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- W38647757 abstract "Macrocyclic lactones are lipophilic molecules bearing a large 12-, 14-, or 16- membered lactone ring substituted with hydroxyl, methyl, and ethyl groups, as well as carbonyl functions with one, two, or three carbohydrate fragments. The first compound of this class, pikromycin, was isolated by Brockman et al. in 1950 []. The past three decades have witnessed the development and extensive use of a group of medium-to-narrow-spectrum antibiotic macrocyclic lac-tones: erythromycin, oleandomycin, leucomycin (kitasamycin), josamycin (leucomycin A3), acetylspiramycin, and midemycin." @default.
- W38647757 created "2016-06-24" @default.
- W38647757 creator A5011704380 @default.
- W38647757 creator A5015092364 @default.
- W38647757 date "2001-01-01" @default.
- W38647757 modified "2023-09-26" @default.
- W38647757 title "The potential role of immunosuppressive macrocyclic lactones" @default.
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- W38647757 doi "https://doi.org/10.1007/978-3-0348-8352-8_4" @default.
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