IL94082A0 - 3-n-substituted carbamoyl-indole derivatives,their preparation and pharmaceutical compositions containing them - Google Patents
3-n-substituted carbamoyl-indole derivatives,their preparation and pharmaceutical compositions containing themInfo
- Publication number
- IL94082A0 IL94082A0 IL94082A IL9408290A IL94082A0 IL 94082 A0 IL94082 A0 IL 94082A0 IL 94082 A IL94082 A IL 94082A IL 9408290 A IL9408290 A IL 9408290A IL 94082 A0 IL94082 A0 IL 94082A0
- Authority
- IL
- Israel
- Prior art keywords
- preparation
- pharmaceutical compositions
- compositions containing
- substituted carbamoyl
- indole derivatives
- Prior art date
Links
- VFHUJFBEFDVZPJ-UHFFFAOYSA-N 1h-indole-2-carboxamide Chemical class C1=CC=C2NC(C(=O)N)=CC2=C1 VFHUJFBEFDVZPJ-UHFFFAOYSA-N 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D471/06—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/06—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/06—Peri-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Quinoline Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL8900963 | 1989-04-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL94082A0 true IL94082A0 (en) | 1991-01-31 |
Family
ID=19854496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL94082A IL94082A0 (en) | 1989-04-18 | 1990-04-13 | 3-n-substituted carbamoyl-indole derivatives,their preparation and pharmaceutical compositions containing them |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5102901A (fr) |
| EP (1) | EP0393766A3 (fr) |
| JP (1) | JPH02292281A (fr) |
| AU (1) | AU634534B2 (fr) |
| CA (1) | CA2014641A1 (fr) |
| IL (1) | IL94082A0 (fr) |
| NZ (1) | NZ233285A (fr) |
| ZA (1) | ZA902794B (fr) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8814277D0 (en) * | 1988-06-16 | 1988-07-20 | Glaxo Group Ltd | Chemical compounds |
| EP0375045A1 (fr) * | 1988-12-22 | 1990-06-27 | Duphar International Research B.V | Dérivés d'indoles annelés |
| US4916129A (en) * | 1989-01-19 | 1990-04-10 | E. I. Du Pont De Nemours And Company | Combination β-blocking/angiotensin II blocking antihypertensives |
| GB8913646D0 (en) * | 1989-06-14 | 1989-08-02 | Glaxo Group Ltd | Chemical compounds |
| HU211081B (en) * | 1990-12-18 | 1995-10-30 | Sandoz Ag | Process for producing indole derivatives as serotonin antagonists and pharmaceutical compositions containing the same |
| EP0914322A1 (fr) * | 1996-05-27 | 1999-05-12 | Fujisawa Pharmaceutical Co., Ltd. | Nouveaux carboxamides d'indolyle et de benzofuranyle utilises comme inhibiteurs de la production d'oxyde nitrique |
| ATE337780T1 (de) * | 2000-11-24 | 2006-09-15 | Smithkline Beecham Plc | Indoly-lsulphonyl-verbindungen zur behandlung von störungen des zns |
| AU2002336749A1 (en) * | 2001-09-21 | 2003-04-01 | Pharmacia And Upjohn Company | Tricyclic indole derivatives as 5-ht ligands |
| BRPI0417626A (pt) | 2003-12-17 | 2007-03-27 | Akzo Nobel Nv | derivado de 1-[(indol-3-il) carbonil] piperazina tricìclica, composição farmacêutica, uso de um derivado de 1-[(indol-3-il) carbonil] piperazina tricìclica |
| DE102004025000A1 (de) * | 2004-05-21 | 2005-12-08 | Bayer Technology Services Gmbh | Verfahren zur Herstellung von chemischen und pharmazeutischen Produkten mit integrierter Mehrsäulen-Chromatographie |
| CN101460458A (zh) | 2006-02-15 | 2009-06-17 | 阿勒根公司 | 具有1-磷酸-鞘氨醇(s1p)受体拮抗剂生物活性的带芳基或者杂芳基基团的吲哚-3-羧酸的酰胺、酯、硫代酰胺和硫羟酸酯化合物 |
| WO2007112322A2 (fr) * | 2006-03-28 | 2007-10-04 | Allergan, Inc. | Composés d'indole présentant une activité biologique agoniste et/ou antagoniste vis-à-vis du récepteur de la sphingosine-1-phosphate (s1p) |
| JP2010515750A (ja) | 2007-01-11 | 2010-05-13 | アラーガン インコーポレイテッド | スフィンゴシン−1−ホスフェート(s1p)受容体アンタゴニスト生物活性を有する6−置換インドール−3−カルボン酸アミド化合物 |
| US8524917B2 (en) * | 2007-01-11 | 2013-09-03 | Allergan, Inc. | 6-substituted indole-3-carboxylic acid amide compounds having sphingosine-1-phosphate (S1P) receptor antagonist biological activity |
| WO2009042485A1 (fr) * | 2007-09-24 | 2009-04-02 | Allergan, Inc. | Composés de type indole porteur de groupes hétéroaryles ayant une activité biologique de récepteur de la sphingosine-1-phosphate (s1p) |
| US8143291B2 (en) | 2008-05-09 | 2012-03-27 | Allergan, Inc. | Indole compounds bearing aryl or heteroaryl groups having sphingosine-1-phosphate (S1P) receptor biological activity |
| KR20110044893A (ko) * | 2008-08-12 | 2011-05-02 | 알러간, 인코포레이티드 | 스핑고신-1-포스페이트 (s1p) 수용체 길항제 및 이의 사용 방법 |
| US20120088800A1 (en) | 2009-06-30 | 2012-04-12 | Allergan, Inc. | 2-(SUBSTITUTED) (ARYLMETHYL, ARYLOXY and ARYLTHIO))-N-(SUBSTITUTED PYRIDIN-2-YL)-2-(SUBSTITUTED ARYL) COMPOUNDS AS SUBTYPE-SELECTIVE MODULATORS OF SPHINGOSINE-1-PHOSPHATE-3 (S1P3) RECEPTORS |
| US8168795B2 (en) * | 2009-08-11 | 2012-05-01 | Allergan, Inc. | Selective sphingosine-1-phosphate receptor antagonists |
| WO2011028927A1 (fr) | 2009-09-04 | 2011-03-10 | Allergan, Inc. | Antagonistes sélectifs des récepteurs de sphingosine-1-phosphate |
| BR112012007095A2 (pt) | 2009-09-29 | 2016-04-19 | Allergan Inc | compostos de anel de piridina condensado como moduladores subtipo-seletivos de receptores de esfingosina-1-fosfato-2 (s1p2) |
| US8741875B2 (en) | 2009-11-24 | 2014-06-03 | Allergan, Inc. | Compounds as receptor modulators with therapeutic utility |
| WO2011066184A1 (fr) * | 2009-11-24 | 2011-06-03 | Allergan, Inc. | Nouveaux composés servant de modulateurs de récepteurs présentant une utilité thérapeutique |
| WO2011082266A2 (fr) | 2009-12-30 | 2011-07-07 | Arqule, Inc. | Composés hétérocycliques substitués |
| CN103328492A (zh) | 2010-11-22 | 2013-09-25 | 阿勒根公司 | 作为受体调节剂具有疗效的新型化合物 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4691016A (en) * | 1981-11-06 | 1987-09-01 | Riker Laboratories, Inc. | Intermediates for the preparation of 8,9-dihalobenzo[ij]quinolizine carboxylic acids |
| US4808581A (en) * | 1986-03-17 | 1989-02-28 | Glaxo Group Limited | Imidazolyl- indolylpropanones as 5-HT3 receptor antagonists |
| DE3885357T2 (de) * | 1987-06-29 | 1994-03-24 | Duphar Int Res | Anellierte Indolderivate. |
| GB2209335B (en) * | 1987-09-03 | 1991-05-29 | Glaxo Group Ltd | Lactam derivatives |
| GB8720693D0 (en) * | 1987-09-03 | 1987-10-07 | Glaxo Group Ltd | Chemical compounds |
| GB8723157D0 (en) * | 1987-10-02 | 1987-11-04 | Beecham Group Plc | Compounds |
| GB8802127D0 (en) * | 1988-02-01 | 1988-03-02 | Glaxo Group Ltd | Chemical compounds |
| GB8814277D0 (en) * | 1988-06-16 | 1988-07-20 | Glaxo Group Ltd | Chemical compounds |
| US4950759A (en) * | 1988-07-07 | 1990-08-21 | Duphar International Research B.V. | Substituted 1,7-annelated 1H-indazoles |
| GB8913646D0 (en) * | 1989-06-14 | 1989-08-02 | Glaxo Group Ltd | Chemical compounds |
-
1990
- 1990-04-11 NZ NZ233285A patent/NZ233285A/en unknown
- 1990-04-11 ZA ZA902794A patent/ZA902794B/xx unknown
- 1990-04-12 EP EP19900200908 patent/EP0393766A3/fr not_active Withdrawn
- 1990-04-13 US US07/508,420 patent/US5102901A/en not_active Expired - Fee Related
- 1990-04-13 IL IL94082A patent/IL94082A0/xx unknown
- 1990-04-17 CA CA002014641A patent/CA2014641A1/fr not_active Abandoned
- 1990-04-17 JP JP2099504A patent/JPH02292281A/ja active Pending
- 1990-04-17 AU AU53614/90A patent/AU634534B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02292281A (ja) | 1990-12-03 |
| AU5361490A (en) | 1990-10-25 |
| EP0393766A2 (fr) | 1990-10-24 |
| ZA902794B (en) | 1991-04-24 |
| AU634534B2 (en) | 1993-02-25 |
| US5102901A (en) | 1992-04-07 |
| EP0393766A3 (fr) | 1991-11-06 |
| CA2014641A1 (fr) | 1990-10-18 |
| NZ233285A (en) | 1992-06-25 |
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