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Non-steroidal CYP17A1 Inhibitors: Discovery and Assessment

机译:非甾体CYP17A1抑制剂的发现和评估

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摘要

CYP17A1 is an enzyme that plays a major role in steroidogenesisand is critically involved in the biosynthesis of steroid hormones.Therefore, it remains an attractive target in several serious hormone-dependentcancer diseases, such as prostate cancer and breast cancer. The medicinalchemistry community has been committed to the discovery and developmentof CYP17A1 inhibitors for many years, particularly for the treatmentof castration-resistant prostate cancer. The current Perspective reflectsupon the discovery and evaluation of non-steroidal CYP17A1 inhibitorsfrom a medicinal chemistry angle. Emphasis is placed on the structuralaspects of the target, key learnings from the presented chemotypes,and design guidelines for future inhibitors.
机译:CYP17A1是一种在类固醇生成中起主要作用的酶,并且积极参与类固醇激素的生物合成。因此,它仍然是几种严重的激素依赖性癌症疾病(如前列腺癌和乳腺癌)的有吸引力的靶点。药物化学界多年来一直致力于CYP17A1抑制剂的发现和开发,特别是用于治疗去势抵抗性前列腺癌。本观点从药物化学角度反思了非甾体CYP17A1抑制剂的发现和评价。重点放在靶点的结构方面,从所提出的化学型中学到的关键知识,以及未来抑制剂的设计指南。

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