1370637-75-4

Upstream product

• 67977-95-1 diphenylmethyl 6β-(4-toluamido)penicillate 1-oxide 
• 104101-66-8 diphenylmethyl 6β-(4-toluamido)penicillanate 
• 6274-27-7 [(2,5-dichlorophenyl)thio]acetic acid 
• 91-01-0 1,1-Diphenylmethanol 
• 91177-27-4 7-(N-4-methylbenzamide)-3-(chloromethyl)-8-oxo-5-oxo-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester 
• 68313-81-5 diphenylmethyl (2R,6R,7R)-3-methylene-7-[(4-methylbenzoyl)amino]-8-oxo-5-oxa-1-azabicyclo[4.2.0]octane-2-carboxylate 
• 67978-05-6 C₂₉H₂₆N₂O₄ 
• 82468-41-5 C₂₉H₂₈N₂O₅S 
• 17028-66-9 6β-(4-toluamido)penicillanic acid 

Downstream Products

• 1370637-94-7 C₃₅H₃₀Cl₂N₃O₆S⁽¹⁺⁾*I^(1-) 
• 1370637-97-0 C₃₈H₃₄Cl₂N₃O₆S⁽¹⁺⁾*I^(1-) 
• 1370638-14-4 C₂₂H₂₀Cl₂N₃O₆S⁽¹⁺⁾*I^(1-) 
• 1370638-15-5 C₂₅H₂₄Cl₂N₃O₆S⁽¹⁺⁾*I^(1-) 
• 1370638-16-6 C₂₃H₂₀Cl₂N₅O₆S⁽¹⁺⁾*I^(1-) 
• 1370638-00-8 C₃₆H₃₀Cl₂N₅O₆S⁽¹⁺⁾*I^(1-) 

Relevant academic research and scientific papers

Design, synthesis and antibacterial activity of novel 1-oxacephem analogs

A series of 1-oxacephem analogs were synthesized and their antibacterial properties against five strains of Gram-positive and Gram-negative bacteria were evaluated in vitro while ceftazidine was selected as control. Some of the tested compounds, compound 12c in particular, showed more active against three selected strains than the standard.