US Patent
US8242104 — Benzoxazepin P13K inhibitor compounds and methods of use
Composition of Matter · Assigned to F Hoffmann La Roche AG · Expires 2030-09-27 · 4y remaining
Vulnerability score
23/100
Ironclad — strong claim type, well-established, deep family
What this patent protects
This patent protects benzoxazepin compounds that inhibit lipid kinases, including p110 alpha and other PI3K isoforms, for treating disorders such as cancer.
USPTO Abstract
Benzoxazepin compounds of Formula I, including stereoisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, wherein: Z 1 is CR 1 or N; Z 2 is CR 2 or N; Z 3 is CR 3 or N; Z 4 is CR 4 or N; and B is a pyrazolyl, imidazolyl, or triazolyl ring fused to the benzoxepin ring, are useful for inhibiting lipid kinases including p110 alpha and other isoforms of PI3K, and for treating disorders such as cancer mediated by lipid kinases. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
Drugs covered by this patent
- Itovebi (INAVOLISIB) · Genentech Inc
Bibliographic data sourced from FDA Orange Book + USPTO public records. Plain-English summary generated by AI grounded in source text. Patent term extensions (PTR, SPC, pediatric) may shift the effective expiry. Not legal advice.
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