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

75 related items for PubMed ID: 21664443

  • 1. Assessment of biological half life using in silico QSPkR approach: a self organizing molecular field analysis (SOMFA) on a series of antimicrobial quinolone drugs.
    Goel H, Sinha VR, Thareja S, Aggarwal S, Kumar M.
    Int J Pharm; 2011 Aug 30; 415(1-2):158-63. PubMed ID: 21664443
    [Abstract] [Full Text] [Related]

  • 2. In silico predicative studies for cytotoxic potential of NSAIDs using self-organizing molecular field analysis.
    Goel H, Thareja S, Malla P, Kumar M, Sinha VR.
    Int J Toxicol; 2012 Aug 30; 31(4):390-6. PubMed ID: 22689635
    [Abstract] [Full Text] [Related]

  • 3. 3D-QSAR studies on unsaturated 4-azasteroids as human 5alpha-reductase inhibitors: a self organizing molecular field analysis approach.
    Aggarwal S, Thareja S, Bhardwaj TR, Kumar M.
    Eur J Med Chem; 2010 Feb 30; 45(2):476-81. PubMed ID: 19906465
    [Abstract] [Full Text] [Related]

  • 4. Self-organizing molecular field analysis of NSAIDs: assessment of pharmacokinetic and physicochemical properties using 3D-QSPkR approach.
    Honey, Thareja S, Kumar M, Sinha VR.
    Eur J Med Chem; 2012 Jul 30; 53():76-82. PubMed ID: 22521372
    [Abstract] [Full Text] [Related]

  • 5. Pharmacokinetic and residue studies of quinolone compounds and olaquindox in poultry.
    Anadón A, Martinez-Larrañaga MR, Diaz MJ, Velez C, Bringas P.
    Ann Rech Vet; 1990 Jul 30; 21 Suppl 1():137S-144S. PubMed ID: 2080842
    [Abstract] [Full Text] [Related]

  • 6. Self-organizing molecular field analysis on human β-secretase nonpeptide inhibitors: 5, 5-disubstituted aminohydantoins.
    Li Z, Zhou M, Wu F, Li R, Ding Z.
    Eur J Med Chem; 2011 Jan 30; 46(1):58-64. PubMed ID: 21093114
    [Abstract] [Full Text] [Related]

  • 7. Self organizing molecular field analysis on a series of human 5alpha-reductase inhibitors: unsaturated 3-carboxysteroid.
    Thareja S, Aggarwal S, Bhardwaj TR, Kumar M.
    Eur J Med Chem; 2009 Dec 30; 44(12):4920-5. PubMed ID: 19716209
    [Abstract] [Full Text] [Related]

  • 8. Self-organizing molecular field analysis on pregnane derivatives as human steroidal 5alpha-reductase inhibitors.
    Aggarwal S, Thareja S, Bhardwaj TR, Kumar M.
    Steroids; 2010 Jun 30; 75(6):411-8. PubMed ID: 20170668
    [Abstract] [Full Text] [Related]

  • 9. Self-organizing molecular field analysis of 2,4-thiazolidinediones: A 3D-QSAR model for the development of human PTP1B inhibitors.
    Thareja S, Aggarwal S, Bhardwaj TR, Kumar M.
    Eur J Med Chem; 2010 Jun 30; 45(6):2537-46. PubMed ID: 20236737
    [Abstract] [Full Text] [Related]

  • 10. Quantitative retention-activity relationship models for quinolones using biopartitioning micellar chromatography.
    Wu LP, Chen Y, Wang SR, Chen C, Ye LM.
    Biomed Chromatogr; 2008 Jan 30; 22(1):106-14. PubMed ID: 17703481
    [Abstract] [Full Text] [Related]

  • 11. Quantitative structure-pharmacokinetic parameters relationships (QSPKR) analysis of antimicrobial agents in humans using simulated annealing k-nearest-neighbor and partial least-square analysis methods.
    Ng C, Xiao Y, Putnam W, Lum B, Tropsha A.
    J Pharm Sci; 2004 Oct 30; 93(10):2535-44. PubMed ID: 15349962
    [Abstract] [Full Text] [Related]

  • 12. Quantitative structure-pharmacokinetic relationship (QSPkP) analysis of the volume of distribution values of anti-infective agents from J group of the ATC classification in humans.
    Louis B, Agrawal VK.
    Acta Pharm; 2012 Nov 30; 62(3):305-23. PubMed ID: 23470345
    [Abstract] [Full Text] [Related]

  • 13. Three-dimensional quantitative structure-selectivity relationships analysis guided rational design of a highly selective ligand for the cannabinoid receptor 2.
    Brogi S, Corelli F, Di Marzo V, Ligresti A, Mugnaini C, Pasquini S, Tafi A.
    Eur J Med Chem; 2011 Feb 30; 46(2):547-55. PubMed ID: 21183257
    [Abstract] [Full Text] [Related]

  • 14. Pharmacokinetic study of danofloxacin in cattle and swine.
    Mann DD, Frame GM.
    Am J Vet Res; 1992 Jun 30; 53(6):1022-6. PubMed ID: 1320812
    [Abstract] [Full Text] [Related]

  • 15. 3D-QSAR CoMFA/CoMSIA studies on 5-aryl-2,2-dialkyl-4-phenyl-3(2H)-furanone derivatives, as selective COX-2 inhibitors.
    Puntambekar DS, Giridhar R, Yadav MR.
    Acta Pharm; 2006 Jun 30; 56(2):157-74. PubMed ID: 16613723
    [Abstract] [Full Text] [Related]

  • 16. CoMFA and CoMSIA 3D-QSAR studies on quionolone caroxylic acid derivatives inhibitors of HIV-1 integrase.
    Lu P, Wei X, Zhang R.
    Eur J Med Chem; 2010 Aug 30; 45(8):3413-9. PubMed ID: 20488589
    [Abstract] [Full Text] [Related]

  • 17. QSAR studies on aminothiazole derivatives as aurora a kinase inhibitors.
    Qin J, Xi L, Du J, Liu H, Yao X.
    Chem Biol Drug Des; 2010 Dec 30; 76(6):527-37. PubMed ID: 21040493
    [Abstract] [Full Text] [Related]

  • 18. Novel fluoroquinolone antibacterial agents containing oxime-substituted (aminomethyl)pyrrolidines: synthesis and antibacterial activity of 7-(4-(aminomethyl)-3-(methoxyimino)pyrrolidin-1-yl)-1-cyclopropyl-6- fluoro-4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxylic acid (LB20304).
    Hong CY, Kim YK, Chang JH, Kim SH, Choi H, Nam DH, Kim YZ, Kwak JH.
    J Med Chem; 1997 Oct 24; 40(22):3584-93. PubMed ID: 9357525
    [Abstract] [Full Text] [Related]

  • 19. Allometric analysis of ciprofloxacin and enrofloxacin pharmacokinetics across species.
    Cox SK, Cottrell MB, Smith L, Papich MG, Frazier DL, Bartges J.
    J Vet Pharmacol Ther; 2004 Jun 24; 27(3):139-46. PubMed ID: 15189299
    [Abstract] [Full Text] [Related]

  • 20. Chemometric studies on the bactericidal activity of quinolones via an extended VolSurf approach.
    Cianchetta G, Mannhold R, Cruciani G, Baroni M, Cecchetti V.
    J Med Chem; 2004 Jun 03; 47(12):3193-201. PubMed ID: 15163198
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.