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Journal Abstract Search
688 related items for PubMed ID: 31865012
41. New 6- and 7-heterocyclyl-1H-indole derivatives as potent tubulin assembly and cancer cell growth inhibitors. La Regina G, Bai R, Coluccia A, Naccarato V, Famiglini V, Nalli M, Masci D, Verrico A, Rovella P, Mazzoccoli C, Da Pozzo E, Cavallini C, Martini C, Vultaggio S, Dondio G, Varasi M, Mercurio C, Hamel E, Lavia P, Silvestri R. Eur J Med Chem; 2018 May 25; 152():283-297. PubMed ID: 29730191 [Abstract] [Full Text] [Related]
42. 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]
43. Novel [1,2,4]triazolo[1,5-a]pyrimidine derivatives as potent antitubulin agents: Design, multicomponent synthesis and antiproliferative activities. Yang F, Yu LZ, Diao PC, Jian XE, Zhou MF, Jiang CS, You WW, Ma WF, Zhao PL. Bioorg Chem; 2019 Nov 15; 92():103260. PubMed ID: 31525523 [Abstract] [Full Text] [Related]
44. 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]
45. Design and synthesis of novel 5-(4-chlorophenyl)furan derivatives with inhibitory activity on tubulin polymerization. Moussa SA, A Osman EE, Eid NM, Abou-Seri SM, El Moghazy SM. Future Med Chem; 2018 Aug 01; 10(16):1907-1924. PubMed ID: 29966433 [Abstract] [Full Text] [Related]
46. Hybrid Pharmacophore Design, Molecular Docking, Synthesis, and Biological Evaluation of Novel Aldimine-Type Schiff Base Derivatives as Tubulin Polymerization Inhibitor. Ameri A, Khodarahmi G, Forootanfar H, Hassanzadeh F, Hakimelahi GH. Chem Biodivers; 2018 Mar 01; 15(3):e1700518. PubMed ID: 29292595 [Abstract] [Full Text] [Related]
47. Discovery of novel tubulin/HDAC dual-targeting inhibitors with strong antitumor and antiangiogenic potency. Wang Y, Sun M, Wang Y, Qin J, Zhang Y, Pang Y, Yao Y, Yang H, Duan Y. Eur J Med Chem; 2021 Dec 05; 225():113790. PubMed ID: 34454126 [Abstract] [Full Text] [Related]
48. Design, synthesis and biological evaluation of quinoline-indole derivatives as anti-tubulin agents targeting the colchicine binding site. Li W, Shuai W, Sun H, Xu F, Bi Y, Xu J, Ma C, Yao H, Zhu Z, Xu S. Eur J Med Chem; 2019 Feb 01; 163():428-442. PubMed ID: 30530194 [Abstract] [Full Text] [Related]
49. Design, synthesis of combretastatin A-4 piperazine derivatives as potential antitumor agents by inhibiting tubulin polymerization and inducing autophagy in HCT116 cells. Zhang H, Li M, Zhou X, Tang L, Chen G, Zhang Y. Eur J Med Chem; 2024 Jun 05; 272():116497. PubMed ID: 38759453 [Abstract] [Full Text] [Related]
50. Identification of new 3-phenyl-1H-indole-2-carbohydrazide derivatives and their structure-activity relationships as potent tubulin inhibitors and anticancer agents: A combined in silico, in vitro and synthetic study. Saruengkhanphasit R, Butkinaree C, Ornnork N, Lirdprapamongkol K, Niwetmarin W, Svasti J, Ruchirawat S, Eurtivong C. Bioorg Chem; 2021 May 05; 110():104795. PubMed ID: 33730670 [Abstract] [Full Text] [Related]
51. Discovery of 6-aryl-2-(3,4,5-trimethoxyphenyl)thiazole[3,2-b][1,2,4]triazoles as potent tubulin polymerization inhibitors. Li N, Guan Q, Hong Y, Zhang B, Li M, Li X, Li B, Wu L, Zhang W. Eur J Med Chem; 2023 Aug 05; 256():115402. PubMed ID: 37182330 [Abstract] [Full Text] [Related]
52. Design, synthesis and biological evaluation of novel thiazole-naphthalene derivatives as potential anticancer agents and tubulin polymerisation inhibitors. Wang G, Liu W, Fan M, He M, Li Y, Peng Z. J Enzyme Inhib Med Chem; 2021 Dec 05; 36(1):1694-1702. PubMed ID: 34309466 [Abstract] [Full Text] [Related]
53. Cytotoxic substituted indolizines as new colchicine site tubulin polymerisation inhibitors. Sardaru MC, Craciun AM, Al Matarneh CM, Sandu IA, Amarandi RM, Popovici L, Ciobanu CI, Peptanariu D, Pinteala M, Mangalagiu II, Danac R. J Enzyme Inhib Med Chem; 2020 Dec 05; 35(1):1581-1595. PubMed ID: 32752898 [Abstract] [Full Text] [Related]
54. Modification of the phenyl ring B of phenyl 4-(2-oxoimidazolidin-1-yl)benzenesulfonates by pyridinyl moiety leads to novel antimitotics targeting the colchicine-binding site. Ouellette V, Bouzriba C, Chavez Alvarez AC, Hamel-Côté G, Fortin S. Bioorg Med Chem Lett; 2024 Jun 01; 105():129745. PubMed ID: 38614151 [Abstract] [Full Text] [Related]
55. Synthesis, biological evaluation and molecular docking studies of aminochalcone derivatives as potential anticancer agents by targeting tubulin colchicine binding site. Wang G, Peng Z, Zhang J, Qiu J, Xie Z, Gong Z. Bioorg Chem; 2018 Aug 01; 78():332-340. PubMed ID: 29627654 [Abstract] [Full Text] [Related]
56. Synthesis and structure-activity relationships of 5-phenyloxazole-2-carboxylic acid derivatives as novel inhibitors of tubulin polymerization. Zhang R, Mo H, Ma YY, Zhao DG, Zhang K, Zhang T, Chen X, Zheng X. Bioorg Med Chem Lett; 2021 May 15; 40():127968. PubMed ID: 33753264 [Abstract] [Full Text] [Related]
57. Synthesis, biological evaluation, and structure-activity relationships of new tubulin polymerization inhibitors based on 5-amino-1,2,4-triazole scaffold. Yang F, Chen L, Lai JM, Jian XE, Lv DX, Yuan LL, Liu YX, Liang FT, Zheng XL, Li XL, Wei LY, You WW, Zhao PL. Bioorg Med Chem Lett; 2021 Apr 15; 38():127880. PubMed ID: 33636303 [Abstract] [Full Text] [Related]
58. Design, synthesis, biological evaluation and cocrystal structures with tubulin of chiral β-lactam bridged combretastatin A-4 analogues as potent antitumor agents. Zhou P, Liang Y, Zhang H, Jiang H, Feng K, Xu P, Wang J, Wang X, Ding K, Luo C, Liu M, Wang Y. Eur J Med Chem; 2018 Jan 20; 144():817-842. PubMed ID: 29306206 [Abstract] [Full Text] [Related]
59. Design, synthesis, and biological evaluation of novel 2,3-Di-O-Aryl/Alkyl sulfonate derivatives of l-ascorbic acid: Efficient access to novel anticancer agents via in vitro screening, tubulin polymerization inhibition, molecular docking study and ADME predictions. Deshmukh SR, Nalkar AS, Sarkate AP, Tiwari SV, Lokwani DK, Thopate SR. Bioorg Chem; 2024 Jun 20; 147():107402. PubMed ID: 38688199 [Abstract] [Full Text] [Related]
60. Discovery of novel 2-(trifluoromethyl)quinolin-4-amine derivatives as potent antitumor agents with microtubule polymerization inhibitory activity. Liu K, Mo M, Yu G, Yu J, Song SM, Cheng S, Li HM, Meng XL, Zeng XP, Xu GC, Luo H, Xu BX. Bioorg Chem; 2023 Oct 20; 139():106727. PubMed ID: 37451147 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]