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Theophylline sodium glycinate
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Theophylline sodium glycinate图片
CAS NO:8000-10-0
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品名称
1,3-Dimethylxanthine sodium glycinate
Theo-24 sodium glycinate
产品介绍
Theophylline (1,3-Dimethylxanthine) sodium glycinate 是有效的磷酸二酯酶 (PDE) 抑制剂,腺苷受体拮抗剂,和组蛋白脱乙酰酶 (HDAC) 活化剂。Theophylline sodium glycinate 抑制 PDE3 活性,放松气道平滑肌。Theophylline sodium glycinate 通过增加 IL-10 和抑制 NF-κ B进入细胞核而具有抗炎活性。Theophyllin sodium glycinate 诱发细胞凋亡 (apoptosis)。Theophylline sodium glycinate 可用于哮喘和慢性阻塞性肺疾病 (COPD) 的研究。
生物活性

Theophylline (1,3-Dimethylxanthine) sodium glycinate is a potentphosphodiesterase (PDE)inhibitor,adenosine receptorantagonist, andhistone deacetylase (HDAC)activator. Theophylline sodium glycinate inhibitsPDE3activity to relax airway smooth muscle. Theophylline sodium glycinate has anti-inflammatory activity by increaseIL-10and inhibitNF-κBinto the nucleus. Theophylline sodium glycinate inducesapoptosis. Theophylline sodium glycinate can be used for asthma and chronic obstructive pulmonary disease (COPD) research[1][2][3][4][5].

体外研究
(In Vitro)

Theophylline sodium glycinate (1-1000 μM) inhibits cAMP hydrolysis by PDE in homogenates of bronchial tissue to relax human bronchus and pulmonary arteries[1].
Theophylline sodium glycinate (10 μg/mL; 24 h) induces apoptosis through a reduction in the antiapoptotic protein Bcl-2 in eosinophils[2].
Theophylline sodium glycinate (0-500 μM; 2 h) inhibits NF-κB activation, I kappa B alpha (I-κBα) degradation and decreases the level of IL-6 in a concentration-dependent manner[3].
Theophylline sodium glycinate (0-1000 μM; 30 min; A549 cells) induces histone deacetylase activity to decrease inflammatory gene expression[4].

Western Blot Analysis[3]

Cell Line:A549 cells
Concentration:0, 20, 100 and 500 μM
Incubation Time:2 hours
Result:Decreased the expression of NF-κB p65 and I-κBα degradation in a dose-dependent manner.
体内研究
(In Vivo)

Theophylline sodium glycinate (100 mg/kg; i.p.; daily, for 9 d) has anti-inflammatory activity in mice and increases IL-6 and IL-10 levels and inhibits TNF-α and NO in male Swiss mice[1].

Animal Model:Male Swiss mice[1]
Dosage:100 mg/kg
Administration:Intraperitoneal injection; daily; for 9 days
Result:Increased IL-6 and IL-10 levels and inhibited TNF-α and NO.
Clinical Trial
分子量

278.22

Formula

C9H13N5NaO4+

CAS 号

8000-10-0

中文名称

茶碱甘氨酸钠

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.