Triazole-Linked Glycolipids Enhance the Susceptibility of MRSA to β-Lactam Antibiotics

Triazole-Linked Glycolipids Enhance the Susceptibility of MRSA to β-Lactam Antibiotics Synthesis and antimicrobial activity of β-lactam–bile acid conjugates linked via triazole Diaryltriazenes as antibacterial agents against methicillin resistant Staphylococcus aureus (MRSA) and Mycobacterium smegmatis 1,2,3-Triazole-containing hybrids with potential antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) 18β-Glycyrrhetinic Acid Derivatives Possessing a Trihydroxylated A Ring Are Potent Gram-Positive Antibacterial Agents Efficient click chemistry towards novel 1H-1,2,3-triazole-tethered 4H-chromene−d-glucose conjugates: Design, synthesis and evaluation of in vitro antibacterial, MRSA and antifungal activities Synthesis of 2,3,6-trideoxy sugar triazole hybrids as potential new broad spectrum antimicrobial agents Design, synthesis, and antibacterial activity ofN-(trifluoromethyl)phenyl substituted pyrazole derivatives Tryptoline-based benzothiazoles re-sensitize MRSA to β-lactam antibiotics Antitubercular activity of 1,2,3-triazolyl fatty acid derivatives