The present disclosure provides conjugate structures and compound structures used to produce these conjugates. Also provided are methods of producing drug-polypeptide or detectable label-polypeptide conjugates linked through a modified amino acid. Structures of the modified amino acids used in producing the conjugates are disclosed.
本公开提供了用于制备这些共轭物的共轭结构和化合物结构。还提供了通过修饰的
氨基酸连接的药物-
多肽或可检测标记-
多肽共轭物的制备方法。公开了用于制备共轭物的修饰
氨基酸的结构。