BRPI0408990A - derivados de pirimidin-4-ona e sua utilização como moduladores da p38-cinase - Google Patents
derivados de pirimidin-4-ona e sua utilização como moduladores da p38-cinaseInfo
- Publication number
- BRPI0408990A BRPI0408990A BRPI0408990-1A BRPI0408990A BRPI0408990A BR PI0408990 A BRPI0408990 A BR PI0408990A BR PI0408990 A BRPI0408990 A BR PI0408990A BR PI0408990 A BRPI0408990 A BR PI0408990A
- Authority
- BR
- Brazil
- Prior art keywords
- compounds
- derivatives
- pyrimidin
- kinase modulators
- methods
- Prior art date
Links
- 102000002574 p38 Mitogen-Activated Protein Kinases Human genes 0.000 title abstract 2
- 108010068338 p38 Mitogen-Activated Protein Kinases Proteins 0.000 title abstract 2
- DNCYBUMDUBHIJZ-UHFFFAOYSA-N 1h-pyrimidin-6-one Chemical class O=C1C=CN=CN1 DNCYBUMDUBHIJZ-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 5
- 238000000034 method Methods 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/34—One oxygen atom
- C07D239/36—One oxygen atom as doubly bound oxygen atom or as unsubstituted hydroxy radical
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Neurosurgery (AREA)
- Toxicology (AREA)
- Emergency Medicine (AREA)
- AIDS & HIV (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
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- Biotechnology (AREA)
Abstract
"DERIVADOS DE PIRIMIDIN-4-ONA E SUA UTILIZAçãO COMO MODULADORES DA P38-CINASE". São descritos compostos de Fórmula I e sais farmaceuticamente aceitáveis destes, em que R~ 1~, R~ 2~, R~ 4~ e R~ 5~ estão aqui definidos. Estes compostos são úteis para tratar doenças e estados provocados ou exacerbados pela atividade não regulada da p38 MAP cinase e/ou TNF. São também descritas formulações farmacêuticas que contêm os compostos, métodos de preparar os compostos e métodos de tratamento utilizando os compostos.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US46012403P | 2003-04-03 | 2003-04-03 | |
PCT/IB2004/001121 WO2004087677A2 (en) | 2003-04-03 | 2004-03-29 | Pyrimidin-4-one derivatives and their use as p38 kinase modulators |
Publications (1)
Publication Number | Publication Date |
---|---|
BRPI0408990A true BRPI0408990A (pt) | 2006-04-04 |
Family
ID=33131912
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0408990-1A BRPI0408990A (pt) | 2003-04-03 | 2004-03-29 | derivados de pirimidin-4-ona e sua utilização como moduladores da p38-cinase |
Country Status (24)
Country | Link |
---|---|
US (1) | US7183287B2 (pt) |
EP (1) | EP1753731A2 (pt) |
JP (1) | JP3981398B1 (pt) |
KR (1) | KR100776120B1 (pt) |
CN (1) | CN1968937A (pt) |
AP (1) | AP2005003403A0 (pt) |
AU (1) | AU2004226165C1 (pt) |
BR (1) | BRPI0408990A (pt) |
CA (1) | CA2521081C (pt) |
CR (1) | CR8007A (pt) |
EA (1) | EA009743B1 (pt) |
EC (1) | ECSP056072A (pt) |
GE (1) | GEP20074255B (pt) |
IS (1) | IS8006A (pt) |
MA (1) | MA27754A1 (pt) |
MX (1) | MXPA05010621A (pt) |
NO (1) | NO20055092L (pt) |
NZ (1) | NZ542139A (pt) |
OA (1) | OA13113A (pt) |
RS (1) | RS20050732A (pt) |
TN (1) | TNSN05250A1 (pt) |
UA (1) | UA81658C2 (pt) |
WO (1) | WO2004087677A2 (pt) |
ZA (1) | ZA200506976B (pt) |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070167621A1 (en) * | 2003-04-03 | 2007-07-19 | Pharmacia Corporation | Substituted pyrimidinones |
ATE412652T1 (de) | 2004-08-12 | 2008-11-15 | Pfizer | Triazolopyridinylsulfanylderivate als inhibitoren der p38-map-kinase |
EP1802589B1 (en) * | 2004-10-13 | 2014-04-09 | Pharmacia & Upjohn Company LLC | Crystalline forms of 3-[5-chloro-4-[(2,4-difluorobenzyl) oxy]-6-oxopyrimidin-1(6h)-yl]-n-(2-hydroxyethyl)-4-methylbenzamide |
WO2006040666A1 (en) * | 2004-10-13 | 2006-04-20 | Pharmacia & Upjohn Company Llc | Substituted n-alkylpyrimidinones |
WO2007081901A2 (en) * | 2006-01-05 | 2007-07-19 | The Scripps Research Institute | Pyrimidinone derivatives as protein kinase inhibitors |
CA2640665A1 (en) * | 2006-02-10 | 2007-08-16 | Pfizer Products Inc. | Pyridinone pyrazole urea and pyrimidinone pyrazole urea derivatives |
US7588924B2 (en) | 2006-03-07 | 2009-09-15 | Procter & Gamble Company | Crystal of hypoxia inducible factor 1 alpha prolyl hydroxylase |
PL3026044T3 (pl) | 2006-06-26 | 2019-04-30 | Akebia Therapeutics Inc | Inhibitory prolilo-hydroksylazy i sposoby ich użycia |
EP2383259A1 (en) | 2006-08-25 | 2011-11-02 | Boehringer Ingelheim International GmbH | New pyridone derivatives with MCH antagonistic activity and medicaments comprising these compounds |
WO2008071646A1 (en) | 2006-12-11 | 2008-06-19 | Boehringer Ingelheim International Gmbh | New pyridazine derivatives with mch antagonistic activity and medicaments comprising these compounds |
TW200845994A (en) * | 2007-01-12 | 2008-12-01 | Smithkline Beecham Corp | N-substituted glycine derivatives: prolyl hydroxylase inhibitors |
WO2008153942A1 (en) * | 2007-06-06 | 2008-12-18 | Xcovery, Inc. | Kinase inhibitor compounds |
WO2010138585A1 (en) * | 2009-05-29 | 2010-12-02 | Merck Sharp & Dohme Corp. | Pyrimidinones as pde10 inhibitors |
EP2649998B1 (en) * | 2009-11-06 | 2015-03-04 | Aerpio Therapeutics Inc. | Prolyl hydroxylase inhibitors |
US8507499B2 (en) | 2010-12-06 | 2013-08-13 | Confluence Life Sciences, Inc. | Substituted indole/indazole-pyrimidinyl compounds |
PL2648516T3 (pl) | 2010-12-06 | 2019-04-30 | Aclaris Therapeutics Inc | Podstawione związki pirydynono-pirydynylowe |
WO2012078673A1 (en) | 2010-12-06 | 2012-06-14 | Confluence Life Sciences, Inc. | Substituted pyridine urea compounds |
US9359300B2 (en) | 2010-12-06 | 2016-06-07 | Confluence Life Sciences, Inc. | Methyl/difluorophenyl-methoxy substituted pyridinone-pyridinyl compounds, methyl-pyridinyl-methoxy substituted pyridinone-pyridinyl compounds, and methyl-pyrimidinyl-methoxy substituted pyridinone-pyridinyl compounds |
NO2686520T3 (pt) | 2011-06-06 | 2018-03-17 | ||
MX2014000536A (es) | 2011-07-13 | 2014-12-05 | Novartis Ag | Compuestos de 4-piperidinilo para usarse como inhibidores de tanquirasa. |
JP2014520860A (ja) | 2011-07-13 | 2014-08-25 | ノバルティス アーゲー | タンキラーゼ阻害剤として使用するための4−オキソ−3,5,7,8−テトラヒドロ−4H−ピラノ{4,3−d}ピルミニジニル化合物 |
WO2013012723A1 (en) | 2011-07-13 | 2013-01-24 | Novartis Ag | Novel 2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors |
US9056110B2 (en) | 2011-12-06 | 2015-06-16 | Confluence Life Sciences, Inc. | Substituted pyrimidinone-phenyl-pyrimidinyl compounds |
US9365540B2 (en) | 2012-01-12 | 2016-06-14 | Takeda Pharmaceutical Company Limited | Benzimidazole derivatives as MCH receptor antagonists |
US9434695B2 (en) | 2012-07-18 | 2016-09-06 | Sunshine Lake Pharma Co., Ltd | Nitrogenous heterocyclic derivatives and their application in drugs |
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JPS61205261A (ja) * | 1985-03-08 | 1986-09-11 | Sagami Chem Res Center | 6―置換―5―フルオロウラシル誘導体 |
AU7798994A (en) * | 1993-10-20 | 1995-05-08 | Upjohn Company, The | Pyrimidinones as antiarthritic and anti-inflammatories |
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WO1999064400A1 (en) * | 1998-06-12 | 1999-12-16 | Vertex Pharmaceuticals Incorporated | INHIBITORS OF p38 |
AU2247701A (en) * | 1999-10-21 | 2001-04-30 | Merck & Co., Inc. | Gram-positive selective antibacterial compounds, compositions containing such compounds and methods of treatment |
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2004
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- 2004-03-29 CN CNA2004800156300A patent/CN1968937A/zh active Pending
- 2004-03-29 UA UAA200508500A patent/UA81658C2/ru unknown
- 2004-03-29 RS YUP-2005/0732A patent/RS20050732A/sr unknown
- 2004-03-29 NZ NZ542139A patent/NZ542139A/en unknown
- 2004-03-29 EA EA200501332A patent/EA009743B1/ru unknown
- 2004-03-29 KR KR1020057018627A patent/KR100776120B1/ko not_active IP Right Cessation
- 2004-03-29 WO PCT/IB2004/001121 patent/WO2004087677A2/en active Application Filing
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- 2004-03-29 JP JP2006506466A patent/JP3981398B1/ja not_active Expired - Fee Related
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EP1753731A2 (en) | 2007-02-21 |
AP2005003403A0 (en) | 2005-12-31 |
AU2004226165C1 (en) | 2008-07-03 |
AU2004226165A1 (en) | 2004-10-14 |
CN1968937A (zh) | 2007-05-23 |
IS8006A (is) | 2005-08-29 |
AU2004226165A2 (en) | 2004-10-14 |
TNSN05250A1 (fr) | 2007-07-10 |
US7183287B2 (en) | 2007-02-27 |
EA009743B1 (ru) | 2008-04-28 |
ECSP056072A (es) | 2006-03-01 |
RS20050732A (en) | 2007-08-03 |
JP3981398B1 (ja) | 2007-09-26 |
CA2521081A1 (en) | 2004-10-14 |
MA27754A1 (fr) | 2006-02-01 |
NO20055092L (no) | 2005-11-01 |
US20040242608A1 (en) | 2004-12-02 |
ZA200506976B (en) | 2006-10-25 |
OA13113A (en) | 2006-11-10 |
MXPA05010621A (es) | 2005-11-23 |
EA200501332A1 (ru) | 2006-06-30 |
GEP20074255B (en) | 2007-12-10 |
KR100776120B1 (ko) | 2007-11-16 |
WO2004087677A3 (en) | 2004-12-16 |
NZ542139A (en) | 2008-11-28 |
JP2007528353A (ja) | 2007-10-11 |
WO2004087677A2 (en) | 2004-10-14 |
KR20060006906A (ko) | 2006-01-20 |
CA2521081C (en) | 2010-09-07 |
CR8007A (es) | 2006-02-13 |
UA81658C2 (en) | 2008-01-25 |
AU2004226165B2 (en) | 2007-11-08 |
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