Compositions and methods for treating cancer
US-2020290978-A1 · Sep 17, 2020 · US
US11377451B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11377451-B2 |
| Application number | US-202117475144-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 14, 2021 |
| Priority date | Mar 15, 2019 |
| Publication date | Jul 5, 2022 |
| Grant date | Jul 5, 2022 |
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The present disclosure relates to compounds, compositions and methods for treating cancer, including compounds that are capable of penetrating the blood brain barrier to modulate the activity of EGFR tyrosine kinase. The disclosure further relates to methods of treating cancer in the brain, including glioblastoma and other EGFR mediated cancers. The disclosure further relates to methods of treating cancers such as glioblastoma and other EGFR mediated cancers that have been determined to have altered glucose metabolism in the presence of inhibitors. The present disclosure also provides methods of administering to a subject a glucose metabolism inhibitor and a cytoplasmic p53 stabilizer.
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We claim: 1. A compound selected from the group consisting of: or a pharmaceutically acceptable salt thereof. 2. The compound of claim 1 , wherein the compound is 3. The compound of claim 1 , wherein the compound is 4. The compound of claim 1 , wherein the compound is 5. The compound of claim 1 , wherein the compound is 6. The compound of claim 1 , wherein the compound is 7. The compound of claim 1 , wherein the compound is 8. The compound of claim 1 , wherein the compound is 9. The compound of claim 1 , wherein the compound is 10. The compound of claim 1 , wherein the compound is 11. The compound of claim 1 , wherein the compound is 12. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 13. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 14. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 15. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 16. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 17. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 18. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 19. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 20. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 21. The compound of claim 1 , wherein the compound is a pharmaceutically acceptable salt of the compound which is 22. A pharmaceutical composition comprising a compound, or pharmaceutically acceptable salt thereof, of claim 1 and a pharmaceutically acceptable excipient.
Antineoplastic agents · CPC title
directly linked by a ring-member-to-ring-member bond · CPC title
with hetero atoms directly attached in positions 2 and 4 · CPC title
with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring · CPC title
not condensed and containing further heterocyclic rings, e.g. timolol · CPC title
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