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Search Results for " adenosine kinase inhibitor "

15

抑制剂 & 化合物

1

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T22554	Adenosine Kinase Inhibitor (hydrate)	Others	Others
	Adenosine kinase is the key metabolizing enzyme regulating cellular adenosine concentrations. Inhibition of adenosine kinase can selectively enhance the protective actions of adenosine during tissue trauma without producing the nonspecific effects associa
T14944	CGS 15943	PI3K; Adenosine Receptor	GPCR/G Protein; Neuroscience; PI3K/Akt/mTOR signaling
	CGS 15943 是一种可口服的非黄嘌呤腺苷受体拮抗剂。在转染的 CHO 细胞中，其对人 A1、A2A、A2B 和 A3 腺苷受体的 Ki 分别为 3.5、4.2、16 和 50 nM。
T4668	ABT-702 dihydrochloride	Adenosine Receptor	GPCR/G Protein; Neuroscience
	ABT-702 dihydrochloride 是腺苷激酶抑制剂，IC50为1.7 nM。
T6745	5-Iodotubercidin 5-碘代杀结核菌素,5-ITu,NSC 113939	Adenosine Receptor	GPCR/G Protein; Neuroscience
	5-Iodotubercidin (NSC-113939) 是一种 ATP 类似物，有效抑制腺苷激酶，IC50为 26 nM。它可以激活磷酸化酶和糖原合成酶，在离体肝细胞中启动糖原合成。它也抑制 CK1、胰岛素受体酪氨酸激酶、磷酸化酶激酶、PKA、CK2、PKC 和 Haspin 。
T21017	5'-Amino-5'-deoxyadenosine 5' Amino 5' deoxyadenosine,5'Amino5'deoxyadenosine,Nsc 238990,NH2dAdo	Apoptosis; Adenosine Receptor	Apoptosis; GPCR/G Protein; Neuroscience
	5'-Amino-5'-deoxyadenosine (NH2dAdo) 是一种针对惰性淋巴系统恶性肿瘤的腺苷激酶抑制剂，具有抗肿瘤和抗癌作用。5'-Amino-5'-deoxyadenosine 的抗癌机制通过抑制 DNA 合成，诱导细胞凋亡 (apoptosis) 等来实现。
T2615	Flavopiridol hydrochloride Alvocidib Hydrochloride,NSC 649890,MDL 107826A,HL 275,FLAVOPIRIDOL HCL,NSC 649890 HCl	HIV Protease; CDK; Autophagy	Autophagy; Cell Cycle/Checkpoint; Microbiology/Virology; Proteases/Proteasome
	Flavopiridol hydrochloride (MDL 107826A) 是一种CDK 的广谱抑制剂，与 ATP 竞争性地抑制 CDK1，CDK2 和 CDK4 的活性，IC50值分别为 30, 170, 100 nM。
T21018	Anisodine hydrobromide
	5'-Amino-5'-deoxyadenosine is an inhibitor of adenosine kinase.
T70617	GP-1-515
	GP-1-515 is an adenosine kinase inhibitor with anti-inflammatory effects.
T38346	ABT 702 hydrochloride
	Potent non-nucleoside adenosine kinase inhibitor (IC50 = 1.7 nM), selective over other sites of adenosine interaction (A1, A2A and A3 receptors, adenosine transporter and adenosine deaminase). Displays oral activity in animal models of pain and inflammation.
T26475	A-286501
	A-286501 is an orally active adenosine kinase inhibitor (IC50=0.47 nM). A-286501 effectively attenuates nociception by a non-opioid, non-non-steroidal anti-inflammatory drug ADO, receptor mediated mechanism.
T35574	Adenosine 5'-phosphosulfate (sodium salt)
	Adenosine 5'-phosphosulfate is an ATP and sulfate competitive inhibitor of ATP sulfurylase in humans, S. cerevisiae, and P. chrysogenum (Ki = 18, 2500, and 1500 nM, respectively). Adenosine 5'-phosphosulfate also inhibits human adenosine 5'-phosphosulfate kinase (Ki = 47.5 μM) to prevent sulfation.
T62227	GP3269
	GP3269 是一种选择性的、有效的、口服具有活力的人腺苷激酶 (AK) 抑制剂 (IC50: 11 nM)，在大鼠中具有抗惊厥作用。
T83805	Rp-Adenosine-5'-O-(1-thiodiphosphate) sodium Rp-ADP-α-S
	Rp-Adenosine-5'-O-(1-thiodiphosphate)（Rp-ADP-α-S）是ADP-α-S的含硫异构体，是磷酸化酶激酶的抑制剂（Ki = 0.53 µM）。此化合物能诱导分离的人类血小板聚集（EC50 = 20 µM），并能引发经卡巴胆碱预收缩的豚鼠乙状结肠松弛（EC50 = 58.9 µM）。
T83806	Sp-Adenosine-5'-O-(1-thiodiphosphate) sodium Sp-ADP-α-S
	Sp-Adenosine-5’-O-(1-thiodiphosphate) (Sp-ADP-α-S) 是硫含量核苷酸衍生物ADP-α-S的一种异构体。它是磷酸化酶激酶的抑制剂（Ki = 0.53 µM）。Sp-ADP-α-S能引起人类孤立血小板聚集（EC50 = 20 µM），并能使羧胺胆碱预收缩的豚鼠taenia coli松弛（EC50 = 58.9 µM）。
T68581	AP23464
	AP23464 is a potent adenosine 5'-triphosphate (ATP)-based inhibitor of Src and Abl kinases, displays antiproliferative activity against a human CML cell line and Bcr-Abl-transduced Ba/F3 cells (IC(50) = 14 nM. AP23464 ablates Bcr-Abl tyrosine phosphorylation, blocks cell cycle progression, and promotes apoptosis of Bcr-Abl-expressing cells. Biochemical assays with purified glutathione S transferase (GST)-Abl kinase domain confirmed that AP23464 directly inhibits Abl activity. Importantly, the lo...

化合物

Adenosine Kinase Inhibitor (hydrate)

Cat.No: T22554

Target: Others

Cat.No: T14944

Target: PI3K, Adenosine Receptor

ABT-702 dihydrochloride

Cat.No: T4668

Target: Adenosine Receptor

5-Iodotubercidin

Cat.No: T6745

Synonym: 5-碘代杀结核菌素,5-ITu,NSC 113939

Target: Adenosine Receptor

5'-Amino-5'-deoxyadenosine

Cat.No: T21017

Synonym: 5' Amino 5' deoxyadenosine,5'Amino5'deoxyadenosine,Nsc 238990,NH2dAdo

Target: Apoptosis, Adenosine Receptor

Flavopiridol hydrochloride

Cat.No: T2615

Synonym: Alvocidib Hydrochloride,NSC 649890,MDL 107826A,HL 275,FLAVOPIRIDOL HCL,NSC 649890 HCl

Target: HIV Protease, CDK, Autophagy

Anisodine hydrobromide

Cat.No: T21018

Cat.No: T70617

ABT 702 hydrochloride

Cat.No: T38346

Cat.No: T26475

Adenosine 5'-phosphosulfate (sodium salt)

Cat.No: T35574

Cat.No: T62227

Rp-Adenosine-5'-O-(1-thiodiphosphate) sodium

Cat.No: T83805

Synonym: Rp-ADP-α-S

Sp-Adenosine-5'-O-(1-thiodiphosphate) sodium

Cat.No: T83806

Synonym: Sp-ADP-α-S

Cat.No: T68581

Cat. No.	Product Name	Target	Signaling Pathways
T17143	Toyocamycin 丰加霉素,Vengicide	Apoptosis; Others; IRE1; Antibiotic; Antifungal	Apoptosis; Cell Cycle/Checkpoint; Microbiology/Virology; Others
	Toyocamycin (Vengicide) 是放线菌类产生的腺苷类似物，为 X 盒结合蛋白 1 (XBP1) 抑制剂，抑制 IRE1α 诱导的 ATP 依赖性 XBP1 mRNA 的断裂，IC50值为 80 nM。它还诱导凋亡。

天然产物

Cat.No: T17143

Synonym: 丰加霉素,Vengicide

Target: Apoptosis, Others, IRE1, Antibiotic, Antifungal

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