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129 related items for PubMed ID: 9719590
1. Conformational analysis of ketolide, conformations of RU 004 in solution and bound to bacterial ribosomes. Bertho G, Gharbi-Benarous J, Delaforge M, Lang C, Parent A, Girault JP. J Med Chem; 1998 Aug 27; 41(18):3373-86. PubMed ID: 9719590 [Abstract] [Full Text] [Related]
2. Conformations in solution and bound to bacterial ribosomes of ketolides, HMR 3647 (telithromycin) and RU 72366: a new class of highly potent antibacterials. Evrard-Todeschi N, Gharbi-Benarous J, Gaillet C, Verdier L, Bertho G, Lang C, Parent A, Girault JP. Bioorg Med Chem; 2000 Jul 27; 8(7):1579-97. PubMed ID: 10976506 [Abstract] [Full Text] [Related]
3. Free and bound state structures of 6-O-methyl homoerythromycins and epitope mapping of their interactions with ribosomes. Novak P, Barber J, Cikos A, Arsic B, Plavec J, Lazarevski G, Tepes P, Kosutić-Hulita N. Bioorg Med Chem; 2009 Aug 15; 17(16):5857-67. PubMed ID: 19628398 [Abstract] [Full Text] [Related]
4. Lincomycin and clindamycin conformations. A fragment shared by macrolides, ketolides and lincosamides determined from TRNOE ribosome-bound conformations. Verdier L, Bertho G, Gharbi-Benarous J, Girault JP. Bioorg Med Chem; 2000 Jun 15; 8(6):1225-43. PubMed ID: 10896103 [Abstract] [Full Text] [Related]
5. Systematic approach to understanding macrolide-ribosome interactions: NMR and modeling studies of oleandomycin and its derivatives. Novak P, Tatić I, Tepes P, Kostrun S, Barber J. J Phys Chem A; 2006 Jan 19; 110(2):572-9. PubMed ID: 16405329 [Abstract] [Full Text] [Related]
6. Synthesis and antibacterial activity of ketolides (6-O-methyl-3-oxoerythromycin derivatives): a new class of antibacterials highly potent against macrolide-resistant and -susceptible respiratory pathogens. Agouridas C, Denis A, Auger JM, Benedetti Y, Bonnefoy A, Bretin F, Chantot JF, Dussarat A, Fromentin C, D'Ambrières SG, Lachaud S, Laurin P, Le Martret O, Loyau V, Tessot N. J Med Chem; 1998 Oct 08; 41(21):4080-100. PubMed ID: 9767644 [Abstract] [Full Text] [Related]
17. Determination of the three-dimensional, solution-phase structure of the macrolide antibiotic oxolide in CD2Cl2 and D2O from NMR constraints. Steinmetz WE, Sparrow A, Somsouk M. Magn Reson Chem; 2005 Jan 01; 43(1):16-20. PubMed ID: 15468276 [Abstract] [Full Text] [Related]
18. Conformational analysis of oleandomycin and its 8-methylene-9-oxime derivative by NMR and molecular modelling. Novak P, Tomisić ZB, Tepes P, Lazarevski G, Plavec J, Turkalj G. Org Biomol Chem; 2005 Jan 07; 3(1):39-47. PubMed ID: 15602597 [Abstract] [Full Text] [Related]
19. On the mechanism of action of 9-O-arylalkyloxime derivatives of 6-O-mycaminosyltylonolide, a new class of 16-membered macrolide antibiotics. Karahalios P, Kalpaxis DL, Fu H, Katz L, Wilson DN, Dinos GP. Mol Pharmacol; 2006 Oct 07; 70(4):1271-80. PubMed ID: 16873579 [Abstract] [Full Text] [Related]