Chemical Compound Review:
Cladinose (3R,4S,5S)-4,5-dihydroxy-3- methoxy-3...
Synonyms:
L-Cladinose, AC1NUTFI, CHEBI:29612, FT-0665074, C11917
- Synthesis and antibacterial activity of ketolides (6-O-methyl-3-oxoerythromycin derivatives): a new class of antibacterials highly potent against macrolide-resistant and -susceptible respiratory pathogens. Agouridas, C., Denis, A., Auger, J.M., Benedetti, Y., Bonnefoy, A., Bretin, F., Chantot, J.F., Dussarat, A., Fromentin, C., D'Ambrières, S.G., Lachaud, S., Laurin, P., Le Martret, O., Loyau, V., Tessot, N. J. Med. Chem. (1998)
- Erythromycin A-derived macrolides modify the functional activities of human neutrophils by altering the phospholipase D-phosphatidate phosphohydrolase transduction pathway: L-cladinose is involved both in alterations of neutrophil functions and modulation of this transductional pathway. Abdelghaffar, H., Vazifeh, D., Labro, M.T. J. Immunol. (1997)
- Ketolides lack inducibility properties of MLS(B) resistance phenotype. Bonnefoy, A., Girard, A.M., Agouridas, C., Chantot, J.F. J. Antimicrob. Chemother. (1997)
- Structure-activity relationships among 9-N-alkyl derivatives of erythromycylamine and their effect on the oxidative burst of human neutrophils in vitro. Abdelghaffar, H., Kirst, H., Soukri, A., Babin-Chevaye, C., Labro, M.T. Journal of chemotherapy (Florence, Italy) (2002)
- Cladinose analogues of sixteen-membered macrolide antibiotics. V. Preparation of unsubstituted L-cladinose analogues: effect of methylation of a 3"-hydroxyl group on the bioactivity. Ajito, K., Shimizu, A., Shibahara, S., Hara, O., Kurihara, K., Araake, M., Tohyama, K., Miyadoh, S., Omoto, S., Inouye, S. J. Antibiot. (1997)