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113 related items for PubMed ID: 27128177
1. Simple avarone mimetics as selective agents against multidrug resistant cancer cells. Jeremić M, Pešić M, Dinić J, Banković J, Novaković I, Šegan D, Sladić D. Eur J Med Chem; 2016 Aug 08; 118():107-20. PubMed ID: 27128177 [Abstract] [Full Text] [Related]
2. Synthesis and biological activity of amino acid derivatives of avarone and its model compound. Vilipić J, Novaković I, Stanojković T, Matić I, Šegan D, Kljajić Z, Sladić D. Bioorg Med Chem; 2015 Nov 01; 23(21):6930-42. PubMed ID: 26476666 [Abstract] [Full Text] [Related]
3. Synthesis and biological activity of derivatives of the marine quinone avarone. Bozić T, Novaković I, Gasić MJ, Juranić Z, Stanojković T, Tufegdzić S, Kljajić Z, Sladić D. Eur J Med Chem; 2010 Mar 01; 45(3):923-9. PubMed ID: 19995673 [Abstract] [Full Text] [Related]
4. Bioconjugate of lysozyme and the antibacterial marine sesquiterpene quinone avarone and its derivatives. Novaković I, Anđelković U, Zlatović M, Gašić MJ, Sladić D. Bioconjug Chem; 2012 Jan 18; 23(1):57-65. PubMed ID: 22148500 [Abstract] [Full Text] [Related]
5. Identification of Novel ROS Inducers: Quinone Derivatives Tethered to Long Hydrocarbon Chains. Hong Y, Sengupta S, Hur W, Sim T. J Med Chem; 2015 May 14; 58(9):3739-50. PubMed ID: 25826398 [Abstract] [Full Text] [Related]
6. Further in vitro evaluation of cytotoxicity of the marine natural product derivative 4'-leucine-avarone. Pejin B, Iodice C, Tommonaro G, Bogdanovic G, Kojic V, De Rosa S. Nat Prod Res; 2014 May 14; 28(5):347-50. PubMed ID: 24422776 [Abstract] [Full Text] [Related]
8. H1, a derivative of Tetrandrine, exerts anti-MDR activity by initiating intrinsic apoptosis pathway and inhibiting the activation of Erk1/2 and Akt1/2. Wei N, Liu GT, Chen XG, Liu Q, Wang FP, Sun H. Biochem Pharmacol; 2011 Dec 01; 82(11):1593-603. PubMed ID: 21864508 [Abstract] [Full Text] [Related]
9. Cytotoxicity of three naturally occurring flavonoid derived compounds (artocarpesin, cycloartocarpesin and isobavachalcone) towards multi-factorial drug-resistant cancer cells. Kuete V, Mbaveng AT, Zeino M, Fozing CD, Ngameni B, Kapche GD, Ngadjui BT, Efferth T. Phytomedicine; 2015 Nov 15; 22(12):1096-102. PubMed ID: 26547532 [Abstract] [Full Text] [Related]
10. Ferrocene-cinchona hybrids with triazolyl-chalcone linkers act as pro-oxidants and sensitize human cancer cell lines to paclitaxel. Podolski-Renić A, Bősze S, Dinić J, Kocsis L, Hudecz F, Csámpai A, Pešić M. Metallomics; 2017 Aug 16; 9(8):1132-1141. PubMed ID: 28737782 [Abstract] [Full Text] [Related]
11. Cytotoxic and multidrug resistance reversal activities of novel 1,4-dihydropyridines against human cancer cells. Shekari F, Sadeghpour H, Javidnia K, Saso L, Nazari F, Firuzi O, Miri R. Eur J Pharmacol; 2015 Jan 05; 746():233-44. PubMed ID: 25445037 [Abstract] [Full Text] [Related]
12. Studies on the interactions of bioactive quinone avarone and its methylamino derivatives with calf thymus DNA. Vujčić MT, Tufegdžić S, Novaković I, Djikanović D, Gašić MJ, Sladić D. Int J Biol Macromol; 2013 Nov 05; 62():405-10. PubMed ID: 24080453 [Abstract] [Full Text] [Related]
13. Cytotoxicity and mode of action of a naturally occurring naphthoquinone, 2-acetyl-7-methoxynaphtho[2,3-b]furan-4,9-quinone towards multi-factorial drug-resistant cancer cells. Kuete V, Mbaveng AT, Sandjo LP, Zeino M, Efferth T. Phytomedicine; 2017 Sep 15; 33():62-68. PubMed ID: 28887921 [Abstract] [Full Text] [Related]
14. Design, Synthesis, Biological Evaluation, and Antioxidant and Cytotoxic Activity of Heteroatom-Substituted 1,4-Naphtho- and Benzoquinones. Deniz NG, Ibis C, Gokmen Z, Stasevych M, Novikov V, Komarovska-Porokhnyavets O, Ozyurek M, Guclu K, Karakas D, Ulukaya E. Chem Pharm Bull (Tokyo); 2015 Sep 15; 63(12):1029-39. PubMed ID: 26633024 [Abstract] [Full Text] [Related]
15. Synthesis and SAR study of novel anticancer and antimicrobial naphthoquinone amide derivatives. Sreelatha T, Kandhasamy S, Dinesh R, Shruthy S, Shweta S, Mukesh D, Karunagaran D, Balaji R, Mathivanan N, Perumal PT. Bioorg Med Chem Lett; 2014 Aug 01; 24(15):3647-51. PubMed ID: 24913712 [Abstract] [Full Text] [Related]
16. Reversal of multidrug resistance in vitro and in vivo by 5-N-formylardeemin, a new ardeemin derivative. Zheng X, Li D, Zhao C, Wang Q, Song H, Qin Y, Liao L, Zhang L, Lin Y, Wang X. Apoptosis; 2014 Aug 01; 19(8):1293-300. PubMed ID: 24858827 [Abstract] [Full Text] [Related]
17. Cytotoxicity and modes of action of 4'-hydroxy-2',6'-dimethoxychalcone and other flavonoids toward drug-sensitive and multidrug-resistant cancer cell lines. Kuete V, Nkuete AH, Mbaveng AT, Wiench B, Wabo HK, Tane P, Efferth T. Phytomedicine; 2014 Oct 15; 21(12):1651-7. PubMed ID: 25442273 [Abstract] [Full Text] [Related]
18. Coumarin derivatives as potential antitumor agents: Growth inhibition, apoptosis induction and multidrug resistance reverting activity. Bisi A, Cappadone C, Rampa A, Farruggia G, Sargenti A, Belluti F, Di Martino RMC, Malucelli E, Meluzzi A, Iotti S, Gobbi S. Eur J Med Chem; 2017 Feb 15; 127():577-585. PubMed ID: 28109950 [Abstract] [Full Text] [Related]
19. Design, synthesis and biological evaluation of thiosemicarbazones, hydrazinobenzothiazoles and arylhydrazones as anticancer agents with a potential to overcome multidrug resistance. Pape VF, Tóth S, Füredi A, Szebényi K, Lovrics A, Szabó P, Wiese M, Szakács G. Eur J Med Chem; 2016 Jul 19; 117():335-54. PubMed ID: 27161177 [Abstract] [Full Text] [Related]
20. In vitro cytotoxic activity of novel protoflavone analogs - selectivity towards a multidrug resistant cancer cell line. Danko B, Martins A, Chuang DW, Wang HC, Amaral L, Molnár J, Chang FR, Wu YC, Hunyadi A. Anticancer Res; 2012 Jul 19; 32(7):2863-9. PubMed ID: 22753749 [Abstract] [Full Text] [Related] Page: [Next] [New Search]