ES2084347T3 - Derivados de 5-heteroil-indol. - Google Patents
Derivados de 5-heteroil-indol.Info
- Publication number
- ES2084347T3 ES2084347T3 ES92904837T ES92904837T ES2084347T3 ES 2084347 T3 ES2084347 T3 ES 2084347T3 ES 92904837 T ES92904837 T ES 92904837T ES 92904837 T ES92904837 T ES 92904837T ES 2084347 T3 ES2084347 T3 ES 2084347T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- hydrogen
- heteroil
- indol
- 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.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Luminescent Compositions (AREA)
Abstract
COMPUESTOS DE FORMULA (I) DONDE R1 ES HIDROGENO, ALKILO C1-C2, FENILO, BENCILO, -COR4, O SO2R4; R2 ES (1), (2) O (3); R3 ES -(CH2)D-Z; Z ES (4); R4 ES ALKILO C1-C6, FENILO, O BENCILO; R5 ES HIDROGENO O ALKILO C1-C6;R6, R7, R11, R12, Y R13, SON CADA UNO INDEPENDIENTEMENTE HIDROGENO O ALKILO C1-C6, O BIEN R8 O R9 ES HIDROGENO, ALKILO C1-C6, ALKILO C1-C6 SUSTITUIDO POR HALOGENO, 1-PIRROLIDINILMETIL, 1-PIPERIDINILMETIL, CICLOPENTILMETIL, CICLOHEXILMETIL O (5) CON EL OTRO SIENDO EL ENLACE ENTRE R3 Y Z; Q ES (6) O (7).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65471291A | 1991-02-12 | 1991-02-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2084347T3 true ES2084347T3 (es) | 1996-05-01 |
Family
ID=24625959
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES92904837T Expired - Lifetime ES2084347T3 (es) | 1991-02-12 | 1992-02-03 | Derivados de 5-heteroil-indol. |
Country Status (24)
| Country | Link |
|---|---|
| EP (1) | EP0571471B1 (es) |
| JP (1) | JPH07121942B2 (es) |
| KR (1) | KR930703305A (es) |
| AT (1) | ATE135005T1 (es) |
| AU (1) | AU655456B2 (es) |
| CA (1) | CA2101521A1 (es) |
| CZ (1) | CZ165693A3 (es) |
| DE (1) | DE69208868T2 (es) |
| DK (1) | DK0571471T3 (es) |
| ES (1) | ES2084347T3 (es) |
| FI (1) | FI933551L (es) |
| GR (1) | GR3019778T3 (es) |
| HU (1) | HUT65766A (es) |
| IE (1) | IE920442A1 (es) |
| IL (1) | IL100888A0 (es) |
| MX (1) | MX9200569A (es) |
| MY (1) | MY131298A (es) |
| NO (1) | NO932859D0 (es) |
| NZ (1) | NZ241584A (es) |
| PT (1) | PT100114A (es) |
| TW (1) | TW263508B (es) |
| WO (1) | WO1992013856A1 (es) |
| YU (1) | YU13792A (es) |
| ZA (1) | ZA92969B (es) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW288010B (es) * | 1992-03-05 | 1996-10-11 | Pfizer | |
| US5747501A (en) * | 1992-04-07 | 1998-05-05 | Pfizer, Inc. | Indole derivatives |
| GB9211277D0 (en) | 1992-05-28 | 1992-07-15 | Glaxo Group Inc | Pharmaceutical compositions |
| GB9226532D0 (en) * | 1992-12-21 | 1993-02-17 | Smithkline Beecham Plc | Compounds |
| GB9226537D0 (en) * | 1992-12-21 | 1993-02-17 | Smithkline Beecham Plc | Compounds |
| ES2070087B1 (es) * | 1993-08-13 | 1996-02-16 | Pfizer | Derivados de indol |
| US6423731B2 (en) | 1994-01-06 | 2002-07-23 | Zeneca Limited | Indole derivatives as prodrugs of 5-HT1-like receptor agonists |
| US5468768A (en) * | 1994-01-06 | 1995-11-21 | Bristol-Myers Squibb Company | Antimigraine derivatives of indolylcycloalkanylamines |
| AU694226B2 (en) * | 1994-05-19 | 1998-07-16 | Merck Sharp & Dohme Limited | Piperazine, piperidine and tetrahydropyridine derivatives ofindol-3-ylalkyl as 5-HT1D-alpha agonists |
| EP0765322B1 (en) * | 1994-06-01 | 2001-07-25 | AstraZeneca AB | Indole derivatives as prodrugs of 5-ht1-like receptor agonists |
| US5521196A (en) * | 1994-10-05 | 1996-05-28 | Eli Lilly And Company | 5-HT1F agonists for the treatment of migraine |
| US5521197A (en) * | 1994-12-01 | 1996-05-28 | Eli Lilly And Company | 3-<1-alkylenearyl>-4-<1,2,3,6-tetrahydropyridinyl>-and 3-<1-alkylenearyl>-4-piperidinyl-1h-indoles: new 5-HT1F agonists |
| GB9501865D0 (en) * | 1995-01-31 | 1995-03-22 | Merck Sharp & Dohme | Therapeutic agents |
| PL322843A1 (en) * | 1995-03-20 | 1998-02-16 | Lilly Co Eli | 5-substituted 3-91,2,3,6-tetrahydropyridin-4-yl)- and 3-9piperydin-4-4-yl0-1h-indoles nevel 5-htif natagonists |
| WO1997013512A1 (en) * | 1995-10-10 | 1997-04-17 | Eli Lilly And Company | N-[2-substituted-3-(2-aminoethyl)-1h-indol-5-yl]-amides: new 5-ht1f agonists |
| GB9523583D0 (en) * | 1995-11-17 | 1996-01-17 | Merck Sharp & Dohme | Therapeutic agents |
| FR2754709B1 (fr) | 1996-10-23 | 1999-03-05 | Sanofi Sa | Composition cosmetique contenant un antagoniste des recepteurs du neuropeptide gamma et alpha 2 antagonistes susceptibles d'etre incorpores dans une telle composition |
| FR2763243A1 (fr) * | 1997-05-14 | 1998-11-20 | Pf Medicament | Utilisation d'amines indoliques comme medicaments antithrombotiques |
| US7189753B1 (en) | 1997-11-06 | 2007-03-13 | Cady Roger K | Preemptive prophylaxis of migraine |
| ATE241615T1 (de) | 1998-03-09 | 2003-06-15 | Lundbeck & Co As H | 5-heteroaryl-substituierte indole |
| ATE252572T1 (de) * | 1998-06-30 | 2003-11-15 | Lilly Co Eli | 5-ht1f agonisten |
| ES2291024T4 (es) * | 1999-04-21 | 2009-03-01 | Nps Allelix Corp. | Compuestos de piperidina-indol con afinidad con 5-ht6. |
| WO2001034146A1 (en) * | 1999-11-08 | 2001-05-17 | Smithkline Beecham Corporation | Novel anti-infectives |
| AU9619301A (en) * | 2000-10-20 | 2002-04-29 | Biovitrum Ab | 2-, 3-, 4-, or 5-substituted-n1-(benzensulfonyl)indoles and their use in therapy |
| DE10121217A1 (de) | 2001-04-30 | 2002-10-31 | Merck Patent Gmbh | 6H-Oxazolo[4,5-e]indol-Derivate als nikotinische Acetylcholinrezeptor Liganden und/oder serotonerge Liganden |
| AU2003239508A1 (en) | 2002-05-21 | 2003-12-12 | Bristol-Myers Squibb Company | Indole compounds useful as impdh inhibitors |
| DK1581492T3 (da) * | 2002-11-28 | 2008-11-10 | Suven Life Sciences Ltd | N-arylsulfonyl-3-substituerede indoler med serotoninreceptoraffinitet, fremgangsmåde til fremstilling heraf og en farmaceutisk sammensætning indeholdende disse |
| US7332508B2 (en) * | 2002-12-18 | 2008-02-19 | Novo Nordisk A/S | Substituted homopiperidine, piperidine or pyrrolidine derivatives |
| WO2005005439A1 (en) * | 2003-07-09 | 2005-01-20 | Suven Life Sciences Limited | Benzothiazino indoles |
| US20050245540A1 (en) * | 2003-12-09 | 2005-11-03 | Fujisawa Pharmaceutical Co., Ltd. | New methods |
| WO2005121132A1 (ja) * | 2004-06-11 | 2005-12-22 | Shionogi & Co., Ltd. | 抗hcv作用を有する縮合ヘテロ環化合物 |
| MX2007012818A (es) | 2005-04-13 | 2008-01-14 | Neuraxon Inc | Compuestos indola sustituidos que tienen actividad inhibidora de nos. |
| AU2006278998A1 (en) * | 2005-07-29 | 2007-02-15 | 4Sc Ag | Novel heterocyclic NF-kB inhibitors |
| US7696229B2 (en) | 2006-02-17 | 2010-04-13 | Memory Pharmaceuticals Corporation | Compounds having 5-HT6 receptor affinity |
| CA2643822A1 (en) | 2006-04-13 | 2007-10-25 | Neuraxon, Inc | 1,5 and 3,6- substituted indole compounds having nos inhibitory activity |
| WO2008021851A2 (en) * | 2006-08-09 | 2008-02-21 | Smithkline Beecham Corporation | Novel compounds as antagonists or inverse agonists for opioid receptors |
| TW200848021A (en) | 2007-03-06 | 2008-12-16 | Wyeth Corp | Sulfonylated heterocycles useful for modulation of the progesterone receptor |
| US8673909B2 (en) | 2007-11-16 | 2014-03-18 | Neuraxon, Inc. | Indole compounds and methods for treating visceral pain |
| US9512111B2 (en) | 2010-11-08 | 2016-12-06 | Lycera Corporation | N-sulfonylated tetrahydroquinolines and related bicyclic compounds for inhibition of RORγ activity and the treatment of disease |
| WO2013169704A2 (en) | 2012-05-08 | 2013-11-14 | Merck Sharp & Dohme Corp. | TETRAHYDRONAPHTHYRIDINE AND RELATED BICYCLIC COMPOUNDS FOR INHIBITION OF RORgamma ACTIVITY AND THE TREATMENT OF DISEASE |
| AU2013259624B2 (en) | 2012-05-08 | 2017-10-19 | Lycera Corporation | Tetrahydro[1,8]naphthyridine sulfonamide and related compounds for use as agonists of RORy and the treatment of disease |
| US9783511B2 (en) | 2013-12-20 | 2017-10-10 | Lycera Corporation | Carbamate benzoxazine propionic acids and acid derivatives for modulation of RORgamma activity and the treatment of disease |
| WO2015095795A1 (en) | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | TETRAHYDRONAPHTHYRIDINE, BENZOXAZINE, AZA-BENZOXAZINE, AND RELATED BICYCLIC COMPOUNDS FOR INHIBITION OF RORgamma ACTIVITY AND THE TREATMENT OF DISEASE |
| US9663502B2 (en) | 2013-12-20 | 2017-05-30 | Lycera Corporation | 2-Acylamidomethyl and sulfonylamidomethyl benzoxazine carbamates for inhibition of RORgamma activity and the treatment of disease |
| US10532088B2 (en) | 2014-02-27 | 2020-01-14 | Lycera Corporation | Adoptive cellular therapy using an agonist of retinoic acid receptor-related orphan receptor gamma and related therapeutic methods |
| EP3209641A4 (en) | 2014-05-05 | 2018-06-06 | Lycera Corporation | Benzenesulfonamido and related compounds for use as agonists of ror and the treatement of disease |
| US9896441B2 (en) | 2014-05-05 | 2018-02-20 | Lycera Corporation | Tetrahydroquinoline sulfonamide and related compounds for use as agonists of RORγ and the treatment of disease |
| JP2018510135A (ja) | 2015-02-11 | 2018-04-12 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | RORγT阻害剤としての置換ピラゾール化合物及びその使用 |
| JP2018515491A (ja) | 2015-05-05 | 2018-06-14 | リセラ・コーポレイションLycera Corporation | RORγの作動薬及び疾患の療法として使用するジヒドロ−2H−ベンゾ[b][1,4]オキサジンスルホンアミド及び関連化合物 |
| JP6838004B2 (ja) | 2015-06-11 | 2021-03-03 | リセラ・コーポレイションLycera Corporation | RORγのアゴニストとしての使用及び疾患の治療のためのアリールジヒドロ−2H−ベンゾ[b][1,4]オキサジンスルホンアミド及び関連化合物 |
| AU2016344115A1 (en) | 2015-10-27 | 2018-05-10 | Merck Sharp & Dohme Corp. | Substituted indazole compounds as rorgammat inhibitors and uses thereof |
| EP3368535B1 (en) | 2015-10-27 | 2020-12-02 | Merck Sharp & Dohme Corp. | Heteroaryl substituted benzoic acids as rorgammat inhibitors and uses thereof |
| JP2018531957A (ja) | 2015-10-27 | 2018-11-01 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | RORγT阻害薬としての置換二環式ピラゾール化合物及びその使用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8332437D0 (en) * | 1983-12-06 | 1984-01-11 | Glaxo Group Ltd | Chemical compounds |
| US4833153A (en) * | 1985-11-08 | 1989-05-23 | Glaxo Group Limited | Indole derivatives |
| GB8600398D0 (en) * | 1986-01-08 | 1986-02-12 | Glaxo Group Ltd | Chemical compounds |
| GB8719167D0 (en) * | 1987-08-13 | 1987-09-23 | Glaxo Group Ltd | Chemical compounds |
| GB8724912D0 (en) * | 1987-10-23 | 1987-11-25 | Wellcome Found | Indole derivatives |
| DK0486666T3 (da) * | 1990-06-07 | 1998-03-30 | Zeneca Ltd | Terapeutisk heterocykliske forbindelser |
-
1992
- 1992-01-28 TW TW081100627A patent/TW263508B/zh active
- 1992-02-03 DK DK92904837.9T patent/DK0571471T3/da active
- 1992-02-03 EP EP92904837A patent/EP0571471B1/en not_active Expired - Lifetime
- 1992-02-03 DE DE69208868T patent/DE69208868T2/de not_active Expired - Fee Related
- 1992-02-03 CA CA002101521A patent/CA2101521A1/en not_active Abandoned
- 1992-02-03 ES ES92904837T patent/ES2084347T3/es not_active Expired - Lifetime
- 1992-02-03 HU HU9302328A patent/HUT65766A/hu unknown
- 1992-02-03 WO PCT/US1992/000556 patent/WO1992013856A1/en not_active Ceased
- 1992-02-03 JP JP4505422A patent/JPH07121942B2/ja not_active Expired - Lifetime
- 1992-02-03 AU AU12637/92A patent/AU655456B2/en not_active Ceased
- 1992-02-03 KR KR1019930702398A patent/KR930703305A/ko not_active Ceased
- 1992-02-03 FI FI933551A patent/FI933551L/fi not_active Application Discontinuation
- 1992-02-03 AT AT92904837T patent/ATE135005T1/de not_active IP Right Cessation
- 1992-02-03 CZ CS931656A patent/CZ165693A3/cs unknown
- 1992-02-06 IL IL100888A patent/IL100888A0/xx unknown
- 1992-02-10 MX MX9200569A patent/MX9200569A/es unknown
- 1992-02-10 PT PT100114A patent/PT100114A/pt not_active Application Discontinuation
- 1992-02-11 NZ NZ241584A patent/NZ241584A/en unknown
- 1992-02-11 YU YU13792A patent/YU13792A/sh unknown
- 1992-02-11 IE IE044292A patent/IE920442A1/en not_active Application Discontinuation
- 1992-02-11 MY MYPI92000204A patent/MY131298A/en unknown
- 1992-02-11 ZA ZA92969A patent/ZA92969B/xx unknown
-
1993
- 1993-08-11 NO NO932859A patent/NO932859D0/no unknown
-
1996
- 1996-04-29 GR GR960401158T patent/GR3019778T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0571471A1 (en) | 1993-12-01 |
| ZA92969B (en) | 1993-08-11 |
| ATE135005T1 (de) | 1996-03-15 |
| JPH06500122A (ja) | 1994-01-06 |
| PT100114A (pt) | 1993-05-31 |
| FI933551A7 (fi) | 1993-08-11 |
| AU655456B2 (en) | 1994-12-22 |
| AU1263792A (en) | 1992-09-07 |
| GR3019778T3 (en) | 1996-07-31 |
| HU9302328D0 (en) | 1993-10-28 |
| IL100888A0 (en) | 1992-11-15 |
| CZ165693A3 (en) | 1994-05-18 |
| DE69208868D1 (de) | 1996-04-11 |
| DK0571471T3 (da) | 1996-04-01 |
| MY131298A (en) | 2007-08-30 |
| NZ241584A (en) | 1994-12-22 |
| KR930703305A (ko) | 1993-11-29 |
| FI933551A0 (fi) | 1993-08-11 |
| IE920442A1 (en) | 1992-08-12 |
| WO1992013856A1 (en) | 1992-08-20 |
| DE69208868T2 (de) | 1996-10-17 |
| YU13792A (sh) | 1994-11-15 |
| TW263508B (es) | 1995-11-21 |
| CA2101521A1 (en) | 1992-08-13 |
| HUT65766A (en) | 1994-07-28 |
| NO932859L (no) | 1993-08-11 |
| EP0571471B1 (en) | 1996-03-06 |
| NO932859D0 (no) | 1993-08-11 |
| JPH07121942B2 (ja) | 1995-12-25 |
| FI933551L (fi) | 1993-08-11 |
| MX9200569A (es) | 1992-08-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2084347T3 (es) | Derivados de 5-heteroil-indol. | |
| ES8603711A1 (es) | Procedimiento para preparar compuestos benzimidazoles 2-piridilmetil-tio y sulfinil substituidos | |
| ATE226201T1 (de) | Substituierte pyridylpyrazole | |
| ES2066991T3 (es) | Agentes hipoglucemiantes de oxazolidinadiona. | |
| ATE31307T1 (de) | Benzofuran- und benzopyrancarboxamid-derivate. | |
| NZ332559A (en) | 3-mercapto-propylamine substituted 4-carbonylamino-5,5-dimethyl-thiazolidine derivatives | |
| DE69728544D1 (de) | Totalsynthese von acylfulvenen mit antitumorwirkung | |
| DE69813605D1 (de) | Benzofuranderivate | |
| NZ528997A (en) | Sulfonamides | |
| DK429089D0 (da) | Alkylbenzylaminer | |
| UY24010A1 (es) | Nuevos pirrolocarbazoles | |
| ES2064618T3 (es) | Agonistas de serotonina de tetrahidrobenz(c,d)indol. | |
| ES2121183T3 (es) | Ligandos selectivos de los receptores 5ht1d-5ht1b derivados de indol-piperacina utiles como medicamentos. | |
| FI834730A0 (fi) | 1-karboxialkanoylperhydro-indol-2-karboxylsyror och deras derivat | |
| NO902336D0 (no) | Antispasmotiske midler. | |
| PE14896A1 (es) | Aminoalcanimidazoles y triazoles acilados | |
| AR247735A1 (es) | Sulfonildiamidas sustituidas, procedimientos para su preparacion, intermediarios utilizados en el procedimiento, y su utilizacion como herbicidas y reguladoras del crecimiento de las plantas | |
| PT87048A (pt) | Process for preparing benzazepine sulfonamides antiarrhythmic agents | |
| ES2092112T3 (es) | Agentes hipoglicemicos de tiazolidindiona. | |
| CO4410332A1 (es) | Oxazoles y tiazoles sustituidos | |
| ATE41149T1 (de) | Substituierte furazane. | |
| US4010175A (en) | Thio-{62 -lactam penicillins | |
| ES2097319T3 (es) | Derivados de isoxazol como agentes protectores de la luz. | |
| ECSP951529A (es) | Compuestos farmaceuticos | |
| ATE130616T1 (de) | Stabiles hexahydrat von etoposid-4'-phosphat- dinatriumsalz. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
Ref document number: 571471 Country of ref document: ES |