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UHPLC Quantitation Method and In vitro Studies of Two New Phthalimide Derivatives Planned to Treat Sickle Cell Disease

机译:计划治疗镰状细胞病的两种新的酞菁衍生物的UHPLC定量方法和体外研究

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Background: Sickle cell disease is characterized by the occurrence of acute disability and progressive organ damage, and it is one of the most common and severe monogenic disorders around the world. Since hydroxycarbamide is the only drug approved by the Food and Drug Administration (FDA) to treat this disease, it is necessary to continue the development of new drug candidates to improve its treatment. Two of a series of phthalimide derivatives have shown great potential as a new drug candidate.
机译:背景:镰状细胞疾病的特征在于急性残疾和进步器官损伤的发生,它是世界上最常见和最严重的单一的单一疾病之一。 由于羟基氨基甲酰胺是食品和药物管理局(FDA)批准的唯一药物治疗这种疾病,因此必须继续开发新的毒品候选者以改善其治疗方法。 一系列邻苯二甲酰亚胺衍生物的两种表现出巨大的潜力作为新的候选人。

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