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产地 | 中国 |
品牌 | 爱必信(absin) |
货号 | abs813925 |
用途 | 见爱必信官网 |
英文名称 | 见爱必信官网 |
包装规格 | 100mg,100mg,100mg,500mg,500mg,500mg,200mg,200mg,200mg,5g,5g,5g |
纯度 | >98%% |
CAS编号 | 204255-11-8 |
别名 | 磷酸奥司他韦;GS 4104 |
是否进口 | 否 |
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抑制剂描述: 产品名称:Oseltamivir phosphate 产品别名:见爱必信官网 英文别名:Oseltamivir phosphate 靶点:Neuraminidase CAS:204255-11-8 纯度:>98% 外观:见爱必信官网 保存方法:Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution. 描述: Oseltamivir phosphate (Tamiflu) is a competitive neuraminidase inhibitor. The prodrug oseltamivir phosphate (Tamiflu) is itself not virally effective; however, once in the liver, it is converted by natural chemical processes, hydrolysed hepatically to its active metabolite, the free carboxylate of oseltamivir (GS4071). Oseltamivir phosphate (Tamiflu) serves as a competitive inhibitor towards sialic acid, found on the surface proteins of normal host cells. By blocking the activity of the viral neuraminidase enzyme, oseltamivir phosphate (Tamiflu) prevents new viral particles from being released by infected cells. Oseltamivir phosphate (Tamiflu) is an antiviral drug that slows the spread of influenza (flu) virus between cells in the body by stopping the virus from chemically cutting ties with its host cell. 溶解性:DMSO :4 mg/mL (9.75 mM) 体外研究:
Oseltamivir Phosphate, anti-Neu1 antibodies, and matrix metalloproteinase-9-specific inhibitor blocks Neu1 activity associated with EGF-stimulated TNBC MDA-MB-231 cells. Oseltamivir slows the spread of influenza (flu) virus between cells in the body by stopping the virus from chemically cutting ties with its host cell. 体内研究:Oseltamivir Phosphate monotherapy may be the effective treatment therapy for TNBC(Triple-negative breast cancers).It is efficacious in treating infections caused by H5N1 and H9N2 influenza viruses in mice.After dosing, the prodrug (Oseltamivir phosphate) is readily absorbed from the gastrointestinal tract and rapidly converted into the active metabolite, OC. In all patient groups, OC has high bioavailability and is systemically distributed to infection sites at concentrations sufficient to inhibit a range of influenza virus neuraminidases.
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