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Synthesis, antiproliferative activity and molecular docking of thiocolchicine urethanes.
Bioorg Chem. 2018 Dec;81:553-566. doi: 10.1016/j.bioorg.2018.09.004. Epub 2018 Sep 12.
Bioorg Chem. 2018.
PMID: 30248507
Synthesis, antiproliferative and antibacterial evaluation of C-ring modified colchicine analogues.
Huczyński A, Rutkowski J, Popiel K, Maj E, Wietrzyk J, Stefańska J, Majcher U, Bartl F.
Huczyński A, et al. Among authors: majcher u.
Eur J Med Chem. 2015 Jan 27;90:296-301. doi: 10.1016/j.ejmech.2014.11.037. Epub 2014 Nov 22.
Eur J Med Chem. 2015.
PMID: 25437616
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Synthesis, antiproliferative activity and molecular docking of Colchicine derivatives.
Huczyński A, Majcher U, Maj E, Wietrzyk J, Janczak J, Moshari M, Tuszynski JA, Bartl F.
Huczyński A, et al. Among authors: majcher u.
Bioorg Chem. 2016 Feb;64:103-12. doi: 10.1016/j.bioorg.2016.01.002. Epub 2016 Jan 12.
Bioorg Chem. 2016.
PMID: 26794327
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Antiproliferative Activity and Molecular Docking of Novel Double-Modified Colchicine Derivatives.
Majcher U, Klejborowska G, Moshari M, Maj E, Wietrzyk J, Bartl F, Tuszynski JA, Huczyński A.
Majcher U, et al.
Cells. 2018 Nov 1;7(11):192. doi: 10.3390/cells7110192.
Cells. 2018.
PMID: 30388878
Free PMC article.
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Synthesis, antiproliferative activity, and molecular docking studies of 4-chlorothiocolchicine analogues.
Klejborowska G, Moshari M, Maj E, Majcher U, Preto J, Wietrzyk J, Tuszynski JA, Huczyński A.
Klejborowska G, et al. Among authors: majcher u.
Chem Biol Drug Des. 2020 Jan;95(1):182-191. doi: 10.1111/cbdd.13618. Epub 2019 Sep 20.
Chem Biol Drug Des. 2020.
PMID: 31483093
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Synthesis and Biological Evaluation of Novel Triple-Modified Colchicine Derivatives as Potent Tubulin-Targeting Anticancer Agents.
Majcher U, Klejborowska G, Kaik M, Maj E, Wietrzyk J, Moshari M, Preto J, Tuszynski JA, Huczyński A.
Majcher U, et al.
Cells. 2018 Nov 19;7(11):216. doi: 10.3390/cells7110216.
Cells. 2018.
PMID: 30463236
Free PMC article.
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