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Journal of Antibiotics, 化学 • 材料, 药化类期刊, - X-M

New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates of VRE J. Antibiot. (IF 2.446) Pub Date : 2019-03-15 ...

New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates of VRE | Zsolt Szűcs .

Request PDF on ResearchGate | New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates of VRE | Ten analogues of a teicoplanin pseudoaglycon derivative have been synthesized with the aim of ...

Lipophilic teicoplanin pseudoaglycon derivatives are active against vancomycin- and teicoplanin-resistant enterococci (pdf) | Paperi

A selection of nine derivatives of teicoplanin pseudoaglycon were tested in vitro against clinical vancomycin-resistant Enterococcus strains possessing vanA, vanB or both genes. The bacteria were characterized by PCR for the identification of their resistance genes.

Medscape | J Antibiot (Tokyo) - Publication Informati

New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates ... Two new phenazine metabolites with antimicrobial activities from soil-derived Streptomyces species. July 01, 2019 [ MEDLINE Abstract] ...

Semisynthetic teicoplanin derivatives as new influenza virus binding inhibitors: Synthesis and antiviral studies, Bioorganic ...- DeepDy

Read "Semisynthetic teicoplanin derivatives as new influenza virus binding inhibitors: Synthesis and antiviral studies, Bioorganic & Medicinal Chemistry Letters" on DeepDyve, the largest online rental service for scholarly research with thousands of academic ...

Semisynthetic teicoplanin derivatives as new influenza virus binding inhibitors: Synthesis and antiviral studi

Semisynthetic teicoplanin derivatives as new influenza virus binding inhibitors: Synthesis and antiviral studies In order to obtain new, cluster-forming antibiotic compounds, teicoplanin pseudoaglycone derivatives containing two lipophilic n-octyl chains have been ...

Inhibition of Hepatitis C Virus Replication by Semisynthetic Derivatives of glycopeptide antibioti

Natural teicoplanins do not have antiviral activity, but their semisynthetic derivatives have been found to exert anti-HIV and anti-coronavirus activity (2,3). Here we studied a series of aglycon teicoplanin derivatives that exhibit good antiviral activity and lack, with ...

Lipophilic teicoplanin pseudoaglycon derivatives are active against vancomycin- and teicoplanin-resistant enterococci | The Journal of Antibioti

Besides others, we have been working on the chemical transformations of glycopeptide antibiotics for a long time. ... New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates of VRE , , , Lajos Nagy, ...

Medscape | J Antibiot (Tokyo) - Publication Informati

New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates ... Two new phenazine metabolites with antimicrobial activities from soil-derived Streptomyces species. July 01, 2019 [ MEDLINE Abstract] ...

J Antibiot (Tokyo) – Infectofor

Related Articles New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates of VRE. ... Related Articles Albumycin, a new isoindolequinone from Streptomyces albus J1074 harboring the fluostatin ...

A. Borbás – Research Output — Hungarian Consorti

New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates of VRE Szűcs, Z., Ostorházi, E., Kicsák, ...

17 research works produced by Erzsébet Rőth | University of Debrecen, Debrecen and other plac

relationship studies of lipophilic teicoplanin pseudoaglycon derivatives as new anti-influenza virus agents Erzsébet Rőth's research while affiliated with University of Debrecen and other places Publications (17) ...

Semisynthetic teicoplanin derivatives as new influenza virus binding inhibitors: synthesis and antiviral studies - CO

Abstract In order to obtain new, cluster-forming antibiotic compounds, teicoplanin pseudoaglycone derivatives containing two lipophilic n-octyl chains have been synthesized. The compounds proved to be poor antibacterials, but, surprisingly, they exhibited potent anti ...

Oritavanc

ABSSSI: Expediting Discharge With Oritavancin Insight is provided regarding the AtlantiCare poster presentation that analyzed oritavancin’s potential to expedite ... New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin ...

New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates of VRE — Hungarian .

Ten analogues of a teicoplanin pseudoaglycon derivative have been synthesized with the aim of optimizing the in vitro activity of the compound against VanA type vancomycin resistant enterococci (VRE) isolated from hospitalized patients. Teicoplanin, vancomycin ...

J Antibiot (Tokyo) – Infectofor

Related Articles New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates of VRE. ... Related Articles Albumycin, a new isoindolequinone from Streptomyces albus J1074 harboring the fluostatin ...

(PDF) In vitro antibacterial activity of LY333328, a new semisynthetic glycopeptide | B. Facinelli - Academia.e

new semisynthetic glycopeptide Antimicrobial agents and chemotherapy, 1997 B. Facinelli F. Biavasco F ... data vancomycin resistance to other organisms is illustrated by have been reported with certain semisynthetic derivatives of the recent ...

Semisynthetic teicoplanin derivatives as new influenza virus binding inhibitors: Synthesis and antiviral studies - ScienceDire

In order to obtain new, cluster-forming antibiotic compounds, teicoplanin pseudoaglycone derivatives containing two lipophilic n-octyl chains have been synthesized. The compounds proved to be poor antibacterials, but, surprisingly, they exhibited potent anti-influenza ...

Synthesis and evaluation of methyl ether derivatives of the vancomycin, teicoplanin, and ristocetin aglycon methyl esters - ScienceDire

A series of methyl ether derivatives of the vancomycin, teicoplanin, and ristocetin aglycon methyl esters was synthesized and their antimicrobial activity was established. These derivatives exhibit increased activity against VanB resistant strains of bacteria equipotent ...

Pharmacological Properties of NAI-603, a Well-Tolerated Semisynthetic Derivative of Ramoplan

Such efficacy is comparable to that of teicoplanin and higher than that of linezolid and vancomycin. ... Synthesis and preliminary biological characterization of new semisynthetic derivatives of ramoplanin. J. Med. Chem. 50:3077–3085. 10.1021/jm070042z [] [] ...

(PDF) Semisynthetic teicoplanin derivatives as new influenza virus binding inhibitors: Synthesis and antiviral studies | Sándor Kéki - Academia.e

Semisynthetic teicoplanin derivatives as new influenza virus binding inhibitors: Synthesis and antiviral ... derivatives Received 29 April 2014 containing two lipophilic n-octyl chains have been synthesized June ...