WO2004018449A8 - Derives de piperidine utilises comme inhibiteurs de la phospodiesterase-4 (pde4) - Google Patents

Derives de piperidine utilises comme inhibiteurs de la phospodiesterase-4 (pde4)

Info

Publication number
WO2004018449A8
WO2004018449A8 PCT/EP2003/008673 EP0308673W WO2004018449A8 WO 2004018449 A8 WO2004018449 A8 WO 2004018449A8 EP 0308673 W EP0308673 W EP 0308673W WO 2004018449 A8 WO2004018449 A8 WO 2004018449A8
Authority
WO
WIPO (PCT)
Prior art keywords
pde4 inhibitors
piperidine
derivatives
meanings
compounds
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/EP2003/008673
Other languages
English (en)
Other versions
WO2004018449A1 (fr
Inventor
Geert Jan Sterk
Steffen Weinbrenner
Armin Hatzelmann
Johannes Barsig
Degenhard Marx
Hans-Peter Kley
Johannes A M Christiaans
Wiro M P B Menge
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Takeda GmbH
Original Assignee
Altana Pharma AG
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 Altana Pharma AG filed Critical Altana Pharma AG
Priority to AU2003255376A priority Critical patent/AU2003255376A1/en
Publication of WO2004018449A1 publication Critical patent/WO2004018449A1/fr
Publication of WO2004018449A8 publication Critical patent/WO2004018449A8/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • 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]
    • 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
    • C07D401/14—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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pain & Pain Management (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Rheumatology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

Ces composés correspondant à la formule (I), formule dans laquelle les substituants sont tels que définis dans le descriptif, sont de nouveaux inhibiteurs efficaces de la PDE4.
PCT/EP2003/008673 2002-08-10 2003-08-06 Derives de piperidine utilises comme inhibiteurs de la phospodiesterase-4 (pde4) Ceased WO2004018449A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2003255376A AU2003255376A1 (en) 2002-08-10 2003-08-06 Piperidine-derivatives as pde4 inhibitors

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP02017979 2002-08-10
EP02017979.2 2002-08-10

Publications (2)

Publication Number Publication Date
WO2004018449A1 WO2004018449A1 (fr) 2004-03-04
WO2004018449A8 true WO2004018449A8 (fr) 2004-05-06

Family

ID=31896829

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2003/008673 Ceased WO2004018449A1 (fr) 2002-08-10 2003-08-06 Derives de piperidine utilises comme inhibiteurs de la phospodiesterase-4 (pde4)

Country Status (2)

Country Link
AU (1) AU2003255376A1 (fr)
WO (1) WO2004018449A1 (fr)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0401334D0 (en) 2004-01-21 2004-02-25 Novartis Ag Organic compounds
EP1716133B1 (fr) 2004-02-04 2008-03-26 Nycomed GmbH Dérivés de 2-(pipéridine-4-yl)-4,5-dihydro-2h-pyridazin-3-one comme inhibiteurs de pde4
GB0411056D0 (en) 2004-05-18 2004-06-23 Novartis Ag Organic compounds
GT200500281A (es) 2004-10-22 2006-04-24 Novartis Ag Compuestos organicos.
GB0424284D0 (en) 2004-11-02 2004-12-01 Novartis Ag Organic compounds
GB0426164D0 (en) 2004-11-29 2004-12-29 Novartis Ag Organic compounds
GB0507577D0 (en) 2005-04-14 2005-05-18 Novartis Ag Organic compounds
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
MY144906A (en) 2005-10-21 2011-11-30 Novartis Ag Human antibodies against il13 and therapeutic uses
GB0526244D0 (en) 2005-12-22 2006-02-01 Novartis Ag Organic compounds
GB0601951D0 (en) 2006-01-31 2006-03-15 Novartis Ag Organic compounds
PE20080361A1 (es) 2006-04-21 2008-06-03 Novartis Ag Compuestos derivados de purina como activadores del receptor de adenosina a2a
RU2009115954A (ru) 2006-09-29 2010-11-10 Новартис АГ (CH) Пиразолопиримидины в качестве ингибиторов липидной киназы р13к
JP2010508315A (ja) 2006-10-30 2010-03-18 ノバルティス アーゲー 抗炎症剤としてのヘテロ環式化合物
DE602007011670D1 (de) 2007-01-10 2011-02-10 Irm Llc Verbindungen und zusammensetzungen als kanal-aktivierende proteasehemmer
US8318935B2 (en) 2007-05-07 2012-11-27 Novartis Ag Organic compounds 75074
KR101601284B1 (ko) * 2007-05-16 2016-03-08 다케다 게엠베하 Ｐｄｅ4 억제제로서 피라졸론 유도체
EP2231280B1 (fr) 2007-12-10 2016-08-10 Novartis AG Pyrazine carboxamides semblable à l'Amiloride en tant que bloqueurs d'ENaC
KR20100113557A (ko) 2008-01-11 2010-10-21 노파르티스 아게 키나제 억제제로서의 피리미딘
BRPI0915018A2 (pt) 2008-06-10 2015-10-27 Novartis Ag compostos orgânicos
AR074318A1 (es) 2008-11-14 2011-01-05 Nycomed Gmbh Derivados heterociclicos de pirazolona, composiciones farmaceuticas que los contienen y uso de los mismos para el tratamiento de enfermedades de las vias respiratorias.
HRP20121006T1 (hr) 2009-01-29 2013-01-31 Novartis Ag Supstituirani benzimidazoli za lijeäśenje astrocitoma
US8389526B2 (en) 2009-08-07 2013-03-05 Novartis Ag 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
CA2770873A1 (fr) 2009-08-12 2011-02-17 Novartis Ag Composes hydrazone heterocycliques et leurs utilisations pour traiter le cancer et l'inflammation
GEP201706639B (en) 2009-08-17 2017-03-27 Intellikine Llc Heterocyclic compounds and uses thereof
CA2771432A1 (fr) 2009-08-20 2011-02-24 Novartis Ag Composes d'oximes heterocycliques
EP2813227A1 (fr) 2009-10-22 2014-12-17 Vertex Pharmaceuticals Incorporated Compositions pour le traitement de la mucoviscidose et d'autres maladies chroniques
US8247436B2 (en) 2010-03-19 2012-08-21 Novartis Ag Pyridine and pyrazine derivative for the treatment of CF
WO2012034095A1 (fr) 2010-09-09 2012-03-15 Irm Llc Composés et compositions comme inhibiteurs de trk
UY33597A (es) 2010-09-09 2012-04-30 Irm Llc Compuestos y composiciones como inhibidores de la trk
US8372845B2 (en) 2010-09-17 2013-02-12 Novartis Ag Pyrazine derivatives as enac blockers
JP2014505088A (ja) 2011-02-10 2014-02-27 ノバルティス アーゲー Ｃ−ＭＥＴチロシンキナーゼ阻害剤としての［１，２，４］トリアゾロ［４，３−ｂ］ピリダジン化合物
JP5808826B2 (ja) 2011-02-23 2015-11-10 インテリカイン， エルエルシー 複素環化合物およびその使用
KR20140014184A (ko) 2011-02-25 2014-02-05 아이알엠 엘엘씨 Trk 억제제로서의 화합물 및 조성물
WO2012171900A1 (fr) 2011-06-17 2012-12-20 Nycomed Gmbh Nouveaux dérivés de phtalazinone-pyrrolopyrimidinecarboxamide
US8883819B2 (en) 2011-09-01 2014-11-11 Irm Llc Bicyclic heterocycle derivatives for the treatment of pulmonary arterial hypertension
AU2012310168B2 (en) 2011-09-15 2015-07-16 Novartis Ag 6 - substituted 3 - (quinolin- 6 - ylthio) - [1,2,4] triazolo [4, 3 -a] pyradines as tyrosine kinase
US9056867B2 (en) 2011-09-16 2015-06-16 Novartis Ag N-substituted heterocyclyl carboxamides
WO2013038373A1 (fr) 2011-09-16 2013-03-21 Novartis Ag Dérivés pyrimidinamides
WO2013038378A1 (fr) 2011-09-16 2013-03-21 Novartis Ag Dérivés pyridinamides
ES2558457T3 (es) 2011-09-16 2016-02-04 Novartis Ag Compuestos heterocíclicos para el tratamiento de fibrosis quística
WO2013038381A1 (fr) 2011-09-16 2013-03-21 Novartis Ag Dérivés d'amide pyridine/pyrazine
US8809340B2 (en) 2012-03-19 2014-08-19 Novartis Ag Crystalline form
EP3964513A1 (fr) 2012-04-03 2022-03-09 Novartis AG Produits combinés comprenant des inhibiteurs de tyrosine kinase et leur utilisation
US9073921B2 (en) 2013-03-01 2015-07-07 Novartis Ag Salt forms of bicyclic heterocyclic derivatives
WO2014151147A1 (fr) 2013-03-15 2014-09-25 Intellikine, Llc Combinaison d'inhibiteurs de kinase et ses utilisations
TW201605450A (zh) 2013-12-03 2016-02-16 諾華公司 Ｍｄｍ２抑制劑與ＢＲＡＦ抑制劑之組合及其用途
BR112016024533A8 (pt) 2014-04-24 2021-03-30 Novartis Ag derivados de amino pirazina como inibidores de fosfatidilinositol 3-cinase ou sal, seu uso, e composição e combinação farmacêuticas
CN106458980A (zh) 2014-04-24 2017-02-22 诺华股份有限公司 作为磷脂酰肌醇3‑激酶抑制剂的氨基吡啶衍生物
KR20160141856A (ko) 2014-04-24 2016-12-09 노파르티스 아게 포스파티딜이노시톨 3-키나제 억제제로서의 피라진 유도체
WO2016011658A1 (fr) 2014-07-25 2016-01-28 Novartis Ag Polythérapie
BR112017001695A2 (pt) 2014-07-31 2017-11-21 Novartis Ag terapia de combinação
KR20220019015A (ko) 2019-06-10 2022-02-15 노파르티스 아게 Cf, copd, 및 기관지확장증 치료를 위한 피리딘 및 피라진 유도체
UY38860A (es) 2019-08-28 2021-02-26 Novartis Ag Derivados de 1,3–fenil heteroarilo sustituidos, composiciones para su uso en el tratamiento de enfermedades y formas cristalinas

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CZ293815B6 (cs) * 1997-01-15 2004-08-18 Altanaápharmaáag Ftalazinonové deriváty
AU1760399A (en) * 1997-12-15 1999-07-05 Byk Gulden Lomberg Chemische Fabrik Gmbh New phthalazinones
US6380196B1 (en) * 1997-12-15 2002-04-30 Byk Gulden Lomberg Chemische Fabrik Gmbh Dihydrobenzofurans
AU3328499A (en) * 1998-03-14 1999-10-11 Byk Gulden Lomberg Chemische Fabrik Gmbh Phthalazinone pde iii/iv inhibitors
WO2001019818A1 (fr) * 1999-09-14 2001-03-22 Byk Gulden Lomberg Chemische Fabrik Gmbh Derives de phthalazinone utilises comme inhibiteurs de pd3/4
HRP20020350A2 (en) * 1999-10-25 2004-02-29 Altana Pharma Ag Tetrahydrothiopy ranphtalazinone derivatives as pde4 inhibitors
US6756371B1 (en) * 1999-10-25 2004-06-29 Altana Pharma Ag Phthalazinone derivatives as PDE4 inhibitors
JP4301812B2 (ja) * 2001-02-15 2009-07-22 ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング Ｐｄｅ４インヒビターとしてのフタラインオン−ピペリジノ−誘導体
SK14342003A3 (sk) * 2001-04-25 2004-05-04 Altana Pharma Ag Ftalazinóny, farmaceutický prostriedok s ich obsahom a ich použitie

Also Published As

Publication number Publication date
AU2003255376A1 (en) 2004-03-11
WO2004018449A1 (fr) 2004-03-04

Similar Documents

Publication Publication Date Title
WO2004018449A8 (fr) Derives de piperidine utilises comme inhibiteurs de la phospodiesterase-4 (pde4)
WO2004018457A8 (fr) Piperidine-phthalazones a substitution pyrrolidinedione utilises comme inhibiteurs de la phosphodiesterase-4 (pde4)
WO2004018451A8 (fr) Derives de pyridazinone utilises comme inhibiteurs de pde4
WO2003093269A3 (fr) Pyrazolopyrimidine-4-one substituee
WO2006058700A8 (fr) Derives d'acetamides employes en tant que fongicides
WO2004014893A3 (fr) Quinolones anti-microbiens, leurs compositions et utilisation
WO2004018431A3 (fr) Nouvelles phenanthridines
AU2003301302A1 (en) Pyradazine compounds as gsk-3 inhibitors
WO2004076450A8 (fr) Derives de pyrazolopyridine
AU2003286711A1 (en) Indazolinone compositions useful as kinase inhibitors
WO2005074603A3 (fr) Utilisation d'aminobenzoxazoles comme agents therapeutiques
WO2001017973A3 (fr) Nouveaux herbicides
WO2005087724A3 (fr) Nouvelles hydroxy-6-phenylphenanthridines a substitution amido
WO2004018465A3 (fr) Nouvelles benzonaphtyridines
WO2005066151A3 (fr) Inhibiteurs d'histone desacetylase
EP1551801A4 (fr) Nouveaux gamma-lactames en tant qu'inhibiteurs de la beta-secretase
WO2002085906A3 (fr) Phtalazinones
ZA200608416B (en) Herbicidal composition
AU2003212310A1 (en) (4,2-disubstituted-thiazol-5-yl)amine compounds as pde7 inhibitors
WO2002064574A3 (fr) Antibactériens à base de pyridoarylphényle oxazolidinone, compositions et procédés associés
HK1047276A1 (zh) 作为pde4抑制剂的四氢噻喃2，3-二氮杂萘酮类衍生物
WO2005028474A3 (fr) Inhibiteurs de chk-1
GB0229081D0 (en) Multifunctional cationic photoinitiators, their preparation and use
WO2005061496A8 (fr) Derives aminopyridines en tant qu'inhibiteurs de la no-synthase inductible-
AU2003215635A1 (en) Thiazol-2-yl-imine compounds as pde-7 inhibitors

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AL AU BA BR CA CN CO DZ EC GE HR ID IL IN IS JP KR LT LV MA MK MX NO NZ PH PL SG TN UA US VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR

121 Ep: the epo has been informed by wipo that ep was designated in this application
CFP Corrected version of a pamphlet front page
CR1 Correction of entry in section i

Free format text: IN PCT GAZETTE 10/2004 REPLACE "(72) INVENTORS " BY "(72) INVENTORS (FOR ALL DESIGNATED STATES EXCEPT CA, PH, US)"

122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase in:

Ref country code: JP

WWW Wipo information: withdrawn in national office

Country of ref document: JP