Inhibitors of P38

Details Inhibitors of P38 Inhibitors of P38

2000-12-21

2003-10-14

Shah, Mukund J. (Department: 1624)

Organic compounds -- part of the class 532-570 series

Organic compounds

Heterocyclic carbon compounds containing a hetero ring...

C546S288000, C546S289000, C544S111000, C544S360000, C540S470000, C540S575000, C514S336000, C514S252130, C514S231500, C514S218000

Reexamination Certificate

active

06632945

ABSTRACT:

TECHNICAL FIELD OF INVENTION
The present invention relates to inhibitors of p38, a mammalian protein kinase involved in cell proliferation, cell death and response to extracellular stimuli. The invention also relates to methods for producing these inhibitors. The invention also provides pharmaceutical compositions comprising the inhibitors of the invention and methods of utilizing those compositions in the treatment and prevention of various disorders.
BACKGROUND OF THE INVENTION
Protein kinases are involved in various cellular responses to extracellular signals. Recently, a family of mitogen-activated protein kinases (MAPK) has been discovered. Members of this family are Ser/Thr kinases that activate their substrates by phosphorylation [B. Stein et al., Ann. Rep. Med. Chem., 31, pp. 289-98 (1996)]. MAPKs are themselves activated by a variety of signals including growth factors, cytokines, UV radiation, and stress-inducing agents.
One particularly interesting MAPK is p38. p38, also known as cytokine suppressive anti-inflammatory drug binding protein (CSBP) and RK, was isolated from murine pre-B cells that were transfected with the lipopolysaccharide (LPS) receptor, CD14, and induced with LPS. p38 has since been isolated and sequenced, as has the cDNA encoding it in humans and mouse. Activation of p38 has been observed in cells stimulated by stress, such as treatment of lipopolysaccharides (LPS), UV, anisomycin, or osmotic shock, and by cytokines, such as IL-1 and TNF.
Inhibition of p38 kinase leads to a blockade on the production of both IL-1 and TNF. IL-1 and TNF stimulate the production of other proinflammatory cytokines such as IL-6 and IL-8 and have been implicated in acute and chronic inflammatory diseases and in post-menopausal osteoporosis [R. B. Kimble et al., Endocrinol., 136, pp. 3054-61 (1995)].
Based upon this finding, it is believed that p38, along with other MAPKs, have a role in mediating cellular response to inflammatory stimuli, such as leukocyte accumulation, macrophage/monocyte activation, tissue resorption, fever, acute phase responses and neutrophilia. In addition, MAPKs, such as p38, have been implicated in cancer, thrombin-induced platelet aggregation, immunodeficiency disorders, autoimmune diseases, cell death, allergies, osteoporosis and neurodegenerative disorders. Inhibitors of p38 have also been implicated in the area of pain management through inhibition of prostaglandin endoperoxide synthase-2 induction. Other diseases associated with Il-1, IL-6, IL-8 or TNF overproduction are set forth in WO 96/21654.
Others have already begun trying to develop drugs that specifically inhibit MAPKs. For example, PCT publication WO 95/31451 describes pyrazole compounds that inhibit MAPKs, and, in particular, p38.However, the efficacy of these inhibitors in vivo is still being investigated.
Accordingly, there is still a great need to develop other potent inhibitors of p38, including p38-specific inhibitors, that are useful in treating various conditions associated with p38 activation.
SUMMARY OF THE INVENTION
The present invention addresses this problem by providing compounds that demonstrate strong inhibition of p38.
These compounds have the general formula:
wherein each of Q
1
and Q
2
are independently selected from a phenyl or 5-6 membered aromatic heterocyclic ring system, or a 8-10 membered bicyclic ring system comprising aromatic carbocyclic rings, aromatic heterocyclic rings or a combination of an aromatic carbocyclic ring and an aromatic heterocyclic ring.
A heterocyclic ring system or a heterocyclic ring contains 1 to 4 heteroatoms, which are independently selected from N, O, S, SO and SO
2
.
The rings that make up Q
1
are substituted with 1 to 4 substituents, each of which is independently selected from halo; C
1
-C
3
alkyl optionally substituted with NR′
2
, OR′, CO
2
R′ or CONR′
2
; O—(C
1
-C
3
)-alkyl optionally substituted with NR′
2
, OR′, CO
2
R′ or CONR′
2
; NR′
2
; OCF
3
; CF
3
; NO
2
; CO
2
R′; CONR′; SR′; S(O
2
)N(R′)
2
; SCF
3
; CN; N(R′)C(O)R
4
; N(R′)C(O)OR
4
; N(R′)C(O)C(O)R
4
; N(R′)S(O
2
)R
4
; N(R′)R
4
; N(R
4
)
2
; OR
4
; OC(O)R
4
; OP(O)
3
H
2
; or N═C—N(R′)
2
.
The rings that make UP Q
2
are optionally substituted with up to 4 substituents, each of which is independently selected from halo; C
1
-C
3
straight or branched alkyl optionally substituted with NR′
2
, OR′, CO
2
R′, S(O
2
)N(R′)
2
, N═C—N(R′)
2
, R
3
, or CONR′
2
; O—(C
1
-C
3
)-alkyl; O—(C
1
-C
3
)-alkyl optionally substituted with NR′
2
, OR′, CO
2
R′, S(O
2
)N(R′)
2
, N═C—N(R′)
2
, R
3
, or CONR′
2
; NR′
2
; OCF
3
; CF
3
; NO
2
; CO
2
R′; CONR′; R
3
; OR
3
; NR
3
; SR
3
; C(O)R C(O)N(R′)R
3
; C(O)OR; SR′; S(O
2
)N(R′)
2
; SCF
3
; N═C—N(R′)
2
; or CN.
Q
2
′ is selected from phenyl or a 5-6 member aromatic heterocyclic ring optionally substituted with 1-3 substituents, each of which is independently selected from halogen; C
1
-C
3
alkyl optionally substituted with NR′
2
, OR′, CO
2
R′, CONR′
2
, or O—P(O
3
)H
2
; O—(C
2
-C
3
)-alkyl optionally substituted with NR′
2
, OR′, CO
2
R′, CONR′
2
, or OP(O
3
)H
2
; OCF
3
; CF
3
; OR
4
; O—CO
2
R
4
; O—P(O
3
) H
2
; CO
2
R′; CONR′; SR′; S(O
2
)N(R′)
2
; SCF
3
; CN; N(R′)C(O)R
4
; N(R′)C(O)OR
4
; N(R′)C(O)C(O)R′; N(R′) S(O
2
) R
4
; N(R′) R
4
; N(R
4
)
2
; OR
4
; OC(O)R
4
; OP(O)
3
H
2
; or N═C—N(R′)
2
; provided that Q
2
′ is not phenyl optionally substituted 1 to 3 substituents independently selected from halo, methoxy, cyano, nitro, amino, hydroxy, methyl or ethyl.
R′ is selected from hydrogen; (C
1
-C
3
)-alkyl; (C
2
-C
3
)-alkenyl or alkynyl; phenyl or phenyl substituted with 1 to 3 substituents independently selected from halo, methoxy, cyano, nitro, amino, hydroxy, methyl or ethyl; or a 5-6 membered heterocyclic ring system optionally substituted with 1 to 3 substituents independently selected from halo, methoxy, cyano, nitro, amino, hydroxy, methyl or ethyl.
R
3
is selected from 5-8 membered aromatic or non-aromatic carbocyclic or heterocyclic ring systems each optionally substituted with R′, R
4
, —C(O)R′, —C(O)R —C(O)OR
4
or —J; or an 8-10 membered bicyclic ring system comprising aromatic carbocyclic rings, aromatic heterocyclic rings or a combination of an aromatic carbocyclic ring and an aromatic heterocyclic ring each optionally substituted with R′, R
4
, —C(O)R′, —C(O)R
4
, —C(O)OR or —J.
R
4
is (C
1
-C
4
)-straight or branched alkyl optionally substituted with N(R′)
2
, OR′, CO
2
R′, CON(R′)
2
, or SO
2
N(R
2)
2
; or a 5-6 membered carbocyclic or heterocyclic ring system optionally substituted with N(R′)
2
, OR′, CO
2
R′, CON(R′)
2
, or SO
2
N(R
2
)
2
.
R
5
is selected from hydrogen; (C
1
-C
3
)-alkyl optionally substituted with R
3
; (C
2
-C
3
)-alkenyl or alkynyl each optionally substituted with R
3
; phenyl or phenyl substituted with 1 to 3 substituents independently selected from halo, methoxy, cyano, nitro, amino, hydroxy, methyl or ethyl; or a 5-6 membered heterocyclic ring system optionally substituted with 1 to 3 substituents independently selected from halo, methoxy, cyano, nitro, amino, hydroxy, methyl or ethyl.
W is selected from N(R
2
) SO
2
—N(R
2
)
2
; N(R
2
)SO
2
—N(R
2
)(R
3
); N(R
2
)C(O)—OR
2
; N(R
2
)C(O)—N(R
2
)
2
; N(R
2
)C(O)—N(R
2
)(R
3
); N(R
2
)C(O)—R
2
; N(R
2
)
2
; C(O)—R
2
; CH(OH)—R
2
; C(O)—N(R
2
)
2
; C(O)—OR
2
; J; or (C
1
-C
4
) straight or branched alkyl optionally substituted with N(R′)
2
, OR′, CO
2
R′, CON(R′)
2
, R
3
, SO
2
N(R
2
)
2
, OC(O)R′, OC(O)R′, OC(O)N(R′)
2
, —N(R′)(R
5
), —C(O)N(R
5
)(R
2
), —C(O)R′, —N(R
2
)C(O)N(R
2
)(R
5
), —NC(O)OR
5
,

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