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6-O-substituted macrolides which have antibacterial activity

机译:具有抗菌活性的6-O-取代的大环内酯类

摘要

The instant invention provides novel macrolide compounds and compositions useful in treating bacterial infections. Also provided are processes for preparing same. These macrolides are substituted on the 6-O-position with X'-Y'-Z', wherein X' is selected from the group consisting of C1-C10 alkyl, C3-C10 alkenyl, and C3-C10 alkynyl; Y' and Z' are independently selected from the group consisting of: (c) optionally substituted aryl, and (d) optionally substituted heteroaryl, with the proviso that both Y' and Z' are not both phenyl, and with the further proviso that Y' is not isoxazole when Z' is thiophenyl.
机译:本发明提供了可用于治疗细菌感染的新型大环内酯化合物和组合物。还提供了其制备方法。这些大环内酯在6-O-位被X'-Y'-Z'取代,其中X'选自C1-C10烷基,C3-C10烯基和C3-C10炔基; Y′和Z′独立地选自:(c)任选取代的芳基,和(d)任选取代的杂芳基,条件是Y′和Z′都不都是苯基,并且另外的条件是当Z′是噻吩基时,Y′不是异恶唑。

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