Search Results - "Isert, D"

Antibacterial activities in vitro and in vivo and pharmacokinetics of cefquinome (HR 111V), a new broad-spectrum cephalosporin by LIMBERT, M, ISERT, D, KLESEL, N, MARKUS, A, SEEGER, K, SEIBERT, G, SCHRINNER, E

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Comparative chemotherapeutic efficacy of balhimycin, desgluco-balhimycin against experimental MSSA and MRSA infection in mice by Chatterjee, D K, Sarma, P, Jani, R H, Klesel, N, Isert, D

“…Balhimycin and desglucobalhimycin are glycopeptide antibiotics isolated from an Amycolatopsis spp during the search for novel antibacterials against MRSA from…”
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Chemotherapeutic activity of levofloxacin (HR 355, DR-3355) against systemic and localized infections in laboratory animals by Klesel, N, Geweniger, K H, Koletzki, P, Isert, D, Limbert, M, Markus, A, Riess, G, Schramm, H, Iyer, P

“…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…”
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Transport theory for a scalar quark & gluon model by Isert, D.S., Klevansky, S.P.

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The in-vitro antibacterial activity of a combination of cefpirome or cefoperazone with vancomycin against enterococci and Staphylococcus aureus by Seibert, G, Isert, D, Klesel, N, Limbert, M, Markus, A, Schrinner, E

“…Cefpirome, cefoperazone and ceftazidime were tested for their in-vitro activity against Enterococcus faecalis and methicillin-resistant Staphylococcus aureus…”
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Pharmacokinetics of cefpirome administered intravenously or intramuscularly to rats and dogs by Isert, D, Klesel, N, Limbert, M, Markus, A, Seibert, G, Schrinner, E

“…The pharmacokinetic profile of cefpirome was evaluated in rats and dogs after a single intravenous or intramuscular dose. A two-compartment open model was used…”
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Activity of levofloxacin, ofloxacin, D-ofloxacin and ciprofloxacin against systemic and respiratory tract infections in laboratory animals by Klesel, N, Geweniger, K H, Koletzki, P, Isert, D, Limbert, M, Markus, A, Riess, G, Schramm, H, Seibert, G, Iyer, P

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RU 29 246, the active compound of the cephalosporin-prodrug-ester HR 916. I. Antibacterial activity in vitro by Bauernfeind, A, Jungwirth, R, Eberlein, E, Klesel, N, Adam, F, Isert, D, Limbert, M, Markus, A, Schrinner, E, Seibert, G

“…The aminothiazolyl-cephalosporin RU 29 246 is the active metabolite of the prodrug-pivaloyl-oxyethyl-ester HR 916. RU 29 246 in vitro activity includes a wide…”
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Antibacterial activity in vitro of cefpirome against clinical isolates causing sexually transmitted diseases by Limbert, M, Seibert, G, Winkler, I, Isert, D, Klesel, N, Markus, A, Schrinner, E

“…The in-vitro activity of cefpirome was compared with other antibiotics against organisms causing sexually transmitted diseases (STD). The excellent activity of…”
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Comparative chemotherapeutic activity of cefpirome and imipenem in experimental infections by Klesel, N, Isert, D, Limbert, M, Markus, A, Seibert, G, Schrinner, E

“…In systemic and local infections, the therapeutic efficacy of cefpirome was compared to that of imipenem and cefotaxime. Murine septicemia induced with…”
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RU 29 246, the active compound of the cephalosporin-prodrug-ester HR 916. II. Stability to beta-lactamases and affinity for penicillin-binding proteins by Markus, A, Klesel, N, Wollmann, T, Isert, D, Limbert, M, Schrinner, E, Seibert, G, Bauernfeind, A, Jungwirth, R, Wilhelm, R

“…The aminothiazolyl-cephalosporin RU 29 246, the active metabolite of the prodrug-ester HR 916, is active against strains producing the widespread…”
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RU 29 246, the active compound of the cephalosporin prodrug-ester HR 916. III. Pharmacokinetic properties and antibacterial activity in vivo by Klesel, N, Adam, F, Isert, D, Limbert, M, Markus, A, Schrinner, E, Seibert, G

“…The pharmacokinetics of the broad spectrum cephem RU 29 246 and its prodrug-ester HR 916 B were investigated in mice, rats and dogs and compared to those of…”
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HRE 664, a new parenteral penem. II. Evaluation of the pharmacokinetic behavior and the chemotherapeutic activity in animals by Klesel, N, Isert, D, Limbert, M, Seibert, G, Schrinner, E, Johnson, C

“…The pharmacokinetic and chemotherapeutic properties of the new penem antibiotic HRE 664 (Fig. 1) were evaluated in experimental animals. High and sustained…”
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Synergistic antibacterial activity of cefotaxime and the penem HRE 664 in an improved in vitro model simulating serum and tissue pharmacokinetics by Isert, D, Klesel, N, Markus, A, Seibert, G, Schrinner, E

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HRE 664, a new parenteral penem. I. Antibacterial activity in vitro by Seibert, G, Isert, D, Klesel, N, Limbert, M, Pries, A, Schrinner, E, Cooke, M, Walmsley, J, Bentley, P H

“…The new penem antibiotic HRE 664 displays potent antibacterial activity in vitro against a broad spectrum of clinically relevant bacterial strains including…”
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The in vitro activity of the combination of cefotaxime and HRE 664 by Limbert, M, Isert, D, Klesel, N, Meichsner, C, Seibert, G, Schrinner, E

“…Cefotaxime (CTX) and HRE 664 (a novel penem antibiotic) possess complementary in vitro properties. Differences can be observed in their antibacterial spectra,…”
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Comparative effects of cefpirome (HR 810) and other cephalosporins on experimentally induced pneumonia in mice by Klesel, N, Isert, D, Limbert, M, Seibert, G, Winkler, I, Schrinner, E

“…The chemotherapeutic efficacy of cefpirome (HR 810), a new polar aminothiazolylcephalosporin and that of ceftazidime, cefotaxime, cefoperazone, latamoxef and…”
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Composite nasal septal graft reconstruction of the partial laryngectomized canine by Duncavage, J A, Toohill, R J, Isert, D R

“…Composite nasal septal grafts provide excellent autogenous replacement tissue for the partial laryngectomy defect. The added factor of a mucosa similar to that…”
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Ustilipids, acylated beta-D-mannopyranosyl D-erythritols from Ustilago maydis and Geotrichum candidum by Kurz, Michael, Eder, Claudia, Isert, Dieter, Li, Ziyu, Paulus, Erich F, Schiell, Matthias, Toti, Luigi, Vértesy, Laszló, Wink, Joachim, Seibert, Gerhard

“…Ustilago species produce an extracellular oil that shows activity in various pharmaceutical assays. We isolated several complexes of this heterogeneous…”
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Mulundocandin, an echinocandin-like lipopeptide antifungal agent: biological activities in vitro by Hawser, S, Borgonovi, M, Markus, A, Isert, D

“…Mulundocandin (MCN) is an antifungal lipopeptide which belongs to the echinocandin class of antimycotic agents. MCN exhibited good in vitro activity against…”
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