ZA928727B - 3-sulfonylamino-2(1H)-quinolone compounds, process for preparing them and pharmaceutical compositions containing them. - Google Patents
3-sulfonylamino-2(1H)-quinolone compounds, process for preparing them and pharmaceutical compositions containing them.Info
- Publication number
- ZA928727B ZA928727B ZA928727A ZA928727A ZA928727B ZA 928727 B ZA928727 B ZA 928727B ZA 928727 A ZA928727 A ZA 928727A ZA 928727 A ZA928727 A ZA 928727A ZA 928727 B ZA928727 B ZA 928727B
- Authority
- ZA
- South Africa
- Prior art keywords
- branched
- linear
- trihalomethyl
- unsubstituted
- substituted
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic 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
- C07D215/16—Heterocyclic 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
- C07D215/38—Nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Quinoline Compounds (AREA)
Abstract
Compounds of formula (I): <IMAGE> in which: X, Y, Z - which are identical or different, represent a hydrogen atom, a halogen atom or a nitro, cyano, azido, trihalomethyl, linear or branched (C1-C6)alkyl, linear or branched (C1-C6)alkoxy, or amino (unsubstituted or substituted by a linear or branched (C1-C6)acyl group) group, - or else, when they are situated on two adjacent carbons, form, with the carbon atoms to which they are attached, a phenyl ring or a 5- or 6-membered heterocycle containing from 1 to 3 hetero atoms, preferably a 1,2,5-oxadiazole ring, R represents a linear or branched (C1-C6)alkyl, trihalomethyl, phenyl (unsubstituted or substituted by one or a number of halogen atoms or linear or branched (C1-C6)alkyl, trihalomethyl or linear or branched (C1-C6)alkoxy groups), 2-thienyl (unsubstituted or substituted by a halogen atom), naphthyl or styryl group, A represents a CH radical or a nitrogen atom. Medicaments.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9113977A FR2683818B1 (en) | 1991-11-14 | 1991-11-14 | NOVEL 3-SULFONYLAMINO-2- (1H) -QUINOLEINONE DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA928727B true ZA928727B (en) | 1993-05-10 |
Family
ID=9418879
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA928727A ZA928727B (en) | 1991-11-14 | 1992-11-12 | 3-sulfonylamino-2(1H)-quinolone compounds, process for preparing them and pharmaceutical compositions containing them. |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP0542609B1 (en) |
JP (1) | JPH06102650B2 (en) |
AT (1) | ATE111082T1 (en) |
AU (1) | AU651255B2 (en) |
CA (1) | CA2082856A1 (en) |
DE (1) | DE69200394T2 (en) |
DK (1) | DK0542609T3 (en) |
ES (1) | ES2064156T3 (en) |
FR (1) | FR2683818B1 (en) |
NZ (1) | NZ245127A (en) |
ZA (1) | ZA928727B (en) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2709489B1 (en) * | 1993-08-31 | 1995-10-20 | Adir | New derivatives of 2- (1H) -quinolineone, their preparation process and the pharmaceutical compositions containing them. |
FR2750988B1 (en) * | 1996-07-11 | 1998-09-18 | Adir | NOVEL 2- (1H) -QUINOLEINONE DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
US20020065296A1 (en) | 1999-01-13 | 2002-05-30 | Bayer Corporation | Heteroaryl ureas containing nitrogen hetero-atoms as p38 kinase inhibitors |
CA2359244C (en) | 1999-01-13 | 2013-10-08 | Bayer Corporation | .omega.-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors |
SI1690853T1 (en) | 1999-01-13 | 2010-07-30 | Bayer Healthcare Llc | Use of omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
BR0013597A (en) | 1999-08-27 | 2002-07-16 | Ligand Pharm Inc | Androgen receptor modulating compounds and methods |
US6566372B1 (en) | 1999-08-27 | 2003-05-20 | Ligand Pharmaceuticals Incorporated | Bicyclic androgen and progesterone receptor modulator compounds and methods |
AU6941200A (en) | 1999-08-27 | 2001-03-26 | Ligand Pharmaceuticals Incorporated | 8-substituted-6-trifluoromethyl-9-pyrido(3,2-g)quinoline compounds as androgen receptor modulators |
PE20010647A1 (en) | 1999-09-14 | 2001-06-23 | Lilly Co Eli | RETINOID X RECEPTOR MODULATORS (RXR) WITH IMPROVED PHARMACOLOGICAL PROFILE |
FR2805262A1 (en) * | 2000-02-18 | 2001-08-24 | Adir | NOVEL PHYPHONIC ARYL OR HETEROARYL QUINOLINYL ACID DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
FR2805260A1 (en) * | 2000-02-18 | 2001-08-24 | Adir | NOVEL 6-SULFAMOYL-3-QUINOLINYL PHOSPHONIC ACID DERIVATIVES, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME |
FR2805261A1 (en) * | 2000-02-18 | 2001-08-24 | Adir | NOVEL 6-AMINO OR 6-HYDRAZINOSULFONYL-3- QUINOLINYL PHOSPHONIC ACID DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
TWI298068B (en) * | 2000-06-21 | 2008-06-21 | Dainippon Sumitomo Pharma Co | Pharmaceutical composition for schizophrenia |
PT1626714E (en) | 2003-05-20 | 2007-08-24 | Bayer Pharmaceuticals Corp | Diaryl ureas for diseases mediated by pdgfr |
CA2536349A1 (en) | 2003-08-22 | 2005-03-03 | Ligand Pharmaceuticals Incorporated | 6-cycloamino-2-quinolinone derivatives as androgen receptor modulator compounds |
JP2009513707A (en) | 2005-10-31 | 2009-04-02 | バイエル ヘルスケア リミティド ライアビリティ カンパニー | Diaryl urea and concomitant drugs |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3066145A (en) * | 1962-02-07 | 1962-11-27 | American Home Prod | 3-amino-6-chloro-4-phenyl-2(1h)-quinolone |
EP0386839B1 (en) * | 1989-03-08 | 1997-01-15 | Merck Sharp & Dohme Ltd. | Tetrahydroquinoline derivatives useful for neurodegenerative disorders |
GB9004288D0 (en) * | 1990-02-26 | 1990-04-18 | Almirall Lab | New 4(1h)quinoline derivatives |
-
1991
- 1991-11-14 FR FR9113977A patent/FR2683818B1/en not_active Expired - Fee Related
-
1992
- 1992-11-09 DE DE69200394T patent/DE69200394T2/en not_active Expired - Fee Related
- 1992-11-09 EP EP92403014A patent/EP0542609B1/en not_active Expired - Lifetime
- 1992-11-09 ES ES92403014T patent/ES2064156T3/en not_active Expired - Lifetime
- 1992-11-09 DK DK92403014.1T patent/DK0542609T3/en active
- 1992-11-09 AT AT92403014T patent/ATE111082T1/en active
- 1992-11-12 ZA ZA928727A patent/ZA928727B/en unknown
- 1992-11-13 CA CA002082856A patent/CA2082856A1/en not_active Abandoned
- 1992-11-13 AU AU28351/92A patent/AU651255B2/en not_active Ceased
- 1992-11-13 NZ NZ24512792A patent/NZ245127A/en unknown
- 1992-11-16 JP JP4305550A patent/JPH06102650B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
AU651255B2 (en) | 1994-07-14 |
DE69200394T2 (en) | 1995-04-27 |
EP0542609A1 (en) | 1993-05-19 |
DE69200394D1 (en) | 1994-10-13 |
AU2835192A (en) | 1993-05-20 |
JPH05221997A (en) | 1993-08-31 |
FR2683818B1 (en) | 1993-12-31 |
ATE111082T1 (en) | 1994-09-15 |
EP0542609B1 (en) | 1994-09-07 |
FR2683818A1 (en) | 1993-05-21 |
CA2082856A1 (en) | 1993-05-15 |
DK0542609T3 (en) | 1995-03-20 |
JPH06102650B2 (en) | 1994-12-14 |
ES2064156T3 (en) | 1995-01-16 |
NZ245127A (en) | 1994-07-26 |
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