AR060875A1 - Derivados de 2-piridona como inhibidores de la neutrofilo elastasa humana - Google Patents
Derivados de 2-piridona como inhibidores de la neutrofilo elastasa humanaInfo
- Publication number
- AR060875A1 AR060875A1 ARP070101994A ARP070101994A AR060875A1 AR 060875 A1 AR060875 A1 AR 060875A1 AR P070101994 A ARP070101994 A AR P070101994A AR P070101994 A ARP070101994 A AR P070101994A AR 060875 A1 AR060875 A1 AR 060875A1
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- Prior art keywords
- alkyl
- ring
- substituted
- alkoxy
- atoms
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/04—Drugs for disorders of the respiratory system for throat disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
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- 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]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Otolaryngology (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Isomeros opticos, racematos y tautomeros de los mismos, y sus sales aceptables para uso farmacéutico, junto con procesos para su preparacion, composiciones farmacéuticas que los contienen su uso en terapia. Los compuestos son inhibidores de la neutrofilo elastasa humana. Reivindicacion 1: Un compuesto caracterizado porque responde a la formula (1) en donde R1 representa hidrogeno o alquilo C1-6; W representa un anillo heterocíclico de 5 miembros que comprende al menos un heteroátomo en el anillo seleccionando entre nitrogeno, oxigeno y azufre, en donde al menos uno de los átomos de carbono del anillo puede ser opcionalmente reemplazado por un grupo carbonilo; y en donde el anillo heterocíclico está opcionalmente sustituido por al menos un sustituyente seleccionado entre halogeno, alquilo C1-4, alcoxi C1-4, CN, OH, NO2, alquilo C1-3 sustituido con uno o más átomos de F, alcoxi C1-3 sustituido con uno o más átomos de F, NR10R11, C:::CR15, CONR16R17, CHO, alcanoilo C2-4, S(O)xR18 y OSO2R19; R14 representa fenilo o un anillo heteroaromático de 6 miembros que comprende entre 1 y 3 átomos de nitrogeno en el anillo; estando dicho anillo opcionalmente sustituido con al menos un sustituyente seleccionado entre halogeno, alquilo C1-4, alcoxi C1-4, CN, OH, NO2, alquilo C1-3 sustituido con uno o más átomos de F, alcoxi C1-3 sustituido con uno o más átomos de F, NR12R13, C:::CR30, CONR31R32, CHO, alcanoilo C2-4, S(O)pR33 y OSO2R34; R10, R11, R12 y R13 en forma independiente representan H, alquilo C1-6, formilo o alcanoilo C2-6; o el grupo -NR10R11 o -NR12R13 juntos representan un anillo azacíclico de 5 a 7 miembros que incorpora opcionalmente un heteroátomo adicional seleccionado entre O, S y NR26; R15 y R30 en forma independiente representan H, alquilo C1-3 o Si(CH3)3; R18, R19, R33 y R34 en forma independiente representan H o alquilo C1-3; estando dicho alquilo opcionalmente sustituido con uno o más átomos de F; R6 representa H o F; R3 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; estando dicho anillo opcionalmente sustituido con al menos un sustituyente seleccionado entre halogeno, alquilo C1-6, ciano, alcoxi C1-6, nitro, metilcarbonilo, NR35R36, alquilo C1-3 sustituido con uno o más átomos de F o alcoxi C1-3 sustituido con uno o más átomos de F; R35 y R36 en forma independiente representan H o alquilo C1-3; estando dicho alquilo opcionalmente sustituido además con uno o más átomos de F; R4 representa hidrogeno o alquilo C1-6 opcionalmente sustituido con al menos un sustituyente seleccionado entre fluoro, hidroxilo y alcoxi C1-6; X representa un enlace simple, O, NR24 o un grupo -alquileno-C1-6-Y-, en donde Y representa un enlace simple, átomo de oxigeno, NR24 o S(O)w; y estando dicho alquileno opcionalmente sustituido además con OH, halogeno, CN, NR37R38, alcoxi C1-3, CONR39R40, CO2R66, SO2R41 y SO2NR42R43; o R4 y X se unen de modo tal que el grupo -NR4X juntos representan un anillo azacíclico de 5 a 7 miembros que incorpora opcionalmente un heteroátomo adicional seleccionado entre O, S y NR44; estando dicho anillo opcionalmente sustituido con alquilo C1-6 o NR45R46; estando dicho alquilo opcionalmente. sustituido además con OH; R5 representa un sistema de anillos monociclico seleccionado entre i) fenoxi, ii) fenilo, iii) un anillo heteroaromático de 5 o 6 miembros que comprende al menos un heteroátomo en el anillo seleccionando entre nitrogeno, oxígeno y azufre, iv) un anillo cicloalquilo C3-6 saturado o parcialmente insaturado, o v) un anillo heterocíclico saturado o parcialmente insaturado de 4 a 7 miembros que comprende al menos un heteroátomo en el anillo seleccionando entre oxígeno, S(O)r y NR20, en donde al menos uno de los átomos de carbono del anillo puede ser opcionalmente reemplazado por un grupo carbonilo, o R5 representa un sistema de anillos bicíclico en el cual los dos anillos se seleccionan en forma independiente entre los sistemas de anillos monocíclicos definidos en ii), iii), iv) y v) precedentemente, en donde los dos anillos están o bien fusionados entre sí, unidos directamente entre sí o están separados uno del otro por un grupo ligante seleccionado entre oxígeno, S(O)t o alquileno C1-6 que comprende opcionalmente uno o más heteroátomos internos o terminales seleccionados entre oxígeno, azufre y NR27 y está opcionalmente sustituido con al menos un sustituyente seleccionado entre hidroxilo, oxo y alcoxi C1-6, el sistema de anillos monociclico o bicíclico está opcionalmente sustituido con al menos un sustituyente seleccionado entre oxigeno, CN, OH, alquilo C1-6, alcoxi C1-6, halogeno, NR47R48, NO2, OSO2R49, CO2R50, C(=NH)NH2, C(O)NR51R52, C(S)NR53R54, SC(=NH)NH2, NR55C(=NH)NH2, S(O)vR21, SO2NR56R57, alcoxi C1-3 sustituido con uno o más átomos de F y alquilo C1-3 sustituido con SO2R58 o con uno o más átomos de F; estando dicho alquilo C1-6 opcionalmente sustituido además con al menos un sustituyente seleccionado entre ciano, hidroxilo, alcoxi C1-6, alquiltio C1-6 y -C(O)NR22R23; o R5 también puede representar H; R20 representa hidrogeno, alquilo C1-6, alquilcarbonilo C1-6 o alcoxicarbonilo C1-6; R21 representa hidrogeno, alquilo C1-6 o cicloalquilo C3-8; estando dicho grupo alquilo o cicloalquilo opcionalmente sustituido además con uno o más sustituyentes seleccionados en forma independiente entre OH, CN, alcoxi C1-3 y CONR59R60; R37 y R38 en forma independiente representan H, alquilo C1-6, formilo o alcanoilo C2-6; R47 y R48 en forma independiente representan H, alquilo C1-6, formilo, alcanoilo C2-6, S(O)qR61 o SO2NR62R63; estando dicho grupo alquilo opcionalmente sustituido además con halogeno, CN, alcoxi C1-4 o CONR64R65; R41 y R61 en forma independiente representan H, alquilo C1-6 o cicloalquilo C3-6; p es 0, 1 o 2; q es 0, 1 o 2; r es 0, 1 o 2; t es 0, 1 o 2; w es 0, 1 o 2; x es 0, 1 o 2; v es 0, 1 o 2; R16, R17, R22, R23, R24, R26, R27, R31, R32, R39, R40, R42, R43, R44, R45, R46, R49, R50, R51, R52, R53, R54, R55, R56, R57, R58, R59, R60, R62, R63, R64, R65 y R66 cada uno en forma independiente representan hidrogeno o alquilo C1-6; o una sal aceptable para uso farmacéutico del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US79878606P | 2006-05-08 | 2006-05-08 |
Publications (1)
Publication Number | Publication Date |
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AR060875A1 true AR060875A1 (es) | 2008-07-16 |
Family
ID=38667997
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP070101994A AR060875A1 (es) | 2006-05-08 | 2007-05-08 | Derivados de 2-piridona como inhibidores de la neutrofilo elastasa humana |
Country Status (21)
Country | Link |
---|---|
US (1) | US7998984B2 (es) |
EP (1) | EP2018375B1 (es) |
JP (1) | JP2009536196A (es) |
KR (1) | KR20090017573A (es) |
CN (1) | CN101490033A (es) |
AR (1) | AR060875A1 (es) |
AT (1) | ATE459615T1 (es) |
AU (1) | AU2007248950B2 (es) |
BR (1) | BRPI0711357A2 (es) |
CA (1) | CA2649813A1 (es) |
CL (1) | CL2007001282A1 (es) |
DE (1) | DE602007005120D1 (es) |
ES (1) | ES2339607T3 (es) |
HK (1) | HK1127599A1 (es) |
IL (1) | IL194948A0 (es) |
MX (1) | MX2008013836A (es) |
NO (1) | NO20084872L (es) |
TW (1) | TW200808763A (es) |
UY (1) | UY30328A1 (es) |
WO (1) | WO2007129962A1 (es) |
ZA (1) | ZA200809024B (es) |
Families Citing this family (24)
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SE0302486D0 (sv) * | 2003-09-18 | 2003-09-18 | Astrazeneca Ab | Novel compounds |
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 |
PT2066662E (pt) * | 2006-09-21 | 2013-02-13 | Kyorin Seiyaku Kk | Inibidores de serina-hidrolase |
DE102007031397A1 (de) | 2007-07-05 | 2009-01-08 | D2O Bioscience Group Ltd. | Verwendung von Deuteriumoxid zur Behandlung von Virus-basierten Erkrankungen der Haut |
PE20091565A1 (es) * | 2007-11-06 | 2009-11-06 | Astrazeneca Ab | Derivados de 2-pirazinona como inhibidores de la elastasa de los neutrofilos |
DK2110132T3 (da) * | 2008-04-20 | 2014-04-28 | D2 Bioscience Group Ltd | Anvendelse af deuteriumoxid som elastasehæmmer |
DE102009003942A1 (de) * | 2009-01-07 | 2010-07-08 | D2O Biosience Group Ltd., Hamilton | Verwendung von Deuteriumoxid zur Behandlung Virus-basierter Erkrankungen des Auges |
TW201036957A (en) * | 2009-02-20 | 2010-10-16 | Astrazeneca Ab | Novel salt 628 |
MX2011012267A (es) * | 2009-05-19 | 2012-04-11 | Vivia Biotech Sl | Metodos para proveer pruebas de medicina personalizadas ex vivo en cuanto a neoplasmas hematologicos. |
CN102639505A (zh) | 2009-10-02 | 2012-08-15 | 阿斯利康(瑞典)有限公司 | 用作嗜中性白细胞弹性蛋白酶抑制剂的吡啶-2-酮化合物 |
DE102010030187A1 (de) | 2010-06-16 | 2011-12-22 | Bayer Schering Pharma Aktiengesellschaft | 4-Cyan-2-sulfonylphenyl)pyrazolyl-substituierte Pyridinone und Pyrazinone und ihre Verwendung |
JP2013177318A (ja) * | 2010-06-30 | 2013-09-09 | Dainippon Sumitomo Pharma Co Ltd | ジヒドロピリミジノン誘導体およびその医薬用途 |
EP2740728A4 (en) | 2011-08-01 | 2015-04-01 | Sumitomo Dainippon Pharma Co Ltd | URACIL DERIVATIVE AND ITS USE FOR MEDICAL PURPOSES |
US20140057920A1 (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 |
US20140057926A1 (en) | 2012-08-23 | 2014-02-27 | Boehringer Ingelheim International Gmbh | Substituted 4-pyridones and their use as inhibitors of neutrophil elastase activity |
US9409870B2 (en) * | 2014-12-15 | 2016-08-09 | Chiesi Farmaceutici S.P.A. | Compounds |
CN108137542B (zh) | 2015-09-02 | 2023-10-27 | 葛兰素史克知识产权第二有限公司 | 用作溴结构域抑制剂的吡啶酮二甲酰胺 |
CN106674098B (zh) * | 2016-12-23 | 2019-07-02 | 中国医科大学 | N-(3-氰基-4-烷氧基苯基)吡啶甲酰胺类化合物及其用途 |
EP3749697A4 (en) | 2018-02-05 | 2021-11-03 | Bio-Rad Laboratories, Inc. | CHROMATOGRAPHIC RESIN WITH A LIGAND WITH ANION EXCHANGE-HYDROPHOBIC MIXED MODE |
EP4031138A1 (en) | 2019-09-17 | 2022-07-27 | Mereo Biopharma 4 Limited | Alvelestat for use in the treatment of graft rejection, bronchiolitis obliterans syndrome and graft versus host disease |
AU2021256835A1 (en) | 2020-04-16 | 2022-10-13 | Mereo Biopharma 4 Limited | Methods involving neutrophil elastase inhibitor alvelestat for treating respiratory disease mediated by alpha-1 antitrypsin deficiency |
WO2023067103A1 (en) | 2021-10-20 | 2023-04-27 | Mereo Biopharma 4 Limited | Neutrophil elastase inhibitors for use in the treatment of fibrosis |
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SE0302323D0 (sv) | 2003-08-28 | 2003-08-28 | Astrazeneca Ab | Novel compounds |
SE0302324D0 (sv) | 2003-08-28 | 2003-08-28 | Astrazeneca Ab | Novel compounds |
SE0302487D0 (sv) | 2003-09-18 | 2003-09-18 | Astrazeneca Ab | Novel compounds |
SE0302486D0 (sv) | 2003-09-18 | 2003-09-18 | Astrazeneca Ab | Novel compounds |
WO2005080372A1 (en) | 2004-02-19 | 2005-09-01 | Bayer Healthcare Ag | Dihydropyridinone derivatives |
CA2557271C (en) | 2004-02-26 | 2012-08-21 | Bayer Healthcare Ag | 1,4-diaryl-dihydropyrimidin-2-ones and their use as human neutrophil elastase inhibitors |
US7173031B2 (en) | 2004-06-28 | 2007-02-06 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
KR200365249Y1 (ko) | 2004-07-28 | 2004-10-21 | 추윤정 | 전동 퍼프 |
GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
GB0502258D0 (en) | 2005-02-03 | 2005-03-09 | Argenta Discovery Ltd | Compounds and their use |
TW200700392A (en) | 2005-03-16 | 2007-01-01 | Astrazeneca Ab | Novel compounds |
JO2787B1 (en) | 2005-04-27 | 2014-03-15 | امجين إنك, | Alternative amide derivatives and methods of use |
GB0512940D0 (en) | 2005-06-24 | 2005-08-03 | Argenta Discovery Ltd | Compounds and their use |
GB0605469D0 (en) | 2006-03-17 | 2006-04-26 | Argenta Discovery Ltd | Multimers of heterocyclic compounds and their use |
MX2008013996A (es) | 2006-05-04 | 2009-01-14 | Argenta Discovery Ltd | Tetrahidropirrolopirimidindionas y su uso como inhibidores de elastasa de neutrofilo humano. |
TW200808763A (en) | 2006-05-08 | 2008-02-16 | Astrazeneca Ab | Novel compounds I |
TW200808771A (en) | 2006-05-08 | 2008-02-16 | Astrazeneca Ab | Novel compounds II |
US20110003858A1 (en) | 2006-09-04 | 2011-01-06 | Bergstroem Lena | Multimeric heterocyclic compounds useful as neutrophil elastase inhibitors |
WO2008104752A1 (en) | 2007-02-26 | 2008-09-04 | Astrazeneca Ab | Dihydropyridones as elastase inhibitors |
WO2009058076A1 (en) | 2007-11-02 | 2009-05-07 | Astrazeneca Ab | 2-pyrazinone derivatives and their use as inhibitors of neutrophile elastase |
PE20091565A1 (es) | 2007-11-06 | 2009-11-06 | Astrazeneca Ab | Derivados de 2-pirazinona como inhibidores de la elastasa de los neutrofilos |
TW201036957A (en) | 2009-02-20 | 2010-10-16 | Astrazeneca Ab | Novel salt 628 |
-
2007
- 2007-04-27 TW TW096115047A patent/TW200808763A/zh unknown
- 2007-05-07 AU AU2007248950A patent/AU2007248950B2/en not_active Ceased
- 2007-05-07 CA CA002649813A patent/CA2649813A1/en not_active Abandoned
- 2007-05-07 CL CL2007001282A patent/CL2007001282A1/es unknown
- 2007-05-07 UY UY30328A patent/UY30328A1/es not_active Application Discontinuation
- 2007-05-07 US US12/299,879 patent/US7998984B2/en not_active Expired - Fee Related
- 2007-05-07 CN CNA2007800259071A patent/CN101490033A/zh active Pending
- 2007-05-07 AT AT07748105T patent/ATE459615T1/de not_active IP Right Cessation
- 2007-05-07 WO PCT/SE2007/000441 patent/WO2007129962A1/en active Application Filing
- 2007-05-07 KR KR1020087029811A patent/KR20090017573A/ko not_active Application Discontinuation
- 2007-05-07 JP JP2009509485A patent/JP2009536196A/ja not_active Withdrawn
- 2007-05-07 ES ES07748105T patent/ES2339607T3/es active Active
- 2007-05-07 DE DE602007005120T patent/DE602007005120D1/de active Active
- 2007-05-07 BR BRPI0711357-9A patent/BRPI0711357A2/pt not_active IP Right Cessation
- 2007-05-07 MX MX2008013836A patent/MX2008013836A/es active IP Right Grant
- 2007-05-07 EP EP07748105A patent/EP2018375B1/en active Active
- 2007-05-08 AR ARP070101994A patent/AR060875A1/es unknown
-
2008
- 2008-10-21 ZA ZA200809024A patent/ZA200809024B/xx unknown
- 2008-10-27 IL IL194948A patent/IL194948A0/en unknown
- 2008-11-19 NO NO20084872A patent/NO20084872L/no not_active Application Discontinuation
-
2009
- 2009-07-22 HK HK09106680.3A patent/HK1127599A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
MX2008013836A (es) | 2008-11-10 |
ATE459615T1 (de) | 2010-03-15 |
CL2007001282A1 (es) | 2008-01-18 |
CA2649813A1 (en) | 2007-11-15 |
KR20090017573A (ko) | 2009-02-18 |
US20090131486A1 (en) | 2009-05-21 |
EP2018375A1 (en) | 2009-01-28 |
NO20084872L (no) | 2009-02-03 |
TW200808763A (en) | 2008-02-16 |
UY30328A1 (es) | 2008-01-02 |
US7998984B2 (en) | 2011-08-16 |
IL194948A0 (en) | 2009-08-03 |
HK1127599A1 (en) | 2009-10-02 |
JP2009536196A (ja) | 2009-10-08 |
EP2018375B1 (en) | 2010-03-03 |
WO2007129962A1 (en) | 2007-11-15 |
AU2007248950A1 (en) | 2007-11-15 |
CN101490033A (zh) | 2009-07-22 |
AU2007248950B2 (en) | 2010-11-18 |
BRPI0711357A2 (pt) | 2011-09-27 |
DE602007005120D1 (de) | 2010-04-15 |
ZA200809024B (en) | 2010-03-31 |
ES2339607T3 (es) | 2010-05-21 |
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