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Journal Abstract Search
512 related items for PubMed ID: 28166995
21. 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; 36(1):640-658. PubMed ID: 33588683 [Abstract] [Full Text] [Related]
22. Design, synthesis and structure-activity relationship of 3,6-diaryl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines as novel tubulin inhibitors. Xu Q, Bao K, Sun M, Xu J, Wang Y, Tian H, Zuo D, Guan Q, Wu Y, Zhang W. Sci Rep; 2017 Sep 20; 7(1):11997. PubMed ID: 28931885 [Abstract] [Full Text] [Related]
23. Synthesis, structure-activity relationships and biological evaluation of 7-phenyl-pyrroloquinolinone 3-amide derivatives as potent antimitotic agents. Carta D, Bortolozzi R, Sturlese M, Salmaso V, Hamel E, Basso G, Calderan L, Quintieri L, Moro S, Viola G, Ferlin MG. Eur J Med Chem; 2017 Feb 15; 127():643-660. PubMed ID: 27823884 [Abstract] [Full Text] [Related]
24. 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]
25. Novel Aldimine-Type Schiff Bases of 4-Amino-5-[(3,4,5-trimethoxyphenyl)methyl]-1,2,4-triazole-3-thione/thiol: Docking Study, Synthesis, Biological Evaluation, and Anti-Tubulin Activity. Ameri A, Khodarahmi G, Hassanzadeh F, Forootanfar H, Hakimelahi GH. Arch Pharm (Weinheim); 2016 Aug 01; 349(8):662-81. PubMed ID: 27320785 [Abstract] [Full Text] [Related]
26. Synthesis and biological evaluation of novel shikonin-benzo[b]furan derivatives as tubulin polymerization inhibitors targeting the colchicine binding site. Shao YY, Yin Y, Lian BP, Leng JF, Xia YZ, Kong LY. Eur J Med Chem; 2020 Mar 15; 190():112105. PubMed ID: 32035399 [Abstract] [Full Text] [Related]
27. Design, Synthesis, and Biological Evaluation of Chalcone-Containing Shikonin Derivatives as Inhibitors of Tubulin Polymerization. Qiu HY, Wang F, Wang X, Sun WX, Qi JL, Pang YJ, Yang RW, Lu GH, Wang XM, Yang YH. ChemMedChem; 2017 Mar 07; 12(5):399-406. PubMed ID: 28211616 [Abstract] [Full Text] [Related]
32. 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]
33. Anticancer properties of indole derivatives as IsoCombretastatin A-4 analogues. Pecnard S, Hamze A, Bignon J, Prost B, Deroussent A, Gallego-Yerga L, Peláez R, Paik JY, Diederich M, Alami M, Provot O. Eur J Med Chem; 2021 Nov 05; 223():113656. PubMed ID: 34171660 [Abstract] [Full Text] [Related]
34. Synthesis and biological evaluation of curcumin inspired indole analogues as tubulin polymerization inhibitors. Sri Ramya PV, Angapelly S, Guntuku L, Singh Digwal C, Nagendra Babu B, Naidu VGM, Kamal A. Eur J Med Chem; 2017 Feb 15; 127():100-114. PubMed ID: 28038323 [Abstract] [Full Text] [Related]
35. Design, synthesis and biological evaluation of novel macrocyclic bisbibenzyl analogues as tubulin polymerization inhibitors. Sun B, Li L, Hu QW, Xie F, Zheng HB, Niu HM, Yuan HQ, Lou HX. Eur J Med Chem; 2016 Oct 04; 121():484-499. PubMed ID: 27318123 [Abstract] [Full Text] [Related]
36. Design, synthesis and anticancer properties of isocombretapyridines as potent colchicine binding site inhibitors. Shuai W, Li X, Li W, Xu F, Lu L, Yao H, Yang L, Zhu H, Xu S, Zhu Z, Xu J. Eur J Med Chem; 2020 Jul 01; 197():112308. PubMed ID: 32339853 [Abstract] [Full Text] [Related]
37. 10-(4-Phenylpiperazine-1-carbonyl)acridin-9(10H)-ones and related compounds: Synthesis, antiproliferative activity and inhibition of tubulin polymerization. Waltemate J, Ivanov I, Ghasemi JB, Aghaee E, Daniliuc CG, Müller K, Prinz H. Bioorg Med Chem Lett; 2021 Jan 15; 32():127687. PubMed ID: 33212157 [Abstract] [Full Text] [Related]