Pyrimidinyl tyrosine kinase inhibitors

US9944622B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9944622-B2
Application numberUS-201615196389-A
CountryUS
Kind codeB2
Filing dateJun 29, 2016
Priority dateJun 8, 2012
Publication dateApr 17, 2018
Grant dateApr 17, 2018

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  1. Title

    What the patent document calls the invention.

  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention provides compounds and compositions thereof which are useful as inhibitors of Bruton's tyrosine kinase and which exhibit desirable characteristics for the same.

First claim

Opening claim text (preview).

What is claimed is: 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 or a pharmaceutically acceptable salt thereof. 3. The compound of claim 1 , wherein the compound is or a pharmaceutically acceptable salt thereof. 4. The compound of claim 1 , wherein the compound is or a pharmaceutically acceptable salt thereof. 5. The compound of claim 1 , wherein the compound is or a pharmaceutically acceptable salt thereof. 6. The compound of claim 1 , wherein the compound is or a pharmaceutically acceptable salt thereof. 7. The compound of claim 1 , wherein the compound is or a pharmaceutically acceptable salt thereof. 8. The compound of claim 1 , wherein the compound is or a pharmaceutically acceptable salt thereof. 9. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier. 10. A method for decreasing the enzymatic activity of Bruton's tyrosine kinase comprising contacting Bruton's tyrosine kinase with an effective amount of a compound of claim 1 or a composition thereof. 11. A method for treating a disorder in a human subject in need of treatment for dysregulation of BCR signaling, the method comprising: administering to the subject an effective amount of a compound of claim 1 or a composition thereof, the compound being a Bruton's tyrosine kinase inhibitor; wherein the disorder is responsive to B-cell depletion. 12. A method for treating a disorder selected from the group consisting of autoimmune disorders, inflammatory disorders, and cancers affiliated with B-cells, the method comprising: administering to a human subject an effective amount of a compound of claim 1 or a composition thereof; wherein the disorder is responsive to B-cell depletion. 13. The method of claim 12 , wherein the disorder is rheumatoid arthritis. 14. The method of claim 12 , wherein the disorder is systemic lupus erythematosus. 15. The method of claim 12 , wherein the disorder is atopic dermatitis. 16. The method of claim 12 , wherein the disorder is leukemia or lymphoma.

Assignees

Inventors

Classifications

  • Antianaemics · CPC title

  • Immunosuppressants, e.g. drugs for graft rejection · CPC title

  • Antiallergic agents (antiasthmatic agents A61P11/06; ophthalmic antiallergics A61P27/14) · CPC title

  • Antineoplastic agents · CPC title

  • specific for leukemia · CPC title

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Frequently asked questions

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What does patent US9944622B2 cover?
The present invention provides compounds and compositions thereof which are useful as inhibitors of Bruton's tyrosine kinase and which exhibit desirable characteristics for the same.
Who is the assignee on this patent?
Biogen Ma Inc, Sunesis Pharmaceuticals Inc
What technology area does this patent fall under?
Primary CPC classification C07D401/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 7 related publications on this page (citations in our corpus or others sharing the same primary CPC).