Heteroaryl substituted pyrrolo[2,3-B]pyridines and pyrrolo[2,3-B]pyrimidines as Janus kinase inhibitors

US8933086B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-8933086-B2
Application numberUS-201314033039-A
CountryUS
Kind codeB2
Filing dateSep 20, 2013
Priority dateDec 13, 2005
Publication dateJan 13, 2015
Grant dateJan 13, 2015

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention provides heteroaryl substituted pyrrolo[2,3-b]pyridines and heteroaryl substituted pyrrolo[2,3-b]pyrimidines that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases, skin disorders, myeloid proliferative disorders, cancer, and other diseases.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of treating pancreatic cancer in a patient, comprising administering to said patient a therapeutically effective amount of a compound that is 3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile, or a pharmaceutically acceptable salt thereof. 2. A method according to claim 1 , wherein said compound is (3R)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile, or a pharmaceutically acceptable salt thereof. 3. A method according to claim 2 , further comprising administering to said patient an additional therapeutic agent. 4. The method according to claim 3 , wherein said additional therapeutic agent is a chemotherapeutic agent. 5. The method according to claim 4 , wherein said method comprises administering said compound, or said salt, and said chemotherapeutic agent simultaneously to the patient. 6. The method according to claim 4 , wherein said method comprises administering said compound, or said salt, and said chemotherapeutic agent sequentially to said patient. 7. The method according to claim 2 , wherein about 5 to about 1000 mg of said compound or said salt is administered to said patient.

Assignees

Inventors

Classifications

  • Antipruritics · CPC title

  • C07D471/04Primary

    Ortho-condensed systems · CPC title

  • Skin, i.e. galenical aspects of topical compositions (non-active ingredients are additionally classified in A61K47/00; A61K9/0009, A61K9/0021, A61K9/7015, A61K9/7023 take precedence; cosmetic preparations A61K8/00, A61Q; preparations for wound dressings or bandages A61L26/00) · CPC title

  • the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline · CPC title

  • Heterocyclic compounds · CPC title

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What does patent US8933086B2 cover?
The present invention provides heteroaryl substituted pyrrolo[2,3-b]pyridines and heteroaryl substituted pyrrolo[2,3-b]pyrimidines that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases, skin disorders, myeloid proliferative disorders, cancer, and other diseases.
Who is the assignee on this patent?
Incyte Corp
What technology area does this patent fall under?
Primary CPC classification C07D471/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 13 2015 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).