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雷帕霉素类似物在化学、生物合成及药理学方面的最新进展。

Recent advances in the chemistry, biosynthesis and pharmacology of rapamycin analogs.

作者信息

Graziani Edmund I

机构信息

Department of Chemical Sciences, Wyeth Research, 401 N. Middletown Rd, Pearl River, NY 10965, USA.

出版信息

Nat Prod Rep. 2009 May;26(5):602-9. doi: 10.1039/b804602f. Epub 2009 Mar 5.

Abstract

Covering: 2003 to 2008. In the period 1998 to 2003, a number of reviews have appeared evaluating the potential of rapamycin and other immunophilin ligands as therapies for cancer, organ transplantation, restenosis prevention, autoimmune disorders, and neurodegenerative diseases. This review aims to evaluate advances in the field since that time, specifically detailing progress in: (i) the role of rapamycin in inhibiting its principal cellular target, the mammalian target of rapamycin (mTOR) in both of its protein complexes, (ii) understanding the role of specific genes in the mechanism of rapamycin biosynthesis, (iii) the production of novel analogs of rapamycin via precursor-directed biosynthesis, (iv) the enzymology of the pipecolate incorporating enzyme (RapL) in vitro, and (v) the pharmacology and mechanistic chemical biology of rapamycin analog mediated neuroprotection and neuroregeneration.

摘要

涵盖范围

2003年至2008年。在1998年至2003年期间,出现了一些综述,评估雷帕霉素和其他亲免素配体作为癌症、器官移植、预防再狭窄、自身免疫性疾病和神经退行性疾病治疗方法的潜力。本综述旨在评估自那时以来该领域的进展,具体详述以下方面的进展:(i)雷帕霉素在抑制其主要细胞靶点——哺乳动物雷帕霉素靶蛋白(mTOR)的两种蛋白复合物中的作用;(ii)了解特定基因在雷帕霉素生物合成机制中的作用;(iii)通过前体导向生物合成生产雷帕霉素的新型类似物;(iv)体外哌啶酸掺入酶(RapL)的酶学;(v)雷帕霉素类似物介导的神经保护和神经再生的药理学和机制化学生物学。

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