4.6 Review

The Structural Diversity and Biological Activity of Steroid Oximes

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MOLECULES
卷 28, 期 4, 页码 -

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MDPI
DOI: 10.3390/molecules28041690

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steroids; oximes; chemistry; antitumor; anti-inflammatory; antibacterial; antifungal; antiviral

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Steroids and their derivatives, including steroidal oximes, have attracted extensive research interest due to their pharmacological properties. Oximes, with the formula R1R2C=N-OH, are colorless crystals that are poorly soluble in water. They can be easily obtained through the condensation of aldehydes or ketones with various amine derivatives, making them interesting in medicinal chemistry for drug design. This review focuses on the biological activities of steroidal oximes, such as anticancer, anti-inflammatory, antibacterial, antifungal, and antiviral activities, as well as their mechanisms of action. It also provides an overview of oxime chemistry and describes several steroidal oximes in clinical trials or used as drugs.
Steroids and their derivatives have been the subject of extensive research among investigators due to their wide range of pharmacological properties, in which steroidal oximes are included. Oximes are a chemical group with the general formula R1R2C=N-OH and they exist as colorless crystals and are poorly soluble in water. Oximes can be easily obtained through the condensation of aldehydes or ketones with various amine derivatives, making them a very interesting chemical group in medicinal chemistry for the design of drugs as potential treatments for several diseases. In this review, we will focus on the different biological activities displayed by steroidal oximes such as anticancer, anti-inflammatory, antibacterial, antifungal and antiviral, among others, as well as their respective mechanisms of action. An overview of the chemistry of oximes will also be reported, and several steroidal oximes that are in clinical trials or already used as drugs are described. An extensive literature search was performed on three main databases-PubMed, Web of Science, and Google Scholar.

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