EA200870521A1 - Замещенные спироциклические антагонисты cgrp-рецепторов - Google Patents
Замещенные спироциклические антагонисты cgrp-рецепторовInfo
- Publication number
- EA200870521A1 EA200870521A1 EA200870521A EA200870521A EA200870521A1 EA 200870521 A1 EA200870521 A1 EA 200870521A1 EA 200870521 A EA200870521 A EA 200870521A EA 200870521 A EA200870521 A EA 200870521A EA 200870521 A1 EA200870521 A1 EA 200870521A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- antagonists
- cgrp receptors
- cgrp
- substituted spirocyclic
- compounds
- Prior art date
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- 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
- C07D401/12—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 chain containing hetero atoms as chain links
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- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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- A—HUMAN NECESSITIES
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P25/08—Antiepileptics; Anticonvulsants
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- 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
- C07D413/12—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 linked by a chain containing hetero atoms as chain links
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- 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
- C07D417/12—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 chain containing hetero atoms as chain links
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- 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
- C07D471/04—Ortho-condensed systems
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- 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
- C07D471/12—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 three hetero rings
- C07D471/20—Spiro-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
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- Dermatology (AREA)
- Immunology (AREA)
- Emergency Medicine (AREA)
- Communicable Diseases (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Psychiatry (AREA)
- Urology & Nephrology (AREA)
- Reproductive Health (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Соединения формулы Iв которой переменные А, А, А, А, М, N, J, Q, R, E, E, E, R, R, R, R, Rи Y принимают значения, описанные в настоящей работе, которые являются антагонистами CGRP-рецепторов и которые применимы в лечении или профилактике заболеваний, таких как мигрень, в которые включен CGRP. Изобретение также относится к фармацевтическим композициям, содержащим данные соединения, и к применению данных соединений и композиций в профилактике или лечении таких заболеваний, в которые включен CGRP.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US79907106P | 2006-05-09 | 2006-05-09 | |
PCT/US2007/010952 WO2007133491A1 (en) | 2006-05-09 | 2007-05-04 | Substituted spirocyclic cgrp receptor antagonists |
Publications (1)
Publication Number | Publication Date |
---|---|
EA200870521A1 true EA200870521A1 (ru) | 2009-04-28 |
Family
ID=38556368
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200870521A EA200870521A1 (ru) | 2006-05-09 | 2007-05-04 | Замещенные спироциклические антагонисты cgrp-рецепторов |
Country Status (23)
Country | Link |
---|---|
US (3) | US7629338B2 (ru) |
EP (2) | EP2024358B1 (ru) |
JP (2) | JP4435288B2 (ru) |
KR (1) | KR20090018107A (ru) |
CN (1) | CN101443323A (ru) |
AR (1) | AR060872A1 (ru) |
AU (1) | AU2007284994B2 (ru) |
BR (1) | BRPI0711352A2 (ru) |
CA (1) | CA2650932C (ru) |
CR (1) | CR10415A (ru) |
DO (1) | DOP2007000093A (ru) |
EA (1) | EA200870521A1 (ru) |
EC (1) | ECSP088872A (ru) |
GE (1) | GEP20115140B (ru) |
HN (1) | HN2008001667A (ru) |
IL (1) | IL195110A0 (ru) |
MA (1) | MA30558B1 (ru) |
MX (1) | MX2008014353A (ru) |
NO (1) | NO20085110L (ru) |
PE (1) | PE20080253A1 (ru) |
TW (1) | TW200813008A (ru) |
WO (2) | WO2007133491A1 (ru) |
ZA (1) | ZA200809275B (ru) |
Families Citing this family (48)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2008512459A (ja) * | 2004-09-09 | 2008-04-24 | メルク エンド カムパニー インコーポレーテッド | アリールスピロラクタムcgrp受容体拮抗薬 |
EP1797073B1 (en) * | 2004-09-13 | 2010-04-14 | Merck Sharp & Dohme Corp. | Bicyclic anilide spirolactam cgrp receptor antagonists |
CN101443323A (zh) * | 2006-05-09 | 2009-05-27 | 默克公司 | 取代的螺环cgrp受体拮抗剂 |
US7951795B2 (en) | 2006-12-08 | 2011-05-31 | Merck Sharp & Dohme Corp. | Constrained spirocyclic compounds as CGRP receptor antagonists |
WO2008112159A2 (en) | 2007-03-12 | 2008-09-18 | Merck & Co., Inc. | Monocyclic anilide spirolactam cgrp receptor antagonists |
GB0706914D0 (en) | 2007-04-10 | 2007-05-16 | Isis Innovation | Novel adenovirus vectors |
EP2146715A4 (en) | 2007-04-11 | 2011-08-31 | Merck Sharp & Dohme | CGRP RECEPTOR ANTAGONISTS COMPRISING TERTIARY AMIDE, SULFAMIDE, CARBAMATE AND UREA TERMINAL GROUPS |
AU2008241500A1 (en) * | 2007-04-16 | 2008-10-30 | Merck Sharp & Dohme Corp. | Aryl heterocyclic CGRP receptor antagonists |
WO2008130512A1 (en) | 2007-04-16 | 2008-10-30 | Merck & Co., Inc. | Bicyclic anilide heterocyclic cgrp receptor antagonists |
WO2008153849A1 (en) * | 2007-06-05 | 2008-12-18 | Merck & Co., Inc. | Carboxamide heterocyclic cgrp receptor antagonists |
JP2010529120A (ja) | 2007-06-07 | 2010-08-26 | メルク・シャープ・エンド・ドーム・コーポレイション | 三環式アニリド複素環cgrp受容体アンタゴニスト |
EP2065381A1 (de) | 2007-10-18 | 2009-06-03 | Boehringer Ingelheim Pharma GmbH & Co. KG | CGRP Antagonisten |
BRPI0817835A2 (pt) | 2007-10-18 | 2015-03-31 | Boehringer Ingelheim Int | Antagonistas cgrp |
WO2009065919A2 (de) | 2007-11-22 | 2009-05-28 | Boehringer Ingelheim International Gmbh | Organische verbindungen |
CA2711367A1 (en) * | 2008-02-19 | 2009-08-27 | Merck Sharp & Dohme Corp. | Imidazobenzazepine cgrp receptor antagonists |
JP2011515480A (ja) * | 2008-03-28 | 2011-05-19 | メルク・シャープ・エンド・ドーム・コーポレイション | 単環式cgrp受容体アンタゴニスト |
US8552023B2 (en) * | 2008-08-20 | 2013-10-08 | Merck Sharp & Dohme Corp. | Non-amidic linkers with branched termini as CGRP receptor antagonists |
WO2010027927A1 (en) * | 2008-09-08 | 2010-03-11 | Merck Sharp & Dohme Corp. | Monocyclic amide cgrp receptor antagonists |
WO2010033421A1 (en) * | 2008-09-18 | 2010-03-25 | Merck Sharp & Dohme Corp. | Bicyclic dihydroimidazolone cgrp receptor antagonists |
EP2340025B1 (en) | 2008-10-03 | 2014-10-15 | Merck Sharp & Dohme Corp. | Cgrp receptor antagonists |
JP2012505217A (ja) * | 2008-10-10 | 2012-03-01 | メルク・シャープ・エンド・ドーム・コーポレイション | Cgrp受容体アンタゴニスト |
WO2010077752A1 (en) | 2008-12-17 | 2010-07-08 | Merck Sharp & Dohme Corp. | Imidazolinone derivatives as cgrp receptor antagonists |
US8765763B2 (en) | 2009-06-05 | 2014-07-01 | Boehringer Ingelheim International Gmbh | Substituted piperazines as CGRP antagonists |
WO2011005731A2 (en) | 2009-07-08 | 2011-01-13 | Merck Sharp & Dohme Corp. | Process for making cgrp receptor antagonist |
US20120121508A1 (en) * | 2009-07-27 | 2012-05-17 | Merck Sharp & Dohme Corp. | Radiolabeled cgrp antagonists |
JP2013528598A (ja) | 2010-05-11 | 2013-07-11 | ファイザー・インク | ミネラルコルチコイド受容体拮抗薬としてのモルホリン化合物 |
WO2011153359A1 (en) | 2010-06-04 | 2011-12-08 | Albany Molecular Research, Inc. | Glycine transporter-1 inhibitors, methods of making them, and uses thereof |
TWI522355B (zh) | 2010-11-12 | 2016-02-21 | 默沙東藥廠 | 六氫吡啶酮甲醯胺氮雜茚滿cgrp受體拮抗劑 |
WO2012087777A1 (en) | 2010-12-22 | 2012-06-28 | Merck Sharp & Dohme Corp. | Fused heterocyclic indane carboxamide cgrp receptor antagonists |
EP2686324B1 (en) * | 2011-03-18 | 2016-01-06 | Merck Sharp & Dohme Corp. | Piperidine carboxamide spirohydantoin cgrp receptor antagonists |
EP2685826B1 (en) * | 2011-03-18 | 2016-02-03 | Merck Sharp & Dohme Corp. | Piperidinone carboxamide spirohydantoin cgrp receptor antagonists |
KR20220164616A (ko) * | 2012-03-14 | 2022-12-13 | 머크 샤프 앤드 돔 코포레이션 | Cgrp 수용체 길항제의 제조 방법 |
US9487523B2 (en) | 2012-03-14 | 2016-11-08 | Merck Sharp & Dohme Corp. | Process for making CGRP receptor antagonists |
US9174989B2 (en) | 2012-05-09 | 2015-11-03 | Merck Sharp & Dohme Corp. | Process for making CGRP receptor antagonists |
US9296750B2 (en) | 2012-05-09 | 2016-03-29 | Merck Sharp & Dohme Corp. | Spirolactam CGRP receptor antagonists |
EP2846798B1 (en) | 2012-05-09 | 2018-04-04 | Merck Sharp & Dohme Corp. | Aliphatic spirolactam cgrp receptor antagonists |
PE20161405A1 (es) * | 2013-12-24 | 2017-01-18 | Harvard College | Analogos de cortistatina y sintesis y usos de los mismos |
CA2937315A1 (en) | 2014-02-05 | 2015-08-13 | Merck Sharp & Dohme Corp. | Tablet formulation for cgrp-active compounds |
JOP20200116A1 (ar) | 2015-04-24 | 2017-06-16 | Amgen Inc | طرق لعلاج أو الوقاية من الصداع النصفي |
EP3313518A1 (en) | 2015-06-29 | 2018-05-02 | Galderma Research & Development | Cgrp receptor antagonist compounds for topical treatment of skin disorders |
EP3366286A1 (en) | 2017-02-22 | 2018-08-29 | Johannes Keller | Compounds for treating sepsis |
GB201707938D0 (en) | 2017-05-17 | 2017-06-28 | Univ Sheffield | Compounds |
JP7339262B2 (ja) | 2018-01-12 | 2023-09-05 | アムジェン インコーポレイテッド | Pac1抗体及びその使用 |
US11717515B2 (en) | 2020-12-22 | 2023-08-08 | Allergan Pharmaceuticals International Limited | Treatment of migraine |
US20240139171A1 (en) | 2021-03-02 | 2024-05-02 | Cgrp Diagnostics Gmbh | Treatment and/or reduction of occurrence of migraine |
WO2023026205A1 (en) | 2021-08-24 | 2023-03-02 | Cgrp Diagnostics Gmbh | Preventative treatment of migraine |
CN117003762A (zh) * | 2022-04-29 | 2023-11-07 | 熙源安健医药(上海)有限公司 | 哌啶甲酰胺氮杂茚满类衍生物及其制备方法和用途 |
CN115947697A (zh) * | 2022-12-28 | 2023-04-11 | 苏州汉德创宏生化科技有限公司 | 一种3-氧代吗啉-4-羧酸叔丁酯的合成方法 |
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2007
- 2007-05-04 CN CNA2007800167648A patent/CN101443323A/zh active Pending
- 2007-05-04 BR BRPI0711352-8A patent/BRPI0711352A2/pt not_active IP Right Cessation
- 2007-05-04 EP EP07776804.2A patent/EP2024358B1/en active Active
- 2007-05-04 WO PCT/US2007/010952 patent/WO2007133491A1/en active Application Filing
- 2007-05-04 WO PCT/US2007/010953 patent/WO2008020902A1/en active Application Filing
- 2007-05-04 CA CA2650932A patent/CA2650932C/en not_active Expired - Fee Related
- 2007-05-04 MX MX2008014353A patent/MX2008014353A/es active IP Right Grant
- 2007-05-04 AU AU2007284994A patent/AU2007284994B2/en not_active Ceased
- 2007-05-04 EP EP07835747.2A patent/EP2029575B1/en active Active
- 2007-05-04 EA EA200870521A patent/EA200870521A1/ru unknown
- 2007-05-04 KR KR1020087029977A patent/KR20090018107A/ko not_active Application Discontinuation
- 2007-05-04 JP JP2009509766A patent/JP4435288B2/ja not_active Expired - Fee Related
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