Covalent linkers in antibody-drug conjugates and methods of making and using the same
The present invention provides novel and advantageous compositions having a linker capable of covalently coupling one or more free thiols of an antibody. Specifically, provided herein are the molecular structures, synthetic pathways, coupling mechanisms, and applications thereof as used in an antibody-drug conjugate (ADC).
1. An antibody-drug conjugate having the following formula:
or a pharmaceutically acceptable salt thereof,
wherein:
L 1 , and L 2 each represent a linker independently selected from C 1 -C 6 alkyls, S, C(═O), and combinations thereof, or can be null;
M represents a linking group of
Q represents an active agent selected from tubulin binders, DNA alkylators, DNA intercalators, enzyme inhibitors, immune modalators, visualization agents, peptides, and nucleotides;
L represents a linker selected from C 1 -C 6 alkyls, S, C(═O), Val-Cit-PAB,
and combinations thereof;
m represents an integer from 0 to 6;
n represents an integer from 0 to 8
A is an antibody or functional fragment thereof
S is a sulfur atom of a thiol group of the targeting moiety; and
each of R 3 and R 4 is
2. The antibody-drug conjugate as claimed in claim 1 , wherein the structure of Formula II is:
3. The antibody-drug conjugate as claimed in claim 1 , wherein the antibody-drug conjugate having the following formula II:
or a pharmaceutically acceptable salt thereof,
Wherein:
A is a targeting moiety;
Q is selected from tubulin binders, DNA alkylators, DNA intercalators, enzyme inhibitors, immune modalators, visualization agents, peptides, and nucleotides;
n represents an integer from 0 to 8.
4. The antibody-drug conjugate as claimed in claim 1 , wherein Q is selected from
5. The antibody-drug conjugate as claimed in claim 1 , wherein the structure of Formula II is:
6. The antibody-drug conjugate as claimed in claim 1 , wherein the structure of Formula II is:
7. The antibody-drug conjugate as claimed in claim 1 , wherein the structure of Formula II is: