Arenavirus growth inhibitor comprising polycyclic carbamoylpyridone derivative
US-11492352-B2 · Nov 8, 2022 · US
US12054496B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12054496-B2 |
| Application number | US-202318334588-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 14, 2023 |
| Priority date | Apr 6, 2022 |
| Publication date | Aug 6, 2024 |
| Grant date | Aug 6, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present disclosure relates generally to compounds, of Formula I Also disclosed are pharmaceutical compositions comprising said compounds and methods of making said compounds. The compounds of the disclosure are useful in treating or preventing human immunodeficiency virus (HIV) infection.
Opening claim text (preview).
We claim: 1. A compound, or a pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of: 2. The compound of claim 1 , or the pharmaceutically acceptable salt thereof, wherein the compound is: 3. The compound of claim 1 , or the pharmaceutically acceptable salt thereof, wherein the compound is: 4. The compound of claim 1 , or the pharmaceutically acceptable salt thereof, wherein the compound is: 5. The compound of claim 1 , or the pharmaceutically acceptable salt thereof, wherein the compound is: 6. The compound of a claim 1 , or the pharmaceutically acceptable salt thereof, wherein the compound is: 7. The compound of a claim 1 , wherein the compound is: 8. The compound of a claim 1 , wherein the compound is: 9. The compound of a claim 1 , wherein the compound is: 10. The compound of a claim 1 , wherein the compound is: 11. The compound of a claim 1 , wherein the compound is: 12. A pharmaceutical composition comprising a therapeutically effective amount of a compound selected from the group consisting of: or a pharmaceutically acceptable salt thereof. 13. The pharmaceutical composition of claim 12 , further comprising an additional therapeutic agent. 14. The pharmaceutical composition of claim 13 , wherein the additional therapeutic agent is an anti-HIV agent. 15. The pharmaceutical composition of claim 12 , wherein the pharmaceutical composition is for oral or parenteral administration. 16. The pharmaceutical composition of claim 12 , wherein the compound is: 17. The pharmaceutical composition of claim 12 , wherein the compound is: 18. The pharmaceutical composition of claim 12 , wherein the compound is: 19. The pharmaceutical composition of claim 12 , wherein the compound is: 20. The pharmaceutical composition of claim 12 , wherein the compound is: 21. A kit comprising a compound selected from the group consisting of: or the pharmaceutically acceptable salt thereof, and instructions for use. 22. A method of treating an HIV infection in a human having the infection, comprising administering to the human a therapeutically effective amount of a compound, or pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of: 23. The method of claim 22 , further comprising administering to the human a therapeutically effective amount of an additional therapeutic agent. 24. The method of claim 23 , wherein the additional therapeutic agent is an anti-HIV agent. 25. The method of claim 22 , wherein the compound is administered to the human by oral, intravenous, subcutaneous, or intramuscular administration. 26. The method of claim 22 , wherein the compound is: 27. The method of claim 22 , wherein the compound is: 28. The method of claim 22 , wherein the compound is: 29. The method of claim 22 , wherein the compound is: 30. The method of claim 22 , wherein the compound is:
Optical isomers · CPC title
for HIV · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
having seven-membered rings, e.g. azelastine, pentylenetetrazole · CPC title
in which the condensed system contains four or more hetero rings · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.