Fluticasone Furoate EP Impurity L is chemically (6S,8S,9R,10S,11S,13S,14S,16R,17R)-6,9-Difluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene-17-carboxylic (6S,8S,9R,10S,11S,13S,14S,16R,17R)-6,9-difluoro-17-((furan-2-carbonyl)oxy)-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene-17-carboxylic dithioperoxyanhydride. Fluticasone Furoate EP Impurity L is supplied with detailed characterization data compliant with regulatory guideline. Fluticasone Furoate EP Impurity L can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Fluticasone.
关键字: 医药对照品;
祥根生物医药于2008年12月成立,是一家集药物研发、生产、销售的创新型医药高科技企业,荣获“国家高新技术企业”和“博士后实践创新基地”等称号。祥根生物医药拥有药物成分标准物质、关键中间体、原料药与药品进出口全产业链平台。祥根是众多全球知名标准品(Aozeal/USP/EP/LGC/Bachem/TLC/TRC/意大利试剂等)和原料药(INKE/Bachem/瑞迪/意迪那等)总代理和授权代理商,处于行业领先水平。
祥根生物医药拥有一个尊重人才、重视绩效、持续创新的平台。 研发团队由多名海外高层次人才领衔,研发人员50余人;获得相关发明专利30余项。祥根生物医药的企业责任是:回报员工、回报合作伙伴、回报社会;企业愿景是:提升药品质量,保护人类健康。