Chemical compounds

US10793559B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10793559-B2
Application numberUS-201916572917-A
CountryUS
Kind codeB2
Filing dateSep 17, 2019
Priority dateFeb 12, 2016
Publication dateOct 6, 2020
Grant dateOct 6, 2020

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  1. Title

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  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

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I): and salts thereof. The compounds of the invention are inhibitors of kinase activity, in particular PI3-kinase activity.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of treating a disorder mediated by inappropriate PI3-kinase activity comprising administering an amount of a compound of formula (I): wherein R 1 is C 1-6 alkoxy or —N(C 1-6 alkyl) 2 , R 2 is hydrogen or C 1-6 alkyl optionally substituted by —C(O)OC 1-6 alkyl or —OC(O)C 1-6 alkyl, R 3 , R 4 , R 5 and R 6 are each independently selected from hydrogen and halogen; R 7 and R 8 are each independently C 1-6 alkyl, or R 7 and R 8 , together with the nitrogen atom to which they are attached, are linked to form a 5- or 6-membered heterocyclyl wherein the 5- or 6-membered heterocyclyl optionally contains a further nitrogen atom and is optionally substituted by C 3-6 cycloalkyl, 4- to 6-membered heterocyclyl containing one or two heteroatoms independently selected from oxygen and nitrogen, or C 1-6 alkyl wherein the C 1-6 alkyl is optionally substituted by hydroxy or C 1-6 alkoxy, or R 7 and R 8 , together with the nitrogen atom to which they are attached, are linked to form a 5- or 6-membered heterocyclyl wherein the 5- or 6-membered heterocyclyl contains an oxygen atom and is optionally substituted by one or two substituents independently selected from C 1-6 alkyl; or a pharmaceutically acceptable salt thereof, to a patient in need thereof, by inhibiting PI3-kinase activity and wherein said disorder mediated by inappropriate PI3-kinase activity is selected from the group consisting of asthma and COPD. 2. A method according to claim 1 wherein the disorder mediated by inappropriate PI3-kinase activity is asthma. 3. A method according to claim 1 wherein the disorder mediated by inappropriate PI3-kinase activity is COPD.

Assignees

Inventors

Classifications

  • C07D213/76Primary

    to which a second hetero atom is attached (nitro radicals C07D213/61) · CPC title

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

  • for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia · CPC title

  • C07D413/14Primary

    containing three or more hetero rings · CPC title

  • Antidepressants · CPC title

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Frequently asked questions

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What does patent US10793559B2 cover?
The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I): and salts thereof. The compounds of the invention are inhibitors of kinase activity, in particular PI3-kinase activity.
Who is the assignee on this patent?
Glaxosmithkline Ip Dev Ltd
What technology area does this patent fall under?
Primary CPC classification C07D213/76. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 06 2020 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).