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Journal Abstract Search
660 related items for PubMed ID: 29031074
1. Synthesis, antiproliferative, anti-tubulin activity, and docking study of new 1,2,4-triazoles as potential combretastatin analogues. Mustafa M, Abdelhamid D, Abdelhafez EMN, Ibrahim MAA, Gamal-Eldeen AM, Aly OM. Eur J Med Chem; 2017 Dec 01; 141():293-305. PubMed ID: 29031074 [Abstract] [Full Text] [Related]
2. Synthesis and biological evaluation of cis-restricted triazole/tetrazole mimics of combretastatin-benzothiazole hybrids as tubulin polymerization inhibitors and apoptosis inducers. Subba Rao AV, Swapna K, Shaik SP, Lakshma Nayak V, Srinivasa Reddy T, Sunkari S, Shaik TB, Bagul C, Kamal A. Bioorg Med Chem; 2017 Feb 01; 25(3):977-999. PubMed ID: 28034647 [Abstract] [Full Text] [Related]
3. Potent combretastatin A-4 analogs containing 1,2,4-triazole: Synthesis, antiproliferative, anti-tubulin activity, and docking study. Mustafa M, Anwar S, Elgamal F, Ahmed ER, Aly OM. Eur J Med Chem; 2019 Dec 01; 183():111697. PubMed ID: 31536891 [Abstract] [Full Text] [Related]
4. Synthesis and biological evaluation of 1,2,3-triazole linked aminocombretastatin conjugates as mitochondrial mediated apoptosis inducers. Kamal A, Shaik B, Nayak VL, Nagaraju B, Kapure JS, Shaheer Malik M, Shaik TB, Prasad B. Bioorg Med Chem; 2014 Oct 01; 22(19):5155-67. PubMed ID: 25192811 [Abstract] [Full Text] [Related]
5. 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 01; 65():126-36. PubMed ID: 26943479 [Abstract] [Full Text] [Related]
6. Design and discovery of new antiproliferative 1,2,4-triazin-3(2H)-ones as tubulin polymerization inhibitors targeting colchicine binding site. Eissa IH, Dahab MA, Ibrahim MK, Alsaif NA, Alanazi AZ, Eissa SI, Mehany ABM, Beauchemin AM. Bioorg Chem; 2021 Jul 01; 112():104965. PubMed ID: 34020238 [Abstract] [Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Synthesis and Preclinical Evaluation of Indole Triazole Conjugates as Microtubule Targeting Agents that are Effective against MCF-7 Breast Cancer Cell Lines. Yele V, Pindiprolu SKSS, Sana S, Ramamurty DSVNM, Madasi JRK, Vadlamani S. Anticancer Agents Med Chem; 2021 Dec 17; 21(8):1047-1055. PubMed ID: 32981511 [Abstract] [Full Text] [Related]
11. Design, synthesis and evaluation of antiproliferative and antitubulin activities of 5-methyl-4-aryl-3-(4-arylpiperazine-1-carbonyl)-4H-1,2,4-triazoles. Wang C, Li Y, Liu T, Wang Z, Zhang Y, Bao K, Wu Y, Guan Q, Zuo D, Zhang W. Bioorg Chem; 2020 Nov 17; 104():103909. PubMed ID: 33142419 [Abstract] [Full Text] [Related]
12. Combretastatin-like chalcones as inhibitors of microtubule polymerization. Part 1: synthesis and biological evaluation of antivascular activity. Ducki S, Rennison D, Woo M, Kendall A, Chabert JF, McGown AT, Lawrence NJ. Bioorg Med Chem; 2009 Nov 15; 17(22):7698-710. PubMed ID: 19837593 [Abstract] [Full Text] [Related]
13. 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]
14. Synthesis and antitumor activity of 1,5-disubstituted 1,2,4-triazoles as cis-restricted combretastatin analogues. Romagnoli R, Baraldi PG, Cruz-Lopez O, Lopez Cara C, Carrion MD, Brancale A, Hamel E, Chen L, Bortolozzi R, Basso G, Viola G. J Med Chem; 2010 May 27; 53(10):4248-58. PubMed ID: 20420439 [Abstract] [Full Text] [Related]
15. Synthesis and antiproliferative activity of conformationally restricted 1,2,3-triazole analogues of combretastatins in the sea urchin embryo model and against human cancer cell lines. Demchuk DV, Samet AV, Chernysheva NB, Ushkarov VI, Stashina GA, Konyushkin LD, Raihstat MM, Firgang SI, Philchenkov AA, Zavelevich MP, Kuiava LM, Chekhun VF, Blokhin DY, Kiselyov AS, Semenova MN, Semenov VV. Bioorg Med Chem; 2014 Jan 15; 22(2):738-55. PubMed ID: 24387982 [Abstract] [Full Text] [Related]
16. Synthesis and biological evaluation of arylcinnamide linked combretastatin-A4 hybrids as tubulin polymerization inhibitors and apoptosis inducing agents. Kamal A, Bajee S, Lakshma Nayak V, Venkata Subba Rao A, Nagaraju B, Ratna Reddy C, Jeevak Sopanrao K, Alarifi A. Bioorg Med Chem Lett; 2016 Jun 15; 26(12):2957-2964. PubMed ID: 27161282 [Abstract] [Full Text] [Related]
17. Design, synthesis and bio-evaluation of novel 2-aryl-4-(3,4,5-trimethoxy-benzoyl)-5-substituted-1,2,3-triazoles as the tubulin polymerization inhibitors. Huang L, Liu M, Man S, Ma D, Feng D, Sun Z, Guan Q, Zuo D, Wu Y, Zhang W, Bao K. Eur J Med Chem; 2020 Jan 15; 186():111846. PubMed ID: 31740055 [Abstract] [Full Text] [Related]
18. 4,5-Diaryl-3H-1,2-dithiole-3-thiones and related compounds as combretastatin A-4/oltipraz hybrids: Synthesis, molecular modelling and evaluation as antiproliferative agents and inhibitors of tubulin. Wang Z, Qi H, Shen Q, Lu G, Li M, Bao K, Wu Y, Zhang W. Eur J Med Chem; 2016 Oct 21; 122():520-529. PubMed ID: 27428395 [Abstract] [Full Text] [Related]
19. 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 21; 92():103260. PubMed ID: 31525523 [Abstract] [Full Text] [Related]