EA200700757A1 - Замещённые дипиперидиновые антагонисты ccr2 - Google Patents
Замещённые дипиперидиновые антагонисты ccr2Info
- Publication number
- EA200700757A1 EA200700757A1 EA200700757A EA200700757A EA200700757A1 EA 200700757 A1 EA200700757 A1 EA 200700757A1 EA 200700757 A EA200700757 A EA 200700757A EA 200700757 A EA200700757 A EA 200700757A EA 200700757 A1 EA200700757 A1 EA 200700757A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- ccr2
- dipiperidine
- replaced
- antagonists
- prevention
- Prior art date
Links
Classifications
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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
- C07D401/06—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
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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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A—HUMAN NECESSITIES
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
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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
- C07D401/14—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
- C07D403/14—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
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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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
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Ophthalmology & Optometry (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Communicable Diseases (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Rheumatology (AREA)
- Neurosurgery (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Otolaryngology (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
Abstract
Замещенные производные дипиперидина формулы (I) или их соли, изомеры, пролекарства, метаболиты или полиморфы, которые являются антагонистами CCR2 и применимы для профилактики, лечения или облегчения CCR2-опосредуемых воспалительных синдромов, расстройств или заболеваний у субъекта, нуждающегося в такой профилактике, лечении или облегчении.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US61392204P | 2004-09-28 | 2004-09-28 | |
PCT/US2005/032500 WO2006036527A1 (en) | 2004-09-28 | 2005-09-12 | Substituted dipiperdine ccr2 antagonists |
Publications (1)
Publication Number | Publication Date |
---|---|
EA200700757A1 true EA200700757A1 (ru) | 2007-10-26 |
Family
ID=35788241
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200700757A EA200700757A1 (ru) | 2004-09-28 | 2005-09-12 | Замещённые дипиперидиновые антагонисты ccr2 |
Country Status (18)
Country | Link |
---|---|
US (1) | US20060069123A1 (ru) |
EP (1) | EP1802602A1 (ru) |
JP (1) | JP2008514700A (ru) |
KR (1) | KR20070063562A (ru) |
CN (1) | CN101065374A (ru) |
AR (1) | AR053413A1 (ru) |
AU (1) | AU2005290028A1 (ru) |
BR (1) | BRPI0516166A (ru) |
CA (1) | CA2582225A1 (ru) |
CR (1) | CR9088A (ru) |
EA (1) | EA200700757A1 (ru) |
EC (1) | ECSP077358A (ru) |
IL (1) | IL182254A0 (ru) |
MX (1) | MX2007003793A (ru) |
NO (1) | NO20072065L (ru) |
TW (1) | TW200621707A (ru) |
WO (1) | WO2006036527A1 (ru) |
ZA (1) | ZA200702544B (ru) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2644761C2 (ru) * | 2012-06-22 | 2018-02-14 | Идорсиа Фармасьютиклз Лтд | Производные 1-[м-карбоксамидо(гетеро)арил-метил]-гетероциклил-карбоксамида |
Families Citing this family (47)
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US20070197590A1 (en) * | 2006-01-31 | 2007-08-23 | Demong Duane E | Substituted dipiperidine ccr2 antagonists |
US20070219245A1 (en) * | 2006-03-14 | 2007-09-20 | Cuifen Hou | Method of use for substituted dipiperidine ccr2 antagonists |
US7687508B2 (en) * | 2006-07-28 | 2010-03-30 | Bristol-Myers Squibb Company | Cyclic derivatives as modulators of chemokine receptor activity |
US7629351B2 (en) * | 2006-07-28 | 2009-12-08 | Bristol-Myers Squibb Company | N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-2-oxo-3-(6-(trifluoromethyl)quinazolin-4-ylamino) pyrrolidin-1-yl)cyclohexyl)acetamide and other modulators of chemokine receptor activity, crystalline forms and process |
US7671062B2 (en) * | 2006-07-28 | 2010-03-02 | Bristol-Myers Squibb Company | Modulators of chemokine receptor activity, crystalline forms and process |
US20080076120A1 (en) * | 2006-09-14 | 2008-03-27 | Millennium Pharmaceuticals, Inc. | Methods for the identification, evaluation and treatment of patients having CC-Chemokine receptor 2 (CCR-2) mediated disorders |
PT2526933E (pt) | 2006-09-22 | 2015-06-23 | Pharmacyclics Inc | Inibidores da tirosina-quinase de bruton |
WO2008109238A1 (en) * | 2007-03-02 | 2008-09-12 | Janssen Pharmaceutica N.V. | Substituted cyclopentyl piperidine ccr2 antagonists |
US20120101113A1 (en) | 2007-03-28 | 2012-04-26 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
IL295053A (en) * | 2007-03-28 | 2022-09-01 | Pharmacyclics Llc | Broton tyrosine kinase inhibitors |
UY31162A1 (es) * | 2007-06-20 | 2008-11-28 | Glaxo Group Ltd | Espiroindolinas como moduladores de receptores de quimioquinas |
WO2009061881A1 (en) * | 2007-11-07 | 2009-05-14 | Glaxo Group Limited | Spirodihydrobenzofurans as modulators of chemokine receptors |
US20100331298A1 (en) * | 2007-12-10 | 2010-12-30 | Cytopathfinder, Inc. | Carboxamide Compounds and Their Use |
RU2010128543A (ru) | 2007-12-11 | 2012-01-20 | Сайтопатфайндер, Инк. (Jp) | Карбоксамидные соединения и их применение в качестве агонистов хемокиновых рецепторов |
CN102131777B (zh) * | 2008-06-23 | 2014-03-19 | 詹森药业有限公司 | Ccr2的哌啶基丙烯酰胺拮抗剂 |
AU2009270856B2 (en) | 2008-07-16 | 2013-07-25 | Pharmacyclics Llc | Inhibitors of Bruton's tyrosine kinase for the treatment of solid tumors |
BRPI0923237A2 (pt) * | 2008-12-10 | 2019-09-24 | Janssen Pharmaceutica Nv | compostos de 4-azetidinil-1-heteroaril-ciclohexanol antagonistas de ccr2 |
NZ595431A (en) * | 2009-04-16 | 2013-12-20 | Janssen Pharmaceutica Nv | 4-azetidinyl-1-heteroaryl-cyclohexane antagonists of ccr2 |
CA2758934A1 (en) * | 2009-04-17 | 2010-10-21 | Janssen Pharmaceutica Nv | 4-azetidinyl-1-phenyl-cyclohexane antagonists of ccr2 |
MX2011010963A (es) * | 2009-04-17 | 2011-11-02 | Janssen Pharmaceutica Nv | Antagonistas del receptor 2 de citocina quimiotrayente de ciclohexano unido al 4-azetidinil-1-heteroatomo. |
KR101151415B1 (ko) | 2009-07-10 | 2012-06-01 | 양지화학 주식회사 | Ccr2 길항제로서의 피페라지닐에틸 3-아미노피롤리딘 유도체 |
US8383812B2 (en) * | 2009-10-13 | 2013-02-26 | Bristol-Myers Squibb Company | N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-3-(7-tert-butylpyrazolo[1,5-A][1,3,5]triazin-4-ylamino)-2-oxopyrrolidin-1-yl)cyclohexyl)acetamide, a dual modulator of chemokine receptor activity, crystalline forms and processes |
EA201890869A3 (ru) | 2010-06-03 | 2019-03-29 | Фармасайкликс, Инк. | Применение ингибиторов тирозинкиназы брутона (btk) |
JP5936608B2 (ja) | 2010-06-17 | 2016-06-22 | ヤンセン ファーマシューティカ エヌ.ベー. | Ccr2のシクロヘキシル−アゼチジニルアンタゴニスト |
TW201204733A (en) | 2010-06-25 | 2012-02-01 | Kowa Co | Novel condensed pyridine or condensed pyrimidine derivative, and medicinal agent comprising same |
KR20130121891A (ko) * | 2010-12-01 | 2013-11-06 | 얀센 파마슈티카 엔.브이. | Ccr2의 4-치환된-사이클로헥실아미노-4-피페리디닐-아세트아미드길항제 |
WO2013010136A2 (en) | 2011-07-13 | 2013-01-17 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
CA2852160A1 (en) | 2011-10-28 | 2013-05-02 | Galderma Research & Development | New leukocyte infiltrate markers for rosacea and uses thereof |
US8377946B1 (en) | 2011-12-30 | 2013-02-19 | Pharmacyclics, Inc. | Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors |
CN102603611B (zh) * | 2012-01-11 | 2014-05-07 | 巨化集团公司 | 一种三氟甲基代哌啶类化合物的制备方法 |
AU2013255050B2 (en) | 2012-05-01 | 2016-07-28 | Translatum Medicus Inc. | Methods for treating and diagnosing blinding eye diseases |
CA3015208C (en) | 2012-06-04 | 2024-01-02 | Pharmacyclics Llc | Crystalline forms of a bruton's tyrosine kinase inhibitor |
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AU2015296215A1 (en) | 2014-08-01 | 2017-03-23 | Pharmacyclics Llc | Inhibitors of bruton's tyrosine kinase |
US9545407B2 (en) | 2014-08-07 | 2017-01-17 | Pharmacyclics Llc | Formulations of a bruton's tyrosine kinase inhibitor |
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KR20170122220A (ko) | 2015-03-03 | 2017-11-03 | 파마싸이클릭스 엘엘씨 | 브루톤 타이로신 키나제 저해제의 약제학적 제제 |
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GB9803228D0 (en) * | 1998-02-17 | 1998-04-08 | Zeneca Ltd | Chemical compounds |
GB0107907D0 (en) * | 2001-03-29 | 2001-05-23 | Smithkline Beecham Plc | Novel compounds |
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- 2005-09-12 AU AU2005290028A patent/AU2005290028A1/en not_active Abandoned
- 2005-09-12 CA CA002582225A patent/CA2582225A1/en not_active Abandoned
- 2005-09-12 MX MX2007003793A patent/MX2007003793A/es unknown
- 2005-09-12 BR BRPI0516166-5A patent/BRPI0516166A/pt not_active IP Right Cessation
- 2005-09-12 WO PCT/US2005/032500 patent/WO2006036527A1/en active Application Filing
- 2005-09-12 JP JP2007534623A patent/JP2008514700A/ja active Pending
- 2005-09-12 EP EP05797411A patent/EP1802602A1/en not_active Withdrawn
- 2005-09-12 EA EA200700757A patent/EA200700757A1/ru unknown
- 2005-09-12 KR KR1020077009314A patent/KR20070063562A/ko not_active Application Discontinuation
- 2005-09-12 CN CNA2005800403016A patent/CN101065374A/zh active Pending
- 2005-09-27 AR ARP050104063A patent/AR053413A1/es not_active Application Discontinuation
- 2005-09-27 TW TW094133431A patent/TW200621707A/zh unknown
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2007
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- 2007-03-27 IL IL182254A patent/IL182254A0/en unknown
- 2007-03-28 EC EC2007007358A patent/ECSP077358A/es unknown
- 2007-04-23 NO NO20072065A patent/NO20072065L/no not_active Application Discontinuation
- 2007-04-27 CR CR9088A patent/CR9088A/es unknown
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RU2644761C2 (ru) * | 2012-06-22 | 2018-02-14 | Идорсиа Фармасьютиклз Лтд | Производные 1-[м-карбоксамидо(гетеро)арил-метил]-гетероциклил-карбоксамида |
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IL182254A0 (en) | 2007-09-20 |
US20060069123A1 (en) | 2006-03-30 |
WO2006036527A1 (en) | 2006-04-06 |
AU2005290028A1 (en) | 2006-04-06 |
CR9088A (es) | 2008-09-09 |
CA2582225A1 (en) | 2006-04-06 |
KR20070063562A (ko) | 2007-06-19 |
EP1802602A1 (en) | 2007-07-04 |
ZA200702544B (en) | 2008-09-25 |
AR053413A1 (es) | 2007-05-09 |
NO20072065L (no) | 2007-06-15 |
BRPI0516166A (pt) | 2008-08-26 |
MX2007003793A (es) | 2007-07-11 |
CN101065374A (zh) | 2007-10-31 |
JP2008514700A (ja) | 2008-05-08 |
TW200621707A (en) | 2006-07-01 |
ECSP077358A (es) | 2007-04-26 |
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