PE20060286A1 - Derivados de piperidina o piperazina como antagonistas del receptor cgrp - Google Patents
Derivados de piperidina o piperazina como antagonistas del receptor cgrpInfo
- Publication number
- PE20060286A1 PE20060286A1 PE2005000346A PE2005000346A PE20060286A1 PE 20060286 A1 PE20060286 A1 PE 20060286A1 PE 2005000346 A PE2005000346 A PE 2005000346A PE 2005000346 A PE2005000346 A PE 2005000346A PE 20060286 A1 PE20060286 A1 PE 20060286A1
- Authority
- PE
- Peru
- Prior art keywords
- piperidin
- piperidine
- indazol
- oxo
- antagonists
- 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
- C07D401/14—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
- 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
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
REFERIDA A UN COMPUESTO DE FORMULA I DONDE V ES -N(R1)(R2) O OR4; R4 ES H, ALQUILO C1-C6, HALOALQUILO C1-C4, ENTRE OTROS; R1 Y R2 SON L1, DONDE L1 ES H, ALQUILO C1-C6, FENILO, ENTRE OTROS; Q ES Q' O Q''; Q' ES ALQUILENO C1-C3-R3, ENTRE OTROS; Q'' ES NH(ALQUILO C1-C3)R3, ENTRE OTROS; R3 ES R3a O R3b; R3a ES FENILO, HIDROXIFENILO, NAFTILO, ENTRE OTROS; R3b ES DIHIDROBENZIMIDAZOLONILO, BENZTIAZOLILO, 1H-INDAZOL-5-IL, ENTRE OTROS; D ES O, NCN O NSO2ALQUILO C1-C3; A ES C, N, CH O COH; m Y n SON 0, 1 O 2; p ES 1, G, J Y E FORMAN AX O AY; AX ES UN HETEROCICLO FUSIONADO QUE TIENE DOS ANILLOS FUSIONADOS CON 5 A 7 MIEMBROS EN CADA UNO DE LOS ANILLOS, EL HETEROCICLO CONTIENE DE 1 A 4 HETEROATOMOS SELECCIONADOS DE O, N Y S; AY ES UN HETEROCICLO DE 4 A 6 MIEMBROS QUE TIENE DE 1 A 3 HETEROATOMOS SELECCIONADOS DE O, N Y S. SON COMPUESTOS PREFERIDOS: 3-(7-METIL-1H-INDAZOL-5-IL)-1-OXO-1-(4-PIPERIDIN-1-IL)PIPERIDIN-1-IL)PROPAN-2-IL 4-(1,2-DIHIDRO-2-OXOQUINAZOLIN-3(4H)-IL)PIPERIDINA-1-CARBOXILATO, (R)-3-(7-METIL-1H-INDAZOL-5-IL)-1-OXO-1-(4-PIPERIDIN-1-IL)PIPERIDIN-1-IL)PROPAN-2-IL 4-(2-OXO-1,2-DIHIDROQUINAZOLIN-3(4H)-IL)PIPERIDINA-1-CARBOXILATO, ENTRE OTROS. TAMBIEN REFERIDA A METODOS DE PREPARACION Y COMPOSICIONES QUE CONTIENEN DICHOS COMPUESTOS, LOS CUALES SON ANTAGONISTAS DE LOS RECEPTORES PEPTIDOS RELACIONADOS CON EL GEN DE CALCITONINA Y SON UTILES EN EL TRATAMIENTO DE LA VASODILATACION NEUROGENICA, MIGRANA, ENTRE OTROS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US55740804P | 2004-03-29 | 2004-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20060286A1 true PE20060286A1 (es) | 2006-04-25 |
Family
ID=34964257
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2005000346A PE20060286A1 (es) | 2004-03-29 | 2005-03-28 | Derivados de piperidina o piperazina como antagonistas del receptor cgrp |
Country Status (16)
Country | Link |
---|---|
US (1) | US7772244B2 (es) |
EP (1) | EP1730137A1 (es) |
JP (1) | JP2007530701A (es) |
KR (1) | KR20070007857A (es) |
CN (1) | CN1972929A (es) |
AR (1) | AR048343A1 (es) |
AU (1) | AU2005228881A1 (es) |
BR (1) | BRPI0509341A (es) |
CA (1) | CA2562039A1 (es) |
IL (1) | IL178291A0 (es) |
NO (1) | NO20064888L (es) |
PE (1) | PE20060286A1 (es) |
RU (1) | RU2006138195A (es) |
TW (1) | TW200533398A (es) |
WO (1) | WO2005095383A1 (es) |
ZA (1) | ZA200608037B (es) |
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TW200524601A (en) | 2003-12-05 | 2005-08-01 | Bristol Myers Squibb Co | Heterocyclic anti-migraine agents |
TW200533398A (en) | 2004-03-29 | 2005-10-16 | Bristol Myers Squibb Co | Novel therapeutic agents for the treatment of migraine |
DE102004015723A1 (de) | 2004-03-29 | 2005-10-20 | Boehringer Ingelheim Pharma | Ausgewählte CGRP-Antagonisten, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel |
DE102004018794A1 (de) * | 2004-04-15 | 2005-10-27 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Ausgewählte CGRP-Antagonisten, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel |
DE102004019492A1 (de) * | 2004-04-22 | 2005-11-10 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Ausgewählte CGRP-Antagonisten, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel |
US7696195B2 (en) | 2004-04-22 | 2010-04-13 | Boehringer Ingelheim International Gmbh | Selected CGRP-antagonists, process for preparing them and their use as pharmaceutical compositions |
US7786141B2 (en) * | 2004-08-19 | 2010-08-31 | Vertex Pharmaceuticals Incorporated | Dihydrospiroindene modulators of muscarinic receptors |
RU2007109794A (ru) * | 2004-08-19 | 2008-09-27 | Вертекс Фармасьютикалз, Инкорпорейтед (Us) | Модуляторы мускариновых рецепторов |
US7384931B2 (en) | 2004-11-03 | 2008-06-10 | Bristol-Myers Squibb Company | Constrained compounds as CGRP-receptor antagonists |
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AU2005309365B2 (en) * | 2004-11-29 | 2011-10-06 | Vertex Pharmaceuticals Incorporated | Modulators of muscarinic receptors |
US7449586B2 (en) * | 2004-12-03 | 2008-11-11 | Bristol-Myers Squibb Company | Processes for the preparation of CGRP-receptor antagonists and intermediates thereof |
EP1770091A1 (de) | 2005-09-29 | 2007-04-04 | Boehringer Ingelheim Pharma GmbH & Co. KG | CGRP-Antagonisten, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel |
CN101146799A (zh) | 2005-03-23 | 2008-03-19 | 贝林格尔·英格海姆国际有限公司 | Cgrp拮抗剂、其制备方法以及其作为药物的用途 |
US7834007B2 (en) | 2005-08-25 | 2010-11-16 | Bristol-Myers Squibb Company | CGRP antagonists |
DE102005050892A1 (de) * | 2005-10-21 | 2007-04-26 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Ausgewählte CGRP-Antagonisten, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel |
US8168592B2 (en) * | 2005-10-21 | 2012-05-01 | Amgen Inc. | CGRP peptide antagonists and conjugates |
AU2006330866A1 (en) * | 2005-12-22 | 2007-07-05 | Vertex Pharmaceuticals Incorporated | Modulators of muscarinic receptors |
EP1988892A2 (en) | 2006-02-22 | 2008-11-12 | Vertex Pharmaceuticals Incorporated | Modulators of muscarinic receptors |
ATE517106T1 (de) * | 2006-02-22 | 2011-08-15 | Vertex Pharma | Kondensierte spiropiperidine als modulatoren muskarinartiger rezeptoren |
CN101500565A (zh) * | 2006-06-29 | 2009-08-05 | 弗特克斯药品有限公司 | 毒蕈碱性受体的调节剂 |
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JP2010501561A (ja) | 2006-08-18 | 2010-01-21 | バーテックス ファーマシューティカルズ インコーポレイテッド | ムスカリン受容体の調節剤 |
JP2010508358A (ja) * | 2006-11-01 | 2010-03-18 | ブリストル−マイヤーズ スクイブ カンパニー | グルココルチコイド受容体、AP−1、および/またはNF−κB活性の調節剤、並びにその使用 |
CA2700724A1 (en) * | 2007-10-03 | 2009-04-09 | Vertex Pharmaceuticals Incorporated | Modulators of muscarinic receptors |
FR3008978A1 (fr) * | 2013-07-23 | 2015-01-30 | Servier Lab | "nouveaux derives d'indole et de pyrrole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent" |
JO3669B1 (ar) | 2015-01-06 | 2020-08-27 | Ferring Bv | بيبتيدات مضَادَّة لببتيد المرتبط بجين الكالسيتونين |
JOP20200116A1 (ar) | 2015-04-24 | 2017-06-16 | Amgen Inc | طرق لعلاج أو الوقاية من الصداع النصفي |
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GB201519195D0 (en) | 2015-10-30 | 2015-12-16 | Heptares Therapeutics Ltd | CGRP Receptor Antagonists |
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US8662081B2 (en) | 2005-02-15 | 2014-03-04 | Yale University | Intrauterine device |
-
2005
- 2005-03-23 TW TW094109010A patent/TW200533398A/zh unknown
- 2005-03-28 KR KR1020067022467A patent/KR20070007857A/ko not_active Application Discontinuation
- 2005-03-28 PE PE2005000346A patent/PE20060286A1/es not_active Application Discontinuation
- 2005-03-28 AR ARP050101201A patent/AR048343A1/es not_active Withdrawn
- 2005-03-28 CA CA002562039A patent/CA2562039A1/en not_active Abandoned
- 2005-03-28 EP EP05731205A patent/EP1730137A1/en not_active Withdrawn
- 2005-03-28 JP JP2007506432A patent/JP2007530701A/ja active Pending
- 2005-03-28 RU RU2006138195/04A patent/RU2006138195A/ru unknown
- 2005-03-28 BR BRPI0509341-4A patent/BRPI0509341A/pt not_active Application Discontinuation
- 2005-03-28 WO PCT/US2005/010330 patent/WO2005095383A1/en active Application Filing
- 2005-03-28 AU AU2005228881A patent/AU2005228881A1/en not_active Abandoned
- 2005-03-28 US US11/091,429 patent/US7772244B2/en active Active
- 2005-03-28 CN CNA2005800169860A patent/CN1972929A/zh active Pending
-
2006
- 2006-09-25 IL IL178291A patent/IL178291A0/en unknown
- 2006-09-27 ZA ZA200608037A patent/ZA200608037B/xx unknown
- 2006-10-26 NO NO20064888A patent/NO20064888L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
JP2007530701A (ja) | 2007-11-01 |
AR048343A1 (es) | 2006-04-19 |
EP1730137A1 (en) | 2006-12-13 |
WO2005095383A1 (en) | 2005-10-13 |
US7772244B2 (en) | 2010-08-10 |
US20050215576A1 (en) | 2005-09-29 |
CA2562039A1 (en) | 2005-10-13 |
RU2006138195A (ru) | 2008-05-10 |
NO20064888L (no) | 2006-10-26 |
KR20070007857A (ko) | 2007-01-16 |
IL178291A0 (en) | 2006-12-31 |
CN1972929A (zh) | 2007-05-30 |
ZA200608037B (en) | 2008-06-25 |
BRPI0509341A (pt) | 2007-09-04 |
AU2005228881A1 (en) | 2005-10-13 |
TW200533398A (en) | 2005-10-16 |
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