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865 related items for PubMed ID: 29306206
21. Design, synthesis, and biological evaluation of 1-substituted -2-aryl imidazoles targeting tubulin polymerization as potential anticancer agents. Li L, Quan D, Chen J, Ding J, Zhao J, Lv L, Chen J. Eur J Med Chem; 2019 Dec 15; 184():111732. PubMed ID: 31610372 [Abstract] [Full Text] [Related]
22. β-Lactams with antiproliferative and antiapoptotic activity in breast and chemoresistant colon cancer cells. Malebari AM, Fayne D, Nathwani SM, O'Connell F, Noorani S, Twamley B, O'Boyle NM, O'Sullivan J, Zisterer DM, Meegan MJ. Eur J Med Chem; 2020 Mar 01; 189():112050. PubMed ID: 31954879 [Abstract] [Full Text] [Related]
23. A 2-step synthesis of Combretastatin A-4 and derivatives as potent tubulin assembly inhibitors. Barnes NG, Parker AW, Ahmed Mal Ullah AA, Ragazzon PA, Hadfield JA. Bioorg Med Chem; 2020 Oct 01; 28(19):115684. PubMed ID: 32912434 [Abstract] [Full Text] [Related]
24. Discovery of novel quinoline-based analogues of combretastatin A-4 as tubulin polymerisation inhibitors with apoptosis inducing activity and potent anticancer effect. Ibrahim TS, Hawwas MM, Malebari AM, Taher ES, Omar AM, Neamatallah T, Abdel-Samii ZK, Safo MK, Elshaier YAMM. J Enzyme Inhib Med Chem; 2021 Dec 01; 36(1):802-818. PubMed ID: 33730937 [Abstract] [Full Text] [Related]
25. Design, synthesis and biological evaluation of novel imidazole-chalcone derivatives as potential anticancer agents and tubulin polymerization inhibitors. Rahimzadeh Oskuei S, Mirzaei S, Reza Jafari-Nik M, Hadizadeh F, Eisvand F, Mosaffa F, Ghodsi R. Bioorg Chem; 2021 Jul 01; 112():104904. PubMed ID: 33933802 [Abstract] [Full Text] [Related]
26. Novel Combretastatin A-4 Analogs-Design, Synthesis, and Antiproliferative and Anti-Tubulin Activity. Jędrzejczyk M, Morabito B, Żyżyńska-Granica B, Struga M, Janczak J, Aminpour M, Tuszynski JA, Huczyński A. Molecules; 2024 May 08; 29(10):. PubMed ID: 38792062 [Abstract] [Full Text] [Related]
27. Synthesis and biological evaluation of 1,2,3-triazole linked aminocombretastatin conjugates as mitochondrial mediated apoptosis inducers. Kamal A, Shaik B, Nayak VL, Nagaraju B, Kapure JS, Shaheer Malik M, Shaik TB, Prasad B. Bioorg Med Chem; 2014 Oct 01; 22(19):5155-67. PubMed ID: 25192811 [Abstract] [Full Text] [Related]
28. Design, synthesis, and biological evaluation of novel benzodiazepine derivatives as anticancer agents through inhibition of tubulin polymerization in vitro and in vivo. Pang Y, Lin H, Ou C, Cao Y, An B, Yan J, Li X. Eur J Med Chem; 2019 Nov 15; 182():111670. PubMed ID: 31499359 [Abstract] [Full Text] [Related]
29. Combretastatin linked 1,3,4-oxadiazole conjugates as a Potent Tubulin Polymerization inhibitors. Kamal A, Srikanth PS, Vishnuvardhan MV, Kumar GB, Suresh Babu K, Hussaini SM, Kapure JS, Alarifi A. Bioorg Chem; 2016 Apr 15; 65():126-36. PubMed ID: 26943479 [Abstract] [Full Text] [Related]
30. Design and synthesis of silicon-containing tubulin polymerization inhibitors: replacement of the ethylene moiety of combretastatin A-4 with a silicon linker. Nakamura M, Kajita D, Matsumoto Y, Hashimoto Y. Bioorg Med Chem; 2013 Dec 01; 21(23):7381-91. PubMed ID: 24139940 [Abstract] [Full Text] [Related]
31. Synthesis and biological evaluation of a series of podophyllotoxins derivatives as a class of potent antitubulin agents. Liu Y, Wei D, Zhao Y, Cheng W, Lu Y, Ma Y, Li X, Han C, Wei Y, Cao H, Zhao C. Bioorg Med Chem; 2012 Nov 01; 20(21):6285-95. PubMed ID: 23022053 [Abstract] [Full Text] [Related]
32. Design and discovery of new antiproliferative 1,2,4-triazin-3(2H)-ones as tubulin polymerization inhibitors targeting colchicine binding site. Eissa IH, Dahab MA, Ibrahim MK, Alsaif NA, Alanazi AZ, Eissa SI, Mehany ABM, Beauchemin AM. Bioorg Chem; 2021 Jul 01; 112():104965. PubMed ID: 34020238 [Abstract] [Full Text] [Related]
33. Design, synthesis and bioevaluation of 2,7-diaryl-pyrazolo[1,5-a]pyrimidines as tubulin polymerization inhibitors. Liu R, Zhang S, Huang M, Guo Z, Li L, Li M, Wu L, Guan Q, Zhang W. Bioorg Chem; 2021 Oct 01; 115():105220. PubMed ID: 34352709 [Abstract] [Full Text] [Related]
34. Synthesis and biological evaluation of 4-phenyl-5-quinolinyl substituted isoxazole analogues as potent cytotoxic and tubulin polymerization inhibitors against ESCC. Jia M, Pei Y, Li N, Zhang Y, Song J, Niu JB, Yang H, Zhang S, Sun M. Eur J Med Chem; 2024 Sep 05; 275():116611. PubMed ID: 38901104 [Abstract] [Full Text] [Related]
35. Design, synthesis, in vitro and in vivo biological evaluation of 2-amino-3-aroylbenzo[b]furan derivatives as highly potent tubulin polymerization inhibitors. Oliva P, Romagnoli R, Manfredini S, Brancale A, Ferla S, Hamel E, Ronca R, Maccarinelli F, Giacomini A, Rruga F, Mariotto E, Viola G, Bortolozzi R. Eur J Med Chem; 2020 Aug 15; 200():112448. PubMed ID: 32417696 [Abstract] [Full Text] [Related]
36. Identification of novel 1-indolyl acetate-5-nitroimidazole derivatives of combretastatin A-4 as potential tubulin polymerization inhibitors. Yao YF, Wang ZC, Wu SY, Li QF, Yu C, Liang XY, Lv PC, Duan YT, Zhu HL. Biochem Pharmacol; 2017 Aug 01; 137():10-28. PubMed ID: 28456516 [Abstract] [Full Text] [Related]
37. Design, concise synthesis and evaluation of novel amide-based combretastatin A-4 analogues as potent tubulin inhibitors. Ma Y, Wang T, Cheng L, Ma X, Li R, Zhang M, Chen J, Zhao P. Bioorg Med Chem Lett; 2024 Aug 01; 108():129816. PubMed ID: 38806101 [Abstract] [Full Text] [Related]
38. Synthesis and biological evaluation of carbamates derived from aminocombretastatin A-4 as vascular disrupting agents. Conesa-Milián L, Falomir E, Murga J, Carda M, Meyen E, Liekens S, Alberto Marco J. Eur J Med Chem; 2018 Mar 10; 147():183-193. PubMed ID: 29432949 [Abstract] [Full Text] [Related]
39. Design, synthesis and bioevaluation of 6-aryl-1-(3,4,5-trimethoxyphenyl)-1H-benzo[d]imidazoles as tubulin polymerization inhibitors. Liu R, Huang M, Zhang S, Li L, Li M, Sun J, Wu L, Guan Q, Zhang W. Eur J Med Chem; 2021 Dec 15; 226():113826. PubMed ID: 34571171 [Abstract] [Full Text] [Related]
40. Synthesis and biological evaluation of 2-amino-3-(3',4',5'-trimethoxybenzoyl)-5-aryl thiophenes as a new class of potent antitubulin agents. Romagnoli R, Baraldi PG, Pavani MG, Tabrizi MA, Preti D, Fruttarolo F, Piccagli L, Jung MK, Hamel E, Borgatti M, Gambari R. J Med Chem; 2006 Jun 29; 49(13):3906-15. PubMed ID: 16789746 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]