Agonists of stimulator of interferon genes sting
The invention provides compounds having STimulator of INterferon Genes (STING) agonistic bioactivity that can be used in the treatment of tumors in patients afflicted therewith. The compounds are of formula (I): as defined herein. Compounds for practice of a method of the invention can be delivered via oral delivery for systemic exposure, as well as delivered intratumorally. Antitumor therapy using a compound of formula (I) can further comprise administration of an effective dose of an immune-checkpoint targeting drug.
1. A method of stimulating expression of interferon genes, comprising administering to a patient an effective dose of a compound of any one of the following formulae:
or a pharmaceutically acceptable salt thereof.
2. The method of claim 1 , wherein administering comprises oral or intratumoral administration, or both.
3. The method of claim 1 , wherein administering comprises administering to the patient as an antibody-drug conjugate, or in a liposomal formulation.
4. The method of claim 1 , further comprising administration of an effective dose of an immune-checkpoint targeting drug.
5. The method of claim 4 , wherein the immune-checkpoint targeting drug comprises an anti-PD-L1 antibody, anti-PD-1 antibody, anti-CTLA-4 antibody, or an anti-4-1BB antibody.
6. The method of claim 1 , further comprising administration of ionizing radiation or anticancer drugs.
7. A method of treating a tumor in a patient, comprising administering to the patient an effective dose of an agonist of the Stimulator of Interferon Genes (STING), comprising a compound of formula (I)
wherein each R 1 is independently (C1-C4)alkyl, or CN, nr1 is 0, 1, 2, or 3, provided that each R 1 is bonded to a carbon atom; and,
AR is a group of formula —C(═O)N(R)Ar 1 ; R is H or (C1-C4)alkyl;
wherein Ar 1 is chosen from the group consisting of:
wherein a wavy line indicates a position of bonding;
wherein any Ar 1 is substituted with nr2 independently selected R 2 groups chosen from the group consisting of:
—(C1-C4)-alkyl, —(C1-C4)-alkylO, —(C1-C4)-alkylOC(O), —CN, -halo, —(C3-C7)cycloalkyl, —(C1-C4)-alkOC(O), —COOH, (C3-C7)-cycloalkylOC(O), —SF 5 , -methylenedioxy, -difluoromethylenedioxy, -ethylenedioxy, —CF 3 , —OCF 3 , —C(O)NH 2 , —C(O)NH(CH 2 ) 2 OH, —CH 2 OH, —NR 2 , —CONH-arginine, —C(O)O(CH 2 ) 2 NR 2 ,
wherein a wavy line indicates a position of bonding; and, nr2=0, 1, 2, or 3;
or,
AR is a group of formula
wherein R 3 is selected from the group consisting of
(C1-C4)-alkyl, (C1-C4)-alkylO, (C1-C4)-alkylOC(O), CN, halo, (C3-C7)cycloalkyl, (C1-C4)-alkOC(O), COOH, (C3-C7)-cycloalkylOC(O), —SF 5 , methylenedioxy, difluoromethylenedioxy, ethylenedioxy, CF 3 , —OCF 3 , CONH 2 , CONH(CH 2 ) 2 OH, CH 2 OH, NR 2 , CONH-arginine, and C(O)O(CH 2 ) 2 NR 2 ; and nr3=0, 1, 2, or 3;
or a pharmaceutically acceptable salt thereof.
8. The method of claim 7 , wherein administering comprises oral or intratumoral administration, or both.
9. The method of claim 7 , wherein administering comprises administering to the patient as an antibody-drug conjugate, or in a liposomal formulation.
10. The method of claim 7 , further comprising administration of an effective dose of an immune-checkpoint targeting drug.
11. The method of claim 10 , wherein the immune-checkpoint targeting drug comprises an anti-PD-L1 antibody, anti-PD-1 antibody, anti-CTLA-4 antibody, or an anti-4-1BB antibody.
12. The method of claim 7 , further comprising administration of ionizing radiation or anticancer drugs.
13. The method of claim 7 , wherein the compound of any one of the following formulas:
or a pharmaceutically acceptable salt thereof.
14. A compound of any one of the following formulae:
or a pharmaceutically acceptable salt thereof.