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- 技术资料
- 保存条件:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 保质期:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 英文名:
Pirfenidone
- 库存:
999
- 供应商:
北京索莱宝科技有限公司
- CAS号:
53179-13-8
- 规格:
50mg/100mg/200mg/500mg/1g
| 规格: | 50mg | 产品价格: | ¥360.00 |
|---|---|---|---|
| 规格: | 100mg | 产品价格: | ¥520.00 |
| 规格: | 200mg | 产品价格: | ¥660.00 |
| 规格: | 500mg | 产品价格: | ¥880.00 |
| 规格: | 1g | 产品价格: | ¥1360.00 |
| CAS | 53179-13-8 |
| 中文名称 | 哌非尼酮 |
| 英文名称 | Pirfenidone |
| 别名 | S-7701;AMR-69;吡非尼酮 |
| 分子式 | C12H11NO |
| 分子量 | 185.22 |
| 规格 | 50mg ; 100mg ; 200mg ; 500mg ; 1g |
| 溶解性 | Soluble in DMSO/Water ≥10mg/mL |
| 纯度 | GC≥98% |
| 级别 | Cell Culture |
| 外观(性状) | White to light yellow Solid |
| 储存条件 | Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year |
| 运输条件 | 冷藏运输 |
| EC | 621-260-7 |
| MDL | MFCD00866047 |
| SMILES | CC1=CN(C(=O)C=C1)C2=CC=CC=C2 |
| InChIKey | ISWRGOKTTBVCFA-UHFFFAOYSA-N |
| InChI | InChI=1S/C12H11NO/c1-10-7-8-12(14)13(9-10)11-5-3-2-4-6-11/h2-9H,1H3 |
| PubChem CID | 40632 |
| Beilstein Number | 21(5)7,197 |
| 靶点 | CCL |
| 通路 | Immunology & Inflammation |
| 背景说明 | 是一种抗纤维化化合物,可减弱纤维细胞中 CCL2 和 CCL12 的产生, 还具有抗炎活性。 |
| 生物活性 | Pirfenidone 是一种抗纤维化药物。Pirfenidone 具有生长抑制作用,可降低人胶质瘤细胞系中的 TGF-β2 蛋白水平。Pirfenidone 具有抗炎活性。[1-4] |
| In Vitro | Pirfenidone elicits growth-inhibitory effects and reduces TGF-beta2 protein levels in human glioma cell lines.[1] In RAW264.7 cells,a murine macrophage-like cell line,pirfenidone suppressed the proinflammatory cytokine tumor necrosis factor-alpha(TNF-alpha)by a translational mechanism.[2] Pirfenidone(0~0.5 mg/ml,24h)inhibits TGF-β2-induced proliferation,migration and epithlial-mesenchymal transition of human lens epithelial cells line SRA01/04 at nontoxic concentrations.[3] Pirfenidone inhibited fibrocyte migration by pirfenidone in vitro.[4] |
| In Vivo | In the murine endotoxin shock model,pirfenidone potently inhibited the production of the proinflammatory cytokines,TNF-alpha,interferon-gamma,and interleukin-6,but enhanced the production of the anti-inflammatory cytokine,interleukin-10.[2] Pirfenidone(300 mg/kg/day; 2 weeks; orally)attenuated the fibrocyte pool size in bleomycin-treated mouse lungs via attenuation of CCL2 and CCL12 production in vivo.[4] |
| 数据来源文献 | [1]. Burghardt I,et al. Pirfenidone inhibits TGF-beta expression in malignant glioma cells. Biochem Biophys Res Commun. 2007 Mar 9;354(2):542-7. [2]. Nakazato H,et al. A novel anti-fibrotic agent pirfenidone suppresses tumor necrosis factor-alpha at the translational level. Eur J Pharmacol. 2002 Jun 20;446(1-3):177-85. [3]. Yang Y,et al. Inhibition of pirfenidone on TGF-beta2 induced proliferation,migration and epithlial-mesenchymal transition of human lens epithelial cells line SRA01/04. PLoS One. 2013;8(2):e56837. |
| 单位 | 瓶 |
| 表格1 | |*|1mg|5mg|10mg|$$|1mM|5.399mL|26.9949mL|53.9898mL|$$|5mM|1.0798mL|5.399mL|10.798mL|$$|10mM|0.5399mL|2.6995mL|5.399mL| |
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IF:
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Publish_to:
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PMID:
37781713
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Author:
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IF:
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Publish_to:
INTERNATIONAL IMMUNOPHARMACOLOGY
PMID:

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哌非尼酮
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