Moshari M - Search Results

1

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. Among authors: moshari m. Cells. 2018 Nov 19;7(11):216. doi: 10.3390/cells7110216. Cells. 2018. PMID: 30463236 Free PMC article.

2

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: moshari m. Bioorg Chem. 2016 Feb;64:103-12. doi: 10.1016/j.bioorg.2016.01.002. Epub 2016 Jan 12. Bioorg Chem. 2016. PMID: 26794327

3

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. Among authors: moshari m. Cells. 2018 Nov 1;7(11):192. doi: 10.3390/cells7110192. Cells. 2018. PMID: 30388878 Free PMC article.

4

Synthesis, biological evaluation and molecular docking studies of new amides of 4-bromothiocolchicine as anticancer agents.

Klejborowska G, Urbaniak A, Preto J, Maj E, Moshari M, Wietrzyk J, Tuszynski JA, Chambers TC, Huczyński A. Klejborowska G, et al. Among authors: moshari m. Bioorg Med Chem. 2019 Dec 1;27(23):115144. doi: 10.1016/j.bmc.2019.115144. Epub 2019 Oct 8. Bioorg Med Chem. 2019. PMID: 31653441 Free article.

5

Synthesis, biological evaluation and molecular docking studies of new amides of 4-chlorothiocolchicine as anticancer agents.

Klejborowska G, Urbaniak A, Maj E, Preto J, Moshari M, Wietrzyk J, Tuszynski JA, Chambers TC, Huczyński A. Klejborowska G, et al. Among authors: moshari m. Bioorg Chem. 2020 Apr;97:103664. doi: 10.1016/j.bioorg.2020.103664. Epub 2020 Feb 13. Bioorg Chem. 2020. PMID: 32106039 Free article.

6

Synthesis, anticancer activity and molecular docking studies of N-deacetylthiocolchicine and 4-iodo-N-deacetylthiocolchicine derivatives.

Klejborowska G, Urbaniak A, Maj E, Wietrzyk J, Moshari M, Preto J, Tuszynski JA, Chambers TC, Huczyński A. Klejborowska G, et al. Among authors: moshari m. Bioorg Med Chem. 2021 Feb 15;32:116014. doi: 10.1016/j.bmc.2021.116014. Epub 2021 Jan 11. Bioorg Med Chem. 2021. PMID: 33465696

7

Synthesis, antiproliferative activity and molecular docking of thiocolchicine urethanes.

Majcher U, Urbaniak A, Maj E, Moshari M, Delgado M, Wietrzyk J, Bartl F, Chambers TC, Tuszynski JA, Huczyński A. Majcher U, et al. Among authors: moshari m. Bioorg Chem. 2018 Dec;81:553-566. doi: 10.1016/j.bioorg.2018.09.004. Epub 2018 Sep 12. Bioorg Chem. 2018. PMID: 30248507

8

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: moshari m. 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

9

An insight into the anticancer potential of carbamates and thiocarbamates of 10-demethoxy-10-methylaminocolchicine.

Krzywik J, Aminpour M, Janczak J, Maj E, Moshari M, Mozga W, Wietrzyk J, Tuszyński JA, Huczyński A. Krzywik J, et al. Among authors: moshari m. Eur J Med Chem. 2021 Apr 5;215:113282. doi: 10.1016/j.ejmech.2021.113282. Epub 2021 Feb 10. Eur J Med Chem. 2021. PMID: 33611191 Free article.

10

Computational Prediction and Experimental Validation of the Unique Molecular Mode of Action of Scoulerine.

Moshari M, Wang Q, Michalak M, Klobukowski M, Tuszynski JA. Moshari M, et al. Molecules. 2022 Jun 21;27(13):3991. doi: 10.3390/molecules27133991. Molecules. 2022. PMID: 35807231 Free PMC article.

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