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

Journal Abstract Search


168 related items for PubMed ID: 12824024

  • 1. Synthesis and antibacterial activity of oxazolidinone containing sulphonyl group.
    Cui Y, Yang Y, Chen K, Ji R, Zhang S.
    Bioorg Med Chem Lett; 2003 Jul 21; 13(14):2311-3. PubMed ID: 12824024
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Synthesis and antibacterial activity of dihydro-1,2-oxazine and 2-pyrazoline oxazolidinones: novel analogs of linezolid.
    D'Andrea S, Zheng ZB, Denbleyker K, Fung-Tomc JC, Yang H, Clark J, Taylor D, Bronson J.
    Bioorg Med Chem Lett; 2005 Jun 02; 15(11):2834-9. PubMed ID: 15911264
    [Abstract] [Full Text] [Related]

  • 5. Synthesis and antibacterial activity of 5-substituted oxazolidinones.
    Phillips OA, Udo EE, Ali AA, Al-Hassawi N.
    Bioorg Med Chem; 2003 Jan 02; 11(1):35-41. PubMed ID: 12467705
    [Abstract] [Full Text] [Related]

  • 6. Synthesis and in vitro activity of new methylenepiperidinyl and methylenepyrrolidinyl oxazolidinone antibacterial agents.
    Kim HY, Lee JS, Cha JH, Pae AN, Cho YS, Chang MH, Koh HY.
    Bioorg Med Chem Lett; 2003 Jul 07; 13(13):2227-30. PubMed ID: 12798339
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Structure-activity relationship (SAR) studies on oxazolidinone antibacterial agents. 1. Conversion of 5-substituent on oxazolidinone.
    Tokuyama R, Takahashi Y, Tomita Y, Suzuki T, Yoshida T, Iwasaki N, Kado N, Okezaki E, Nagata O.
    Chem Pharm Bull (Tokyo); 2001 Apr 07; 49(4):347-52. PubMed ID: 11310656
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Synthesis and antibacterial activity of pyrroloaryl-substituted oxazolidinones.
    Paget SD, Foleno BD, Boggs CM, Goldschmidt RM, Hlasta DJ, Weidner-Wells MA, Werblood HM, Wira E, Bush K, Macielag MJ.
    Bioorg Med Chem Lett; 2003 Dec 01; 13(23):4173-7. PubMed ID: 14622996
    [Abstract] [Full Text] [Related]

  • 11. Synthesis and in vitro activity of novel 1,2,4-triazolo[4,3-a]pyrimidine oxazolidinone antibacterial agents.
    Khera MK, Cliffe IA, Mathur T, Prakash O.
    Bioorg Med Chem Lett; 2011 May 15; 21(10):2887-9. PubMed ID: 21507643
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Effects of positional and geometrical isomerism on the biological activity of some novel oxazolidinones.
    Das J, Rao CV, Sastry TV, Roshaiah M, Sankar PG, Khadeer A, Kumar MS, Mallik A, Selvakumar N, Iqbal J, Trehan S.
    Bioorg Med Chem Lett; 2005 Jan 17; 15(2):337-43. PubMed ID: 15603950
    [Abstract] [Full Text] [Related]

  • 16. Synthesis and biological evaluation of benzazepine oxazolidinone antibacterials.
    Johnson PD, Aristoff PA, Zurenko GE, Schaadt RD, Yagi BH, Ford CW, Hamel JC, Stapert D, Moerman JK.
    Bioorg Med Chem Lett; 2003 Dec 01; 13(23):4197-200. PubMed ID: 14623000
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Structure-activity relationship in the oxazolidinone-quinolone hybrid series: influence of the central spacer on the antibacterial activity and the mode of action.
    Hubschwerlen C, Specklin JL, Baeschlin DK, Borer Y, Haefeli S, Sigwalt C, Schroeder S, Locher HH.
    Bioorg Med Chem Lett; 2003 Dec 01; 13(23):4229-33. PubMed ID: 14623007
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 9.