AR046394A1 - Derivados de quinolinas y quinazolinas, metodo de preparacion de los mismos y composiciones farmaceuticas que los contienen. - Google Patents

Derivados de quinolinas y quinazolinas, metodo de preparacion de los mismos y composiciones farmaceuticas que los contienen.

Info

Publication number
AR046394A1
AR046394A1 ARP040102527A ARP040102527A AR046394A1 AR 046394 A1 AR046394 A1 AR 046394A1 AR P040102527 A ARP040102527 A AR P040102527A AR P040102527 A ARP040102527 A AR P040102527A AR 046394 A1 AR046394 A1 AR 046394A1
Authority
AR
Argentina
Prior art keywords
alkyl
cyano
alkoxy
halogen
alkanoyl
Prior art date
Application number
ARP040102527A
Other languages
English (en)
Original Assignee
Glaxo Group Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of AR046394A1 publication Critical patent/AR046394A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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 chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/632Organic additives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/38Nitrogen atoms

Abstract

Composición farmacéutica que comprende un compuesto de fórmula (1), junto con un vehículo o excipiente farmacéuticamente aceptable, y procedimiento para preparar esta composición farmacéutica. Reivindicación 1: Un compuesto de quinolina y quinazolina caracterizado porque tiene la fórmula (1) o una sal farmacéuticamente aceptable del mismo, en la que: R1 es halógeno, ciano, alquilo C1-6, alcoxi C1-6, haloalcoxi C1-6 o haloalquilo C1-6; m es 0, 1, 2, 3 ó 4; X es N o CH; R2 es halógeno, ciano, alquilo C1-6, alcoxi C1-6, haloalcoxi C1-6 o haloalquilo C1-6; n es 0, 1 ó 2; W es -CH2-, -CH(alquilo C1-6)- o -C(alquilo C1-6)(alquilo C1-6)-; p es 0, 1, 2 ó 3; Y y Z juntos forman un grupo cicloalquileno C3-7, o Y es -CH2-, -CH(alquilo C1- 6)- o -C(alquilo C1-6)(alquilo C1-6) y Z es -CH2-, -CHOH-, -CHR6- o -CR6R7- (en el que R6 y R7 son independientemente halógeno, ciano, alquilo C1-6 o alcoxi C1-6); R3 y R4 son independientemente hidrógeno, alquilo C1-6, alquil C1-6sulfonilo o un grupo que tiene la fórmula (2), en la que: r es 0, 1, 2, 3 ó 4; A es oxígeno o azufre; B es un enlace simple o -NR8- (en el que R8 es hidrógeno, arilo o alquilo C1-6, en el que el arilo está opcionalmente sustituido por uno o más sustituyentes independientemente seleccionados entre halógeno, oxo, alquilo C1-6, CF3, ciano, hidroxi, alcanoilo C1-6 y alcoxi C1-6); D es -(CH2)t-, -(CH2)tO- o -O(CH2)t-, en el que t es 0, 1, 2, 3 ó 4; y E es alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-7 (opcionalmente sustituido por uno o más sustituyentes independiente seleccionados entre halógeno, hidroxi, oxo, alquilo C1-6, ciano, CF3, OCF3, alcoxi C1-6 y alcanoilo C1-6), arilo (opcionalmente sustituido por uno o más sustituyentes independientemente seleccionados entre halógeno, oxo, alquilo C1-6, CF3, ciano, hidroxi, alcanoilo C1-6 y alcoxi C1-6), o E es -NR9R10, en el que R9 y R10 se seleccionan independientemente entre hidrógeno, alquilo C1-6 y arilo (opcionalmente sustituido por uno o más sustituyentes independientemente seleccionados entre halógeno, oxo, alquilo C1-6, -CF3, ciano, hidroxi, alcanoilo C1-6 y alcoxi C1-6); o R3 y R4, juntos con el átomo de nitrógeno al que están acoplados R3 y R4, forman un grupo heterocíclico de 3-7 miembros monocíclico o un grupo heterocíclico de 8-11 miembros bicíclico, en el que cada grupo está opcionalmente sustituido por uno o más sustituyentes seleccionados entre halógeno, oxo, alquilo C1-6, ciano, CF3, alcoxi C1-6, alcanoilo C1-6, arilo y arilalquilo C1-6 (en el que el arilo y el arilalquilo C1-6 están además opcionalmente sustituidos por uno o más de halógeno, oxo, alquilo C1-6, ciano, CF3, alcoxi C1-6 o alcanoilo C1-6); y R5 es independientemente halógeno, ciano, alquilo C1-6 o alcoxi C1-6; y q es 0, 1, 2, 3 ó 4.
ARP040102527A 2003-07-18 2004-07-16 Derivados de quinolinas y quinazolinas, metodo de preparacion de los mismos y composiciones farmaceuticas que los contienen. AR046394A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0316915.8A GB0316915D0 (en) 2003-07-18 2003-07-18 Compounds

Publications (1)

Publication Number Publication Date
AR046394A1 true AR046394A1 (es) 2005-12-07

Family

ID=27764115

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP040102527A AR046394A1 (es) 2003-07-18 2004-07-16 Derivados de quinolinas y quinazolinas, metodo de preparacion de los mismos y composiciones farmaceuticas que los contienen.

Country Status (29)

Country Link
US (5) US7279481B2 (es)
EP (3) EP1876174B1 (es)
JP (1) JP2006528146A (es)
KR (1) KR20060041242A (es)
CN (1) CN100441571C (es)
AR (1) AR046394A1 (es)
AT (2) ATE448205T1 (es)
AU (1) AU2004263268B2 (es)
BR (1) BRPI0412695A (es)
CA (1) CA2532452A1 (es)
CY (1) CY1107974T1 (es)
DE (2) DE602004024141D1 (es)
DK (1) DK1646613T3 (es)
ES (2) ES2336148T3 (es)
GB (1) GB0316915D0 (es)
HK (1) HK1089438A1 (es)
HR (1) HRP20080226T3 (es)
IL (1) IL173036A0 (es)
IS (1) IS2744B (es)
MA (1) MA27926A1 (es)
MX (1) MXPA06000716A (es)
NO (1) NO20060774L (es)
NZ (1) NZ544586A (es)
PL (1) PL1646613T3 (es)
PT (1) PT1646613E (es)
RU (1) RU2402533C2 (es)
SI (1) SI1646613T1 (es)
TW (1) TW200521115A (es)
WO (1) WO2005014552A1 (es)

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0316915D0 (en) * 2003-07-18 2003-08-20 Glaxo Group Ltd Compounds
DK1765327T3 (da) * 2004-06-17 2014-11-03 Cytokinetics Inc Forbindelser, sammensætninger og fremgangsmåder
KR100817538B1 (ko) * 2006-07-05 2008-03-27 한국화학연구원 신규 치환된―1h―퀴나졸린―2,4―디온 유도체, 이의제조방법 및 이를 함유하는 약학적 조성물
US20100041689A1 (en) * 2006-12-19 2010-02-18 University Of Virginia Patent Foundation Combined Effects of Topiramate and Ondansetron on Alcohol Consumption
CA2677205A1 (en) * 2007-01-31 2008-08-07 University Of Virginia Patent Foundation Topiramate plus naltrexone for the treatment of addictive disorders
ES2359170T3 (es) 2007-07-19 2011-05-19 Laboratorios Del Dr. Esteve S.A. Compuestos tetrahidro-quinolín-sulfonamida sustituidos, su preparación y uso como medicamentos.
US20110065628A1 (en) * 2007-08-27 2011-03-17 University Of Virginia Patent Foundation Medication Combinations for the Treatment of Alcoholism and Drug Addiction
JP2011515076A (ja) * 2008-02-28 2011-05-19 ユニバーシティ オブ バージニア パテント ファウンデーション セロトニン輸送体遺伝子およびアルコール中毒症の処置
JP2011518836A (ja) 2008-04-24 2011-06-30 インサイト・コーポレイション 大環状化合物およびそれらのキナーゼ阻害剤としての使用
EP2298199B1 (en) * 2008-05-06 2012-05-23 Biedermann Technologies GmbH & Co. KG Rod-shaped implant, in particular for the dynamic stabilization of the spine
US20100298397A1 (en) * 2009-05-19 2010-11-25 Singh Nikhilesh N Method of treatment of obsessive compulsive disorder with ondansetron
CN101671336B (zh) 2009-09-23 2013-11-13 辽宁利锋科技开发有限公司 芳杂环并嘧啶衍生物和类似物及其制备方法和用途
EP2308850A1 (en) * 2009-10-06 2011-04-13 Laboratorios Del. Dr. Esteve, S.A. Heterocycyl-substituted-alkylamino phenyl derivatives, their preparation and use as medicaments
DK2801625T3 (en) 2010-07-02 2018-02-05 Univ Virginia Patent Foundation Molecular genetic approach to the treatment and diagnosis of alcohol and drug dependence
KR20140052018A (ko) 2011-08-09 2014-05-02 다케다 야쿠힌 고교 가부시키가이샤 시클로프로판아민 화합물
EP2751137A4 (en) 2011-09-09 2015-06-03 Univ Virginia Patent Found MOLECULAR GENETIC APPROACH FOR THE TREATMENT AND DIAGNOSIS OF ALCOHOL DEPENDENCE AND PHARMACODEPPENDANCE
GB201117313D0 (en) 2011-10-07 2011-11-16 Gt Biolog Ltd Bacterium for use in medicine
JP6345651B2 (ja) * 2012-05-09 2018-06-20 サノビオン ファーマシューティカルズ インクSunovion Pharmaceuticals Inc. ヘテロアリール化合物及びその使用方法
CN103508927A (zh) * 2012-06-25 2014-01-15 天津药物研究院 一种2-甲磺酰氨基二苯醚的制备方法
JP6325449B2 (ja) 2012-10-12 2018-05-16 武田薬品工業株式会社 シクロプロパンアミン化合物およびその用途
GB201306536D0 (en) 2013-04-10 2013-05-22 Gt Biolog Ltd Polypeptide and immune modulation
RU2701861C1 (ru) 2013-11-20 2019-10-02 Санва Кагаку Кенкюсо Ко., Лтд. Новое производное 3-азабицикло[3.1.0]гексана и его применение в медицинских целях
CN106459024B (zh) 2014-04-11 2019-11-05 武田药品工业株式会社 环丙胺化合物及其用途
WO2016075314A1 (fr) 2014-11-13 2016-05-19 Institut National De La Recherche Agronomique Identification de facteurs de transcription de yarrowia lipolytica affectant la production de proteines
FR3028527A1 (fr) 2014-11-13 2016-05-20 Pivert Identification de facteurs de transcription de yarrowia lipolytica
HUE037476T2 (hu) 2014-12-23 2018-08-28 4D Pharma Res Ltd Pirin polipeptid és immunmodulálás
KR20220151045A (ko) 2014-12-23 2022-11-11 4디 파마 리서치 리미티드 면역 조정
MA41060B1 (fr) 2015-06-15 2019-11-29 4D Pharma Res Ltd Compositions comprenant des souches bactériennes
EA201890050A1 (ru) 2015-06-15 2018-06-29 4Д Фарма Рисёрч Лимитед Композиции, содержащие бактериальные штаммы
EA201890048A1 (ru) 2015-06-15 2018-06-29 4Д Фарма Рисёрч Лимитед Композиции, содержащие бактериальные штаммы
ME03511B (me) 2015-06-15 2020-04-20 4D Pharma Res Ltd Kompozicije koje sadrže bakterijske sojeve
MA41010B1 (fr) 2015-06-15 2020-01-31 4D Pharma Res Ltd Compositions comprenant des souches bactériennes
GB201520497D0 (en) 2015-11-20 2016-01-06 4D Pharma Res Ltd Compositions comprising bacterial strains
EP3209310B1 (en) 2015-11-20 2018-01-31 4D Pharma Research Limited Compositions comprising bacterial strains
LT3313423T (lt) 2016-03-04 2019-06-25 4D Pharma Plc Kompozicijos, apimančios bakterinius blautia kamienus, skirtos visceralinio hiperjautrumo gydymui
GB201612191D0 (en) 2016-07-13 2016-08-24 4D Pharma Plc Compositions comprising bacterial strains
TWI802545B (zh) 2016-07-13 2023-05-21 英商4D製藥有限公司 包含細菌菌株之組合物
GB201621123D0 (en) 2016-12-12 2017-01-25 4D Pharma Plc Compositions comprising bacterial strains
RS61872B1 (sr) 2017-05-22 2021-06-30 4D Pharma Res Ltd Kompozicije koje sadrže bakterijske sojeve
EP3630942B1 (en) 2017-05-24 2022-11-30 4D Pharma Research Limited Compositions comprising bacterial strain
EP3638271B1 (en) 2017-06-14 2020-10-14 4D Pharma Research Limited Compositions comprising bacterial strains
AU2018285453B2 (en) 2017-06-14 2020-03-19 Cj Bioscience, Inc. Compositions comprising a bacterial strain of the genus Megasphaera and uses thereof
CN108047143A (zh) * 2017-12-18 2018-05-18 刘凤娟 一种用于治疗功能性胃肠病的5-羟色胺受体拮抗剂的合成方法
DK3814348T3 (da) 2018-06-27 2023-10-30 Bristol Myers Squibb Co Substituerede naphthyridinonforbindelser, der er anvendelige som t-celleaktivatorer
EA202190137A1 (ru) 2018-06-27 2021-05-17 Бристол-Маерс Сквибб Компани Нафтиридиноновые соединения для применения в качестве активаторов t-клеток
AR119821A1 (es) 2019-08-28 2022-01-12 Bristol Myers Squibb Co Compuestos de piridopirimidinonilo sustituidos útiles como activadores de células t
AR120823A1 (es) 2019-12-23 2022-03-23 Bristol Myers Squibb Co Compuestos bicíclicos sustituidos útiles como activadores de células t

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2641602A (en) 1950-11-29 1953-06-09 Eastman Kodak Co 1, 8-dihydroxy-5-nitro-4-hydroxyethylphenyl aminoanthraquinone compounds
US3992537A (en) 1971-06-07 1976-11-16 Boehringer Ingelheim Gmbh Pharmaceutical compositions containing an N-phenyl-imidazolidine-2-one and method of use
US3975525A (en) 1971-06-07 1976-08-17 Boehringer Ingelheim Gmbh N-[4'-Imidazolidinon-(2)-yl-phenethyl]-N'-pyridyl-piperazines and salts thereof
US3937708A (en) 1971-06-07 1976-02-10 Boehringer Ingelheim Gmbh N-phenyl-imidazolidine-1-ones
JPS5883677A (ja) 1981-11-11 1983-05-19 Otsuka Pharmaceut Co Ltd カルボスチリル誘導体
US4891275A (en) * 1982-10-29 1990-01-02 Norsk Hydro A.S. Aluminum shapes coated with brazing material and process of coating
JPS6354363A (ja) 1986-08-26 1988-03-08 Ss Pharmaceut Co Ltd キノリン誘導体
FI95572C (fi) 1987-06-22 1996-02-26 Eisai Co Ltd Menetelmä lääkeaineena käyttökelpoisen piperidiinijohdannaisten tai sen farmaseuttisen suolan valmistamiseksi
US4933447A (en) 1987-09-24 1990-06-12 Ss Pharmaceutical Co., Ltd. Quinoline derivatives
US4891375A (en) 1988-01-13 1990-01-02 Pfizer Inc. Arylpiperazinyl-alkylene-phenyl-heterocyclic compounds
JP2777159B2 (ja) 1988-12-22 1998-07-16 エーザイ株式会社 環状アミン誘導体を含有する医薬
GB9300195D0 (en) 1993-01-06 1993-03-03 Wyeth John & Brother Ltd Piperazine derivatives
GB9300194D0 (en) 1993-01-06 1993-03-03 Wyeth John & Brother Ltd Piperazine derivatives
GB9308725D0 (en) 1993-04-27 1993-06-09 Wyeth John & Brother Ltd Piperazine derivatives
SK285119B6 (sk) 1996-03-29 2006-06-01 Duphar International Research B. V. Piperazínové a piperidínové zlúčeniny, spôsob ich prípravy, farmaceutické kompozície, ktoré ich obsahujú, a ich použitie
WO1997041108A1 (en) 1996-04-30 1997-11-06 Warner-Lambert Company Substituted piperazines and piperidines as central nervous system agents
GB2312843A (en) 1996-05-07 1997-11-12 Merck & Co Inc Method of treating rheumatoid arthritis
WO1998025617A1 (en) 1996-12-13 1998-06-18 Merck & Co., Inc. Substituted aryl piperazines as modulators of chemokine receptor activity
ATE253058T1 (de) 1997-09-02 2003-11-15 Duphar Int Res Piperidin- und piperazin derivate als 5-ht1- rezeptor-agonisten
EP0900792B1 (en) 1997-09-02 2003-10-29 Duphar International Research B.V Piperazine and piperidine derivatives as 5-HT1A and dopamine D2-receptor (ant)agonists
DK1027336T3 (da) 1997-10-27 2005-01-24 Neurosearch As Heteroaryldiazacycloalkaner, deres fremstilling og anvendelse
JP2002508366A (ja) 1997-12-12 2002-03-19 スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー キノリンピペラジンおよびキノリンピペリジン誘導体、それらの製造方法、ならびに複合的5−ht1a、5−ht1bおよび5−ht1d受容体アンタゴニストとしてのそれらの用途
UA62015C2 (en) * 1998-12-28 2003-12-15 Pfizer Prod Inc Benzoizoxazol derivatives, a pharmaceutical composition (variants) based thereon (variants) and a method for treatment (variants)
CN1158258C (zh) 1999-06-24 2004-07-21 东丽株式会社 肾上腺素能α1B受体拮抗药
ES2234683T3 (es) * 1999-11-05 2005-07-01 Smithkline Beecham Plc Derivados de isoquinolina y quinazolina con actividad combinada sobre los receptores 5ht1a, 5ht1b y 5ht1d.
JP4242643B2 (ja) 2000-10-26 2009-03-25 スミスクライン ビーチャム ピー エル シー ベンズオキサジノン誘導体、その製造および使用
CA2364211A1 (en) 2000-12-05 2002-06-05 Phillip Branch Chappell Combination treatment for depression, anxiety and psychosis
GB0106419D0 (en) * 2001-03-15 2001-05-02 Smithkline Beecham Plc Novel compounds
UY27304A1 (es) 2001-05-24 2002-12-31 Avanir Pharmaceuticals Inhibidores del factor inhibidor de la migración de los macrófagos y métodos para su identificación
GB0203804D0 (en) 2002-02-18 2002-04-03 Glaxo Group Ltd Compounds
GB0224084D0 (en) 2002-10-16 2002-11-27 Glaxo Group Ltd Novel compounds
WO2004041793A1 (en) 2002-11-08 2004-05-21 Warner-Lambert Company Llc Phenylalkyl and pyridylalkyl piperazine derivatives
GB0227240D0 (en) 2002-11-21 2002-12-31 Glaxo Group Ltd Compounds
TW200418829A (en) 2003-02-14 2004-10-01 Avanir Pharmaceutics Inhibitors of macrophage migration inhibitory factor and methods for identifying the same
US6759435B1 (en) * 2003-07-03 2004-07-06 A.P. Group Inc. Antidepressant drugs and methods
GB0316915D0 (en) 2003-07-18 2003-08-20 Glaxo Group Ltd Compounds
US20050124625A1 (en) 2003-10-21 2005-06-09 Salvati Mark E. Piperazine derivatives and their use as modulators of nuclear hormone receptor function
WO2005087742A1 (en) 2004-03-08 2005-09-22 Exelixis, Inc. Metabolic kinase modulators and methods of use as pesticides
AU2005221832A1 (en) 2004-03-10 2005-09-22 Nycomed Gmbh Novel amido-substituted hydroxy-6-phenylphenanthridines and their use as PDE4 inhibitors
PE20060653A1 (es) 2004-08-31 2006-09-27 Glaxo Group Ltd Derivados triciclicos condensados como moduladores del receptor 5-ht1

Also Published As

Publication number Publication date
PT1646613E (pt) 2008-06-19
IS2744B (is) 2011-08-15
US20100204273A1 (en) 2010-08-12
ES2302543T3 (es) 2008-07-16
EP1876174B1 (en) 2009-11-11
NO20060774L (no) 2006-04-06
MA27926A1 (fr) 2006-06-01
ATE448205T1 (de) 2009-11-15
CN1852896A (zh) 2006-10-25
US20080280919A1 (en) 2008-11-13
MXPA06000716A (es) 2006-03-30
ES2336148T3 (es) 2010-04-08
US7732600B2 (en) 2010-06-08
HK1089438A1 (en) 2006-12-01
JP2006528146A (ja) 2006-12-14
EP1876174A1 (en) 2008-01-09
ATE389637T1 (de) 2008-04-15
KR20060041242A (ko) 2006-05-11
DK1646613T3 (da) 2008-07-14
US20070167423A1 (en) 2007-07-19
DE602004012564T2 (de) 2009-04-30
US20090312546A1 (en) 2009-12-17
IL173036A0 (en) 2006-06-11
AU2004263268B2 (en) 2010-12-16
GB0316915D0 (en) 2003-08-20
IS8304A (is) 2006-02-15
AU2004263268A1 (en) 2005-02-17
US7279481B2 (en) 2007-10-09
EP2145622A1 (en) 2010-01-20
CN100441571C (zh) 2008-12-10
NZ544586A (en) 2009-05-31
CA2532452A1 (en) 2005-02-17
PL1646613T3 (pl) 2008-08-29
SI1646613T1 (sl) 2008-08-31
US7592346B2 (en) 2009-09-22
DE602004012564D1 (de) 2008-04-30
DE602004024141D1 (de) 2009-12-24
TW200521115A (en) 2005-07-01
RU2402533C2 (ru) 2010-10-27
HRP20080226T3 (en) 2008-06-30
CY1107974T1 (el) 2013-09-04
BRPI0412695A (pt) 2006-10-03
US20060229312A1 (en) 2006-10-12
WO2005014552A1 (en) 2005-02-17
EP1646613A1 (en) 2006-04-19
EP1646613B1 (en) 2008-03-19
RU2006104993A (ru) 2006-08-10
US7459456B2 (en) 2008-12-02

Similar Documents

Publication Publication Date Title
AR046394A1 (es) Derivados de quinolinas y quinazolinas, metodo de preparacion de los mismos y composiciones farmaceuticas que los contienen.
AR066669A1 (es) Derivados de imidazolona como inhibidores de bencimidazolona quimasa. composiciones farmaceuticas.
AR109958A1 (es) Lactamas bicíclicas de piridona y sus métodos de uso
CO6160229A2 (es) Ciclopenta [d] pirimidinas como inhibidores de proteina quinasa akt
AR063601A1 (es) Arilamidas sustituidas por tiazol u oxazol
ECSP034475A (es) Derivados de 4-fenil-piridin como antagonistas del receptor de neuroquinina-1
AR049443A1 (es) Derivados de pirrolpiridinas
AR077434A1 (es) Compuestos para la reduccion de produccion de beta - amiloide
AR038235A1 (es) Compuestos de espiropiperidina n-sustituidos como ligandos para el receptor orl-1
AR085615A1 (es) Derivados de fluoropiridinona utiles como agentes antibacterianos y composiciones farmaceuticas que los contienen
AR060173A1 (es) Derivados de piridina y de pirimidina como antagonistas del mglur2, metodos para su preparacion, composiciones farmaceuticas que los contienen y su uso en la fabricacion de medicamentos para el tratamiento de trastornos del snc.
AR055878A1 (es) Derivados de ciclopropanocarboxamida
AR044011A1 (es) Antagonistas de mchr1 heterociclicos
AR052215A1 (es) 3-aminociclopentancarboxamidas como moduladores de receptores de quimioquinas, su uso en el tratamiento de enfermedades relacionadas y composiciones farmacéuticas que las contienen.
AR019115A1 (es) Derivados de la 1-[(1-sustituido-4-piperidinil)metil]-4-piperidina, procesos para la preparacion de los mismos, composiciones farmaceuticas que loscontienen y los compuestos intermedios para prepararlos
AR044614A1 (es) Composiciones de sulfonamida que modulan la actividad del receptor de quinioquinas (ccr4)
AR061369A1 (es) Derivados de pirimidina y composiciones farmaceuticas que los comprenden
AR045931A1 (es) Derivados de piperazina
AR081932A1 (es) Derivados de heteroaril imidazolona, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de enfermedades neoplasicas y autoinmunes
AR064414A1 (es) Derivados de 1-azoniabiciclo[2, 2, 2]octano y 1-azabiciclo[2, 2, 2]oct-3-ilo, un proceso para su preparacion, una composicion farmaceutica que los comprende, procedimiento de obtencion de la misma, su uso en la elaboracion de un medicamento para el tratamiento de epoc y un producto farmaceutico que
AR044134A1 (es) Derivados de quinuclidina, metodo de preparacion y composiciones farmaceuticas.
AR041246A1 (es) Derivados de piridina; un procedimiento de preparacion de los mismos y composicion farmaceutica que los contiene
AR046085A1 (es) Agonistas etilamino amino sustituidos del receptor beta 2 adrenergico
AR069814A1 (es) Derivados de 4 amino-pirimidina, proceso de preparacion y composiciones farmaceuticas que los contienen
CO5650235A2 (es) Derivados de imidazol

Legal Events

Date Code Title Description
FA Abandonment or withdrawal