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Journal Abstract Search
752 related items for PubMed ID: 29627654
1. 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; 78():332-340. PubMed ID: 29627654 [Abstract] [Full Text] [Related]
2. Design, synthesis and biological evaluation of a series of pyrano chalcone derivatives containing indole moiety as novel anti-tubulin agents. Wang G, Li C, He L, Lei K, Wang F, Pu Y, Yang Z, Cao D, Ma L, Chen J, Sang Y, Liang X, Xiang M, Peng A, Wei Y, Chen L. Bioorg Med Chem; 2014 Apr 01; 22(7):2060-79. PubMed ID: 24629450 [Abstract] [Full Text] [Related]
3. 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]
4. Synthesis, biological evaluation, and molecular modelling of new naphthalene-chalcone derivatives as potential anticancer agents on MCF-7 breast cancer cells by targeting tubulin colchicine binding site. Wang G, Liu W, Gong Z, Huang Y, Li Y, Peng Z. J Enzyme Inhib Med Chem; 2020 Dec 01; 35(1):139-144. PubMed ID: 31724435 [Abstract] [Full Text] [Related]
9. Design and synthesis of novel imidazole-chalcone derivatives as microtubule protein polymerization inhibitors to treat cervical cancer and reverse cisplatin resistance. Liu Z, Yang Z, Ablise M. Bioorg Chem; 2024 Jun 01; 147():107310. PubMed ID: 38583249 [Abstract] [Full Text] [Related]
10. Synthesis and biological evaluation of curcumin inspired imidazo[1,2-a]pyridine analogues as tubulin polymerization inhibitors. Ramya PVS, Guntuku L, Angapelly S, Digwal CS, Lakshmi UJ, Sigalapalli DK, Babu BN, Naidu VGM, Kamal A. Eur J Med Chem; 2018 Jan 01; 143():216-231. PubMed ID: 29174816 [Abstract] [Full Text] [Related]
11. Synthesis and biological evaluation of novel benzo[c]acridine-diones as potential anticancer agents and tubulin polymerization inhibitors. Behbahani FS, Tabeshpour J, Mirzaei S, Golmakaniyoon S, Tayarani-Najaran Z, Ghasemi A, Ghodsi R. Arch Pharm (Weinheim); 2019 Jun 01; 352(6):e1800307. PubMed ID: 31012156 [Abstract] [Full Text] [Related]
12. (E)-N-Aryl-2-oxo-2-(3,4,5-trimethoxyphenyl)acetohydrazonoyl cyanides as tubulin polymerization inhibitors: Structure-based bioisosterism design, synthesis, biological evaluation, molecular docking and in silico ADME prediction. Wang G, Peng Z, Peng S, Qiu J, Li Y, Lan Y. Bioorg Med Chem Lett; 2018 Nov 01; 28(20):3350-3355. PubMed ID: 30197030 [Abstract] [Full Text] [Related]
13. Design, synthesis, and anticancer evaluation of benzophenone derivatives bearing naphthalene moiety as novel tubulin polymerization inhibitors. Wang G, Liu W, Tang J, Ma X, Gong Z, Huang Y, Li Y, Peng Z. Bioorg Chem; 2020 Nov 01; 104():104265. PubMed ID: 32919128 [Abstract] [Full Text] [Related]
15. Design, Synthesis and Cytotoxic Evaluation of Novel Chalcone Derivatives Bearing Triazolo[4,3-a]-quinoxaline Moieties as Potent Anticancer Agents with Dual EGFR Kinase and Tubulin Polymerization Inhibitory Effects. Alswah M, Bayoumi AH, Elgamal K, Elmorsy A, Ihmaid S, Ahmed HEA. Molecules; 2017 Dec 27; 23(1):. PubMed ID: 29280968 [Abstract] [Full Text] [Related]
16. Discovery of new quinolines as potent colchicine binding site inhibitors: design, synthesis, docking studies, and anti-proliferative evaluation. Hagras M, El Deeb MA, Elzahabi HSA, Elkaeed EB, Mehany ABM, Eissa IH. J Enzyme Inhib Med Chem; 2021 Dec 27; 36(1):640-658. PubMed ID: 33588683 [Abstract] [Full Text] [Related]
17. Synthesis, Anticancer Activity and Molecular Modeling Studies of Novel Chalcone Derivatives Containing Indole and Naphthalene Moieties as Tubulin Polymerization Inhibitors. Wang G, Peng Z, Li Y. Chem Pharm Bull (Tokyo); 2019 Jul 01; 67(7):725-728. PubMed ID: 30982797 [Abstract] [Full Text] [Related]
18. Synthesis, biological evaluation, and molecular docking investigation of 3-amidoindoles as potent tubulin polymerization inhibitors. Chen P, Zhuang YX, Diao PC, Yang F, Wu SY, Lv L, You WW, Zhao PL. Eur J Med Chem; 2019 Jan 15; 162():525-533. PubMed ID: 30472600 [Abstract] [Full Text] [Related]
19. Design, synthesis and biological evaluation of millepachine derivatives as a new class of tubulin polymerization inhibitors. Wang G, Peng F, Cao D, Yang Z, Han X, Liu J, Wu W, He L, Ma L, Chen J, Sang Y, Xiang M, Peng A, Wei Y, Chen L. Bioorg Med Chem; 2013 Nov 01; 21(21):6844-54. PubMed ID: 23993668 [Abstract] [Full Text] [Related]