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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

93 related items for PubMed ID: 21397509

  • 21. Access to functionalized 3H-pyrrolo[2,3-c]quinolin-4(5H)-ones and thieno[2,3-c]quinolin-4(5H)-ones via domino reaction of 4-alkynyl-3-bromoquinolin-2(1H)-ones.
    Wang Z, Xue L, He Y, Weng L, Fang L.
    J Org Chem; 2014 Oct 17; 79(20):9628-38. PubMed ID: 25244431
    [Abstract] [Full Text] [Related]

  • 22. Design, synthesis, and biological evaluation of pyrrolo[2,1-c][1,4]benzodiazepine and indole conjugates as anticancer agents.
    Wang JJ, Shen YK, Hu WP, Hsieh MC, Lin FL, Hsu MK, Hsu MH.
    J Med Chem; 2006 Feb 23; 49(4):1442-9. PubMed ID: 16480280
    [Abstract] [Full Text] [Related]

  • 23. 3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 2. Effect of pyrrole-C2 and/or -C4 substitutions on biological activity.
    Mai A, Massa S, Cerbara I, Valente S, Ragno R, Bottoni P, Scatena R, Loidl P, Brosch G.
    J Med Chem; 2004 Feb 26; 47(5):1098-109. PubMed ID: 14971890
    [Abstract] [Full Text] [Related]

  • 24. A general intramolecular Friedel-Crafts approach to functionalized pyrrolo[3,2,1-ij]quinolin-4-ones.
    Patil DV, Cavitt MA, Grzybowski P, France S.
    Chem Commun (Camb); 2012 Oct 25; 48(83):10337-9. PubMed ID: 22968155
    [Abstract] [Full Text] [Related]

  • 25. Synthesis and antiproliferative activity of 2,4-disubstituted 6-aryl-7H-pyrrolo[3,2-d]pyrimidin-7-one 5-oxides.
    Pudziuvelyte E, Ríos-Luci C, León LG, Cikotiene I, Padrón JM.
    Bioorg Med Chem; 2009 Jul 15; 17(14):4955-60. PubMed ID: 19527934
    [Abstract] [Full Text] [Related]

  • 26. Novel cyano- and N-isopropylamidino-substituted derivatives of benzo[b]thiophene-2-carboxanilides and benzo[b]thieno[2,3-c]quinolones: synthesis, photochemical synthesis, crystal structure determination, and antitumor evaluation. 2.
    Jarak I, Kralj M, Suman L, Pavlović G, Dogan J, Piantanida I, Zinić M, Pavelić K, Karminski-Zamola G.
    J Med Chem; 2005 Apr 07; 48(7):2346-60. PubMed ID: 15801828
    [Abstract] [Full Text] [Related]

  • 27. Novel angular furo and thieno-quinolinones: synthesis and preliminary photobiological studies.
    Fossa P, Mosti L, Menozzi G, Marzano C, Baccichetti F, Bordin F.
    Bioorg Med Chem; 2002 Mar 07; 10(3):743-51. PubMed ID: 11814864
    [Abstract] [Full Text] [Related]

  • 28. 1,4,8-trimethylfuro[2,3-H]quinolin-2(1H)-one, a new furocoumarin bioisoster.
    Marzano C, Chilin A, Baccichetti F, Bettio F, Guiotto A, Miolo G, Bordin F.
    Eur J Med Chem; 2004 May 07; 39(5):411-9. PubMed ID: 15110967
    [Abstract] [Full Text] [Related]

  • 29. Synthesis and benzodiazepine receptors affinity of 2,3-dihydro-9-phenyl-1H-pyrrolo[3,4-b]quinolin-1-one and 3-carbethoxy-4-phenylquinoline derivatives.
    Anzini M, Cappelli A, Vomero S, Cagnotto A, Skorupska M.
    Farmaco; 1992 Feb 07; 47(2):191-202. PubMed ID: 1324688
    [Abstract] [Full Text] [Related]

  • 30. Antiproliferative activity in HL60 cells by tetrasubstituted pyrroles: a structure-activity relationship study.
    Padrón JM, Tejedor D, Santos-Expósito A, García-Tellado F, Martín VS, Villar J.
    Bioorg Med Chem Lett; 2005 May 16; 15(10):2487-90. PubMed ID: 15863302
    [Abstract] [Full Text] [Related]

  • 31. Synthesis of novel pyrrole and pyrrolo[2,3-d]pyrimidine derivatives bearing sulfonamide moiety for evaluation as anticancer and radiosensitizing agents.
    Ghorab MM, Ragab FA, Heiba HI, Youssef HA, El-Gazzar MG.
    Bioorg Med Chem Lett; 2010 Nov 01; 20(21):6316-20. PubMed ID: 20850308
    [Abstract] [Full Text] [Related]

  • 32. Novel acetylcholinesterase inhibitor as increasing agent on rhythmic bladder contractions: SAR of 8-{3-[1-(3-fluorobenzyl)piperidin-4-yl]propanoyl}-1,2,5,6-tetrahydro-4H-pyrrolo[3,2,1-ij]quinolin-4-one (TAK-802) and related compounds.
    Ishichi Y, Sasaki M, Setoh M, Tsukamoto T, Miwatashi S, Nagabukuro H, Okanishi S, Imai S, Saikawa R, Doi T, Ishihara Y.
    Bioorg Med Chem; 2005 Mar 15; 13(6):1901-11. PubMed ID: 15727846
    [Abstract] [Full Text] [Related]

  • 33. Pyrano[2,3-e]isoindol-2-ones, new angelicin heteroanalogues.
    Barraja P, Spanò V, Patrizia D, Carbone A, Cirrincione G, Vedaldi D, Salvador A, Viola G, Dall'acqua F.
    Bioorg Med Chem Lett; 2009 Mar 15; 19(6):1711-4. PubMed ID: 19230658
    [Abstract] [Full Text] [Related]

  • 34. Synthesis and in vitro and in vivo antitumor activity of 2-phenylpyrroloquinolin-4-ones.
    Ferlin MG, Chiarelotto G, Gasparotto V, Dalla Via L, Pezzi V, Barzon L, Palù G, Castagliuolo I.
    J Med Chem; 2005 May 05; 48(9):3417-27. PubMed ID: 15857148
    [Abstract] [Full Text] [Related]

  • 35. Antiproliferative effects of some novel synthetic solanidine analogs on HL-60 human leukemia cells in vitro.
    Minorics R, Szekeres T, Krupitza G, Saiko P, Giessrigl B, Wölfling J, Frank E, Zupkó I.
    Steroids; 2011 Jan 05; 76(1-2):156-62. PubMed ID: 20974162
    [Abstract] [Full Text] [Related]

  • 36. Pyrrolo-1,5-benzoxazepines induce apoptosis in HL-60, Jurkat, and Hut-78 cells: a new class of apoptotic agents.
    Zisterer DM, Campiani G, Nacci V, Williams DC.
    J Pharmacol Exp Ther; 2000 Apr 05; 293(1):48-59. PubMed ID: 10734152
    [Abstract] [Full Text] [Related]

  • 37. Pyrimido[4,5-c]quinolin-1(2H)-ones as a novel class of antimitotic agents: Synthesis and in vitro cytotoxic activity.
    Metwally K, Pratsinis H, Kletsas D.
    Eur J Med Chem; 2007 Mar 05; 42(3):344-50. PubMed ID: 17141923
    [Abstract] [Full Text] [Related]

  • 38. Synthesis of a new class of pyrrolo[3,4-h]quinazolines with antimitotic activity.
    Spanò V, Montalbano A, Carbone A, Parrino B, Diana P, Cirrincione G, Castagliuolo I, Brun P, Issinger OG, Tisi S, Primac I, Vedaldi D, Salvador A, Barraja P.
    Eur J Med Chem; 2014 Mar 03; 74():340-57. PubMed ID: 24486413
    [Abstract] [Full Text] [Related]

  • 39. Synthesis and structure-activity relationship of 4-substituted 2-(2-acetyloxyethyl)-8-(morpholine-4-sulfonyl)pyrrolo[3,4-c]quinoline-1,3-diones as potent caspase-3 inhibitors.
    Kravchenko DV, Kuzovkova YA, Kysil VM, Tkachenko SE, Maliarchouk S, Okun IM, Balakin KV, Ivachtchenko AV.
    J Med Chem; 2005 Jun 02; 48(11):3680-3. PubMed ID: 15916416
    [Abstract] [Full Text] [Related]

  • 40. Structure-activity relationships of N-acyl pyrroloquinolone PDE-5 inhibitors.
    Lanter JC, Sui Z, Macielag MJ, Fiordeliso JJ, Jiang W, Qiu Y, Bhattacharjee S, Kraft P, John TM, Haynes-Johnson D, Craig E, Clancy J.
    J Med Chem; 2004 Jan 29; 47(3):656-62. PubMed ID: 14736245
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.