[EN] DIRECTED CONJUGATION TECHNOLOGIES<br/>[FR] TECHNOLOGIES DE CONJUGAISON DIRIGÉE
申请人:KLEO PHARMACEUTICALS INC
公开号:WO2021102052A1
公开(公告)日:2021-05-27
Among other things, the present disclosure provides technologies for site-directed conjugation of various moieties of interest to target agents. In some embodiments, the present disclosure utilizes target binding moieties to provide high conjugation efficiency and selectivity. In some embodiments, provided technologies are useful for preparing antibody conjugates.
Spontaneous and promoted association of linear oligoglycines
作者:I. V. Gorokhova、A. A. Chinarev、A. B. Tuzikov、S. V. Tsygankova、N. V. Bovin
DOI:10.1134/s1068162006050049
日期:2006.9
Linear oligoglycines of various lengths bearing a carboxyl or an amide group at their C-termini and also their poly(acrylamide) conjugates were synthesized. No self-assembly into supramolecular structures was observed for free oligoglycines H-(Gly)m-OH (m = 3–5). At the same time, oligoglycylamides H-(Gly)m-NH2 (m = 3–5) demonstrated ability for both self-assembly in aqueous solution and assembly promoted
合成了在其 C 末端带有羧基或酰胺基团的各种长度的线性寡甘氨酸以及它们的聚(丙烯酰胺)缀合物。对于游离寡甘氨酸 H-(Gly)m-OH (m = 3-5),未观察到自组装成超分子结构。同时,低聚甘氨酰胺 H-(Gly)m-NH2 (m = 3-5) 展示了在水溶液中自组装和通过与表面的额外相互作用促进组装的能力。在聚合物结合的低聚甘氨酸(及其酰胺)的情况下,正如预期的那样,没有观察到肽链的分子内聚集。这意味着在一个中心存在多个相互结合的寡聚甘氨酸链并不是多聚甘氨酸 II 型结合的必要先决条件。
10.1021/jo0623311
作者:Pritz, Stephan、Wolf, Yvonne、Kraetke, Oliver、Klose, Jana、Bienert, Michael、Beyermann, Michael