Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ivan Kompis"'
Autor:
Peter Hartman, Rudolf L. Then, Clemens Broger, Hanno Langen, Malcolm G. P. Page, R. Dehoogt, Hans Locher, Allan D'Arcy, Beat Wipf, Glenn E. Dale, Synese Jolidon, A. M. Labhardt, Christian Oefner, Dietrich Stüber, Ivan Kompis
Publikováno v:
Journal of Molecular Biology. 266:23-30
A single amino acid substitution, Phe98 to Tyr98, in dihydrofolate reductase (DHFR) is the molecular origin of trimethoprim (TMP) resistance in Staphylococcus aureus. This active site amino acid substitution was found in all S. aureus TMP-resistant c
Autor:
Christian Hubschwerlen, Malcolm G. P. Page, Valerie Runtz, Paul Hebeisen, Ingrid Heinze-Krauss, Henri Stalder, Hans Richter, Peter Angehrn, Urs Weiss, Wei Chung-Chen, Philippe Guerry, Ivan Kompis
Publikováno v:
Journal of Medicinal Chemistry. 39:1864-1871
The synthesis and structure−activity relationships of a new class of vinylcephalosporins substituted with a lactamyl residue (1) are described. These compounds show excellent activity against enterococci and retain the broad spectrum activity of th
Autor:
Ivan Kompis, Vladimir I. Polshakov, Berry Birdsall, William D. Morgan, Dasa Lipovsek Sali, James Feeney
Publikováno v:
Biochemistry. 34:11690-11702
Two-dimensional (2D) double-quantum-filtered correlation spectroscopy (DQF-COSY), total correlation spectroscopy (TOCSY), nuclear Overhauser effect spectroscopy (NOESY), and rotating-frame NOESY (ROESY) spectra were used to assign essentially all the
Publikováno v:
Helvetica Chimica Acta. 77:1057-1064
Substituted 4-oxoquinoline-3- (1a) and 4-oxo-1,8-naphthyridine-3- (1b) carboxylic acids are clinically useful antibacterial agents exerting their activity by inhibiting the subunit A of DNA gyrase. Recently, pyrimido-[1,6-a]benzimidazoles 2 were foun
Autor:
Hans Gmuender, Peter Angehrn, Christian Hubschwerlen, Philippe Pflieger, Klaus Gubernator, Jean-Luc Specklin, Ivan Kompis
Publikováno v:
ChemInform. 24
Substituted 4-quinolone- (1, A = CH) and 1,8-naphthyrid-4-one- (1, A = N) 3-carboxylic acids are currently the only classes of clinically useful antibacterial agents exerting their activity by inhibiting the subunit A of DNA gyrase. Pyrimido[1,6-alph
Publikováno v:
ChemInform. 25
Substituted 4-oxoquinoline-3- (1a) and 4-oxo-1,8-naphthyridine-3- (1b) carboxylic acids are clinically useful antibacterial agents exerting their activity by inhibiting the subunit A of DNA gyrase. Recently, pyrimido-[1,6-a]benzimidazoles 2 were foun
Autor:
Christian Hubschwerlen, Henri Stalder, Urs Weiss, Philippe Guerry, Wei Chung-Chen, Hans Richter, Paul Hebeisen, Valerie Runtz, Peter Angehrn, Ivan Kompis, Malcolm G. P. Page, Ingrid Heinze-Krauss
Publikováno v:
ChemInform. 27
The synthesis and structure−activity relationships of a new class of vinylcephalosporins substituted with a lactamyl residue (1) are described. These compounds show excellent activity against enterococci and retain the broad spectrum activity of th
Autor:
Hans Gmuender, Klaus Gubernator, Jean-Luc Specklin, Peter Angehrn, Christian Hubschwerlen, Ivan Kompis, Philippe Pflieger
Publikováno v:
Journal of Medicinal Chemistry. 35:1385-1392
Substituted 4-quinolone- (1, A = CH) and 1,8-naphthyrid-4-one- (1, A = N) 3-carboxylic acids are currently the only classes of clinically useful antibacterial agents exerting their activity by inhibiting the subunit A of DNA gyrase. Pyrimido[1,6-alph
Publikováno v:
Helvetica Chimica Acta. 69:887-897
Based on a computer-assisted analysis of the three-dimensional structure of the binary complex of E.coli dihydrofolate reductase (DHFR) with methotrexate, 5-(N-arylnortropan-3-yl)- and 5-(N-arylpiperidin-4-yl)-2,4-diaminopyrimidines 2 and 4 were desi
Publikováno v:
Helvetica Chimica Acta. 63:504-522
15N-NMR. spectra of mono- and diaminopyridines, and mono-, di- and triaminopyrimidines including trimethoprim and other dihydrofolate reductase inhibitors have been studied in neutral and acidic media. Complete chemical shift assignments are given. R