LV12090B - DERIVATIVES OF IMIDAZOL, TRIAZOL AND TETRAZOL - Google Patents
DERIVATIVES OF IMIDAZOL, TRIAZOL AND TETRAZOL Download PDFInfo
- Publication number
- LV12090B LV12090B LVP-98-54A LV980054A LV12090B LV 12090 B LV12090 B LV 12090B LV 980054 A LV980054 A LV 980054A LV 12090 B LV12090 B LV 12090B
- Authority
- LV
- Latvia
- Prior art keywords
- indol
- formula
- group
- ylmethyl
- ethylamine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07D409/04—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 directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Neurosurgery (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pain & Pain Management (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Epoxy Resins (AREA)
- Paints Or Removers (AREA)
- Lubricants (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Photoreceptors In Electrophotography (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Dental Preparations (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB919102222A GB9102222D0 (en) | 1991-02-01 | 1991-02-01 | Therapeutic agents |
GB919106917A GB9106917D0 (en) | 1991-04-03 | 1991-04-03 | Therapeutic agents |
GB919113415A GB9113415D0 (en) | 1991-06-21 | 1991-06-21 | Therapeutic agents |
GB919122451A GB9122451D0 (en) | 1991-10-23 | 1991-10-23 | Therapeutic agents |
Publications (2)
Publication Number | Publication Date |
---|---|
LV12090A LV12090A (lv) | 1998-07-20 |
LV12090B true LV12090B (en) | 1998-09-20 |
Family
ID=27450619
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
LVP-98-54A LV12090B (en) | 1991-02-01 | 1998-03-17 | DERIVATIVES OF IMIDAZOL, TRIAZOL AND TETRAZOL |
Country Status (30)
Country | Link |
---|---|
US (4) | US5298520A (zh) |
EP (2) | EP0778275B1 (zh) |
JP (1) | JP2500280B2 (zh) |
KR (1) | KR100212111B1 (zh) |
CN (4) | CN1038681C (zh) |
AT (1) | ATE158582T1 (zh) |
BG (1) | BG62024B2 (zh) |
CA (2) | CA2238140C (zh) |
CY (1) | CY2095B1 (zh) |
CZ (1) | CZ283018B6 (zh) |
DE (2) | DE19975007I2 (zh) |
DK (1) | DK0497512T3 (zh) |
ES (2) | ES2162188T3 (zh) |
FI (1) | FI107154B (zh) |
GR (2) | GR3025026T3 (zh) |
HR (1) | HRP930777B1 (zh) |
HU (2) | HU222350B1 (zh) |
IE (1) | IE920342A1 (zh) |
IL (1) | IL100756A (zh) |
LU (1) | LU90338I2 (zh) |
LV (1) | LV12090B (zh) |
MX (1) | MX9200405A (zh) |
NL (1) | NL980019I1 (zh) |
NO (2) | NO180447C (zh) |
NZ (1) | NZ241394A (zh) |
SA (1) | SA94140534B1 (zh) |
SG (1) | SG50409A1 (zh) |
SI (1) | SI9210101B (zh) |
SK (1) | SK278998B6 (zh) |
YU (1) | YU48236B (zh) |
Families Citing this family (123)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ238424A (en) * | 1990-06-07 | 1993-12-23 | Wellcome Found | 3,5-substituted indole derivatives; medicaments and preparatory processes. |
US5607951A (en) * | 1990-10-15 | 1997-03-04 | Pfizer Inc | Indole derivatives |
US5545644A (en) * | 1990-10-15 | 1996-08-13 | Pfizer Inc. | Indole derivatives |
US5559246A (en) * | 1990-10-15 | 1996-09-24 | Pfizer Inc. | Indole derivatives |
US5578612A (en) * | 1990-10-15 | 1996-11-26 | Pfizer Inc. | Indole derivatives |
US5559129A (en) * | 1990-10-15 | 1996-09-24 | Pfizer Inc | Indole derivatives |
EP0596933A1 (en) * | 1991-08-03 | 1994-05-18 | Smithkline Beecham Plc | 5-ht4 receptor antagonists |
GB9201038D0 (en) * | 1992-01-16 | 1992-03-11 | Glaxo Group Ltd | Chemical compounds |
TW288010B (zh) * | 1992-03-05 | 1996-10-11 | Pfizer | |
EP0630374B1 (en) * | 1992-03-13 | 2001-09-05 | MERCK SHARP & DOHME LTD. | Imidazole, triazole and tetrazole derivatives |
GB9207396D0 (en) * | 1992-04-03 | 1992-05-13 | Merck Sharp & Dohme | Therapeutic agents |
US6380233B1 (en) | 1992-04-07 | 2002-04-30 | Pfizer Inc | Indole derivatives as 5-HT1 agonists |
JP2644088B2 (ja) | 1992-04-07 | 1997-08-25 | フアイザー・インコーポレイテツド | 5−ht1作動薬としてのインドール誘導体 |
GB9207930D0 (en) * | 1992-04-10 | 1992-05-27 | Pfizer Ltd | Indoles |
NZ251047A (en) * | 1992-04-10 | 1996-09-25 | Pfizer | Acylaminoindole derivatives and medicaments |
GB9208463D0 (en) * | 1992-04-16 | 1992-06-03 | Merck Sharp & Dohme | Therapeutic agents |
GB9210400D0 (en) * | 1992-05-15 | 1992-07-01 | Merck Sharp & Dohme | Therapeutic agents |
GB9211277D0 (en) | 1992-05-28 | 1992-07-15 | Glaxo Group Inc | Pharmaceutical compositions |
HUT71403A (en) * | 1992-06-05 | 1995-11-28 | Merck Sharp & Dohme | The sulphate salt of a substituted triazole, pharmaceutical compositions thereof, and their use in therapy |
GB9215526D0 (en) * | 1992-07-22 | 1992-09-02 | Merck Sharp & Dohme | Chemical process |
AU672802B2 (en) * | 1992-07-24 | 1996-10-17 | Merck Sharp & Dohme Limited | Imidazole, triazole and tetrazole derivatives |
IL106445A (en) * | 1992-07-30 | 1998-01-04 | Merck Sharp & Dohme | History of 1,2,4-Trans-Triazole 4-Transform, Preparation and Pharmaceutical Preparations Containing Them |
TW251284B (zh) * | 1992-11-02 | 1995-07-11 | Pfizer | |
GB9226537D0 (en) * | 1992-12-21 | 1993-02-17 | Smithkline Beecham Plc | Compounds |
FR2701026B1 (fr) * | 1993-02-02 | 1995-03-31 | Adir | Nouveaux dérivés de l'indole, de l'indazole et du benzisoxazole, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent. |
US6060473A (en) * | 1993-04-01 | 2000-05-09 | Ucb S.A. - Dtb | 7-azabicyclo[2.2.1]-heptane and -heptene derivatives as cholinergic receptor ligands |
US5817679A (en) * | 1993-04-01 | 1998-10-06 | University Of Virginia | 7-Azabicyclo 2.2.1!-heptane and -heptene derivatives as cholinergic receptor ligands |
AU686654B2 (en) * | 1993-08-31 | 1998-02-12 | Pfizer Inc. | 5-arylindole derivatives |
HUT74949A (en) | 1993-09-10 | 1997-03-28 | Cytomed | Epibatidine and derivatives thereof as cholinergic receptor agonists and antagonists |
GB9402016D0 (en) * | 1994-02-02 | 1994-03-30 | Merck Sharp & Dohme | Therapeutic agents |
GB9402011D0 (en) * | 1994-02-02 | 1994-03-30 | Merck Sharp & Dohme | Therapeutic agents |
US6117889A (en) * | 1994-04-01 | 2000-09-12 | University Of Virginia | 7-Azabicyclo-[2.2.1]-heptane and -heptene derivatives as analgesics and anti-inflammatory agents |
US5552402A (en) * | 1994-05-19 | 1996-09-03 | Merck, Sharp & Dohme Ltd. | Five-membered heteroaromatic compounds as 5-HT receptor agonists |
US5807857A (en) * | 1994-05-19 | 1998-09-15 | Merck Sharp & Dohme Ltd. | Piperazine, piperidine and tetrahydropyridine derivative of indol-3-alkyl as 5-HT1D-α agonists |
GB9410031D0 (en) * | 1994-05-19 | 1994-07-06 | Merck Sharp & Dohme | Therapeutic agents |
US5567824A (en) * | 1994-05-24 | 1996-10-22 | Merck & Co., Inc. | Palladium catalyzed ring closure of triazolyltryptamine |
WO1996003400A1 (en) * | 1994-07-26 | 1996-02-08 | Pfizer Inc. | 4-indole derivatives as serotonin agonists and antagonists |
WO1996004274A1 (en) * | 1994-08-02 | 1996-02-15 | Merck Sharp & Dohme Limited | Azetidine, pyrrolidine and piperidine derivatives |
GB9417310D0 (en) | 1994-08-27 | 1994-10-19 | Pfizer Ltd | Therapeutic agents |
US5521196A (en) * | 1994-10-05 | 1996-05-28 | Eli Lilly And Company | 5-HT1F agonists for the treatment of migraine |
GB9423460D0 (en) * | 1994-11-21 | 1995-01-11 | Merck Sharp & Dohme | Therapeutic agents |
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 |
US5484763A (en) * | 1995-02-10 | 1996-01-16 | American Cyanamid Company | Substituted benzisoxazole and benzisothiazole herbicidal agents |
TR199700993T1 (xx) * | 1995-03-20 | 1998-03-21 | Eli Lilly And Company | 5-ikameli-3-(1,2,3,6-tetrahidropridin-4-il)- ve 3-(piperidin-4-il)-1H-indoller: yeni 5-HT1F agonistler. |
US5602168A (en) * | 1995-07-10 | 1997-02-11 | Neurogen Corporation | 1-(N'-(arylalkylaminoalkyl)) aminoisoindoles; dopamine receptor subtype specific ligands |
US5656632A (en) * | 1995-06-05 | 1997-08-12 | Neurogen Corporation | 1-(N'-(arylalkylaminoalkyl)) aminoisoindoles; dopamine receptor subtype specific ligands |
US6245768B1 (en) | 1995-06-05 | 2001-06-12 | Neurogen Corporation | 1-(N′-(arylalkylaminoalkyl)) aminoisoindoles; a new class of dopamine receptor subtype specific ligands |
WO1997003068A1 (en) * | 1995-07-11 | 1997-01-30 | Merck & Co., Inc. | A triazolylmethyl-indole ethylamine bisulfate salt |
ZA965837B (en) * | 1995-07-11 | 1997-01-31 | Merck & Co Inc | A triazolylmethyl-indole ethylamine bisulfate salt |
US5942536A (en) * | 1995-10-10 | 1999-08-24 | Eli Lilly And Company | N- 2-substituted-3-(2-aminoethyl)-1H-indol-5-YL!-Amides: new 5-HT1F agonists |
US5998415A (en) * | 1995-11-02 | 1999-12-07 | Merck Sharp & Dohme Ltd. | Bicyclic heteroaryl-alkylene-(homo)piperazinones and thione analogues thereof, their preparation, and their use of as selective agonists of 5-HT1 -like receptors |
GB9523583D0 (en) * | 1995-11-17 | 1996-01-17 | Merck Sharp & Dohme | Therapeutic agents |
GB9610978D0 (en) * | 1996-05-24 | 1996-07-31 | Merck Sharp & Dohme | Therapeutic agents |
US5811551A (en) * | 1996-08-13 | 1998-09-22 | Merck & Co., Inc. | Palladium catalyzed indolization |
US5808064A (en) * | 1996-08-13 | 1998-09-15 | Merck & Co., Inc. | Palladium catalyzed indolization |
US5877329A (en) * | 1996-08-13 | 1999-03-02 | Merck & Co., Inc. | Palladium catalyzed indolization |
EP0944428B1 (de) | 1996-08-19 | 2013-06-26 | Volkswagen Aktiengesellschaft | Verfahren zum Betrieb einer Brennkraftmaschine mit einen NOx-Adsorber |
DE59712848D1 (de) | 1996-08-19 | 2007-07-05 | Volkswagen Ag | Fremdgezündete Brennkraftmaschine mit einem NOx-Absorber |
GB9620777D0 (en) * | 1996-10-07 | 1996-11-20 | Merck Sharp & Dohme | Therapeutic use |
US5998438A (en) * | 1996-11-26 | 1999-12-07 | Allelix Biopharmaceuticals, Inc. | 5-cyclo indole compounds |
US6066092A (en) * | 1997-11-06 | 2000-05-23 | Cady; Roger K. | Preemptive prophylaxis of migraine device and method |
US7189753B1 (en) | 1997-11-06 | 2007-03-13 | Cady Roger K | Preemptive prophylaxis of migraine |
EP1068198B1 (en) * | 1998-03-09 | 2003-05-28 | H.Lundbeck A/S | 5-heteroaryl substituted indoles |
DE69922688T2 (de) * | 1998-11-02 | 2005-12-01 | Merck & Co. Inc. | Zusammensetzungen aus einem 5ht1b/1d agonisten und einem selektiven cox-2 hemmer zur behandlung von migräne |
US5994352A (en) * | 1998-11-13 | 1999-11-30 | Pfizer Inc. | 5-arylindole derivatives |
CO5190664A1 (es) * | 1999-06-30 | 2002-08-29 | Pfizer Prod Inc | Terapia de combinacion para el tratamiento de migrana administracion de un receptor 5ht, cafeina y un inhibidor de ciclooxigenasa-2 |
EP1341777B1 (en) * | 2000-11-29 | 2007-09-26 | Eli Lilly And Company | 1-(2-m-methanesulfonamidophenylethyl)-4-(m-trifluoromethylphenyl)piperazine and pharmaceutically acceptable salts and solvates thereof and their use in the treatement of incontinence |
WO2002079153A1 (en) * | 2001-03-28 | 2002-10-10 | Biocatalytics, Inc. | Method for producing tryptamine derivatives |
CN1649614A (zh) | 2002-02-22 | 2005-08-03 | 新河药品股份有限公司 | 活性剂传递系统和保护及施用活性剂的方法 |
DE10214228A1 (de) * | 2002-03-22 | 2003-10-02 | Bdd Group Holding Ag Zug | Deuterierte substitutierte Indole sowie diese Verbindungen enthaltende Arzneimittel |
AU2003249582B2 (en) | 2002-06-21 | 2006-08-03 | Suven Life Sciences Limited | Tetracyclic arylsulfonyl indoles having serotonin receptor affinity |
BR0312175A (pt) | 2002-06-21 | 2005-04-05 | Suven Life Sciences Ltd | Composto, composição farmacêutica, uso de um composto, método para o tratamento e método para reduzir a morbidez e a mortalidade associadas com o excesso de peso |
ES2204303B2 (es) | 2002-08-07 | 2004-12-16 | Laboratorios Vita, S.A. | Procedimiento para la obtencion de un compuesto farmaceuticamente activo. |
ES2310243T3 (es) | 2002-11-28 | 2009-01-01 | Suven Life Sciences Limited | Indoles n-aril-3-sulfonil sustituidos que tienen afinidad por receptores de serotonina, proceso para su preparacion y composicion farmaceutica que los contiene. |
KR100776118B1 (ko) | 2002-11-28 | 2007-11-15 | 수벤 라이프 사이언시스 리미티드 | 엔-아릴술포닐-3-아미노알콕시인돌 |
JP4571507B2 (ja) | 2002-12-18 | 2010-10-27 | スベン ライフ サイエンシズ リミティド | セロトニン受容体親和性を有する四環系3−置換インドール |
EP1572647B1 (en) | 2002-12-20 | 2016-09-21 | Basf Se | Synthesis of amines and intermediates for the synthesis thereof |
KR100572325B1 (ko) * | 2003-12-17 | 2006-04-19 | 삼성전자주식회사 | 이온 주입 장치 및 이를 이용한 이온 주입 방법 |
CA2552663A1 (en) | 2004-01-09 | 2005-07-28 | Ratiopharm Gmbh | Crystalline forms of rizatriptan benzoate |
WO2005075422A1 (en) * | 2004-01-28 | 2005-08-18 | Ratiopharm Gmbh | Synthesis methods and intermediates for the manufacture of rizatriptan |
WO2006053116A2 (en) * | 2004-11-10 | 2006-05-18 | Dr. Reddy's Laboratories Ltd. | Rizatriptan process |
KR101374553B1 (ko) * | 2004-11-18 | 2014-03-17 | 신타 파마슈티칼스 코프. | Hsp90 활성을 조절하는 트리아졸 화합물 |
WO2006082598A2 (en) * | 2005-02-01 | 2006-08-10 | Natco Pharma Limited | Novel crystalline forms of rizatriptan benzoate |
WO2006137083A1 (en) * | 2005-06-20 | 2006-12-28 | Natco Pharma Limited | Improved process for the preparation of rizatriptan benzoate |
ES2270717B1 (es) * | 2005-08-08 | 2008-03-01 | Ragactives, S.L. | Procedimiento para la obtencion de derivados de triptamina. |
EP1915369A4 (en) * | 2005-08-11 | 2010-09-08 | Merck Frosst Canada Ltd | NEW SUBSTITUTED 1,2,3-TRIAZOLYLMETHYLBENZOTHIOPHENE OR ENDOLE AND THEIR USE AS INHIBITORS OF LEUKOTRIENBIOSYNTHESIS |
JP5118039B2 (ja) * | 2005-08-18 | 2013-01-16 | シンタ ファーマシューティカルズ コーポレーション | Hsp90活性を調節するトリアゾール化合物 |
EP1951713A1 (en) * | 2005-11-14 | 2008-08-06 | Matrix Laboratories Ltd | Process for the large scale production of rizatriptan benzoate |
WO2007083320A2 (en) | 2006-01-19 | 2007-07-26 | Matrix Laboratories Ltd | Conversion of aromatic diazonium salt to aryl hydrazine |
AU2007267847B2 (en) | 2006-05-25 | 2012-04-12 | Synta Pharmaceuticals Corp. | Triazole compounds that modulate Hsp90 activity |
EP2035396B1 (en) | 2006-05-25 | 2014-05-14 | Synta Pharmaceuticals Corp. | Triazole compounds that modulate hsp90 activity |
CA2653327A1 (en) * | 2006-05-25 | 2007-12-06 | Synta Pharmaceuticals Corp. | Compounds that modulate hsp90 activity and methods for identifying same |
EP2038262B1 (en) * | 2006-05-25 | 2014-11-12 | Synta Pharmaceuticals Corp. | Triazole compounds that modulate hsp90 activity |
SI2124556T1 (sl) | 2006-10-09 | 2015-01-30 | Charleston Laboratories, Inc. | Farmacevtske sestave |
EP2160390A1 (en) * | 2007-06-04 | 2010-03-10 | Generics Ýuk¨Limited | Novel process |
AU2008310883A1 (en) * | 2007-10-09 | 2009-04-16 | Hamann, Mark T | Method to use compositions having antidepressant anxiolytic and other neurological activity and compositions of matter |
US8124126B2 (en) | 2008-01-09 | 2012-02-28 | Charleston Laboratories, Inc. | Pharmaceutical compositions |
US20090294028A1 (en) * | 2008-06-03 | 2009-12-03 | Nanochip, Inc. | Process for fabricating high density storage device with high-temperature media |
EP2451274B1 (en) | 2009-07-08 | 2017-10-04 | Charleston Laboratories, Inc. | Pharmaceutical compositions |
EP2482744A4 (en) * | 2009-10-02 | 2017-01-04 | Cardiofocus, Inc. | Cardiac ablation system with inflatable member having multiple inflation settings |
EP2533640B1 (en) * | 2010-02-08 | 2016-09-28 | Medivation Technologies, Inc. | Processes of synthesizing dihydropyridophthalazinone derivatives |
US9205086B2 (en) | 2010-04-19 | 2015-12-08 | Synta Pharmaceuticals Corp. | Cancer therapy using a combination of a Hsp90 inhibitory compounds and a EGFR inhibitor |
CA2853806C (en) | 2011-11-02 | 2020-07-14 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitors with platinum-containing agents |
WO2013067162A1 (en) | 2011-11-02 | 2013-05-10 | Synta Pharmaceuticals Corp. | Cancer therapy using a combination of hsp90 inhibitors with topoisomerase i inhibitors |
AU2012339679A1 (en) | 2011-11-14 | 2014-06-12 | Synta Pharmaceuticals Corp. | Combination therapy of Hsp90 inhibitors with BRAF inhibitors |
WO2013120045A1 (en) * | 2012-02-10 | 2013-08-15 | University Of Utah Research Foundation | Substituted 1h-indazol-1-ol analogs as inhibitors of beta catenin/tcf protein-protein interactions |
CN103739594A (zh) * | 2012-10-17 | 2014-04-23 | 南京大学 | 一类含吡嗪环和三氮唑结构的席夫碱类衍生物及其制法 |
RS60353B1 (sr) | 2015-05-20 | 2020-07-31 | Amgen Inc | Agonisti triazola apj receptora |
WO2017072584A1 (en) * | 2015-10-28 | 2017-05-04 | Dr. Reddy's Laboratories Ltd. | Pharmaceutical compositions for rizatriptan |
EP3407869A1 (en) | 2016-01-27 | 2018-12-05 | Instar Technologies A.S. | Oromucosal nanofiber carriers for therapeutic treatment |
JP2019507181A (ja) | 2016-03-04 | 2019-03-14 | チャールストン ラボラトリーズ,インコーポレイテッド | 医薬組成物 |
GB2570382B (en) | 2016-04-27 | 2020-07-29 | Univ Puerto Rico | 1,5-disubstituted 1,2,3-triazoles are inhibitors of Rac/Cdc42 GTPases |
WO2017192485A1 (en) | 2016-05-03 | 2017-11-09 | Amgen Inc. | Heterocyclic triazole compounds as agonists of the apj receptor |
MA46827A (fr) | 2016-11-16 | 2019-09-25 | Amgen Inc | Composés de triazole à substitution cycloalkyle en tant qu'agonistes du récepteur apj |
WO2018097944A1 (en) | 2016-11-16 | 2018-05-31 | Amgen Inc. | Triazole furan compounds as agonists of the apj receptor |
MA46824A (fr) | 2016-11-16 | 2019-09-25 | Amgen Inc | Composés de triazole substitués par alkyle en tant qu'agonistes du récepteur apj |
US10906890B2 (en) | 2016-11-16 | 2021-02-02 | Amgen Inc. | Triazole phenyl compounds as agonists of the APJ receptor |
EP3541805B1 (en) | 2016-11-16 | 2020-10-14 | Amgen Inc. | Heteroaryl-substituted triazoles as apj receptor agonists |
WO2018093580A1 (en) | 2016-11-16 | 2018-05-24 | Amgen Inc. | Triazole pyridyl compounds as agonists of the apj receptor |
MA50509A (fr) | 2017-11-03 | 2021-06-02 | Amgen Inc | Agonistes de triazole fusionnés du récepteur apj |
MA52487A (fr) | 2018-05-01 | 2021-03-10 | Amgen Inc | Pyrimidinones substituées en tant qu'agonistes du récepteur apj |
EP3766483A1 (en) | 2019-07-19 | 2021-01-20 | BioPharma Synergies, S. L. | Orodispersible powder composition comprising a triptan |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3475437A (en) * | 1964-06-05 | 1969-10-28 | Boehringer Sohn Ingelheim | 3-tertiary amino lower alkylpseudoindoles |
GB1237008A (en) * | 1968-12-18 | 1971-06-30 | Pfizer Ltd | Novel indoline derivatives |
US3686213A (en) * | 1970-08-28 | 1972-08-22 | American Cyanamid Co | Substituted aminoethyl indoles |
DE2520816C3 (de) * | 1975-05-09 | 1979-02-15 | Bayer Ag, 5090 Leverkusen | Methinfarbstoffe |
ZA795239B (en) * | 1978-10-12 | 1980-11-26 | Glaxo Group Ltd | Heterocyclic compounds |
BE889931A (fr) * | 1980-08-12 | 1982-02-11 | Glaxo Group Ltd | Derives indoliques, leur preparation et leurs applications en tant que medicaments |
ZW19381A1 (en) * | 1980-08-12 | 1983-03-09 | Glaxo Group Ltd | Heterocyclic compounds |
NZ197998A (en) * | 1980-08-12 | 1985-08-16 | Glaxo Group Ltd | 5-amino(methyl)-1h-indol-3-ylalkaneamines |
IT1171449B (it) * | 1980-08-12 | 1987-06-10 | Glaxo Group Ltd | Composti eterociclici indolici procedimento per produrli e composizioni farmaceutiche che li contengono |
US4453001A (en) * | 1982-02-22 | 1984-06-05 | Sandoz, Inc. | Isoxazolyl indolamines as intermediates |
JPS58150576A (ja) * | 1982-03-03 | 1983-09-07 | Sumitomo Chem Co Ltd | 新規な1,2,4−オキサジアゾ−ル誘導体 |
US4692531A (en) * | 1984-06-22 | 1987-09-08 | Bristol-Myers Company | Substituted 3,4-diamino-1,2,5-thiadiazoles having histamine H2 -receptor antagonist activity |
GB8419575D0 (en) * | 1984-08-01 | 1984-09-05 | Glaxo Group Ltd | Chemical compounds |
DE3430284A1 (de) * | 1984-08-17 | 1986-02-27 | Troponwerke GmbH & Co KG, 5000 Köln | Neue tryptamin-derivate, ein verfahren zu ihrer herstellung und ihre verwendung |
US4663526A (en) * | 1984-12-26 | 1987-05-05 | Emil Kamieniecki | Nondestructive readout of a latent electrostatic image formed on an insulating material |
IE58370B1 (en) * | 1985-04-10 | 1993-09-08 | Lundbeck & Co As H | Indole derivatives |
DE3531658A1 (de) * | 1985-09-05 | 1987-03-12 | Boehringer Mannheim Gmbh | Heterocyclisch substituierte indole, zwischenprodukte, verfahren zu ihrer herstellung und arzneimittel |
GB8527619D0 (en) * | 1985-11-08 | 1985-12-11 | Glaxo Group Ltd | Chemical compounds |
US4833153A (en) * | 1985-11-08 | 1989-05-23 | Glaxo Group Limited | Indole derivatives |
US4881967A (en) * | 1986-12-10 | 1989-11-21 | E. I. Du Pont De Nemours And Company | Heterocyclic 2,3-dihydrobenzofuran herbicides |
US5225431A (en) * | 1987-10-23 | 1993-07-06 | Burroughs Wellcome Co. | Therapeutic substituted indole compounds and compositions thereof |
GB8724912D0 (en) * | 1987-10-23 | 1987-11-25 | Wellcome Found | Indole derivatives |
NZ227841A (en) * | 1988-02-12 | 1991-08-27 | Merck Sharp & Dohme | Heterocyclic compounds with at least two non-condensed five membered rings and pharmaceutical compositions |
NZ238424A (en) * | 1990-06-07 | 1993-12-23 | Wellcome Found | 3,5-substituted indole derivatives; medicaments and preparatory processes. |
EP0596933A1 (en) * | 1991-08-03 | 1994-05-18 | Smithkline Beecham Plc | 5-ht4 receptor antagonists |
KR930011238A (ko) * | 1991-11-12 | 1993-06-24 | 오리 노리오 | 스태틱 알에이엠(ram)의 메모리셀 및 그 메모리셀어레이 |
US5436246A (en) * | 1992-09-17 | 1995-07-25 | Merrell Dow Pharmaceuticals Inc. | Serotonin receptor agents |
-
1992
- 1992-01-23 CZ CS92198A patent/CZ283018B6/cs not_active IP Right Cessation
- 1992-01-23 SK SK198-92A patent/SK278998B6/sk not_active IP Right Cessation
- 1992-01-24 AT AT92300617T patent/ATE158582T1/de active
- 1992-01-24 EP EP97200467A patent/EP0778275B1/en not_active Expired - Lifetime
- 1992-01-24 SG SG1996000418A patent/SG50409A1/en unknown
- 1992-01-24 DE DE1999175007 patent/DE19975007I2/de active Active
- 1992-01-24 NZ NZ241394A patent/NZ241394A/en not_active IP Right Cessation
- 1992-01-24 ES ES97200467T patent/ES2162188T3/es not_active Expired - Lifetime
- 1992-01-24 DE DE69222329T patent/DE69222329T2/de not_active Expired - Lifetime
- 1992-01-24 ES ES92300617T patent/ES2106822T3/es not_active Expired - Lifetime
- 1992-01-24 IL IL10075692A patent/IL100756A/en not_active IP Right Cessation
- 1992-01-24 DK DK92300617.5T patent/DK0497512T3/da active
- 1992-01-24 EP EP92300617A patent/EP0497512B1/en not_active Expired - Lifetime
- 1992-01-28 CA CA002238140A patent/CA2238140C/en not_active Expired - Lifetime
- 1992-01-28 CA CA002060139A patent/CA2060139C/en not_active Expired - Lifetime
- 1992-01-28 US US07/827,187 patent/US5298520A/en not_active Expired - Lifetime
- 1992-01-30 YU YU10192A patent/YU48236B/sh unknown
- 1992-01-30 SI SI9210101A patent/SI9210101B/sl unknown
- 1992-01-30 MX MX9200405A patent/MX9200405A/es unknown
- 1992-01-31 JP JP4059849A patent/JP2500280B2/ja not_active Expired - Lifetime
- 1992-01-31 IE IE034292A patent/IE920342A1/en active Protection Beyond IP Right Term
- 1992-01-31 NO NO920424A patent/NO180447C/no not_active IP Right Cessation
- 1992-01-31 HU HU9200299A patent/HU222350B1/hu active IP Right Grant
- 1992-01-31 FI FI920442A patent/FI107154B/fi active Protection Beyond IP Right Term
- 1992-02-01 CN CN92101189A patent/CN1038681C/zh not_active Expired - Lifetime
- 1992-02-01 KR KR1019920001592A patent/KR100212111B1/ko not_active IP Right Cessation
-
1993
- 1993-04-02 HR HR930777A patent/HRP930777B1/xx not_active IP Right Cessation
- 1993-07-14 BG BG097943A patent/BG62024B2/bg unknown
- 1993-11-22 US US08/156,140 patent/US5451588A/en not_active Expired - Lifetime
-
1994
- 1994-01-30 SA SA94140534A patent/SA94140534B1/ar unknown
-
1995
- 1995-05-10 US US08/438,621 patent/US5602162A/en not_active Expired - Lifetime
- 1995-05-25 US US08/452,185 patent/US5602163A/en not_active Expired - Lifetime
- 1995-06-28 HU HU95P/P00500P patent/HU211516A9/hu unknown
-
1996
- 1996-11-25 CN CN96121796A patent/CN1060479C/zh not_active Expired - Lifetime
- 1996-11-25 CN CN96121797A patent/CN1128617C/zh not_active Expired - Lifetime
- 1996-11-25 CN CN96117268A patent/CN1061654C/zh not_active Expired - Lifetime
-
1997
- 1997-10-15 GR GR970402671T patent/GR3025026T3/el unknown
-
1998
- 1998-03-17 LV LVP-98-54A patent/LV12090B/en unknown
- 1998-06-08 NL NL980019C patent/NL980019I1/nl unknown
- 1998-07-17 CY CY9800017A patent/CY2095B1/xx unknown
-
1999
- 1999-01-13 LU LU90338C patent/LU90338I2/fr unknown
- 1999-04-09 NO NO1999005C patent/NO1999005I1/no unknown
-
2001
- 2001-10-11 GR GR20010401586T patent/GR3036864T3/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
LV12090B (en) | DERIVATIVES OF IMIDAZOL, TRIAZOL AND TETRAZOL | |
AU672802B2 (en) | Imidazole, triazole and tetrazole derivatives | |
AU669160B2 (en) | Imidazole, triazole and tetrazole derivatives | |
US5514682A (en) | Fused imidazole and triazole derivatives as 5-HT1 receptor agonists | |
CA2101219A1 (en) | 4-substituted 1,2,4-triazole derivatives | |
US5902819A (en) | Triazole derivatives | |
GB2289465A (en) | Five-membered heteroaromatic 5-HT receptor agonists | |
LT3594B (en) | Imidazole,triazole and tetrazole derivatives | |
SI9300375A (sl) | Derivati imidazola,triazola in tetrazola | |
RO110945B1 (ro) | Derivați de imidazol, triazol și tetrazol, procedee pentru prepararea acestora, compoziții farmaceutice și metodă pentru tratamentul migrenelor și afecțiunilor asociate | |
WO1997016445A1 (en) | Azetidine, pyrrolidine and piperidine derivatives |