Zobrazeno 1 - 10 of 22 pro vyhledávání: '"Dieter Isert"'
1
Ustilipids, Acylated .BETA.-D-Mannopyranosyl D-Erythritols from Ustilago maydis and Geotrichum candidum
Autor: Michael Kurz, Ziyu Li, Luigi Toti, Claudia Eder, Dieter Isert, Matthias Schiell, Joachim Wink, Erich F. Paulus, Laszlo Vertesy, Gerhard Seibert
Publikováno v: The Journal of Antibiotics. 56:91-101
Ustilago species produce an extracellular oil that shows activity in various pharmaceutical assays. We isolated several complexes of this heterogeneous glycolipid from cultures of Ustilago maydis DSM 11494 and Geotrichum candidum ST 002515, and deter
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b11c2fae47cddf71e466099714b7c373
https://doi.org/10.7164/antibiotics.56.91
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2
Mulundocandin, an Echinocandin-like Lipopeptide Antifungal Agent: Biological Activities In Vitro
Autor: Stephen Hawser, Markus Astrid, Dieter Isert, Monica Borgonovi
Publikováno v: The Journal of Antibiotics. 52:305-310
Mulundocandin (MCN) is an antifungal lipopeptide which belongs to the echinocandin class of antimycotic agents. MCN exhibited good in vitro activity against Candida albicans and C. glabrata isolates with MIC ranges of 0.5-4.0 microg/ml and 2.0-4.0 mi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03a3b338beae533ee20f0793dc0d4b9f
https://doi.org/10.7164/antibiotics.52.305
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3
Synthesis of HR 916 K: An Efficient Route to the Pure Diastereomers of the 1-(Pivaloyloxy)ethyl Esters of Cephalosporins
Autor: Norbert Krass, Dieter Isert, Rolf Horlein, Fischer Gerd, Theo Wollmann, Uwe Gerlach, Ulrich Stache, Elisabeth Defoßa, Rudolf Lattrell
Publikováno v: Liebigs Annalen. 1996:1743-1749
HR 916 K (5), the 1-(S)-(pivaloyloxy)ethyl prodrug ester of the cephalosporin cefdaloxime, exhibits a significantly higher oral bioavailability than the 1-(R) diastereomer HR 916 J. An efficient synthesis of HR 916 K was developed. The separation of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7ced9b6c375c1c441b4b7c9c015448a6
https://doi.org/10.1002/jlac.199619961107
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5
Chemotherapeutic activity of levofloxacin (HR 355, DR-3355) against systemic and localized infections in laboratory animals
Autor: Markus Astrid, K. H. Geweniger, Dieter Isert, N. Klesel, P. Koletzki, H. Schramm, M. Limbert, G. Riess, P. Iyer
Publikováno v: Journal of Antimicrobial Chemotherapy. 35:805-819
Ofloxacin, its optical isomers levofloxacin (HR 355, DR-3355) and D-ofloxacin (DR-3354) and ciprofloxacin were administered orally to mice and rats which had systemic and localized infections. Both levofloxacin and ciprofloxacin were equally effectiv
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f319522ffcb3a2357724296c6838545
https://doi.org/10.1093/jac/35.6.805
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7
ChemInform Abstract: 3874 H1 and H3, Novel Antifungal Heptaene Antibiotics Produced by Streptomyces sp. HAG 003874
Autor: Stephen Hawser, Eberhard Ehlers, Werner Aretz, Michael Kurz, Joachim Wink, Dieter Isert, Matthias Schiell, Laszlo Vertesy, Martin Knauf, Martin Vogel
Publikováno v: ChemInform. 30
New antifungal antibiotics, designated as 3874 H1 and H3, were discovered in the fermentation broth of the strain Streptomyces sp. HAG 003874. The compounds were obtained as yellow powders after sequential purification by chromatography on MCI Gel CH
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::94142ec28ae96cb04a6a1901772d6edc
https://doi.org/10.1002/chin.199912247
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8
ChemInform Abstract: Mulundocandin, an Echinocandin-Like Lipopeptide Antifungal Agent: Biological Activities in vitro
Autor: Stephen Hawser, Markus Astrid, Monica Borgonovi, Dieter Isert
Publikováno v: ChemInform. 30
Mulundocandin (MCN) is an antifungal lipopeptide which belongs to the echinocandin class of antimycotic agents. MCN exhibited good in vitro activity against Candida albicans and C. glabrata isolates with MIC ranges of 0.5-4.0μg/ml and 2.0-4.0μg/ml,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8e8ba707408ceb46d12c392d987b194a
https://doi.org/10.1002/chin.199932214
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9
The in-vitro antibacterial activity of a combination of cefpirome or cefoperazone with vancomycin against enterococci and Staphylococcus aureus
Autor: N. Klesel, M. Limbert, Markus Astrid, Elmar Dr Schrinner, G. Seibert, Dieter Isert
Publikováno v: Journal of Antimicrobial Chemotherapy. 29:25-30
Cefpirome, cefoperazone and ceftazidime were tested for their in-vitro activity against Enterococcus faecalis and methicillin-resistant Staphylococcus aureus (MRSA) isolates. Cefpirome was the most active cephalosporin followed by cefoperazone. Cefta
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25bc905d6a4c864bd78de62165fe3085
https://doi.org/10.1093/jac/29.suppl_a.25
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10
Antibacterial activity in vitro of cefpirome against clinical isolates causing sexually transmitted diseases
Autor: Markus Astrid, M. Limbert, I. Winkler, Elmar Dr Schrinner, Dieter Isert, G. Seibert, N. Klesel
Publikováno v: Journal of Antimicrobial Chemotherapy. 29:13-17
The in-vitro activity of cefpirome was compared with other antibiotics against organisms causing sexually transmitted diseases (STD). The excellent activity of cefpirome against Neisseria gonorrhoeae (MIC90 1.0 mg/L), Haemophilus ducreyi (MIC90 0.5 m
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff0390410a69142ae3dabb25e9eac75e
https://doi.org/10.1093/jac/29.suppl_a.13
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