Chemistry:Tiazofurin
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Short description: Chemical compound
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Other names | 2-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3-thiazole-4-carboxamide |
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Formula | C9H12N2O5S |
Molar mass | 260.26 g·mol−1 |
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Tiazofurin is a drug which acts as an inhibitor of the enzyme IMP dehydrogenase. Tiazofurin and its analogues were under investigation for potential use in the treatment of cancer,[1] though side effects such as pleuropericarditis and a flu-like syndrome precluded further development. They also show antiviral effects and may be reevaluated as potential options in the treatment of newly emerging viral diseases.[2]
References
- ↑ "Synthesis and antiproliferative activity of two new tiazofurin analogues with 2'-amido functionalities". Bioorg. Med. Chem. Lett. 16 (10): 2773–6. 2006. doi:10.1016/j.bmcl.2006.02.001. PMID 16495053.
- ↑ "C-Nucleosides To Be Revisited". Journal of Medicinal Chemistry 59 (6): 2301–11. March 2016. doi:10.1021/acs.jmedchem.5b01157. PMID 26513594.
Original source: https://en.wikipedia.org/wiki/Tiazofurin.
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