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 *

140 related articles for article (PubMed ID: 15624920)

  • 1. A concise synthesis of a novel antiangiogenic tyrosine kinase inhibitor.
    Payack JF; Vazquez E; Matty L; Kress MH; McNamara J
    J Org Chem; 2005 Jan; 70(1):175-8. PubMed ID: 15624920
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis of 3-substituted-2-oxoindole analogues and their evaluation as kinase inhibitors, anticancer and antiangiogenic agents.
    Abadi AH; Abou-Seri SM; Abdel-Rahman DE; Klein C; Lozach O; Meijer L
    Eur J Med Chem; 2006 Mar; 41(3):296-305. PubMed ID: 16494969
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Design, synthesis, and biological evaluation of 3,4-diarylmaleimides as angiogenesis inhibitors.
    Peifer C; Stoiber T; Unger E; Totzke F; Schächtele C; Marmé D; Brenk R; Klebe G; Schollmeyer D; Dannhardt G
    J Med Chem; 2006 Feb; 49(4):1271-81. PubMed ID: 16480264
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Design, synthesis, and biological evaluation of novel 3-aryl-4-(1H-indole-3yl)-1,5-dihydro-2H-pyrrole-2-ones as vascular endothelial growth factor receptor (VEGF-R) inhibitors.
    Peifer C; Selig R; Kinkel K; Ott D; Totzke F; Schächtele C; Heidenreich R; Röcken M; Schollmeyer D; Laufer S
    J Med Chem; 2008 Jul; 51(13):3814-24. PubMed ID: 18529047
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis and structure-activity relationships of indole and benzimidazole piperazines as histamine H(4) receptor antagonists.
    Terzioglu N; van Rijn RM; Bakker RA; De Esch IJ; Leurs R
    Bioorg Med Chem Lett; 2004 Nov; 14(21):5251-6. PubMed ID: 15454206
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis and biological evaluation of 5-[(aryl)(1H-imidazol-1-yl)methyl]-1H-indoles: potent and selective aromatase inhibitors.
    Lézé MP; Le Borgne M; Pinson P; Palusczak A; Duflos M; Le Baut G; Hartmann RW
    Bioorg Med Chem Lett; 2006 Mar; 16(5):1134-7. PubMed ID: 16380254
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Practical asymmetric synthesis of a potent Cathepsin K inhibitor. Efficient palladium removal following Suzuki coupling.
    Chen CY; Dagneau P; Grabowski EJ; Oballa R; O'Shea P; Prasit P; Robichaud J; Tillyer R; Wang X
    J Org Chem; 2003 Apr; 68(7):2633-8. PubMed ID: 12662032
    [TBL] [Abstract][Full Text] [Related]  

  • 8. RO4383596, an orally active KDR, FGFR, and PDGFR inhibitor: synthesis and biological evaluation.
    McDermott LA; Simcox M; Higgins B; Nevins T; Kolinsky K; Smith M; Yang H; Li JK; Chen Y; Ke J; Mallalieu N; Egan T; Kolis S; Railkar A; Gerber L; Luk KC
    Bioorg Med Chem; 2005 Aug; 13(16):4835-41. PubMed ID: 15953730
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Concise total synthesis of (+)-WIN 64821 and (-)-ditryptophenaline.
    Movassaghi M; Schmidt MA; Ashenhurst JA
    Angew Chem Int Ed Engl; 2008; 47(8):1485-7. PubMed ID: 18189262
    [No Abstract]   [Full Text] [Related]  

  • 10. Total synthesis of ageladine A, an angiogenesis inhibitor from the marine sponge Agelas nakamurai.
    Meketa ML; Weinreb SM
    Org Lett; 2006 Mar; 8(7):1443-6. PubMed ID: 16562912
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Selective NR1/2B N-methyl-D-aspartate receptor antagonists among indole-2-carboxamides and benzimidazole-2-carboxamides.
    Borza I; Bozó E; Barta-Szalai G; Kiss C; Tárkányi G; Demeter A; Gáti T; Háda V; Kolok S; Gere A; Fodor L; Nagy J; Galgóczy K; Magdó I; Agai B; Fetter J; Bertha F; Keserü GM; Horváth C; Farkas S; Greiner I; Domány G
    J Med Chem; 2007 Mar; 50(5):901-14. PubMed ID: 17290978
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inhibitors of HIV-1 attachment. Part 3: A preliminary survey of the effect of structural variation of the benzamide moiety on antiviral activity.
    Meanwell NA; Wallace OB; Wang H; Deshpande M; Pearce BC; Trehan A; Yeung KS; Qiu Z; Wright JJ; Robinson BA; Gong YF; Wang HG; Spicer TP; Blair WS; Shi PY; Lin PF
    Bioorg Med Chem Lett; 2009 Sep; 19(17):5136-9. PubMed ID: 19632112
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis of dragmacidin D via direct C-H couplings.
    Mandal D; Yamaguchi AD; Yamaguchi J; Itami K
    J Am Chem Soc; 2011 Dec; 133(49):19660-3. PubMed ID: 22074290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis and anti-tyrosine kinase activity of 3-(substituted-benzylidene)-1, 3-dihydro-indolin derivatives: investigation of their role against p60c-Src receptor tyrosine kinase with the application of receptor docking studies.
    Olgen S; Akaho E; Nebioglu D
    Farmaco; 2005; 60(6-7):497-506. PubMed ID: 15927182
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis and biological evaluation of novel N
    Nirogi RV; Bandyala TR; Gangadasari PR; Khagga M
    J Enzyme Inhib Med Chem; 2016; 31(sup1):1-15. PubMed ID: 27806648
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A highly selective tandem cross-coupling of gem-dihaloolefins for a modular, efficient synthesis of highly functionalized indoles.
    Fang YQ; Lautens M
    J Org Chem; 2008 Jan; 73(2):538-49. PubMed ID: 18154302
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Concise syntheses of N-aryl-5,6,7-trimethoxyindoles as antimitotic and vascular disrupting agents: application of the copper-mediated Ullmann-type arylation.
    Lee HY; Chang JY; Chang LY; Lai WY; Lai MJ; Shih KH; Kuo CC; Chang CY; Liou JP
    Org Biomol Chem; 2011 May; 9(9):3154-7. PubMed ID: 21416070
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Discovery and evaluation of 3-(5-thien-3-ylpyridin-3-yl)-1H-indoles as a novel class of KDR kinase inhibitors.
    Fraley ME; Arrington KL; Hambaugh SR; Hoffman WF; Cunningham AM; Young MB; Hungate RW; Tebben AJ; Rutledge RZ; Kendall RL; Huckle WR; McFall RC; Coll KE; Thomas KA
    Bioorg Med Chem Lett; 2003 Sep; 13(18):2973-6. PubMed ID: 12941314
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Combined directed ortho and remote metalation-cross-coupling strategies. General method for benzo[a]carbazoles and the synthesis of an unnamed indolo[2,3-a]carbazole alkaloid.
    Cai X; Snieckus V
    Org Lett; 2004 Jul; 6(14):2293-5. PubMed ID: 15228262
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 2-Hydroxy-4,6-diamino-[1,3,5]triazines: a novel class of VEGF-R2 (KDR) tyrosine kinase inhibitors.
    Baindur N; Chadha N; Brandt BM; Asgari D; Patch RJ; Schalk-Hihi C; Carver TE; Petrounia IP; Baumann CA; Ott H; Manthey C; Springer BA; Player MR
    J Med Chem; 2005 Mar; 48(6):1717-20. PubMed ID: 15771417
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.