Prodrugs of NRF2 activating compounds and uses thereof
Aspects of the present disclosure include prodrugs of compounds that activate Nrf2. Such prodrugs find use in the treatment of autoimmune and inflammatory diseases and disorders, such as for example psoriasis and multiple sclerosis. Embodiments of the present disclosure also relate to pharmaceutical compositions that include these prodrugs, methods of using these prodrugs in the treatment of various diseases and disorders, processes for preparing these prodrugs and intermediates useful in these processes.
1. A compound of formula (I):
wherein:
R 2 is selected from the group consisting of sulfonyl, carboxyl, carboxyl ester, and aminoacyl;
R 3 is selected from the group consisting of an active agent, an antioxidant, an amino acid, an amino acid derivative, a peptide, and a peptide derivative;
R 4 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, heterocyclyl, substituted heterocyclyl, aryl, substituted aryl, heteroaryl, and substituted heteroaryl;
X 1 and X 2 are each independently selected from N and CH, wherein at least one of X 1 and X 2 is N; and
n is an integer from 1 to 6,
or a salt or a stereoisomer thereof.
2. The compound of claim 1 , wherein R 2 is sulfonyl or carboxyl ester.
3. The compound of claim 1 , wherein the compound is a compound of formula (II):
wherein:
R 3 is selected from the group consisting of an active agent, an antioxidant, an amino acid, an amino acid derivative, a peptide, and a peptide derivative;
R 4 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, heterocyclyl, substituted heterocyclyl, aryl, substituted aryl, heteroaryl, and substituted heteroaryl;
R 5 is selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, heterocyclyl, substituted heterocyclyl, aryl, substituted aryl, heteroaryl, and substituted heteroaryl;
X 1 and X 2 are each independently selected from N and CH, wherein at least one of X 1 and X 2 is N; and
n is an integer from 1 to 6,
or a salt or a stereoisomer thereof.
4. The compound of claim 3 , wherein R 5 is aryl or substituted aryl.
5. The compound of claim 1 , wherein n is 1.
6. The compound of claim 1 , wherein n is 2.
7. The compound of claim 1 , wherein R 3 is glutathione.
8. The compound of claim 1 , wherein R 3 is an amino acid or an amino acid derivative.
9. The compound of claim 1 , wherein X 1 is N and X 2 is N.
10. The compound of claim 1 , wherein X 1 is N and X 2 is CH.
11. The compound of claim 1 , wherein the compound is selected from the group consisting of:
12. An isolated compound, wherein the isolated compound is selected from the group consisting of:
13. A pharmaceutical composition comprising a compound of claim 1 , and a pharmaceutically acceptable carrier.
14. A method of treating a disease or disorder in a subject in need thereof, the method comprising:
administering to the subject a pharmaceutically effective amount of a compound of claim 1 sufficient to treat the disease or disorder in the subject,
wherein the disease or disorder is an autoimmune disease or an inflammatory disease.
15. The method of claim 14 , wherein the disease or disorder is psoriasis or multiple sclerosis.