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盐酸非那吡啶 /Phenazopyridine hydrochloride {[allProObj[0].p_purity_real_show]}

货号:A416289 同义名: Phenazopyridine HCl;Phenazopyridine (hydrochloride)

Phenazopyridine HCl 是一种用于泌尿道疾病的局部麻醉剂。

Phenazopyridine hydrochloride 化学结构 CAS号:136-40-3
Phenazopyridine hydrochloride 化学结构
CAS号:136-40-3
Phenazopyridine hydrochloride 3D分子结构
CAS号:136-40-3
Phenazopyridine hydrochloride 化学结构 CAS号:136-40-3
Phenazopyridine hydrochloride 3D分子结构 CAS号:136-40-3
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Phenazopyridine hydrochloride 纯度/质量文件 产品仅供科研

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Phenazopyridine hydrochloride 生物活性

描述 Phenazopyridine hydrochloride is a chemical, which has a local analgesic effect, often used to alleviate the pain, irritation, discomfort, or urgency caused by urinary tract infections, surgery, or injury to the urinary tract. Preoperative oral phenazopyridine is effective in more than 90% of cases to detect during gynecologic surgery. A higher phenazopyridine dose and lower intraoperative urine output were associated with increased efficacy[3]. Phenazopyridine hydrochloride was carcinogenic in Fischer 344 rats, inducing adenocarcinomas of the colon in both males and females. Although phenazopyridine hydrochloride was not carcinogenic in male B6C3F1 mice, the chemical was carcinogenic in females, inducing hepatocellular adenomas and carcinomas[4]. Dose-inhibition curves showed that three of these kinases interacted with phenazopyridine with sub-micromolar binding affinities: cyclin-G-associated kinase, and the two phosphatidylinositol kinases PI4KB and PIP4K2C, the latter being known for participating in pain induction. Docking revealed that phenazopyridine forms strong H-bonds with the hinge region of the ATP-binding pocket of these kinases. Phenazopyridine is a kinase inhibitor, impacting notably phosphatidylinositol kinases involved in nociception[5]. Phenazopyridine: (i) enhanced neuronal differentiation, (ii) increased cell survival, (iii) decreased the amount of non-neuronal and undifferentiated cells and (iv) synchronized the cellular differentiation state[6].

Phenazopyridine hydrochloride 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT02476448 Injury of Ureter Not Applicable Completed - United States, Florida ... 展开 >> Cleveland Clinic Florida Weston, Florida, United States, 33331 收起 <<
NCT00305071 Pyuria Urinar... 展开 >>y Tract Infections 收起 << Phase 2 Unknown - Taiwan ... 展开 >> Min-Sheng General Hospital Not yet recruiting Taoyuan City, Taiwan, 320 Contact: Po-Chien Huang, MD    886-3-3179599 ext 8223    m001435@e-ms.com.tw 收起 <<
NCT02380573 Mild Cognitive Impairment ... 展开 >> MCI Aging Alzheimer's Disease AD 收起 << Phase 2 Active, not recruiting July 2019 United States, Texas ... 展开 >> Research Imaging Institute, The University of Texas Health Science Center at San Antonio San Antonio, Texas, United States, 78229 收起 <<

Phenazopyridine hydrochloride 参考文献

[1]Aizawa N, Wyndaele JJ. Effects of phenazopyridine on rat bladder primary afferent activity, and comparison with lidocaine and acetaminophen. Neurourol Urodyn. 2010 Nov;29(8):1445-50.

[2]Suter DM, Preynat-Seauve O, et al. Phenazopyridine induces and synchronizes neuronal differentiation of embryonic stem cells. J Cell Mol Med. 2009 Sep;13(9B):3517-27.

[3]Strom EM, Chaudhry ZQ, Guo R, Maisonet AJ, Holschneider CH, Wieslander CK. Effectiveness of Assessing Ureteral Patency Using Preoperative Phenazopyridine. Female Pelvic Med Reconstr Surg. 2019 Jul/Aug;25(4):289-293

[4]National Toxicology Program. Bioassay of phenazopyridine hydrochloride for possible carcinogenicity. Natl Cancer Inst Carcinog Tech Rep Ser. 1978;99:1-115

[5]Preynat-Seauve O, Nguyen EB, Westermaier Y, Héritier M, Tardy S, Cambet Y, Feyeux M, Caillon A, Scapozza L, Krause KH. Novel Mechanism for an Old Drug: Phenazopyridine is a Kinase Inhibitor Affecting Autophagy and Cellular Differentiation. Front Pharmacol. 2021 Aug 4;12:664608

[6]Suter DM, Preynat-Seauve O, Tirefort D, Feki A, Krause KH. Phenazopyridine induces and synchronizes neuronal differentiation of embryonic stem cells. J Cell Mol Med. 2009 Sep;13(9B):3517-27

Phenazopyridine hydrochloride 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.00mL

0.80mL

0.40mL

20.02mL

4.00mL

2.00mL

40.05mL

8.01mL

4.00mL

Phenazopyridine hydrochloride 技术信息

CAS号136-40-3
分子式C11H12ClN5
分子量 249.7
别名 Phenazopyridine HCl;Phenazopyridine (hydrochloride)
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Sealed in dry,2-8°C

溶解方案

DMSO: 25 mg/mL(100.12 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 1 mg/mL(4 mM),配合低频超声,并水浴加热至45℃助溶

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案一
方案二
动物实验配方
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