Pyrazole or triazole compounds and their use for the manufacture of a medicament for treating somatic mutation related diseases

US9051342B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9051342-B2
Application numberUS-57717705-A
CountryUS
Kind codeB2
Filing dateOct 13, 2005
Priority dateOct 13, 2004
Publication dateJun 9, 2015
Grant dateJun 9, 2015

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention relates to methods, compounds, and compositions for treating or preventing diseases associated with nonsense mutations in an mRNA by administering the compounds or compositions of the present invention. More particularly, the present invention relates to methods, compounds, and compositions for suppressing premature translation termination associated with a nonsense mutation in an mRNA.

First claim

Opening claim text (preview).

What is claimed is: 1. A compound of Formula 1-A-10 or 1-A-11: wherein: n is 0, 1, or 2; R 1 is carboxy, cyano, or a carbonyl group which is optionally substituted with a C 1 -C 4 alkoxy group; R 2 is absent or a nitro; R is hydrogen; a —R a group; or two R groups, where R may also include an oxy group, together with the phenyl to which they are attached form a ring structure selected from RR; wherein: RR is a nine to ten membered bicyclic ring structure optionally substituted with one or more halogens, C 1 -C 4 alkyl groups, C 1 -C 4 haloalkyl groups, C 1 -C 4 alkoxy groups, oxo groups, or C 1 -C 4 haloalkoxy groups; R a is selected from the group consisting of: a hydroxy group; a halogen; a C 1 -C 4 alkyl which is substituted with one or more independently selected halogen or hydroxy groups; a C 1 -C 4 alkoxy which is substituted with one or more independently selected halogen or phenyl groups; a C 4 -C 8 cycloalkyl which is optionally substituted with one or more independently selected C 1 -C 4 alkyl groups; an —R b group; a —O—R b group; a four to six-membered heterocycle which is optionally substituted with one or more independently selected C 1 -C 4 alkyl, oxo, or —R b groups; a nine to ten membered heterocycle having two ring structures; a carbonyl which is optionally substituted with a hydroxy, a C 1 -C 4 alkyl, or a C 1 -C 4 alkoxy group; a carbamoyl which is optionally substituted with one or two C 1 -C 4 alkyl groups; a nitro group; a thio which is optionally substituted with a hydroxy, a C 1 -C 4 alkyl, or —R b group; a sulfonyl which is optionally substituted with a hydroxy, a C 1 -C 4 alkyl, or —R b group; or an amino which is optionally substituted with one or two independently selected C 1 -C 4 alkyl, sulfonyl, or carbonyl groups, wherein the aminosulfonyl group is optionally substituted with a hydroxy, a C 1 -C 4 alkyl, or —R b group and wherein the aminocarbonyl group is optionally substituted with a C 1 -C 4 alkyl, a C 1 -C 4 haloalkyl, a benzoxy, or an amino group which is optionally substituted with an —R b group; wherein —R b is a C 6 -C 8 aryl which is optionally substituted with one or more of the following: a hydroxy, a halogen, a C 1 -C 4 alkyl group, a C 1 -C 4 haloalkyl group, a C 1 -C 4 alkoxy group, or an amino group which is optionally substituted with one or more C 1 -C 4 alkyl groups; or a pharmaceutically acceptable salt thereof. 2. A compound selected from the group consisting of: and pharmaceutically acceptable salts thereof. 3. The compound of claim 1 , wherein RR is selected from: wherein the * indicates the bond of attachment of RR to the compound of Formula 1-A-10 or 1-A-11. 4. A compound selected from: or a pharmaceutically acceptable salt thereof.

Assignees

Inventors

Classifications

  • Drugs for disorders of the cardiovascular system · CPC title

  • of the thyroid hormones, e.g. T3, T4 · CPC title

  • for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis · CPC title

  • Antihyperlipidemics · CPC title

  • for hyperglycaemia, e.g. antidiabetics · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9051342B2 cover?
The present invention relates to methods, compounds, and compositions for treating or preventing diseases associated with nonsense mutations in an mRNA by administering the compounds or compositions of the present invention. More particularly, the present invention relates to methods, compounds, and compositions for suppressing premature translation termination associated with a nonsense mutati…
Who is the assignee on this patent?
Almstead Neil, Karp Gary M, Wilde Richard, and 5 more
What technology area does this patent fall under?
Primary CPC classification C07D271/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 09 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).