Oxazole and isoxazole-containing pharmaceuticals: targets, pharmacological activities, and their SAR studies

Abstract

Oxazole, a five-membered aromatic heterocycle featuring a nitrogen and an oxygen atom separated by a carbon atom, and its isomer isoxazole, with directly attached oxygen and nitrogen atoms, have been pivotal in medicinal chemistry. Over the past few decades, the U.S. Food and Drug Administration (FDA) has approved more than 20 drugs containing these nuclei for various clinical conditions, including Tafamidis and Oxaprozin. Due to their unique physicochemical properties, these drugs often exhibit superior pharmacokinetic profiles and pharmacological effects compared to those with similar heterocycles. This review provides a comprehensive overview of all FDA-approved drugs containing oxazole and isoxazole nuclei, focusing on their pharmacological activities and structure–activity relationships.

Graphical abstract: Oxazole and isoxazole-containing pharmaceuticals: targets, pharmacological activities, and their SAR studies

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Review Article
Submitted
05 Oct 2024
Accepted
18 Feb 2025
First published
19 Feb 2025

RSC Med. Chem., 2025, Advance Article

Oxazole and isoxazole-containing pharmaceuticals: targets, pharmacological activities, and their SAR studies

S. Li, Y. Mei, L. Jiang, X. Yang, W. Zeng and Y. Du, RSC Med. Chem., 2025, Advance Article , DOI: 10.1039/D4MD00777H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements