69976-10-9Relevant academic research and scientific papers
10A-AZALIDE COMPOUND HAVING 4-MEMBERED RING STRUCTURE
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Page/Page column 57, (2011/04/14)
A 10a-azalide compound having a 4-membered ring structure crosslinked at the 10a- and 12-positions, which is represented by the formula (I), and is effective on even Haemophilus influenzae, or erythromycin resistant bacteria (e.g., resistant pneumococci and streptococci).
3-descladinose-2,3-anhydroerythromycin derivatives
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, (2008/06/13)
Novel 3-descladinose-2,3-anhydroerythromycin compounds and pharmaceutically acceptable salts and esters thereof having antibacterial activity.
Anhydrolide macrolides. 2. Synthesis and antibacterial activity of 2,3- anhydro-6-O-methyl 11,12-carbazate erythromycin A analogues
Griesgraber, George,Kramer, Mark J.,Elliott, Richard L.,Nilius, Angela M.,Ewing, Patty J.,Raney, Patti M.,Bui, Mai-Ha,Flamm, Robert K.,Chu, Daniel T.W.,Plattner, Jacob J.,Or, Yat Sun
, p. 1660 - 1670 (2007/10/03)
A series of 3-descladinosyl-2,3-anhydro-6-O-methylerythromycin A 11,12- cyclic carbazate analogues was prepared and evaluated for antibacterial activity. These 2,3-anhydro macrolides were found to be potent antibacterial agents in vitro against macrolide-susceptible organisms including Staphylococcus aureus 6538P, Streptococcus pyogenes EES61, and Streptococcus pneumoniae ATCC6303. These compounds were also very active against some organisms that show macrolide resistance (S. aureus A5177, S. pyogenes PIU2584, and S. pneumoniae 5649). The compounds generally showed poor activity against organisms with constitutive MLS resistance. Selected compounds were evaluated in vivo in mouse protection studies. Although most of the compounds tested in vivo showed poor efficacy, two compounds, 38 and 57, were more active than clarithromycin against S. pneumoniae ATCC6303.
