IP Library Granted Patent US 7,342,037
Granted Patent B2
US 7,342,037 · App. 11/450,840 · Granted Mar 11, 2008

Anti-inflammatory medicaments

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Quick Facts
Patent No.
US 7,342,037
App. No.
11/450,840
Granted
Mar 11, 2008
Kind
B2
Abstract

Novel compounds and methods of using those compounds for the treatment of inflammatory conditions are provided. In a preferred embodiment, modulation of the activation state of p38 kinase protein comprises the step of contacting the kinase protein with the novel compounds.

Claims (52)

1. A compound having the formula

wherein:

A is selected from the group consisting of phenyl, naphthyl, pyridyl, pyrimidyl, thienyl, furyl, pyrrolyl, thiazolyl, oxazolyl, imidazolyl, indolyl, indazolyl, benzimidazolyl, benzotriazolyl, isoquinolyl, quinolyl, benzothiazolyl, benzofuranyl, benzothienyl, pyrazolylpyrimidinyl, imidazopyrimidinyl, purinyl, and

where each W 1 is individually selected from the group consisting of —CH— and —N—;

D is selected from the group consisting of phenyl, pyrazolyl, pyrrolyl, imidazolyl, oxazolyl, thiazolyl, furyl, oxadiazolyl, thiadiazolyl, thienyl, pyridyl, and pyrimidyl;

G is —CH 2 —, N(R 6 ), O;

Q is

each R 4 group is individually selected from the group consisting of —H, alkyls, aminoalkyls, alkoxyalkyls, aryls, aralkyls, heterocyclyls, and heterocyclylalkyls except when the R 4 substituent places a heteroatom on an alpha-carbon directly attached to a ring nitrogen on Q;

when two R 4 groups are bonded with the same atom, the two R 4 groups optionally form an alicyclic or heterocyclic 4-7 membered ring;

each R 6 is individually selected from the group consisting of —H and alkyls;

each Z is individually selected from the group consisting of —O— and —N(R 4 )—;

R 7 ″ is selected from the group consisting of alkyls, aryls, heterocyclyls, and perfluoroalkyls;

wherein A or Q is optionally substituted with one or more R 7 ′ substituents selected from the group consisting of —H, alkyls, aryls, heterocyclyls, alkylaminos, arylaminos, cycloalkylaminos, heterocyclylaminos, hydroxys, alkoxys, aryloxys, alkylthios, arthylthios, cyanos, halogens, nitros, alkylsulfinyls, alkylsulfonyls, aminosulfonyls, and perfluoroalkyls;

and each R 9 ′ is individually and independently selected from the group consisting of F and alkyls, wherein when two R 9 ′ groups are alkyl groups, said alkyl groups may be cyclized to form a 3-6 membered ring.

2. The compound of claim 1 , wherein A is phenyl substituted by one or more R 7 ′ substituents, said R 7 ′ substituents being halogens.

3. The compound of claim 1 , wherein A is an R 7 ′-substituted naphthyl.

4. The compound of claim 1 , where R 7 ″ is selected from the group consisting of aryls and heterocyclyls.

5. A method of modulating the activation state of a p38-alpha kinase comprising the step of contacting said kinase with a molecule having the formula

wherein:

A is selected from the group consisting of phenyl, naphthyl, pyridyl, pyrimidyl, thienyl, furyl, pyrrolyl, thiazolyl, oxazolyl, imidazolyl, indolyl, indazolyl, benzimidazolyl, benzotriazolyl, isoquinolyl, quinolyl, benzothiazolyl, benzofuranyl, benzothienyl, pyrazolylpyrimidinyl, imidazopyrimidinyl, purinyl, and

where each W 1 is individually selected from the group consisting of —CH— and —N—;

D is selected from the group consisting of phenyl, pyrazolyl, pyrrolyl, imidazolyl, oxazolyl, thiazolyl, furyl, oxadiazolyl, thiadiazolyl, thienyl, pyridyl, and pyrimidyl;

G is —CH 2 —, N(R 6 ), O;

Q is

each R 4 group is individually selected from the group consisting of —H, alkyls, aminoalkyls, alkoxyalkyls, aryls, aralkyls, heterocyclyls, and heterocyclylalkyls except when the R 4 substituent places a heteroatom on an alpha-carbon directly attached to a ring nitrogen on Q;

when two R 4 groups are bonded with the same atom, the two R 4 groups optionally form an alicyclic or heterocyclic 4-7 membered ring;

each R 6 is individually selected from the group consisting of —H, alkyls, allyls, and β-trimethylsilylethyl;

each Z is individually selected from the group consisting of —O— and —N(R 4 )—;

R 7 ″ is selected from the group consisting of alkyls, aryls, heterocyclyls, and perfluoroalkyls;

wherein A or Q is optionally substituted with one or more R 7 ′ substituents selected from the group consisting of —H, alkyls, aryls, heterocyclyls, alkylaminos, arylaminos, cycloalkylaminos, heterocyclylaminos, hydroxys, alkoxys, aryloxys, alkylthios, arthylthios, cyanos, halogens, nitros, alkylsulfinyls, alkylsulfonyls, aminosulfonyls, and perfluoroalkyls;

and each R 9 ′ is individually and independently selected from the group consisting of F and alkyls, wherein when two R 9 ′ groups are alkyl groups, said alkyl groups may be cyclized to form a 3-6 membered ring.

6. The method of claim 5 , wherein A is phenyl substituted by one or more R 7 ′ substituents, said R 7 ′ substituents being halogens.

7. The method of claim 5 , wherein A is an R 7 ′-substituted naphthyl.

8. The method of claim 5 , where R 7 ″ is selected from the group consisting of aryls and heterocyclyls.

9. An adduct comprising a molecule bound with a kinase, said molecule having the formula

wherein:

A is selected from the group consisting of phenyl, naphthyl, pyridyl, pyrimidyl, thienyl, furyl, pyrrolyl, thiazolyl, oxazolyl, imidazolyl, indolyl, indazolyl, benzimidazolyl, benzotriazolyl, isoquinolyl, quinolyl, benzothiazolyl, benzofuranyl, benzothienyl, pyrazolylpyrimidinyl, imidazopyrimidinyl, purinyl, and

where each W 1 is individually selected from the group consisting of —CH— and —N—;

D is selected from the group consisting of phenyl, pyrazolyl, pyrrolyl, imidazolyl, oxazolyl, thiazolyl, furyl, oxadiazolyl, thiadiazolyl, thienyl, pyridyl, and pyrimidyl;

G is —CH 2 —, N(R 6 ), O;

Q is

each R 4 group is individually selected from the group consisting of —H, alkyls, aminoalkyls, alkoxyalkyls, aryls, aralkyls, heterocyclyls, and heterocyclylalkyls except when the R 4 substituent places a heteroatom on an alpha-carbon directly attached to a ring nitrogen on Q;

when two R 4 groups are bonded with the same atom, the two R 4 groups optionally form an alicyclic or heterocyclic 4-7 membered ring;

each R 6 is individually selected from the group consisting of —H, alkyls, allyls, and β-trimethylsilylethyl;

each Z is individually selected from the group consisting of —O— and —N(R 4 )—;

R 7 ″ is selected from the group consisting of alkyls, aryls, heterocyclyls, and perfluoroalkyls;

wherein A or Q is optionally substituted with one or more R 7 ′ substituents selected from the group consisting of —H, alkyls, aryls, heterocyclyls, alkylaminos, arylaminos, cycloalkylaminos, heterocyclylaminos, hydroxys, alkoxys, aryloxys, alkylthios, arthylthios, cyanos, halogens, nitros, alkylsulfinyls, alkylsulfonyls, aminosulfonyls, and perfluoroalkyls;

and each R 9 ′ is individually and independently selected from the group consisting of F and alkyls, wherein when two R 9 ′ groups are alkyl groups, said alkyl groups may be cyclized to form a 3-6 membered ring.

10. The adduct of claim 9 , wherein A is phenyl substituted by one or more R 7 ′ substituents, said R 7 ′ substituents being halogens.

11. The adduct of claim 9 , wherein A is an R 7 ′-substituted naphthyl.

12. The adduct of claim 9 , where R 7 ″ is selected from the group consisting of aryls and heterocyclyls.

13. A method of treating an individual suffering from a condition selected from the group consisting of human inflammation, rheumatoid arthritis, rheumatoid spondylitis, osteo-arthritis, asthma, gouty arthritis, sepsis, septic shock, endotoxic shock, Gram-negative sepsis, toxic shock syndrome, adult respiratory distress syndrome, stroke, reperfusion injury, neural trauma, neural ischemia, psoriasis, restenosis, chronic pulmonary inflammatory disease, bone resorptive diseases, graft-versus-host reaction, Crohn's disease, ulcerative colitis, inflammatory bowel disease, pyresis, and combinations thereof, said method comprising the step of administering to said individual a compound of the formula of claim 1 .

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Dec 24, 2015
From: BRIGHTSTAR ASSOCIATES, LLC
To: DECIPHERA PHARMACEUTICALS, LLC
Reel/Frame 037359/0831 →
RELEASE OF SECURITY INTEREST Recorded Dec 24, 2015
From: BRIGHTSTAR ASSOCIATES, LLC
To: DECIPHERA PHARMACEUTICALS, LLC
Reel/Frame 037359/0866 →
SECURITY INTEREST Recorded Aug 10, 2015
From: DECIPHERA PHARMACEUTICALS, LLC
To: BRIGHTSTAR ASSOCIATES LLC
Reel/Frame 036288/0037 →
SECURITY INTEREST Recorded Aug 10, 2015
From: DECIPHERA PHARMACEUTICALS, LLC
To: BRIGHTSTAR ASSOCIATES LLC
Reel/Frame 036315/0091 →
SECURITY INTEREST Recorded Aug 10, 2015
From: DECIPHERA PHARMACEUTICALS, LLC
To: BRIGHTSTAR ASSOCIATES LLC
Reel/Frame 036315/0188 →
SECURITY AGREEMENT Recorded Jul 5, 2012
From: DECIPHERA PHARMACEUTICALS, LLC
To: BRIGHTSTAR ASSOCIATES LLC
Reel/Frame 028503/0011 →