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Journal Abstract Search
459 related items for PubMed ID: 23666368
1. Development of a novel class of tubulin inhibitors with promising anticancer activities. Xi J, Zhu X, Feng Y, Huang N, Luo G, Mao Y, Han X, Tian W, Wang G, Han X, Luo R, Huang Z, An J. Mol Cancer Res; 2013 Aug; 11(8):856-64. PubMed ID: 23666368 [Abstract] [Full Text] [Related]
2. Induction of apoptosis through tubulin inhibition in human cancer cells by new chromene-based chalcones. Aryapour H, Riazi GH, Ahmadian S, Foroumadi A, Mahdavi M, Emami S. Pharm Biol; 2012 Dec; 50(12):1551-60. PubMed ID: 22984888 [Abstract] [Full Text] [Related]
3. Molecular modelling studies on Arylthioindoles as potent inhibitors of tubulin polymerization. Coluccia A, Sabbadin D, Brancale A. Eur J Med Chem; 2011 Aug; 46(8):3519-25. PubMed ID: 21621885 [Abstract] [Full Text] [Related]
4. Synthesis of a terphenyl substituted 4-aza-2,3-didehydropodophyllotoxin analogues as inhibitors of tubulin polymerization and apoptosis inducers. Kamal A, Tamboli JR, Nayak VL, Adil SF, Vishnuvardhan MV, Ramakrishna S. Bioorg Med Chem; 2014 May 01; 22(9):2714-23. PubMed ID: 24721832 [Abstract] [Full Text] [Related]
5. 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]
6. New indole-based chalconoids as tubulin-targeting antiproliferative agents. Mirzaei H, Shokrzadeh M, Modanloo M, Ziar A, Riazi GH, Emami S. Bioorg Chem; 2017 Dec 01; 75():86-98. PubMed ID: 28922629 [Abstract] [Full Text] [Related]
7. A novel synthetic compound exerts effective anti-tumour activity in vivo via the inhibition of tubulin polymerisation in A549 cells. Yan J, Pang Y, Sheng J, Wang Y, Chen J, Hu J, Huang L, Li X. Biochem Pharmacol; 2015 Sep 01; 97(1):51-61. PubMed ID: 26212540 [Abstract] [Full Text] [Related]
8. Structure-based virtual screening of novel tubulin inhibitors and their characterization as anti-mitotic agents. Kim ND, Park ES, Kim YH, Moon SK, Lee SS, Ahn SK, Yu DY, No KT, Kim KH. Bioorg Med Chem; 2010 Oct 01; 18(19):7092-100. PubMed ID: 20810285 [Abstract] [Full Text] [Related]
9. BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo. Kuo CC, Hsieh HP, Pan WY, Chen CP, Liou JP, Lee SJ, Chang YL, Chen LT, Chen CT, Chang JY. Cancer Res; 2004 Jul 01; 64(13):4621-8. PubMed ID: 15231674 [Abstract] [Full Text] [Related]
10. Indicine N-oxide binds to tubulin at a distinct site and inhibits the assembly of microtubules: a mechanism for its cytotoxic activity. Appadurai P, Rathinasamy K. Toxicol Lett; 2014 Feb 10; 225(1):66-77. PubMed ID: 24300171 [Abstract] [Full Text] [Related]
11. A-204197, a new tubulin-binding agent with antimitotic activity in tumor cell lines resistant to known microtubule inhibitors. Tahir SK, Han EK, Credo B, Jae HS, Pietenpol JA, Scatena CD, Wu-Wong JR, Frost D, Sham H, Rosenberg SH, Ng SC. Cancer Res; 2001 Jul 15; 61(14):5480-5. PubMed ID: 11454695 [Abstract] [Full Text] [Related]
12. Novel shikonin derivatives targeting tubulin as anticancer agents. Guo J, Chen XF, Liu J, Lin HY, Han HW, Liu HC, Huang SC, Shahla BK, Kulek A, Qi JL, Wang XM, Ling LJ, Yang YH. Chem Biol Drug Des; 2014 Nov 15; 84(5):603-15. PubMed ID: 24797889 [Abstract] [Full Text] [Related]
13. Design, synthesis and biological evaluation of a novel tubulin inhibitor 7a3 targeting the colchicine binding site. Lai Q, Wang Y, Wang R, Lai W, Tang L, Tao Y, Liu Y, Zhang R, Huang L, Xiang H, Zeng S, Gou L, Chen H, Yao Y, Yang J. Eur J Med Chem; 2018 Aug 05; 156():162-179. PubMed ID: 30006162 [Abstract] [Full Text] [Related]
14. Discovery of a Series of Acridinones as Mechanism-Based Tubulin Assembly Inhibitors with Anticancer Activity. Magalhaes LG, Marques FB, da Fonseca MB, Rogério KR, Graebin CS, Andricopulo AD. PLoS One; 2016 Aug 05; 11(8):e0160842. PubMed ID: 27508497 [Abstract] [Full Text] [Related]
15. 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 05; 65():126-36. PubMed ID: 26943479 [Abstract] [Full Text] [Related]
16. Binding of dihydroxynaphthyl aryl ketones to tubulin colchicine site inhibits microtubule assembly. Gutierrez E, Benites J, Valderrama JA, Calderon PB, Verrax J, Nova E, Villanelo F, Maturana D, Escobar C, Lagos R, Monasterio O. Biochem Biophys Res Commun; 2015 Oct 23; 466(3):418-25. PubMed ID: 26365353 [Abstract] [Full Text] [Related]
17. The novel microtubule-destabilizing drug BAL27862 binds to the colchicine site of tubulin with distinct effects on microtubule organization. Prota AE, Danel F, Bachmann F, Bargsten K, Buey RM, Pohlmann J, Reinelt S, Lane H, Steinmetz MO. J Mol Biol; 2014 Apr 17; 426(8):1848-60. PubMed ID: 24530796 [Abstract] [Full Text] [Related]
18. Novel Benzo[B]Furans with Anti-Microtubule Activity Upregulate Expression of Apoptotic Genes and Arrest Leukemia Cells in G2/M Phase. Królewska-Golińska K, Cieślak MJ, Sobczak M, Dolot R, Radzikowska-Cieciura E, Napiórkowska M, Wybrańska I, Nawrot B. Anticancer Agents Med Chem; 2019 Apr 17; 19(3):375-388. PubMed ID: 30465514 [Abstract] [Full Text] [Related]
19. Identification of tubulin as the molecular target of proapoptotic pyrrolo-1,5-benzoxazepines. Mulligan JM, Greene LM, Cloonan S, Mc Gee MM, Onnis V, Campiani G, Fattorusso C, Lawler M, Williams DC, Zisterer DM. Mol Pharmacol; 2006 Jul 17; 70(1):60-70. PubMed ID: 16571652 [Abstract] [Full Text] [Related]
20. Synthesis of phenstatin/isocombretastatin-chalcone conjugates as potent tubulin polymerization inhibitors and mitochondrial apoptotic inducers. Kamal A, Kumar GB, Vishnuvardhan MV, Shaik AB, Reddy VS, Mahesh R, Sayeeda IB, Kapure JS. Org Biomol Chem; 2015 Apr 07; 13(13):3963-81. PubMed ID: 25721862 [Abstract] [Full Text] [Related] Page: [Next] [New Search]