| CPC A61K 51/065 (2013.01) [A61K 31/43 (2013.01); A61K 31/7076 (2013.01); A61K 38/12 (2013.01); A61K 38/14 (2013.01); A61K 47/54 (2017.08); A61K 47/542 (2017.08); A61K 47/545 (2017.08); A61K 47/61 (2017.08); A61K 47/665 (2017.08); A61K 47/6903 (2017.08); A61K 49/0041 (2013.01); A61K 49/0043 (2013.01); A61K 49/0052 (2013.01); A61K 49/0054 (2013.01); A61K 49/0073 (2013.01); A61K 51/0482 (2013.01); A61K 51/0495 (2013.01); A61K 51/1213 (2013.01); C07D 257/08 (2013.01); C07D 311/82 (2013.01); C07D 499/74 (2013.01); C07H 7/02 (2013.01); C07H 15/24 (2013.01); C07H 19/167 (2013.01); C07H 19/213 (2013.01)] | 20 Claims |
|
1. A solid support composition comprising:
a biocompatible solid support;
at least one binding agent; and
a linker comprising from about 1 to about 10 linking atoms, covalently linking each binding agent to the biocompatible solid support,
wherein the binding agent and the linker together have the structure selected from the group consisting of:
![]() |