AR046083A1 - Derivados de 2 piridona como inhibidores de la elastasa de neutrofilos - Google Patents
Derivados de 2 piridona como inhibidores de la elastasa de neutrofilosInfo
- Publication number
- AR046083A1 AR046083A1 ARP040103354A ARP040103354A AR046083A1 AR 046083 A1 AR046083 A1 AR 046083A1 AR P040103354 A ARP040103354 A AR P040103354A AR P040103354 A ARP040103354 A AR P040103354A AR 046083 A1 AR046083 A1 AR 046083A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- optionally further
- further substituted
- independently selected
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 18
- 229910052760 oxygen Inorganic materials 0.000 abstract 16
- 229910052717 sulfur Inorganic materials 0.000 abstract 16
- 125000005842 heteroatom Chemical group 0.000 abstract 14
- 125000000217 alkyl group Chemical group 0.000 abstract 12
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 11
- 125000001072 heteroaryl group Chemical group 0.000 abstract 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 9
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 8
- 229920006395 saturated elastomer Polymers 0.000 abstract 8
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 229910052757 nitrogen Inorganic materials 0.000 abstract 7
- 125000001589 carboacyl group Chemical group 0.000 abstract 5
- 125000004429 atom Chemical group 0.000 abstract 4
- 125000001153 fluoro group Chemical group F* 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- -1 CO2R47 Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
- C07D213/85—Nitriles in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/02—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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto caracterizado porque responde a la fórmula (1), en donde: Y representa CR3 o N; R1 representa H o (C1-6) alquilo; R2 representa: i) CN, NO2, OH, OSO2R47, O-(C2-6) alcanoilo, CO2R47, CHO o (C2-6) alcanoilo; o ii) (C1-6) alcoxi opcionalmente sustituido por OH, (C1-6) alcoxi, CN, NR54R55, CONR54R55, OCOR47 o uno o más átomos de F; o iii) (C3-6) cicloalquilo saturado o parcialmente insaturado opcionalmente sustituido adicionalmente por (C1-6) alquilo; o iv) un anillo heterocíclico (C4-7) saturado o parcialmente insaturado que contiene entre 1 y 3 heteroátomos seleccionados en forma independiente entre O, S(O)m y NR62 opcionalmente sustituido adicionalmente por (C1-6) alquilo; o v) CONR48R49, CONR50NR48R49, C(=NOR52)R53, C(=NH)NHOR52 o NR48R49; o (C2-6) alquenilo o (C2-6) alquinilo; estando dicho grupo alquenilo o alquinilo opcionalmente sustituido adicionalmente por (C1-6) alcoxi o fenilo o un anillo heteroaromático de cinco o seis miembros que contiene entre 1 y 3 heteroátomos seleccionados en forma independiente entre O, S y N; estando dicho anillo fenilo o heteroaromático opcionalmente sustituido adicionalmente por halógeno, CN, (C1-6) alquilo o (C1-6) alcoxi; o vii) (C1-6) alquilo sustituido por uno o más átomos de F; o viii) (C1-6) alquilo sustituido por uno o más grupos seleccionados entre halógeno, OH, oxo, azido, R48R49, (C1-6) alcoxi y (C1-6) alcoxi sustituido por uno o más átomos de F; o ix) (C1-6) alquilo sustituido por fenilo o un anillo heteroaromático de cinco o seis miembros que contiene entre 1 y 3 heteroátomos seleccionados en forma independiente entre O, S y N; estando dicho anillo fenilo o heteroaromático opcionalmente sustituido adicionalmente por halógeno, CN, (C1-6) alquilo o (C1-6) alcoxi; R48 y R49 en forma independiente representan H, OH, (C1-6) alcoxi, (C3-6) cicloalquilo, CHO, (C2-6) alcanoilo, CO2R50, C(X)NR63R64 o (C1-6) alquilo; estando dicho alquilo opcionalmente sustituido adicionalmente por OH, (C1-4) alcoxi, (C3-6) cicloalquilo, CN, o fenilo o un anillo heteroaromático de cinco o seis miembros que contiene entre 1 y 3 heteroátomos seleccionados en forma independiente entre O, S y N; estando dicho alcanoilo opcionalmente sustituido adicionalmente por CN; X representa O o S; o el grupo R48R49 en conjunto representa un anillo azacíclico saturado o parcialmente insaturado de 5 a 7 miembros que incorpora opcionalmente un heteroátomo adicional seleccionado entre O, S y NR56; estando dicho anillo azacíclico opcionalmente sustituido adicionalmente por uno o más sustituyentes seleccionados entre OR57 y (C1-4) alquilo; estando dicho alquilo opcionalmente sustituido adicionalmente por OR57; R3 representa H o F; G1 representa fenilo o un anillo heteroaromático de cinco o seis miembros que contiene entre 1 y 3 heteroátomos seleccionados en forma independiente entre O, S y N; R5 representa H, halógeno, (C1-6) alquilo, CN, (C1-6) alcoxi, NO2, NR14R15, (C1- 3) alquilo sustituido por uno o más átomos de F o (C1-3) alcoxi sustituido por uno o más átomos de F; R14 y R15 en forma independiente representan H o (C1-3) alquilo; estando dicho alquilo opcionalmente sustituido adicionalmente por uno o más átomos de F; n representan un entero 1, 2 ó 3 y cuando n representa 2 ó 3, cada grupo R5 se selecciona en forma independiente; R4 representa H o (C1-6) alquilo, estando dicho alquilo opcionalmente sustituido adicionalmente por OH o (C1-6) alcoxi; o R4 y L están unidos de forma tal que el grupo -R4L representan un anillo azacíclico de 5 a 7 miembros que incorpora opcionalmente un heteroátomo adicional seleccionado entre O, S y NR16; estando dicho anillo opcionalmente sustituido adicionalmente por (C1- 6) alquilo o NR60R61; estando dicho alquilo opcionalmente sustituido adicionalmente por OH; L representa un enlace, O, NR29 o (C1-6) alquilo; donde dicho alquilo incorpora opcionalmente un heteroátomo seleccionado entre O, S y NR16; y estando dicho alquilo opcionalmente sustituido adicionalmente por OH o OMe; G2 representa un sistema de anillo monocíclico seleccionado entre: i) fenilo o fenoxi; ii) un anillo heteroaromático de 5 ó 6 miembros que contiene entre uno y tres heteroátomos seleccionados en forma independiente entre O, S y N; iii) un cicloalquilo (C3-6) saturado o parcialmente insaturado; o iv) un anillo heterocíclico (C4-7) saturado o parcialmente insaturado que contiene uno o dos heteroátomos seleccionados en forma independiente entre O, S(O)p y NR17 y que opcionalmente incorpora además un grupo carbonilo; o G2 representa un sistema de anillo bicíclico en donde cada uno de los dos anillos se selecciona en forma independiente entre: i) fenilo; ii) un anillo heteroaromático de 5 ó 6 miembros que contiene entre uno y tres heteroátomos seleccionados en forma independiente entre O, S y N; iii) un cicloalquilo (C3-6) saturado o parcialmente insaturado; o iv) un anillo heterocíclico (C4-7) saturado o parcialmente insaturado que contiene uno o dos heteroátomos seleccionados en forma independiente entre O, S(O)p y NR17 y que opcionalmente incorpora además un grupo carbonilo; y los dos anillos o bien están fusionados, o están unidos directamente juntos o están separados por un grupo ligante seleccionado entre O, S(O)q o CH2; estando dicho sistema de anillo monocíclico o bicíclico opcionalmente sustituido adicionalmente por entre uno y tres sustituyentes seleccionados en forma independiente entre CN, OH, (C1-6) alquilo, (C1-6) alcoxi, halógeno, NR18R19, NO2, OSO2R38, CO2R20, C(=NH)NH2, C(O)NR21R22, C(S)NR23R24, SC(=NH)NH2, NR31C(=NH)NH2, S(O)SR25, SO2NR26R27, (C1-3) alcoxi sustituido por uno o más átomos de F y (C1-3) alquilo sustituido por SO2R39 o por uno o más átomos de F; o cuando L no representa un enlace, G2 también puede representar H; en cada caso m, p, q, s y t en forma independiente representa un entero 0, 1 ó 2; R18 yR19 en forma independiente representan H, (C1-6) alquilo, formilo, (C2-6) alcanoilo, S(O)tR32 o SO2NR33R34; estando dicho grupo alquilo opcionalmente sustituido adicionalmente por halógeno, CN, (C1-4) alcoxi o COR41R42; R25 representa H, (C1-6) alquilo o (C3-6) cicloalquilo; estando dicho grupo alquilo opcionalmente sustituido adicionalmente por uno o más sustituyentes seleccionados en forma independiente entre OH, CN, CONR35R36, CO2R37, OCOR40, (C3-6) cicloalquilo, un anillo heterocíclico saturado de C4-7 que contiene uno o dos heteroátomos seleccionados en forma independiente entre O, S(O)p y R43 y fenilo o un anillo heteroaromático de 5 ó 6 miembros que contiene entre uno y tres heteroátomos seleccionados en forma independiente entre O, S y N; estando dicho anillo aromático opcionalmente sustituido adicionalmente por uno o más sustituyentes seleccionados en forma independiente entre halógeno, CN, (C1-4) alquilo, (C1-4) alcoxi, OH, CONR44R45, CO2R46, S(O)SR65 y NHCOCH3; R32 representa H, (C1-6) alquilo o (C3- 6) cicloalquilo; R16, R17, R20, R21, R22, R23, R24, R26, R27, R29, R31, R33, R34, R35, R36, R37, R38, 39, R40, R41, R42, R43, R44, R45, R46, R47, R50, R52, R53, R54, R55, R56, R57, R60, R61, R62, R63, R64 y R65 en forma independiente representan H o (C1-6) alquilo; y sus sales aceptables para uso farmacéutico.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0302487A SE0302487D0 (sv) | 2003-09-18 | 2003-09-18 | Novel compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR046083A1 true AR046083A1 (es) | 2005-11-23 |
Family
ID=29212489
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040103354A AR046083A1 (es) | 2003-09-18 | 2004-09-17 | Derivados de 2 piridona como inhibidores de la elastasa de neutrofilos |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US20070043036A1 (es) |
| EP (1) | EP1663974B1 (es) |
| JP (1) | JP2007505902A (es) |
| KR (1) | KR20060096995A (es) |
| CN (1) | CN100439339C (es) |
| AR (1) | AR046083A1 (es) |
| AT (1) | ATE420861T1 (es) |
| AU (1) | AU2004272485B2 (es) |
| BR (1) | BRPI0414570A (es) |
| CA (1) | CA2538410A1 (es) |
| CO (1) | CO5670357A2 (es) |
| DE (1) | DE602004019110D1 (es) |
| ES (1) | ES2319300T3 (es) |
| IL (1) | IL173986A0 (es) |
| IS (1) | IS8394A (es) |
| MX (1) | MXPA06002723A (es) |
| NO (1) | NO20061700L (es) |
| RU (1) | RU2348617C2 (es) |
| SA (1) | SA04250300B1 (es) |
| SE (1) | SE0302487D0 (es) |
| TW (1) | TW200526579A (es) |
| UA (1) | UA84878C2 (es) |
| UY (1) | UY28513A1 (es) |
| WO (1) | WO2005026124A1 (es) |
| ZA (1) | ZA200602262B (es) |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200500341A (en) * | 2002-11-12 | 2005-01-01 | Astrazeneca Ab | Novel compounds |
| SE0302486D0 (sv) * | 2003-09-18 | 2003-09-18 | Astrazeneca Ab | Novel compounds |
| US7459562B2 (en) | 2004-04-23 | 2008-12-02 | Bristol-Myers Squibb Company | Monocyclic heterocycles as kinase inhibitors |
| TW200538453A (en) | 2004-04-26 | 2005-12-01 | Bristol Myers Squibb Co | Bicyclic heterocycles as kinase inhibitors |
| US7432373B2 (en) | 2004-06-28 | 2008-10-07 | Bristol-Meyers Squibb Company | Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors |
| US20050288290A1 (en) | 2004-06-28 | 2005-12-29 | Borzilleri Robert M | Fused heterocyclic kinase inhibitors |
| US7439246B2 (en) | 2004-06-28 | 2008-10-21 | Bristol-Myers Squibb Company | Fused heterocyclic kinase inhibitors |
| TW200700392A (en) * | 2005-03-16 | 2007-01-01 | Astrazeneca Ab | Novel compounds |
| PT1928454E (pt) * | 2005-05-10 | 2014-12-04 | Intermune Inc | Derivativos da piridona para modulação do sistema de proteína quinase ativada pelo stress |
| GB0516313D0 (en) | 2005-08-08 | 2005-09-14 | Argenta Discovery Ltd | Azole derivatives and their uses |
| US7994211B2 (en) | 2005-08-08 | 2011-08-09 | Argenta Discovery Limited | Bicyclo[2.2.1]hept-7-ylamine derivatives and their uses |
| JP2009509979A (ja) * | 2005-09-29 | 2009-03-12 | ユニバーシティ オブ アルバータ | グランザイムb阻害のための組成物および方法 |
| GB0605469D0 (en) * | 2006-03-17 | 2006-04-26 | Argenta Discovery Ltd | Multimers of heterocyclic compounds and their use |
| TW200808771A (en) * | 2006-05-08 | 2008-02-16 | Astrazeneca Ab | Novel compounds II |
| TW200808763A (en) * | 2006-05-08 | 2008-02-16 | Astrazeneca Ab | Novel compounds I |
| US8470859B2 (en) | 2006-10-23 | 2013-06-25 | Takeda Pharmaceutical Company Limited | Iminopyridine derivative and use thereof |
| PT2089364E (pt) | 2006-11-08 | 2013-08-26 | Bristol Myers Squibb Co | Compostos de piridinona |
| CL2008003301A1 (es) | 2007-11-06 | 2009-10-16 | Astrazeneca Ab | Compuestos derivados de 3,4-dihidropirazina-2-carboxamida, inhibidores de la elastasa de neutrofilos humanos; composiciones farmacéuticas; procesos de preparación de compuestos y composición farmacéutica; y uso en el tratamiento de síndrome de dificultad respiratoria de los adultos, fibrosis quística, cáncer, entre otras. |
| CN101970405A (zh) | 2007-12-14 | 2011-02-09 | 普尔马金医疗(哮喘)有限公司 | 吲哚及其治疗用途 |
| AU2009206440B2 (en) | 2008-01-23 | 2013-08-15 | Bristol-Myers Squibb Company | 4-pyridinone compounds and their use for cancer |
| US8481569B2 (en) | 2008-04-23 | 2013-07-09 | Takeda Pharmaceutical Company Limited | Iminopyridine derivatives and use thereof |
| EP2296653B1 (en) | 2008-06-03 | 2016-01-27 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
| GB0902648D0 (en) | 2009-02-17 | 2009-04-01 | Argenta Discovery Ltd | Pharmaceutical compounds and compositions |
| JP2012517992A (ja) | 2009-02-17 | 2012-08-09 | チェシ ファーマスーティシ エス.ピー.エイ. | P38mapキナーゼインヒビターとしてのトリアゾロピリジン誘導体 |
| TW201036957A (en) | 2009-02-20 | 2010-10-16 | Astrazeneca Ab | Novel salt 628 |
| RU2012116877A (ru) * | 2009-10-02 | 2013-11-10 | Астразенека Аб | Соединения 2-пиридона, применяемые в качестве ингибиторов нейтрофильной эластазы |
| GB0918922D0 (en) | 2009-10-28 | 2009-12-16 | Vantia Ltd | Aminopyridine derivatives |
| GB0918924D0 (en) | 2009-10-28 | 2009-12-16 | Vantia Ltd | Azaindole derivatives |
| GB0918923D0 (en) | 2009-10-28 | 2009-12-16 | Vantia Ltd | Aminothiazole derivatives |
| IN2012DN05081A (es) * | 2009-12-08 | 2015-10-09 | Boehringer Ingelheim Int | |
| GB201009731D0 (en) | 2010-06-10 | 2010-07-21 | Pulmagen Therapeutics Inflamma | Kinase inhibitors |
| EP2740728A4 (en) | 2011-08-01 | 2015-04-01 | Sumitomo Dainippon Pharma Co Ltd | URACIL DERIVATIVE AND ITS USE FOR MEDICAL PURPOSES |
| SG10201604656YA (en) | 2011-12-09 | 2016-07-28 | Chiesi Farma Spa | Kinase inhibitors |
| PT2788349T (pt) | 2011-12-09 | 2017-02-02 | Chiesi Farm Spa | Inibidores de cinase |
| BR112014013178A2 (pt) | 2011-12-09 | 2017-06-13 | Chiesi Farm Spa | composto, composição farmacêutica e uso de um composto |
| US20140057926A1 (en) | 2012-08-23 | 2014-02-27 | Boehringer Ingelheim International Gmbh | Substituted 4-pyridones and their use as inhibitors of neutrophil elastase activity |
| US9102624B2 (en) | 2012-08-23 | 2015-08-11 | Boehringer Ingelheim International Gmbh | Substituted 4-pyridones and their use as inhibitors of neutrophil elastase activity |
| US20140057920A1 (en) | 2012-08-23 | 2014-02-27 | Boehringer Ingelheim International Gmbh | Substituted 4-pyridones and their use as inhibitors of neutrophil elastase activity |
| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
| BR112015029970A2 (pt) | 2013-06-06 | 2017-07-25 | Chiesi Farm Spa | inibidores de cinase |
| US9221807B2 (en) * | 2014-02-21 | 2015-12-29 | Boehringer Ingelheim International Gmbh | Substituted pyridones and pyrazinones and their use as inhibitors of neutrophil elastase activity |
| WO2015153683A1 (en) | 2014-04-02 | 2015-10-08 | Intermune, Inc. | Anti-fibrotic pyridinones |
| AR105875A1 (es) | 2015-09-02 | 2017-11-15 | GLAXOSMITHKLINE INTELLECTUAL PROPERTY (Nº 2) LTD | Derivados de 2-oxo-1,2-dihidropiridina como inhibidores de bromodominio |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9207145D0 (en) * | 1991-04-18 | 1992-05-13 | Ici Plc | Heterocyclic amides |
| US5521179A (en) * | 1991-04-18 | 1996-05-28 | Zeneca Limited | Heterocyclic amides |
| FR2687674B1 (fr) * | 1992-02-07 | 1995-05-19 | Roussel Uclaf | Nouveaux derives de la pyridone, leur procede de preparation, les nouveaux intermediaires obtenus, leur application a titre de medicaments et les compositions pharmaceutiques les renfermant. |
| EP0729464A1 (en) * | 1993-11-19 | 1996-09-04 | PARKE, DAVIS & COMPANY | 5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents |
| RU2067579C1 (ru) * | 1994-10-07 | 1996-10-10 | Пермский фармацевтический институт | 3-(2'-нафтоилметилен)-пиперазинон-2 и 1-n-фенил-3-фенацилиденпиперазинон-2, проявляющие противовоспалительную активность |
| KR100828982B1 (ko) * | 2000-12-28 | 2008-05-14 | 시오노기세이야쿠가부시키가이샤 | 칸나비노이드 2형 수용체 친화 작용을 갖는 피리돈 유도체 |
| GB0129260D0 (en) * | 2001-12-06 | 2002-01-23 | Eisai London Res Lab Ltd | Pharmaceutical compositions and their uses |
| EP1458682B1 (en) * | 2001-12-20 | 2006-08-30 | Bayer HealthCare AG | 1,4-dihydro-1,4-diphenylpyridine derivatives |
| GB2383326A (en) * | 2001-12-20 | 2003-06-25 | Bayer Ag | Antiinflammatory dihydropyridines |
| TW200500341A (en) * | 2002-11-12 | 2005-01-01 | Astrazeneca Ab | Novel compounds |
| SE0302486D0 (sv) * | 2003-09-18 | 2003-09-18 | Astrazeneca Ab | Novel compounds |
-
2003
- 2003-09-18 SE SE0302487A patent/SE0302487D0/xx unknown
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2004
- 2004-09-13 TW TW093127678A patent/TW200526579A/zh unknown
- 2004-09-15 RU RU2006112427/04A patent/RU2348617C2/ru not_active IP Right Cessation
- 2004-09-15 EP EP04775439A patent/EP1663974B1/en not_active Expired - Lifetime
- 2004-09-15 ES ES04775439T patent/ES2319300T3/es not_active Expired - Lifetime
- 2004-09-15 KR KR1020067005458A patent/KR20060096995A/ko not_active Withdrawn
- 2004-09-15 CA CA002538410A patent/CA2538410A1/en not_active Abandoned
- 2004-09-15 WO PCT/SE2004/001336 patent/WO2005026124A1/en not_active Ceased
- 2004-09-15 CN CNB2004800275174A patent/CN100439339C/zh not_active Expired - Fee Related
- 2004-09-15 JP JP2006526856A patent/JP2007505902A/ja active Pending
- 2004-09-15 UY UY28513A patent/UY28513A1/es unknown
- 2004-09-15 UA UAA200602252A patent/UA84878C2/ru unknown
- 2004-09-15 BR BRPI0414570-4A patent/BRPI0414570A/pt not_active IP Right Cessation
- 2004-09-15 US US10/572,640 patent/US20070043036A1/en not_active Abandoned
- 2004-09-15 AU AU2004272485A patent/AU2004272485B2/en not_active Ceased
- 2004-09-15 DE DE602004019110T patent/DE602004019110D1/de not_active Expired - Fee Related
- 2004-09-15 AT AT04775439T patent/ATE420861T1/de not_active IP Right Cessation
- 2004-09-15 MX MXPA06002723A patent/MXPA06002723A/es unknown
- 2004-09-17 AR ARP040103354A patent/AR046083A1/es not_active Application Discontinuation
- 2004-09-18 SA SA4250300A patent/SA04250300B1/ar unknown
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2006
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- 2006-03-15 CO CO06026211A patent/CO5670357A2/es not_active Application Discontinuation
- 2006-03-17 ZA ZA200602262A patent/ZA200602262B/xx unknown
- 2006-03-31 IS IS8394A patent/IS8394A/is unknown
- 2006-04-18 NO NO20061700A patent/NO20061700L/no not_active Application Discontinuation
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| IS8394A (is) | 2006-03-31 |
| TW200526579A (en) | 2005-08-16 |
| IL173986A0 (en) | 2006-07-05 |
| EP1663974A1 (en) | 2006-06-07 |
| MXPA06002723A (es) | 2006-06-06 |
| CN1856467A (zh) | 2006-11-01 |
| JP2007505902A (ja) | 2007-03-15 |
| HK1089167A1 (en) | 2006-11-24 |
| EP1663974B1 (en) | 2009-01-14 |
| DE602004019110D1 (de) | 2009-03-05 |
| SE0302487D0 (sv) | 2003-09-18 |
| ATE420861T1 (de) | 2009-01-15 |
| CN100439339C (zh) | 2008-12-03 |
| CO5670357A2 (es) | 2006-08-31 |
| UY28513A1 (es) | 2005-04-29 |
| UA84878C2 (ru) | 2008-12-10 |
| AU2004272485B2 (en) | 2008-03-13 |
| ES2319300T3 (es) | 2009-05-06 |
| RU2006112427A (ru) | 2007-11-10 |
| NO20061700L (no) | 2006-04-18 |
| BRPI0414570A (pt) | 2006-11-07 |
| WO2005026124A1 (en) | 2005-03-24 |
| US20070043036A1 (en) | 2007-02-22 |
| ZA200602262B (en) | 2007-07-25 |
| CA2538410A1 (en) | 2005-03-24 |
| SA04250300B1 (ar) | 2008-09-07 |
| KR20060096995A (ko) | 2006-09-13 |
| RU2348617C2 (ru) | 2009-03-10 |
| AU2004272485A1 (en) | 2005-03-24 |
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