FR2447376A1 - Nouveaux derives de 1,2-dihydro-2-oxo-4-phenyl-3-quinoleinecarbonitrile, utiles notamment comme agents anti-inflammatoires - Google Patents
Nouveaux derives de 1,2-dihydro-2-oxo-4-phenyl-3-quinoleinecarbonitrile, utiles notamment comme agents anti-inflammatoiresInfo
- Publication number
- FR2447376A1 FR2447376A1 FR8001874A FR8001874A FR2447376A1 FR 2447376 A1 FR2447376 A1 FR 2447376A1 FR 8001874 A FR8001874 A FR 8001874A FR 8001874 A FR8001874 A FR 8001874A FR 2447376 A1 FR2447376 A1 FR 2447376A1
- Authority
- FR
- France
- Prior art keywords
- quinoleinecarbonitrile
- dihydro
- oxo
- phenyl
- derivatives
- 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.)
- Withdrawn
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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
-
- 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
- C07D281/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D281/02—Seven-membered rings
- C07D281/04—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D281/08—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D281/10—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with one six-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (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)
- Quinoline Compounds (AREA)
Abstract
LES MEDICAMENTS SELON L'INVENTION REPONDENT A LA FORMULE GENERALE: (CF DESSIN DANS BOPI) DANS LAQUELLE (CH) EST UNE CHAINE DROITE EN C-C ET R ET R SONT IDENTIQUES OU DIFFERENTS ET REPRESENTENT CHACUN L'HYDROGENE OU UN ALKYLE INFERIEUR, AVEC LA CONDITION QUE L'UN AU MOINS DES RESTES R ET R EST UN ALKYLE INFERIEUR, OU BIEN R ET R, PRIS ENSEMBLE AVEC L'ATOME D'AZOTE, FORMENT UN RADICAL HETEROCYCLIQUE A 5 OU 6CHAINONS, ET R ET R SONT IDENTIQUES OU DIFFERENTS ET PEUVENT ETRE UN ATOME D'HYDROGENE OU D'HALOGENE OU UN GROUPE ALKYLE INFERIEUR, ALCOXY INFERIEUR OU TRIFLUOROMETHYLE. ON PEUT LES ADMINISTRER EN TABLETTES, CAPSULES OU SOLUBLES OU SUSPENSIONS INJECTABLES, POUR DES DOSES JOURNALIERES SIMPLES OU MULTIPLES D'ENVIRON1 A 150MGKG, EN UNE OU EN DEUX A QUATRE PRISES PAR JOUR.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/007,069 US4232027A (en) | 1979-01-29 | 1979-01-29 | 1,2-Dihydro-2-oxo-4-phenyl-3-quinolinecarbonitrile derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
FR2447376A1 true FR2447376A1 (fr) | 1980-08-22 |
Family
ID=21724050
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR8001874A Withdrawn FR2447376A1 (fr) | 1979-01-29 | 1980-01-29 | Nouveaux derives de 1,2-dihydro-2-oxo-4-phenyl-3-quinoleinecarbonitrile, utiles notamment comme agents anti-inflammatoires |
Country Status (6)
Country | Link |
---|---|
US (1) | US4232027A (fr) |
JP (1) | JPS55102568A (fr) |
DE (1) | DE3003146A1 (fr) |
FR (1) | FR2447376A1 (fr) |
GB (1) | GB2041361B (fr) |
IT (1) | IT1145403B (fr) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0024638A1 (fr) * | 1979-08-30 | 1981-03-11 | Byk Gulden Lomberg Chemische Fabrik GmbH | Acides quinoléinone alkylcarboxyliques substitués, leur préparation et médicaments les contenant |
JPH03181465A (ja) * | 1989-12-11 | 1991-08-07 | Takeda Chem Ind Ltd | キノリン誘導体 |
US5650410A (en) * | 1994-03-08 | 1997-07-22 | Takeda Chemical Industries, Ltd. | Pharmaceutical composition containing quinoline or quinazoline derivatives and derivatives therefor |
US7825131B2 (en) * | 2003-09-23 | 2010-11-02 | Merck Sharp & Dohme Corp. | Quinoline potassium channel inhibitors |
HUE056777T2 (hu) | 2016-12-22 | 2022-03-28 | Amgen Inc | Benzizotiazol-, izotiazolo[3,4-b]piridin-, kinazolin-, ftálazin-, pirido[2,3-d]piridazin- és pirido[2,3-d]pirimidin-származékok mint KRAS G12C inhibitorok tüdõ-, hasnyálmirigy- vagy vastagbélrák kezelésére |
JOP20190272A1 (ar) | 2017-05-22 | 2019-11-21 | Amgen Inc | مثبطات kras g12c وطرق لاستخدامها |
MA50077A (fr) | 2017-09-08 | 2020-07-15 | Amgen Inc | Inhibiteurs de kras g12c et leurs procédés d'utilisation |
CA3098574A1 (fr) | 2018-05-04 | 2019-11-07 | Amgen Inc. | Inhibiteurs de kras g12c et leurs procedes d'utilisation |
MX2020011582A (es) | 2018-05-04 | 2020-11-24 | Amgen Inc | Inhibidores de kras g12c y metodos para su uso. |
MA52564A (fr) | 2018-05-10 | 2021-03-17 | Amgen Inc | Inhibiteurs de kras g12c pour le traitement du cancer |
MA52765A (fr) | 2018-06-01 | 2021-04-14 | Amgen Inc | Inhibiteurs de kras g12c et leurs procédés d'utilisation |
AU2019284472B2 (en) * | 2018-06-11 | 2024-05-30 | Amgen Inc. | KRAS G12C inhibitors for treating cancer |
CA3100390A1 (fr) | 2018-06-12 | 2020-03-12 | Amgen Inc. | Inhibiteurs de kras g12c regroupant un cycle de piperazine et utilisation dans le traitement du cancer |
JP7516029B2 (ja) | 2018-11-16 | 2024-07-16 | アムジエン・インコーポレーテツド | Kras g12c阻害剤化合物の重要な中間体の改良合成法 |
MX2021005700A (es) | 2018-11-19 | 2021-07-07 | Amgen Inc | Inhibidores de kras g12c y metodos de uso de los mismos. |
JP7377679B2 (ja) | 2018-11-19 | 2023-11-10 | アムジエン・インコーポレーテツド | がん治療のためのkrasg12c阻害剤及び1種以上の薬学的に活性な追加の薬剤を含む併用療法 |
EP3738593A1 (fr) | 2019-05-14 | 2020-11-18 | Amgen, Inc | Dosage d'inhibiteur de kras pour le traitement de cancers |
US11236091B2 (en) | 2019-05-21 | 2022-02-01 | Amgen Inc. | Solid state forms |
US20240190842A1 (en) * | 2022-11-09 | 2024-06-13 | Accutar Biotechnology Inc. | Substituted quinolinone-8-carbonitrile derivatives having androgen degradation activity and uses thereof |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3210358A (en) * | 1961-08-09 | 1965-10-05 | Geigy Chem Corp | Substituted 4-amino carbostyrils |
CH471784A (de) * | 1966-01-26 | 1969-04-30 | Bayer Ag | Verfahren zur Herstellung von Carbostyrilderivaten |
US3763153A (en) * | 1972-02-22 | 1973-10-02 | Squibb & Sons Inc | Benzothiazines |
US3895006A (en) * | 1974-04-19 | 1975-07-15 | Squibb & Sons Inc | 5-(Substituted amino)alkyl)-2-aryl-3-halo-1,5-benzothiazepin-4(5H)-ones |
US3994900A (en) * | 1976-01-23 | 1976-11-30 | E. R. Squibb & Sons, Inc. | 6-(Or 8)-[[(substituted amino)alkyl]oxy(or thio)]-3,4-dihydro-4-phenyl-2(1H)-quinolinones |
-
1979
- 1979-01-29 US US06/007,069 patent/US4232027A/en not_active Expired - Lifetime
-
1980
- 1980-01-03 GB GB8000160A patent/GB2041361B/en not_active Expired
- 1980-01-11 IT IT8047580A patent/IT1145403B/it active
- 1980-01-28 JP JP923380A patent/JPS55102568A/ja active Pending
- 1980-01-29 FR FR8001874A patent/FR2447376A1/fr not_active Withdrawn
- 1980-01-29 DE DE19803003146 patent/DE3003146A1/de not_active Withdrawn
Non-Patent Citations (1)
Title |
---|
CA1973 * |
Also Published As
Publication number | Publication date |
---|---|
IT8047580A0 (it) | 1980-01-11 |
JPS55102568A (en) | 1980-08-05 |
GB2041361B (en) | 1982-12-08 |
IT1145403B (it) | 1986-11-05 |
GB2041361A (en) | 1980-09-10 |
DE3003146A1 (de) | 1980-08-07 |
US4232027A (en) | 1980-11-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
RE | Withdrawal of published application |