In this article, we are going to address the topic of RU-22930 from different perspectives and angles, with the aim of providing a comprehensive and complete view on this topic. We will analyze its impact in different contexts, its evolution over time, as well as the different opinions and positions that exist on the matter. RU-22930 is a topic of current relevance that arouses great interest and debate, which is why it is essential to address it in a rigorous and exhaustive manner. Through this article, we aim to offer our readers a detailed and enriching vision of RU-22930, with the aim of contributing to the knowledge and understanding of this particular topic.
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Clinical data | |
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Other names | 5,6-Dihydro-2-methyl-4--2H-1,2,4-oxadiazin-3-(4H)-one[1] |
Drug class | Nonsteroidal antiandrogen |
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Chemical and physical data | |
Formula | C11H10F3N3O4 |
Molar mass | 305.213 g·mol−1 |
3D model (JSmol) | |
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RU-22930 is a nonsteroidal antiandrogen (NSAA) related to the NSAAs flutamide and nilutamide (RU-23908) and was developed by Roussel Uclaf but was never marketed.[2][3] It is a selective antagonist of the androgen receptor and consequently has progonadotropic effects by increasing gonadotropin and testosterone levels via disinhibition of the hypothalamic-pituitary-gonadal axis.[2] Unlike flutamide and nilutamide, the drug is said to be short-acting and inactive by injection, but it has been found to be active topically in animals, and hence could be useful for the treatment of androgen-dependent skin conditions.[2][4]