药物发现中的体外生物转化

S. Ravindran, Rutuja Rokade, J. Suthar, Pooja Singh, Pooja Deshpande, Rajeshree Khambadkar, Srushti Utekar
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引用次数: 5

摘要

体外生物转化研究在决定新化学实体(NCE)命运的药物发现程序中起着至关重要的作用。富含酶的基质如微粒体、肝细胞、肝组分和S9组分将新的化学实体转化为不同的代谢物。代谢物可能具有重要的药理学意义,也可能具有毒性。采用液相色谱-质谱联用技术鉴定新形成的代谢物。确定新化学实体中的生物转化位点有助于药物化学家对其结构进行优化,并将其开发为药用药物。使用体外生物转化研究筛选药物有助于选择正确的新化学实体,用于进一步的动物系统体内研究和后来的人体临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vitro Biotransformation in Drug Discovery
In vitro Biotransformation studies play a crucial role in drug discovery program that determine the fate of the new chemical entities (NCE’s). Enzyme rich matrices such as microsomes, hepatocytes, liver fractions and S9 fractions transform the new chemical entities to different metabolites. Metabolites could be pharmacologically important or toxic. Newly formed metabolites are identified using liquid chromatography interfaced with mass spectrometry. Identification of the biotransformation sites in the new chemical entity helps the medicinal chemists to optimize its structure and develop the NCE as a pharmaceutical drug. Screening pharmaceutical drugs using in vitro biotransformation studies assist in selecting the right new chemical entity for further in vivo studies in animal systems and later in human clinical trials.
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