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Journal Abstract Search
257 related items for PubMed ID: 26602827
1. Synthesis and bio-evaluation of novel quinolino-stilbene derivatives as potential anticancer agents. Srivastava V, Lee H. Bioorg Med Chem; 2015 Dec 15; 23(24):7629-40. PubMed ID: 26602827 [Abstract] [Full Text] [Related]
2. 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 15; 36(1):802-818. PubMed ID: 33730937 [Abstract] [Full Text] [Related]
3. Synthesis and biological evaluation of quinoline analogues of flavones as potential anticancer agents and tubulin polymerization inhibitors. Shobeiri N, Rashedi M, Mosaffa F, Zarghi A, Ghandadi M, Ghasemi A, Ghodsi R. Eur J Med Chem; 2016 May 23; 114():14-23. PubMed ID: 26974371 [Abstract] [Full Text] [Related]
4. Design, synthesis, and biological evaluation of novel combretastatin A-4 thio derivatives as microtubule targeting agents. Stefański T, Mikstacka R, Kurczab R, Dutkiewicz Z, Kucińska M, Murias M, Zielińska-Przyjemska M, Cichocki M, Teubert A, Kaczmarek M, Hogendorf A, Sobiak S. Eur J Med Chem; 2018 Jan 20; 144():797-816. PubMed ID: 29291446 [Abstract] [Full Text] [Related]
5. 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]
6. Synthesis, anticancer activity and molecular docking studies on a series of heterocyclic trans-cyanocombretastatin analogues as antitubulin agents. Penthala NR, Zong H, Ketkar A, Madadi NR, Janganati V, Eoff RL, Guzman ML, Crooks PA. Eur J Med Chem; 2015 Mar 06; 92():212-20. PubMed ID: 25557492 [Abstract] [Full Text] [Related]
7. Design, synthesis and biological evaluation of novel acridine and quinoline derivatives as tubulin polymerization inhibitors with anticancer activities. Ren Y, Ruan Y, Cheng B, Li L, Liu J, Fang Y, Chen J. Bioorg Med Chem; 2021 Sep 15; 46():116376. PubMed ID: 34455231 [Abstract] [Full Text] [Related]
8. 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]
9. Synthesis, biological evaluation and molecular docking studies of resveratrol derivatives possessing curcumin moiety as potent antitubulin agents. Ruan BF, Lu X, Li TT, Tang JF, Wei Y, Wang XL, Zheng SL, Yao RS, Zhu HL. Bioorg Med Chem; 2012 Jan 15; 20(2):1113-21. PubMed ID: 22189271 [Abstract] [Full Text] [Related]
10. Design, synthesis, biological evaluation, and 3D-QSAR analysis of podophyllotoxin-dioxazole combination as tubulin targeting anticancer agents. Wang ZZ, Sun WX, Wang X, Zhang YH, Qiu HY, Qi JL, Pang YJ, Lu GH, Wang XM, Yu FG, Yang YH. Chem Biol Drug Des; 2017 Aug 15; 90(2):236-243. PubMed ID: 28079286 [Abstract] [Full Text] [Related]
11. 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]
12. Design, synthesis and antiproliferative activity of the new conjugates of E7010 and resveratrol as tubulin polymerization inhibitors. Kamal A, Ashraf M, Basha ST, Ali Hussaini SM, Singh S, Vishnuvardhan MV, Kiran B, Sridhar B. Org Biomol Chem; 2016 Jan 28; 14(4):1382-94. PubMed ID: 26676480 [Abstract] [Full Text] [Related]
13. Synthesis of Combretastatin-A4 Carboxamidest that Mimic Sulfonyl Piperazines by a Molecular Hybridization Approach: in vitro Cytotoxicity Evaluation and Inhibition of Tubulin Polymerization. Jadala C, Sathish M, Anchi P, Tokala R, Lakshmi UJ, Reddy VG, Shankaraiah N, Godugu C, Kamal A. ChemMedChem; 2019 Dec 17; 14(24):2052-2060. PubMed ID: 31674147 [Abstract] [Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Design, Synthesis and Antitumor Activity of Novel link-bridge and B-Ring Modified Combretastatin A-4 (CA-4) Analogues as Potent Antitubulin Agents. Duan YT, Man RJ, Tang DJ, Yao YF, Tao XX, Yu C, Liang XY, Makawana JA, Zou MJ, Wang ZC, Zhu HL. Sci Rep; 2016 May 03; 6():25387. PubMed ID: 27138035 [Abstract] [Full Text] [Related]
18. 2-amino and 2'-aminocombretastatin derivatives as potent antimitotic agents. Chang JY, Yang MF, Chang CY, Chen CM, Kuo CC, Liou JP. J Med Chem; 2006 Oct 19; 49(21):6412-5. PubMed ID: 17034147 [Abstract] [Full Text] [Related]
19. 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]