Combination therapies comprising antibody molecules to pd-1
US-2018222982-A1 · Aug 9, 2018 · US
US12358918B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12358918-B2 |
| Application number | US-201917293255-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 14, 2019 |
| Priority date | Nov 14, 2018 |
| Publication date | Jul 15, 2025 |
| Grant date | Jul 15, 2025 |
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The present disclosure relates to compositions and methods for the diagnosis and treatment or prevention of cancers, particularly cancers that exhibit elevated expression of FOXA1 and/or FOXA1 gene targets, such as certain breast, liver and/or prostate cancers, including luminal and/or ER-positive forms of breast cancer. Three previously identified adenosine receptor antagonists, CGS-15943, MRS-1220 and SCH-58261, as well as furan ring moiety-possessing derivatives of CGS-15943 are specifically provided for killing cancer cells in a manner that appears to involve activation of the aryl hydrocarbon receptor (AHR) by such compounds. The instant disclosure therefore provides for selecting and/or administering CGS-15943, MRS-1220, SCH-58261 and/or a furan-possessing derivative of CGS-15943, MRS-1220 and/or SCH-58261 as a therapeutic agent to target a cancer cell and/or subject having or at risk of developing a cancer. Methods and compositions for therapies that include such compounds are also provided.
Opening claim text (preview).
We claim: 1. A compound having a structure of formula I: wherein: R 1 , R 2 , and R 3 independently represent H or Me, wherein R 1 , R 2 , and R 3 independently represent H; or wherein R 1 represents methyl and R 2 and R 3 each represents H; or wherein R 3 represents methyl and R 1 and R 2 each represents H; or wherein both R 1 and R 3 represent methyl and R 2 represents H; or wherein R 2 and R 3 together with the other atoms to which they are bound form an optionally substituted phenyl group; R 4 represents H, methyl, or NR 5 R 6 wherein R 5 and R 6 independently represent H, methyl, or phenyl, provided that only one of R 5 and R 6 may represent phenyl; and wherein R 7 , R 8 , and R 9 independently represent H, F, Cl, Br, methoxy, or optionally substituted C 1 -C 3 alkyl, X represents O or N—R 10 , wherein R 10 represents H or methyl; X 1 represents C—O or CR 4 ; X 2 represents N or NH; and X 3 represents CR 7 or N, provided that X 2 represents NH when X 1 represents C═O, at least one of R 7 , R 8 , and R 9 represents F, Cl, Br, methoxy, or optionally substituted C 1 -C 3 alkyl; and further provided that if R 1 , R 2 and R 3 independently represent H and R 5 represents Cl, R 4 cannot represent NR 5 R 6 wherein R 5 and R 6 both represent H; or a pharmaceutically acceptable salt, ester, amide, prodrug or stereoisomer thereof. 2. The compound of claim 1 , wherein: R 4 is H; R 4 represents methyl; R 4 represents NR 5 R 6 , R 5 represents H and R 6 represents Me; R 4 represents NR 5 R 6 , and R 5 and R 6 represent Me; R 4 represents NR 5 R 6 , R 5 represents H and R 6 represents phenyl; R 4 represents NR 5 R 6 , R 5 represents methyl and R 6 represents phenyl; R 8 represents Cl and R 7 and R 9 each represents H; R 8 represents F and R 7 and R 9 each represents H; R 8 represents Br and R 7 and R 9 each represents H; R 8 represents CF 3 and R 7 and R 9 each represents H; R 8 represents methoxy and R 7 and R 8 each represents H; R 9 represents CF 3 and R 7 and R 8 each represents H; R 9 represents methoxy and R 7 and R 8 each represents H; X represents O; X represents NR 10 , wherein R 10 represents methyl; X 1 represents C═O and X 2 represents NH; and/or X 3 represents N. 3. A compound selected from the group consisting of: or a pharmaceutically acceptable salt, ester, amide, prodrug or stereoisomer thereof.
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