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Semi-synthetic desmethyl-vancomycin-based glycopeptide with antibacterial activity

机译:具有抗菌活性的半合成去甲基万古霉素基糖肽

摘要

Semi-synthetic glycopeptides that have antibacterial activity are based on modifications of the desmethyl-vancomycin scaffold, in particular, acylation of the amino substituent on the amino-substituted sugar moiety on this scaffold with certain acyl groups; and/or conversion of the acid moiety on the macrocyclic ring of this scaffolds to certain substituted amides. In addition, compounds of the invention include desmethyl-vancomycin scaffolds on which the acid moiety on the macrocyclic ring is converted to certain substituted amides and the amino substituent on the amino-substituted sugar moiety is alkylated with certain alkyl groups. Also provided are methods for synthesis of the compounds, pharmaceutical compositions containing the compounds, and methods of use of the compounds for the treatment and/or prophylaxis of diseases, especially bacterial infections.
机译:具有抗菌活性的半合成糖肽基于去甲基万古霉素骨架的修饰,特别是基于该骨架上氨基取代糖部分的氨基取代基被某些酰基酰化;和/或该支架大环上的酸部分转化为某些取代的酰胺。另外,本发明的化合物包括去甲基-万古霉素骨架,在其上大环上的酸部分被转化为某些取代的酰胺,并且在氨基取代的糖部分上的氨基取代基被某些烷基烷基化。还提供了化合物的合成方法,包含该化合物的药物组合物,以及将该化合物用于治疗和/或预防疾病,特别是细菌感染的方法。

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