These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 23061567)

  • 1. Synthesis and evaluation of water-soluble etoposide esters of malic acid as prodrugs.
    Chen J; Du W
    Med Chem; 2013 Aug; 9(5):740-7. PubMed ID: 23061567
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis and evaluation of water-soluble docetaxel prodrugs-docetaxel esters of malic acid.
    Du W; Hong L; Yao T; Yang X; He Q; Yang B; Hu Y
    Bioorg Med Chem; 2007 Sep; 15(18):6323-30. PubMed ID: 17624790
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Paclitaxel esters of malic acid as prodrugs with improved water solubility.
    Damen EW; Wiegerinck PH; Braamer L; Sperling D; de Vos D; Scheeren HW
    Bioorg Med Chem; 2000 Feb; 8(2):427-32. PubMed ID: 10722165
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Design, synthesis and antitumor activity of valproic acid salicylanilide esters].
    Yuan M; Li JM; He GW; Zhong GC; Zhang YC
    Yao Xue Xue Bao; 2013 Jun; 48(6):874-80. PubMed ID: 23984521
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis and biological activity of prodrug inhibitors of the thioredoxin-thioredoxin reductase system.
    Wipf P; Lynch SM; Powis G; Birmingham A; Englund EE
    Org Biomol Chem; 2005 Nov; 3(21):3880-2. PubMed ID: 16240002
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Design, synthesis and evaluation of carbamate-bridged amino acid prodrugs of cycloicaritin with improved antitumor activity, aqueous solubility and phase II metabolic stability.
    Wang W; Fan J; Li F; Gan S; Zhang J; Wang Y; Li Y; Li W; He Z; Ding H; Sun Y; Zhang T; Jiang Q
    Eur J Med Chem; 2024 Oct; 276():116646. PubMed ID: 38972080
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Carbonate esters turn camptothecin-unsaturated fatty acid prodrugs into nanomedicines for cancer therapy.
    Li Y; Kang T; Wu Y; Chen Y; Zhu J; Gou M
    Chem Commun (Camb); 2018 Feb; 54(16):1996-1999. PubMed ID: 29411840
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New 3'-O-aromatic acyl-5-fluoro-2'-deoxyuridine derivatives as potential anticancer agents.
    Szymańska-Michalak A; Wawrzyniak D; Framski G; Kujda M; Zgoła P; Stawinski J; Barciszewski J; Boryski J; Kraszewski A
    Eur J Med Chem; 2016 Jun; 115():41-52. PubMed ID: 26994842
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis and evaluation of water-soluble paclitaxel prodrugs.
    Feng X; Yuan YJ; Wu JC
    Bioorg Med Chem Lett; 2002 Nov; 12(22):3301-3. PubMed ID: 12392737
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prodrug forms of N-[(4-deoxy-4-amino-10-methyl)pteroyl]glutamate-gamma-[psiP(O)(OH)]-glutarate, a potent inhibitor of folylpoly-gamma-glutamate synthetase: synthesis and hydrolytic stability.
    Feng Y; Coward JK
    J Med Chem; 2006 Jan; 49(2):770-88. PubMed ID: 16420062
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prodrugs of 4'-demethyl-4-deoxypodophyllotoxin: synthesis and evaluation of the antitumor activity.
    Kim Y; You YJ; Nam NH; Ahn BZ
    Bioorg Med Chem Lett; 2002 Dec; 12(23):3435-8. PubMed ID: 12419378
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Design, synthesis, and evaluation of water-soluble morpholino-decorated paclitaxel prodrugs with remarkably decreased toxicity.
    Feng S; Chen K; Wang C; Jiang X; Dong H; Gong Z; Liu K
    Bioorg Med Chem Lett; 2016 Aug; 26(15):3598-602. PubMed ID: 27311893
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Combination of amino acid/dipeptide with nitric oxide donating oleanolic acid derivatives as PepT1 targeting antitumor prodrugs.
    Fang L; Wang M; Gou S; Liu X; Zhang H; Cao F
    J Med Chem; 2014 Feb; 57(3):1116-20. PubMed ID: 24422538
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prodrug Mono Therapy: synthesis and biological evaluation of an etoposide glucuronide-prodrug.
    Schmidt F; Monneret C
    Bioorg Med Chem; 2003 May; 11(10):2277-83. PubMed ID: 12713838
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Self-assembling nanowires of an amphiphilic camptothecin prodrug derived from homologous derivative conjugation.
    He D; Zhang W; Deng H; Huo S; Wang YF; Gong N; Deng L; Liang XJ; Dong A
    Chem Commun (Camb); 2016 Dec; 52(98):14145-14148. PubMed ID: 27869268
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Extended scaffold glucuronides: en route to the universal synthesis of O-aryl glucuronide prodrugs.
    Walther R; Jarlstad Olesen MT; Zelikin AN
    Org Biomol Chem; 2019 Jul; 17(29):6970-6974. PubMed ID: 31290904
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis and biological studies of the thiols-triggered anticancer prodrug for a more effective cancer therapy.
    Xu Y; Chen J; Li Y; Peng S; Gu X; Sun M; Gao K; Fang J
    Org Biomol Chem; 2015 Mar; 13(9):2634-9. PubMed ID: 25581090
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Design, Synthesis, and Biological Evaluation of Potential Prodrugs Related to the Experimental Anticancer Agent Indotecan (LMP400).
    Lv PC; Elsayed MS; Agama K; Marchand C; Pommier Y; Cushman M
    J Med Chem; 2016 May; 59(10):4890-9. PubMed ID: 27097152
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Synthesis of new lipophilic ipomeanol analogues and their cytotoxic activities.
    Krauss J; Unterreitmeier D
    Arch Pharm (Weinheim); 2005 Jan; 338(1):44-8. PubMed ID: 15674804
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel nanoassemblies composed of squalenoyl-paclitaxel derivatives: synthesis, characterization, and biological evaluation.
    Dosio F; Reddy LH; Ferrero A; Stella B; Cattel L; Couvreur P
    Bioconjug Chem; 2010 Jul; 21(7):1349-61. PubMed ID: 20597546
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.