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FDA 的批准印章:揭示心血管疾病、ACE、HIV、CNS 等领域的肽类突破。

FDA's stamp of approval: Unveiling peptide breakthroughs in cardiovascular diseases, ACE, HIV, CNS, and beyond.

机构信息

School of Pharmacy, Newcastle upon Tyne, UK.

Department of Chemical Engineering, Imperial College London, London, UK.

出版信息

J Pept Sci. 2024 Nov;30(11):e3627. doi: 10.1002/psc.3627. Epub 2024 Jun 17.

Abstract

Peptides exhibit significant specificity and effective interaction with therapeutic targets, positioning themselves as key players in the global pharmaceutical market. They offer potential treatments for a wide range of diseases, including those that pose significant challenges. Notably, the peptide trofinetide (Daybue) marked a groundbreaking achievement by providing the first-ever cure for Rett syndrome, and several peptides have secured FDA approval as first-in-class medications. Furthermore, peptides are expanding their presence in areas traditionally dominated by either small or large molecules. A noteworthy example is the FDA approval of motixafortide (Aphexda) as the first peptide-based chemokine antagonist. Here, the focus will be on the analysis of FDA-approved peptides, particularly those targeting cardiovascular diseases, human immunodeficiency, central nervous system diseases, and various other intriguing classes addressing conditions such as osteoporosis, thrombocytopenia, Cushing's disease, and hypoglycemia, among others. The review will explore the chemical structures of the peptides, their indications and modes of action, the developmental trajectory, and potential adverse effects.

摘要

肽类药物与治疗靶点具有显著的特异性和有效性,是全球制药市场的重要参与者。它们为多种疾病提供了潜在的治疗方法,包括那些具有重大挑战的疾病。值得注意的是,肽类药物替度鲁肽(Daybue)的出现标志着治疗雷特综合征的首个突破,并且有几种肽类药物已被 FDA 批准为同类首创药物。此外,肽类药物正在扩大其在传统上由小分子或大分子主导的领域的应用。一个值得注意的例子是 FDA 批准 motixafortide(Aphexda)作为首个基于肽的趋化因子拮抗剂。本综述将重点分析 FDA 批准的肽类药物,特别是针对心血管疾病、人类免疫缺陷、中枢神经系统疾病以及其他各种有趣的类别,如骨质疏松症、血小板减少症、库欣病和低血糖症等疾病的肽类药物。本综述将探讨这些肽类药物的化学结构、适应证和作用机制、研发轨迹以及潜在的不良反应。

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