BG104786A - Дихидробензо (1,4) оксазини и тетрахидрохиноксалини - Google Patents
Дихидробензо (1,4) оксазини и тетрахидрохиноксалиниInfo
- Publication number
- BG104786A BG104786A BG104786A BG10478600A BG104786A BG 104786 A BG104786 A BG 104786A BG 104786 A BG104786 A BG 104786A BG 10478600 A BG10478600 A BG 10478600A BG 104786 A BG104786 A BG 104786A
- Authority
- BG
- Bulgaria
- Prior art keywords
- linkage
- ny4y5
- alkyl
- compounds
- ny1y2
- Prior art date
Links
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)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Изобретението се отнася до физиологично активни съединения с формула@@в която R1 представлява R3-Z3-, R3-L2-R4-Z3-, R3-L3-Ar1-L4-Z3- или R3-L3-Ar1-L2-R4-Z3-; R2 означава водород, халоген, по-нисш алкил или по-нисш алкокси; А1 е правоверижна С2-3 алкиленова връзка, допълнително заместена с една или повече групи, избрани от алкил, арил, арилалкил, хетероарил, хетероарилалкил, имино, оксо, тиоксо или алкил, заместен с -ZR6, -NY1Y2, -CO2R6 или -С(=O)-NY1Y2; L1 представлява алкениленова, алкиленова,алкиниленова, циклоалкениленова, циклоалкиленова,хетероарилдиилова, хетероциклоалкиленова или ариленова връзка, всяка допълнително заместена с: (а) киселинна функционална група, циано, оксо, -S(O)mR9, R3, -C(=O)-R3, -C(=O)-OR3, -N(R8)-C(=O)-R9, -N(R8)-C(=O)-OR9, -N(R8)-SO2-R9, -NY4Y5 или -[C(=O)-N(R10)-C(R5)(R11)]p-C(=O)-NY4Y5, или (б) алкил, заместен с киселинна функционална група или -S(O)mR9,-C(=O)-NY4Y5 или -NY4Y5; -[C(=O)-N(R10)-C(R5)(R11)]p връзка; -Z2-R12-връзка; -С(=O)-CH2-C(=O)- връзка; -R12-Z2-R12- връзка; -С(R4)(R13)-[C(=O)-N(R10)-C(R5)(R11)]p- връзка или -L5-L6-L7- връзка; Z1 представлява NR17 или О; Y е карбоксигрупа (или кисел биоизостер). Изобретението се отнася и до съответните N-оксиди и техните пролекарствени средства, до фармацевтично приемливи соли и солвати на такива съединения и техните N-оксиди и пролекарствени средства. Посочените съединения имат ценни фармацевтични свойства, особено възможността да регулират взаимодействието на VCAM-1 и фибронектин с интегрина VLA-4 (алфа4 бе
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 (en) | 1998-12-23 | 1999-12-23 | Dihydro-benzo(1,4)oxazines and tetrahydroquinoxalines |
Publications (1)
Publication Number | Publication Date |
---|---|
BG104786A true BG104786A (bg) | 2001-04-30 |
Family
ID=26314897
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BG104786A BG104786A (bg) | 1998-12-23 | 2000-09-20 | Дихидробензо (1,4) оксазини и тетрахидрохиноксалини |
Country Status (10)
Country | Link |
---|---|
US (1) | US6632814B1 (bg) |
EP (1) | EP1056728B1 (bg) |
AP (1) | AP2000001924A0 (bg) |
AU (1) | AU1881900A (bg) |
BG (1) | BG104786A (bg) |
DE (1) | DE69937603T2 (bg) |
ES (1) | ES2297943T3 (bg) |
HU (1) | HUP0200481A3 (bg) |
SK (1) | SK14192000A3 (bg) |
WO (1) | WO2000039103A1 (bg) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU4591800A (en) * | 1999-05-05 | 2000-11-21 | Aventis Pharma Limited | Ureas as cell adhesion modulators |
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 |
EP3241833A1 (en) | 2010-10-18 | 2017-11-08 | Cerenis Therapeutics Holding SA | Compounds, compositions and methods useful for cholesterol mobilisation |
JP5903499B2 (ja) | 2011-12-22 | 2016-04-13 | ノバルティス アーゲー | ジヒドロ−ベンゾ−オキサジンおよびジヒドロ−ピリド−オキサジン誘導体 |
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 |
US9422281B2 (en) | 2013-11-18 | 2016-08-23 | Forma Therapeutics, Inc. | Benzopiperazine compositions as BET bromodomain inhibitors |
HUE053645T2 (hu) | 2013-11-18 | 2021-07-28 | Forma Therapeutics Inc | Tetrahidrokinolin kompozíciók mint BET bromodomén inhibitorok |
Family Cites Families (26)
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. |
KR920011020B1 (ko) * | 1989-07-03 | 1992-12-26 | 요시또미세이야꾸 가부시끼가이샤 | 벤즈아진 화합물 및 그의 의약용도 |
GB9320277D0 (en) | 1993-10-01 | 1993-11-17 | Nycomed Salutar Inc | Chelants |
ATE205837T1 (de) | 1991-04-15 | 2001-10-15 | Aventis Pharma Gmbh | Chinoxaline, verfahren zu ihrer herstellung und ihre verwendung |
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 (bg) * | 1993-03-09 | 1997-04-01 | Takeda Pharm Industry Co Ltd | |
WO1994020473A1 (en) | 1993-03-11 | 1994-09-15 | Yamanouchi Pharmaceutical Co., Ltd. | Compound with vasopressin antagonism |
US5334598A (en) | 1993-03-19 | 1994-08-02 | Merck & Co., Inc. | Six-membered ring fused imidazoles substituted with phenoxyphenylacetic acid derivatives |
AU693143B2 (en) * | 1993-12-06 | 1998-06-25 | Cytel Corporation | CS-1 peptidomimetics, compositions and methods of using the same |
WO1995029177A1 (en) | 1994-04-23 | 1995-11-02 | Smithkline Beecham P.L.C. | Tricyclic derivatives as 5ht2c and 5ht2b antagonists |
US6083961A (en) | 1994-08-03 | 2000-07-04 | Fujisawa Pharmaceutical Co., Ltd. | Benzimidazole compounds as bradykinin antagonists |
KR970707098A (ko) | 1994-10-27 | 1997-12-01 | 후지야마 아키라 | 브라디키닌 길항제로서 피리도피리미돈, 퀴놀린 및 융합된 N-헤테로사이클(Pyridopyrimidones, quinolines and fused N-heterocycles as bradykinin antagonists) |
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 |
DE69706407T2 (de) * | 1996-03-29 | 2002-05-29 | 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 |
CA2307613A1 (en) | 1997-10-22 | 1999-04-29 | Eisai Co., Ltd. | Retinoic acid agonist as a prophylactic and therapeutic agent for nephritis |
CA2303848C (en) * | 1997-10-31 | 2008-09-30 | Rhone-Poulenc Rorer Limited | Substituted anilides |
CA2316235A1 (en) * | 1997-12-23 | 1999-07-08 | Aventis Pharma Limited | Substituted .beta.-alanines |
AU3716499A (en) * | 1998-04-21 | 1999-11-08 | Aventis Pharma Limited | Substituted diamines and their use as cell adhesion inhibitors |
-
1999
- 1999-12-23 HU HU0200481A patent/HUP0200481A3/hu unknown
- 1999-12-23 ES ES99962463T patent/ES2297943T3/es not_active Expired - Lifetime
- 1999-12-23 AU AU18819/00A patent/AU1881900A/en not_active Abandoned
- 1999-12-23 DE DE69937603T patent/DE69937603T2/de not_active Expired - Lifetime
- 1999-12-23 AP APAP/P/2000/001924A patent/AP2000001924A0/en unknown
- 1999-12-23 WO PCT/GB1999/004430 patent/WO2000039103A1/en active IP Right Grant
- 1999-12-23 SK SK1419-2000A patent/SK14192000A3/sk unknown
- 1999-12-23 EP EP99962463A patent/EP1056728B1/en not_active Expired - Lifetime
-
2000
- 2000-08-23 US US09/644,308 patent/US6632814B1/en not_active Expired - Fee Related
- 2000-09-20 BG BG104786A patent/BG104786A/bg unknown
Also Published As
Publication number | Publication date |
---|---|
AP2000001924A0 (en) | 2000-09-30 |
AU1881900A (en) | 2000-07-31 |
SK14192000A3 (sk) | 2001-07-10 |
US6632814B1 (en) | 2003-10-14 |
DE69937603T2 (de) | 2008-10-23 |
EP1056728B1 (en) | 2007-11-21 |
EP1056728A1 (en) | 2000-12-06 |
DE69937603D1 (de) | 2008-01-03 |
ES2297943T3 (es) | 2008-05-01 |
WO2000039103A1 (en) | 2000-07-06 |
HUP0200481A2 (en) | 2002-06-29 |
WO2000039103B1 (en) | 2000-09-28 |
HUP0200481A3 (en) | 2002-12-28 |
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