SK14192000A3 - Dihydro-benzo(1,4)oxazíny a tetrahydrochinoxalíny, ich použitie a farmaceutický prostriedok obsahujúci tieto zlúčeniny - Google Patents

Dihydro-benzo(1,4)oxazíny a tetrahydrochinoxalíny, ich použitie a farmaceutický prostriedok obsahujúci tieto zlúčeniny Download PDF

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Publication number
SK14192000A3
SK14192000A3 SK1419-2000A SK14192000A SK14192000A3 SK 14192000 A3 SK14192000 A3 SK 14192000A3 SK 14192000 A SK14192000 A SK 14192000A SK 14192000 A3 SK14192000 A3 SK 14192000A3
Authority
SK
Slovakia
Prior art keywords
group
alkyl
substituted
optionally substituted
compound
Prior art date
Application number
SK1419-2000A
Other languages
English (en)
Slovak (sk)
Inventor
Jean-Dominique Bourzat
Alain Commercon
Bruno Jacques Christophe FILOCHE
Neil Harris
Thomas David Pallin
Keith Alfred James Stuttle
Original Assignee
Aventis Pharma Limited
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
Priority claimed from GBGB9828417.7A external-priority patent/GB9828417D0/en
Application filed by Aventis Pharma Limited filed Critical Aventis Pharma Limited
Publication of SK14192000A3 publication Critical patent/SK14192000A3/sk

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • 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
    • 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]
    • A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/34—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
    • C07D265/36—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings condensed with one six-membered ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Pulmonology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
SK1419-2000A 1998-12-23 1999-12-23 Dihydro-benzo(1,4)oxazíny a tetrahydrochinoxalíny, ich použitie a farmaceutický prostriedok obsahujúci tieto zlúčeniny SK14192000A3 (sk)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB9828417.7A GB9828417D0 (en) 1998-12-23 1998-12-23 Chemical compounds
US12608499P 1999-03-25 1999-03-25
PCT/GB1999/004430 WO2000039103A1 (fr) 1998-12-23 1999-12-23 Dihydro-benzo(1,4)oxazines et tetrahydroquinoxalines

Publications (1)

Publication Number Publication Date
SK14192000A3 true SK14192000A3 (sk) 2001-07-10

Family

ID=26314897

Family Applications (1)

Application Number Title Priority Date Filing Date
SK1419-2000A SK14192000A3 (sk) 1998-12-23 1999-12-23 Dihydro-benzo(1,4)oxazíny a tetrahydrochinoxalíny, ich použitie a farmaceutický prostriedok obsahujúci tieto zlúčeniny

Country Status (10)

Country Link
US (1) US6632814B1 (fr)
EP (1) EP1056728B1 (fr)
AP (1) AP2000001924A0 (fr)
AU (1) AU1881900A (fr)
BG (1) BG104786A (fr)
DE (1) DE69937603T2 (fr)
ES (1) ES2297943T3 (fr)
HU (1) HUP0200481A3 (fr)
SK (1) SK14192000A3 (fr)
WO (1) WO2000039103A1 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2370805C (fr) * 1999-05-05 2012-07-03 Aventis Pharma Limited Urees en tant que modulateurs de l'adhesion cellulaire
US6750215B2 (en) 2001-08-08 2004-06-15 Pharmacia & Upjohn, S.P.A. Substituted benzoxazines as integrin antagonists
US6794385B2 (en) 2001-08-08 2004-09-21 Pharmacia & Upjohn, S.P.A. Benzoxazine derivatives useful as integrin receptor antagonists
NZ607928A (en) * 2010-10-18 2014-03-28 Cerenis Therapeutics Holding Sa Compounds, compositions and methods useful for cholesterol mobilisation
PL2794600T3 (pl) 2011-12-22 2018-06-29 Novartis Ag Pochodne 2,3-dihydro-benzo[1,4]oksazyny i powiązane związki jako inhibitory kinazy fosfoinozytydu-3 (PI3K) do leczenia np. reumatoidalnego zapalenia stawów
CN103275021B (zh) * 2013-05-24 2015-05-20 东北农业大学 N-二氯乙酰基-6,7-二氯-1,2,3,4-四氢喹喔啉及其制备方法
MX370535B (es) 2013-11-18 2019-12-17 Forma Therapeutics Inc Compuestos de tetrahidroquinolina como inhibidores del bromodominio extra terminal y bromo (bet) y el uso de los mismos en el tratamiento de cáncer.
CN106029076B (zh) 2013-11-18 2019-06-07 福马疗法公司 作为bet溴域抑制剂的苯并哌嗪组合物

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS588016A (ja) 1981-07-06 1983-01-18 Mitsubishi Chem Ind Ltd 強心剤
DE3338846A1 (de) 1982-10-29 1984-05-03 Toyama Chemical Co. Ltd., Tokyo Neue 4-oxo-1,4-dihydronicotinsaeurederivate und salze derselben, verfahren zu ihrer herstellung und antibakterielle mittel mit einem gehalt derselben
US4582909A (en) 1984-02-02 1986-04-15 Warner-Lambert Company Benzobicyclic lactam acids and derivatives as cognition activators
AU626881B2 (en) 1988-07-14 1992-08-13 F. Hoffmann-La Roche Ag Benzofused heterocyclics used as pharmaceuticals
ES2014560A6 (es) 1988-12-30 1990-07-16 Marga Investigacion Proceso para la preparacion de un nuevo reactivo organo-sililpolifosforico y su aplicacion al proceso de sontesis de 3-carboxi-quinolonas o azaquinolonas y sus sales.
EP0407137B1 (fr) * 1989-07-03 1996-05-01 Yoshitomi Pharmaceutical Industries, Ltd. Dérivés de benzazine et leurs applications pharmaceutiques
GB9320277D0 (en) 1993-10-01 1993-11-17 Nycomed Salutar Inc Chelants
DK0509398T3 (da) 1991-04-15 2002-01-14 Aventis Pharma Gmbh Quinoxaliner, fremgangsmåder til deres fremstilling samt deres anvendelse
AU1493092A (en) * 1991-04-18 1992-10-22 Ortho Pharmaceutical Corporation (+) and (-) enantiomers of 5-aliphatic-6-(benzoxazinyl- or benzothiazinyl)-2,3,4,5-tetrahydropyridazin-3-ones
TW301607B (fr) * 1993-03-09 1997-04-01 Takeda Pharm Industry Co Ltd
WO1994020473A1 (fr) 1993-03-11 1994-09-15 Yamanouchi Pharmaceutical Co., Ltd. Compose avec action antagoniste de la vasopressine
US5334598A (en) 1993-03-19 1994-08-02 Merck & Co., Inc. Six-membered ring fused imidazoles substituted with phenoxyphenylacetic acid derivatives
WO1995015973A1 (fr) * 1993-12-06 1995-06-15 Cytel Corporation Peptidomimetiques cs-1, compositions et procedes pour les utiliser
EP0757687A1 (fr) 1994-04-23 1997-02-12 Smithkline Beecham Plc Derives tricycliques antagonistes de 5ht2c et de 5ht2b
EP0774462A4 (fr) 1994-08-03 1997-10-29 Fujisawa Pharmaceutical Co Compose heterocyclique
CA2203659A1 (fr) 1994-10-27 1996-05-09 Teruo Oku Pyridopyrimidones, quinoleines et heterocycles azotes fusionnes comme antagonistes de la bradykinine
US5977125A (en) 1994-10-31 1999-11-02 Eisai Co., Ltd. Mono-or polyenic carboxylic acid derivatives
US6248713B1 (en) * 1995-07-11 2001-06-19 Biogen, Inc. Cell adhesion inhibitors
GB9605883D0 (en) 1996-03-20 1996-05-22 Smithkline Beecham Plc Novel compounds
ATE204857T1 (de) * 1996-03-29 2001-09-15 Searle & Co Meta-substituierte phenylenderivate und ihre verwendung als alphavbeta3 intergrin-antagonisten oder inhibitoren
JPH10158192A (ja) 1996-10-03 1998-06-16 Eisai Co Ltd 移植片対宿主疾患（ｇｖｈｄ）の治療および臓器移植時の移植片拒絶反応抑制のための医薬組成物
DE19647381A1 (de) * 1996-11-15 1998-05-20 Hoechst Ag Neue Heterocyclen als Inhibitoren der Leukozytenadhäsion und VLA-4-Antagonisten
WO1999020309A1 (fr) 1997-10-22 1999-04-29 Eisai Co., Ltd. Agonistes de l'acide retinoique, agents preventifs et therapeutiques des nephrites
EP1027328B1 (fr) * 1997-10-31 2006-08-23 Aventis Pharma Limited Anilides substituees
EP1042279B1 (fr) * 1997-12-23 2005-03-02 Aventis Pharma Limited Beta-alanines substituees
WO1999054321A1 (fr) * 1998-04-21 1999-10-28 Aventis Pharma Limited Diamines substituees et leur utilisation en tant qu'inhibiteurs d'adhesion cellulaire

Also Published As

Publication number Publication date
ES2297943T3 (es) 2008-05-01
HUP0200481A3 (en) 2002-12-28
WO2000039103B1 (fr) 2000-09-28
HUP0200481A2 (en) 2002-06-29
BG104786A (en) 2001-04-30
WO2000039103A1 (fr) 2000-07-06
DE69937603D1 (de) 2008-01-03
AU1881900A (en) 2000-07-31
DE69937603T2 (de) 2008-10-23
AP2000001924A0 (en) 2000-09-30
EP1056728B1 (fr) 2007-11-21
US6632814B1 (en) 2003-10-14
EP1056728A1 (fr) 2000-12-06

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