1. GPCR/G Protein Neuronal Signaling Immunology/Inflammation
  2. Histamine Receptor
  3. Antazoline phosphate

Antazoline phosphate  (Synonyms: Phenazoline phosphate)

目录号: HY-B1067B
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Antazoline phosphate 是一种组胺 H1 受体拮抗剂 (histamine H1 receptor),具有抗胆碱能和抗病毒作用。Antazoline phosphate 通过可逆性竞争作用于靶细胞的组胺受体位点,阻止组胺作用于靶细胞。Antazoline phosphate 啉通过阻断和抑制H1受体,发挥抗过敏作用,防止生理反应的发生。Antazoline phosphate 能剂量依赖性地有效降低细胞外上清液中的 HBV DNA,在 HepAD38 细胞中的 EC50 为 2.910 μmol/L。Antazoline phosphate 对 Huh7 细胞外上清液中的 HBV DNA 也有显著的抑制作用 (EC50 = 2.349 μmol/L)。Antazoline phosphate 对急性心肌梗死具有抗心律失常作用。Antazoline phosphate 可用于心血管疾病和乙型肝炎 (HBV) 的研究。

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Antazoline phosphate

Antazoline phosphate Chemical Structure

CAS No. : 154-68-7

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Antazoline phosphate is an H1 receptor antagonist that affects the activity of the central nervous system, has a potent antiarrhythmic effect[1][2][3]. Antazoline phosphate is a histamine H1 receptor antagonist with anticholinergic and antiviral properties. Antazoline phosphate can prevent histamine from acting on target cells through a reversible competition effect on histamine receptor sites of these cells. Antazoline phosphate can exert an antiallegic effect and prevent the occurrence of physiological reactions from the effect of blocking as well as inhibiting H1 receptor. Antazoline phosphate can effectively reduce HBV DNA in the extracellular supernatant in a dose-dependent manner, with EC50 of 2.910 μmol/L in HepAD38 cells. Antazoline phosphate also has a significant inhibitory effect on HBV DNA in the extracellular supernatant of Huh7 cells (EC50 = 2.349 μmol/L). Antazoline phosphate has anti-arrhythmic effect in acute myocardial infarctions. Antazoline phosphate can be studied in research for cardiovascular diseases, and HBV[1][2][3].

体外研究
(In Vitro)

Antazoline phosphate shows good inhibitory effect on HBV DNA in the supernatant of HepAD38 and Huh7 cells with the value of EC50 is 2.910 μmol/L and 2.349 μmol/L, respectively[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[2]

Cell Line: HepAD38 cells
Concentration: 10 μmol/L
Incubation Time: 5 days
Result: Exhibited no significant cytotoxicity at a concentration of 10μmol/L and had a dose-dependent inhibition of HBV DNA in the supernatant.

RT-PCR[2]

Cell Line: Huh7 cells
Concentration: 30 μmol/L, 10 μmol/L, 3.33 μmol/L, 1.1 μmol/L, 0.370 μmol/L, and 0.123 μmol/L
Incubation Time: 4 days
Result: Had a significant inhibitory effect on HBV DNA in supernatants in a dose-dependent manner.
体内研究
(In Vivo)

Antazoline phosphate (IP; 0.01 ml/g; 30min) as H1 receptor antagonists diminishes the anticonvulsant activity of carbamazepine and diphenylhydantoin[3].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Swiss mice[3]
Dosage: 0.01 mL/g
Administration: IP; 0.01 ml/g; 30min
Result: Showed some proconvulsive activity.
Clinical Trial
分子量

363.35

Formula

C17H22N3O4P

CAS 号
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.

纯度 & 产品资料
参考文献
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Antazoline phosphate
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HY-B1067B
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