184 related articles for article (PubMed ID: 33465696)
1. 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
Bioorg Med Chem; 2021 Feb; 32():116014. PubMed ID: 33465696
[TBL] [Abstract][Full Text] [Related]
2. 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
Bioorg Chem; 2018 Dec; 81():553-566. PubMed ID: 30248507
[TBL] [Abstract][Full Text] [Related]
3. 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
Chem Biol Drug Des; 2020 Jan; 95(1):182-191. PubMed ID: 31483093
[TBL] [Abstract][Full Text] [Related]
4. Carbamate derivatives of colchicine show potent activity towards primary acute lymphoblastic leukemia and primary breast cancer cells-in vitro and ex vivo study.
Urbaniak A; Jousheghany F; Piña-Oviedo S; Yuan Y; Majcher-Uchańska U; Klejborowska G; Moorjani A; Monzavi-Karbassi B; Huczyński A; Chambers TC
J Biochem Mol Toxicol; 2020 Jun; 34(6):e22487. PubMed ID: 32141170
[TBL] [Abstract][Full Text] [Related]
5. 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
Bioorg Med Chem; 2019 Dec; 27(23):115144. PubMed ID: 31653441
[TBL] [Abstract][Full Text] [Related]
6. 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
Bioorg Chem; 2020 Apr; 97():103664. PubMed ID: 32106039
[TBL] [Abstract][Full Text] [Related]
7. Synthesis and antitumor activity of nitrogen-based thiocolchicine derivatives.
Wang B; Pan XD; Liu HY; Yang J; Lü ZY; Zhao JH
Yao Xue Xue Bao; 2006 Nov; 41(11):1057-63. PubMed ID: 17262947
[TBL] [Abstract][Full Text] [Related]
8. Synthesis of thiocolchicine amine derivatives and evaluation of their antiproliferative activity.
Czerwonka D; Maj E; Wietrzyk J; Huczyński A
Bioorg Med Chem Lett; 2021 Nov; 52():128382. PubMed ID: 34592435
[TBL] [Abstract][Full Text] [Related]
9. 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
Cells; 2018 Nov; 7(11):. PubMed ID: 30463236
[TBL] [Abstract][Full Text] [Related]
10. Synthesis, Antiproliferative Activity and Molecular Docking Studies of Novel Doubly Modified Colchicine Amides and Sulfonamides as Anticancer Agents.
Krzywik J; Mozga W; Aminpour M; Janczak J; Maj E; Wietrzyk J; Tuszyński JA; Huczyński A
Molecules; 2020 Apr; 25(8):. PubMed ID: 32295119
[TBL] [Abstract][Full Text] [Related]
11. New Series of Double-Modified Colchicine Derivatives: Synthesis, Cytotoxic Effect and Molecular Docking.
Krzywik J; Aminpour M; Maj E; Mozga W; Wietrzyk J; Tuszyński JA; Huczyński A
Molecules; 2020 Aug; 25(15):. PubMed ID: 32748887
[TBL] [Abstract][Full Text] [Related]
12. 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
Cells; 2018 Nov; 7(11):. PubMed ID: 30388878
[TBL] [Abstract][Full Text] [Related]
13. 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
Bioorg Chem; 2016 Feb; 64():103-12. PubMed ID: 26794327
[TBL] [Abstract][Full Text] [Related]
14. N-acetylcolchinol O-methyl ether and thiocolchicine, potent analogs of colchicine modified in the C ring. Evaluation of the mechanistic basis for their enhanced biological properties.
Kang GJ; Getahun Z; Muzaffar A; Brossi A; Hamel E
J Biol Chem; 1990 Jun; 265(18):10255-9. PubMed ID: 2191947
[TBL] [Abstract][Full Text] [Related]
15. Synthesis and Antiproliferative Screening Of Novel Analogs of Regioselectively Demethylated Colchicine and Thiocolchicine.
Czerwonka D; Sobczak S; Maj E; Wietrzyk J; Katrusiak A; Huczyński A
Molecules; 2020 Mar; 25(5):. PubMed ID: 32151042
[TBL] [Abstract][Full Text] [Related]
16. A novel microtubule depolymerizing colchicine analogue triggers apoptosis and autophagy in HCT-116 colon cancer cells.
Kumar A; Singh B; Sharma PR; Bharate SB; Saxena AK; Mondhe DM
Cell Biochem Funct; 2016 Mar; 34(2):69-81. PubMed ID: 26919061
[TBL] [Abstract][Full Text] [Related]
17. 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
Eur J Med Chem; 2021 Apr; 215():113282. PubMed ID: 33611191
[TBL] [Abstract][Full Text] [Related]
18. Synthesis and antiproliferative screening of novel doubly modified colchicines containing urea, thiourea and guanidine moieties.
Krzywik J; Maj E; Nasulewicz-Goldeman A; Mozga W; Wietrzyk J; Huczyński A
Bioorg Med Chem Lett; 2021 Sep; 47():128197. PubMed ID: 34116158
[TBL] [Abstract][Full Text] [Related]
19. N-deacetyl-N-aminoacylthiocolchicine derivatives: synthesis and biological evaluation on MDR-positive and MDR-negative human cancer cell lines.
Gelmi ML; Mottadelli S; Pocar D; Riva A; Bombardelli E; De Vincenzo R; Scambia G
J Med Chem; 1999 Dec; 42(25):5272-6. PubMed ID: 10602712
[TBL] [Abstract][Full Text] [Related]
20. 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
Eur J Med Chem; 2015 Jan; 90():296-301. PubMed ID: 25437616
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]