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Corrigendum to "Design, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity" [Bioorg. Chem. 121 (2022) 105691].
Bioorg Chem. 2022 Oct;127:105984. doi: 10.1016/j.bioorg.2022.105984. Epub 2022 Jun 28.
Bioorg Chem. 2022.
PMID: 35777235
No abstract available.
Heteroannelated and 7-deoxygenated goniofufurone mimics with antitumour activity: design, synthesis and preliminary SAR studies.
Popsavin V, Francuz J, Srećo Zelenović B, Benedeković G, Popsavin M, Kojić V, Bogdanović G.
Popsavin V, et al. Among authors: sreco zelenovic b.
Bioorg Med Chem Lett. 2013 Oct 15;23(20):5507-10. doi: 10.1016/j.bmcl.2013.08.069. Epub 2013 Aug 22.
Bioorg Med Chem Lett. 2013.
PMID: 24021462
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Design, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity.
Svirčev M, Popsavin M, Pavić A, Vasiljević B, Rodić MV, Djokić S, Kesić J, Srećo Zelenović B, Popsavin V, Kojić V.
Svirčev M, et al. Among authors: sreco zelenovic b.
Bioorg Chem. 2022 Apr;121:105691. doi: 10.1016/j.bioorg.2022.105691. Epub 2022 Feb 18.
Bioorg Chem. 2022.
PMID: 35217378
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Synthesis and biological activity of thiophene bioisosteres of natural styryl lactone goniofufurone and related compounds.
Popsavin M, Djokić S, Kovačević I, Stanisavljević SM, Kojić V, Rodić MV, Aleksić L, Kesić J, Srećo Zelenović B, Popsavin V, Jakimov DS.
Popsavin M, et al. Among authors: sreco zelenovic b.
Eur J Med Chem. 2024 Apr 5;269:116340. doi: 10.1016/j.ejmech.2024.116340. Epub 2024 Mar 21.
Eur J Med Chem. 2024.
PMID: 38527380
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