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 *

124 related articles for article (PubMed ID: 18007362)

  • 1. Simple and efficient synthesis of 2,7-difunctionalized-1,8-naphthyridines.
    Goswami S; Mukherjee R; Mukherjee R; Jana S; Maity AC; Adak AK
    Molecules; 2005 Aug; 10(8):929-36. PubMed ID: 18007362
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Naphthyridines part 4: unprecedented synthesis of polyfunctionally substituted benzo[c][2,7]naphthyridines and benzo[c]pyrimido[4,5,6-ij][2,7]naphthyridines with structural analogy to pyrido[4,3,2-mn]acridines present in the marine tetracyclic pyridoacridine alkaloids.
    Mekheimer RA; Al-Sheikh MA; Medrasi HY; Bahatheg GA
    Mol Divers; 2018 Feb; 22(1):159-171. PubMed ID: 29164475
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Arylbenzo[h][1, 6]naphthyridine derivatives: synthesis and photophysical properties.
    Toche RB; Janrao RA; Bagul SM; Patil SP; Pagar BP; Nikam PS
    J Fluoresc; 2011 Jul; 21(4):1617-24. PubMed ID: 21301938
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Efficient synthesis of functionalized benzo[b][1,8]naphthyridine derivatives via three-component reaction catalyzed by L-proline.
    Fu L; Lin W; Hu MH; Liu XC; Huang ZB; Shi DQ
    ACS Comb Sci; 2014 May; 16(5):238-43. PubMed ID: 24669887
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Efficient method for the synthesis of pyranoquinoline, thiopyranoquinoline, thienoquinoline, and naphtho[2,7]naphthyridine derivatives catalyzed by iodine.
    Wang XS; Li Q; Wu JR; Tu SJ
    J Comb Chem; 2009; 11(3):433-7. PubMed ID: 19374375
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An efficient Bi(NO3)3 x 5H2O catalyzed multi component one-pot synthesis of novel naphthyridines.
    Ravikumar Naik TR; Bhojya Naik HS
    Mol Divers; 2008 May; 12(2):139-42. PubMed ID: 18587659
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.
    Li J; Yu Y; Tu MS; Jiang B; Wang SL; Tu SJ
    Org Biomol Chem; 2012 Jul; 10(28):5361-5. PubMed ID: 22546930
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis of 1-Amino-3-oxo-2,7-naphthyridines
    Sirakanyan SN; Spinelli D; Geronikaki A; Zuppiroli L; Zuppiroli R; Kartsev VG; Hakobyan EK; Yegoryan HA; Hovakimyan AA
    Int J Mol Sci; 2022 May; 23(11):. PubMed ID: 35682584
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Studies on the syntheses and reaction of nitrogen-containing heterocyclic compounds centered the naphthyridines].
    Hamada Y; Takeuchi I
    Yakugaku Zasshi; 2000 Feb; 120(2):206-23. PubMed ID: 10689967
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fused 1,5-Naphthyridines: Synthetic Tools and Applications.
    Masdeu C; Fuertes M; Martin-Encinas E; Selas A; Rubiales G; Palacios F; Alonso C
    Molecules; 2020 Jul; 25(15):. PubMed ID: 32752070
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis, DNA binding, docking and photoclevage studies of novel benzo[b][1,8]naphthyridines.
    Naik TR; Naik HS; Naik HR; Bindu PJ; Harish BG; Krishna V
    Med Chem; 2009 Sep; 5(5):411-8. PubMed ID: 19534683
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.
    Wang W; Feng X; Du H
    Org Biomol Chem; 2016 Jul; 14(28):6683-6. PubMed ID: 27334098
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Methods for the synthesis of 5,6,7,8-tetrahydro-1,8-naphthyridine fragments for alphaVbeta3 integrin antagonists.
    Hartner FW; Hsiao Y; Eng KK; Rivera NR; Palucki M; Tan L; Yasuda N; Hughes DL; Weissman S; Zewge D; King T; Tschaen D; Volante RP
    J Org Chem; 2004 Dec; 69(25):8723-30. PubMed ID: 15575749
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis and characteristics of novel fluorescence dyes based on chromeno[4,3,2-de][1,6]naphthyridine framework.
    Wang H; Shi J; Wang C; Zhang X; Zhao L; Wan Y; Wu H
    Spectrochim Acta A Mol Biomol Spectrosc; 2013 Feb; 103():62-7. PubMed ID: 23257331
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthetic Strategies, Reactivity and Applications of 1,5-Naphthyridines.
    Fuertes M; Masdeu C; Martin-Encinas E; Selas A; Rubiales G; Palacios F; Alonso C
    Molecules; 2020 Jul; 25(14):. PubMed ID: 32708796
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Simple Precursor for Highly Functionalized Fused Imidazo[4,5-b]pyridines and Imidazo[4,5-b]-1,8-naphthyridine.
    Al-Duaij OK; Zaki ME; El Gazzar AB
    Molecules; 2016 Dec; 21(12):. PubMed ID: 27916964
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diversity synthesis of pyrimido[4,5-b][1,6]naphthyridine and its derivatives under microwave irradiation.
    Han ZG; Zhang G; Jiang B; Ma N; Shi F; Tu SJ
    J Comb Chem; 2009; 11(5):809-12. PubMed ID: 19694422
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Unexpected behavior of enaminones: interesting new routes to 1,6-naphthyridines, 2-oxopyrrolidines and pyrano[4,3,2-de][1,6]naphthyridines.
    Moustafa MS; Al-Mousawi SM; Hilmy NM; Ibrahim YA; Liermann JC; Meier H; Elnagdi MH
    Molecules; 2012 Dec; 18(1):276-86. PubMed ID: 23271466
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Straightforward synthesis and biological evaluation as topoisomerase I inhibitors and antiproliferative agents of hybrid Chromeno[4,3-b][1,5]Naphthyridines and Chromeno[4,3-b][1,5]Naphthyridin-6-ones.
    Martín-Encinas E; Rubiales G; Knudssen BR; Palacios F; Alonso C
    Eur J Med Chem; 2019 Sep; 178():752-766. PubMed ID: 31229877
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Library synthesis using 5,6,7,8-tetrahydro-1,6-naphthyridines as scaffolds.
    Zhou Y; Beeler AB; Cho S; Wang Y; Franzblau SG; Snyder JK
    J Comb Chem; 2008; 10(4):534-40. PubMed ID: 18517255
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.