Comprehensive review on the anti-bacterial activity of 1, 2, 3-triazole hybrids

B Zhang - European Journal of Medicinal Chemistry, 2019 - Elsevier
Bacterial infections, caused predominately by Gram-positive and Gram-negative organisms,
are proliferation of harmful strains of bacteria on or inside the body. Hospital-acquired and …

Mechanism of action of oritavancin and related glycopeptide antibiotics

NE Allen, TI Nicas - FEMS microbiology reviews, 2003 - academic.oup.com
Oritavancin (LY333328) is a semisynthetic glycopeptide antibiotic having excellent
bactericidal activity against glycopeptide-susceptible and-resistant Gram-positive bacteria …

Telavancin, a Multifunctional Lipoglycopeptide, Disrupts both Cell Wall Synthesis and Cell Membrane Integrity in Methicillin-Resistant Staphylococcus aureus

DL Higgins, R Chang, DV Debabov… - Antimicrobial agents …, 2005 - Am Soc Microbiol
The emergence and spread of multidrug-resistant gram-positive bacteria represent a serious
clinical problem. Telavancin is a novel lipoglycopeptide antibiotic that possesses rapid in …

Glycopeptide antibiotics: from conventional molecules to new derivatives

F Van Bambeke, Y Van Laethem, P Courvalin… - Drugs, 2004 - Springer
Vancomycin and teicoplanin are still the only glycopeptide antibiotics available for use in
humans. Emergence of resistance in enterococci and staphylococci has led to restriction of …

Telavancin: a novel lipoglycopeptide

LD Saravolatz, GE Stein… - Clinical infectious …, 2009 - academic.oup.com
Telavancin, a derivative of vancomycin, is a lipoglycopeptide antibiotic that has been shown
to be effective for the treatment of complicated skin and skin-structure infections. It has also …

Recent advances in the synthesis of new glycopeptide antibiotics

PA Ashford, SP Bew - Chemical Society Reviews, 2012 - pubs.rsc.org
The vancomycin family of glycopeptide antibiotics has been inspiring research in the field of
synthetic chemistry since the 1980s. Recent studies have moved away from the focus of total …

Why are membrane targets discovered by phenotypic screens and genome sequencing in Mycobacterium tuberculosis?

RC Goldman - Tuberculosis, 2013 - Elsevier
High through put screening (HTS) was extensively used in attempts to discover new TB
drugs from libraries of pure small molecule compounds many of which complied with the …

Novel inhibitors of bacterial cell wall synthesis

LL Silver - Current opinion in microbiology, 2003 - Elsevier
Over the past forty years, efforts to discover antibacterials have yielded a wide variety of
chemical structures, almost exclusively natural products, which inhibit many steps in cell wall …

Structures of Staphylococcus aureus Cell-Wall Complexes with Vancomycin, Eremomycin, and Chloroeremomycin Derivatives by 13C{19F} and 15N{19F} …

SJ Kim, L Cegelski, M Preobrazhenskaya… - Biochemistry, 2006 - ACS Publications
Solid-state NMR has been used to examine isolated cell walls and intact whole cells of
Staphylococcus aureus complexed to five different vancomycin, eremomycin, and …

Antiretroviral activity of semisynthetic derivatives of glycopeptide antibiotics

J Balzarini, C Pannecouque, E De Clercq… - Journal of medicinal …, 2003 - ACS Publications
A variety of semisynthetic derivatives of natural antibacterial glycopeptide antibiotics such as
vancomycin, eremomycin, ristocetin A, teicoplanin A2-2, DA-40926, their aglycons, and also …