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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Deuterated drugs and biomarkers in the COVID-19 pandemic</dc:title><dc:creator>Jansen-van Vuuren,	Ross D.	(Avtor)
	</dc:creator><dc:creator>Jedlovčnik,	Luka	(Avtor)
	</dc:creator><dc:creator>Košmrlj,	Janez	(Avtor)
	</dc:creator><dc:creator>Massey,	Thomas E.	(Avtor)
	</dc:creator><dc:creator>Derdau,	Volker	(Avtor)
	</dc:creator><dc:subject>COVID-19</dc:subject><dc:subject>hydrogen isotopes</dc:subject><dc:subject>inhibitors</dc:subject><dc:subject>metabolism</dc:subject><dc:subject>pharmaceuticals</dc:subject><dc:description>Coronavirus disease 2019 (COVID-19) is a highly contagious disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Initially identified in Wuhan (China) in December 2019, COVID-19 rapidly spread globally, resulting in the COVID-19 pandemic. Carriers of the SARS-CoV-2 can experience symptoms ranging from mild to severe (or no symptoms whatsoever). Although vaccination provides extra immunity toward SARS-CoV-2, there has been an urgent need to develop treatments for COVID-19 to alleviate symptoms for carriers of the disease. In seeking a potential treatment, deuterated compounds have played a critical role either as therapeutic agents or as internal MS standards for studying the pharmacological properties of new drugs by quantifying the parent compounds and metabolites. We have identified &gt;70 examples of deuterium-labeled compounds associated with treatment of COVID-19. Of these, we found 9 repurposed drugs and &gt;20 novel drugs studied for potential therapeutic roles along with a total of 38 compounds (drugs, biomarkers, and lipids) explored as internal mass spectrometry standards. This review details the synthetic pathways and modes of action of these compounds (if known), and a brief analysis of each study.</dc:description><dc:date>2022</dc:date><dc:date>2023-02-14 11:29:22</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>144314</dc:identifier><dc:identifier>UDK: 547.8:546.11</dc:identifier><dc:identifier>ISSN pri članku: 2470-1343</dc:identifier><dc:identifier>DOI: 10.1021/acsomega.2c04160</dc:identifier><dc:identifier>COBISS_ID: 131181827</dc:identifier><dc:language>sl</dc:language></metadata>
