Pfeiffer R R
Rev Infect Dis. 1981 Nov-Dec;3 suppl:S205-9.
Recent analytical methods have advanced knowledge of the structure of vancomycin from a description of only several molecular fragments to a complete understanding of the intact molecule. The molecular weight is 1,448. The molecule consists of a seven-membered peptide chain that is formed by parts of three phenylglycine systems, two chlorinated tyrosine units, aspartic acid, and N-methylleucine. Two ether bonds and a carbon-carbon bond join the various substituents on the peptide chain into three large rings. A disaccharide, composed of glucose and vancosamine, is also present but is not part of the cyclic structure. Details of the vancomycin structure have been related to hydrogen bonding between the antibiotic and bacterial cell-wall precursors that have a D-alanyl-D-alanine carboxyl terminus; such bonding would provide a molecular basis for the cell-wall mode of action for vancomycin. With one carboxyl, two amino, and three phenolic groups, vancomycin undergoes a variety of ionic interactions in solutions of different pH and composition.
最近的分析方法使万古霉素的结构知识从仅对几个分子片段的描述发展到对完整分子的全面理解。其分子量为1448。该分子由一条七元肽链组成,该肽链由三个苯甘氨酸系统的部分、两个氯化酪氨酸单元、天冬氨酸和N-甲基亮氨酸构成。两个醚键和一个碳-碳键将肽链上的各种取代基连接成三个大环。还存在由葡萄糖和万古糖胺组成的二糖,但它不是环状结构的一部分。万古霉素结构的细节与抗生素和具有D-丙氨酰-D-丙氨酸羧基末端的细菌细胞壁前体之间的氢键有关;这种结合将为万古霉素的细胞壁作用模式提供分子基础。万古霉素有一个羧基、两个氨基和三个酚羟基,在不同pH值和组成的溶液中会发生多种离子相互作用。