No: T72000

Cat.No: T24384

Synonym: L97-1,L 97-1

Adenosine receptor antagonist 2

Cat.No: T62611

Cat.No: T70648

Adenosine receptor inhibitor 1

Cat.No: T61850

A1AR antagonist 2

Cat.No: T60580

A1AR antagonist 1

Cat.No: T60687

A1AR antagonist 6

Cat.No: T60615

A1AR antagonist 4

Cat.No: T61536

A1AR antagonist 5

Cat.No: T60915

A2AAR antagonist 1

Cat.No: T60591

A1/A3 AR antagonist 1

Cat.No: T62134

Cat.No: T26855

Synonym: BMS665053

Cat.No: T37014

A2A/A3 AR antagonist-1

Cat.No: T74606

Cyclazosin Free Base

Cat.No: T70770

A2AR-antagonist-1

Cat.No: T72626

Target: Adenosine Receptor

hA2A/hCA XII modulator 1

Cat.No: T63400

Theophylline sodium glycinate

Cat.No: T60511

Rp-cAMPS sodium salt

Cat.No: T36679

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