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6698-26-6

中文名称 2',5'-DIDEOXYADENOSINE
英文名称 2',5'-DIDEOXYADENOSINE
CAS 6698-26-6
分子式 C10H13N5O2
分子量 235.24
MOL 文件 6698-26-6.mol
更新日期 2024/04/27 22:04:59
6698-26-6 结构式 6698-26-6 结构式

基本信息

中文别名
2',5'-二脱氧腺苷
2',5'-双脱氧腺苷
化合物2',5'-DIDEOXYADENOSINE
英文别名
NSC 95943
2',5'-DD-ADO
2',5'-DIDEOXYADENOSINE
Adenosine, 2',5'-dideoxy-
2',5'-Dideoxyadenosine >=95% (HPLC), solid
2,5-Dideoxyadenosine - CAS 6698-26-6 - Calbiochem
5-(6-AMINOPURIN-9-YL)-2-METHYLTETRAHYDROFURAN-3-OL
(2R,3S,5R)-5-(6-aMino-9H-purin-9-yl)-2-Methyltetrahydrofuran-3-ol
NSC 95943 2',5'-DIDEOXYADENOSINE
phosphoric acid [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-2-oxolanyl]methyl [hydroxy(phosphonooxy)phosphoryl] [(2R,3S,4R,5R)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl] ester

物理化学性质

沸点547.0±60.0 °C(Predicted)
密度1.77±0.1 g/cm3(Predicted)
储存条件-20°C
溶解度DMSO: soluble
酸度系数(pKa)14.06±0.60(Predicted)
形态solid
颜色white

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335
WGK Germany3
海关编码29349990

常见问题列表

生物活性
2',5'-Dideoxyadenosine 是一种有效且非竞争性的腺苷酸环化酶 (adenylyl cyclase) 抑制剂,可以有效结合 P 位点,IC50 为 3 µM。2',5'-Dideoxyadenosine 是核苷类似物,在心脏中发挥强大的抗肾上腺素 (antiadrenergic) 作用。
靶点

IC50: 3 µM (adenylyl cyclase)

体外研究

2',5'-Dideoxyadenosine (10 μM, 30 min) reduces cAMP production and blocks the phosphorylation of GluA1 at Ser845 induced by carbachol (CCh).
2',5'-Dideoxyadenosine (10 μM, 30 min) blocks CCh-induced increase of phosphorylation of Akt and attenuates CCh-induced phosphorylation of Ser2448.
2',5'-Dideoxyadenosine (20-150 mM), like adenosine, dependently and reversibly inhibits the positive inotropic and chronotropic effect of beta-adrenergic stimulation with isoproterenol (8-54 pmol) up to 70% and 50%, respectively.

Western Blot Analysis

Cell Line: Primary hippocampal neurons
Concentration: 10 μM
Incubation Time: 30 min
Result: Reduced cAMP production and blocked the phosphorylation of GluA1 at Ser845 induced by carbachol (CCh).
体内研究

2',5'-Dideoxyadenosine (0.1 mg/kg; IP; 15 min pre-treated) fully inhibits the diuretic, natriuretic and K + and Cl - sparing effect of Fr•EtOAc in rats.

Animal Model: Male Wistar rats (3-4 months old)
Dosage: 0.1 mg/kg
Administration: IP; 15 min pre-treated
Result: Fully inhibited the diuretic, natriuretic and K + and Cl - sparing effect of Fr•EtOAc in rats.
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