CL2008002073A1 - Compuestos derivados de lactama tetraciclicos, inhibidores de mk-2; procedimiento de praparacion; composicion farmaceutica; y su uso en el tratamiento de artritis, sinovitis aguda, tendinitis, soriasis, miocarditis, caquexia, asma, cancer, entre otras. - Google Patents
Compuestos derivados de lactama tetraciclicos, inhibidores de mk-2; procedimiento de praparacion; composicion farmaceutica; y su uso en el tratamiento de artritis, sinovitis aguda, tendinitis, soriasis, miocarditis, caquexia, asma, cancer, entre otras.Info
- Publication number
- CL2008002073A1 CL2008002073A1 CL2008002073A CL2008002073A CL2008002073A1 CL 2008002073 A1 CL2008002073 A1 CL 2008002073A1 CL 2008002073 A CL2008002073 A CL 2008002073A CL 2008002073 A CL2008002073 A CL 2008002073A CL 2008002073 A1 CL2008002073 A1 CL 2008002073A1
- Authority
- CL
- Chile
- Prior art keywords
- tendonitis
- myocarditis
- cachexia
- psoriasis
- asthma
- Prior art date
Links
Classifications
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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
- C07D471/14—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
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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
- 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
- C07D471/22—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 systems contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
-
- 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
- C07D491/22—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 four or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
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- Hematology (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Endocrinology (AREA)
- Heart & Thoracic Surgery (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Transplantation (AREA)
- AIDS & HIV (AREA)
- Hospice & Palliative Care (AREA)
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Abstract
Compuestos derivados de lactama tetracíclicos; procedimiento de preparación; composición farmacéutica que comprende a dicho compuesto; y uso del compuesto en el tratamiento de artritis, sinovitis aguda, tendinitis, soriasis, miocarditis, caquexia, asma, cáncer, entre otras.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07112549 | 2007-07-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2008002073A1 true CL2008002073A1 (es) | 2009-02-20 |
Family
ID=38792023
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2008002073A CL2008002073A1 (es) | 2007-07-16 | 2008-07-15 | Compuestos derivados de lactama tetraciclicos, inhibidores de mk-2; procedimiento de praparacion; composicion farmaceutica; y su uso en el tratamiento de artritis, sinovitis aguda, tendinitis, soriasis, miocarditis, caquexia, asma, cancer, entre otras. |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US7838674B2 (es) |
| EP (1) | EP2178874A1 (es) |
| JP (1) | JP2010533674A (es) |
| KR (1) | KR20100031619A (es) |
| CN (1) | CN101687869A (es) |
| AR (1) | AR067535A1 (es) |
| AU (1) | AU2008277676A1 (es) |
| BR (1) | BRPI0814426A2 (es) |
| CA (1) | CA2693904A1 (es) |
| CL (1) | CL2008002073A1 (es) |
| EA (1) | EA201000100A1 (es) |
| MX (1) | MX2009014247A (es) |
| PE (1) | PE20090480A1 (es) |
| TW (1) | TW200904818A (es) |
| WO (1) | WO2009010488A1 (es) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8494544B2 (en) * | 2009-12-03 | 2013-07-23 | Osocad Remote Limited Liability Company | Method, apparatus and computer program to perform location specific information retrieval using a gesture-controlled handheld mobile device |
| AU2010333024B2 (en) | 2009-12-14 | 2014-09-18 | Merck Sharp & Dohme B.V. | MK2 inhibitors |
| AU2014277711B2 (en) * | 2009-12-14 | 2016-10-27 | Merck Sharp & Dohme B.V. | MK2 inhibitors |
| AR080865A1 (es) | 2010-03-31 | 2012-05-16 | Array Biopharma Inc | Derivados de espirotetrahidronaftaleno, composiciones farmaceuticas que los contienen, proceso de preparacion y uso de los mismos para tratar enfermedades neurodegenerativas,tal como alzheimer. |
| EP2619181A1 (en) | 2010-09-23 | 2013-07-31 | Syngenta Participations AG | Novel microbiocides |
| EP2668188B1 (en) * | 2011-01-26 | 2016-05-18 | Nerviano Medical Sciences S.r.l. | Tricyclic derivatives, process for their preparation and their use as kinase inhibitors |
| RU2591191C2 (ru) * | 2011-01-26 | 2016-07-10 | НЕРВИАНО МЕДИКАЛ САЙЕНСИЗ С.р.л. | Трициклические пирроло производные, способ их получения и их применение в качестве ингибиторов киназы |
| WO2012117021A2 (en) | 2011-03-03 | 2012-09-07 | Syngenta Participations Ag | Novel microbiocidal oxime ethers |
| US20140113824A1 (en) | 2011-05-10 | 2014-04-24 | Bayer Intellectual Property Gmbh | Bicyclic (thio)carbonylamidines |
| WO2013092460A1 (en) | 2011-12-20 | 2013-06-27 | Syngenta Participations Ag | Cyclic bisoxime microbicides |
| EP2641901A1 (en) | 2012-03-22 | 2013-09-25 | Syngenta Participations AG. | Novel microbiocides |
| KR101561330B1 (ko) | 2012-09-19 | 2015-10-16 | 주식회사 두산 | 인돌로인돌계 유기 발광 화합물 및 이를 이용한 유기 전계 발광 소자 |
| CN102936216B (zh) * | 2012-12-05 | 2015-03-04 | 南京药石药物研发有限公司 | 7,9-二氧代-2,6-氮杂-螺[3.5]壬-2-甲酸叔丁酯及其中间体的制备方法 |
| PT2953942T (pt) | 2013-02-06 | 2018-01-17 | Bayer Cropscience Ag | Derivados de pirazol substituídos com halogéneo como agentes pesticidas |
| EP2968339A4 (en) * | 2013-03-15 | 2017-02-15 | Celgene Avilomics Research, Inc. | Mk2 inhibitors and uses thereof |
| AU2015317741B2 (en) | 2014-09-17 | 2020-01-16 | Bristol-Myers Squibb Company | MK2 inhibitors and uses thereof |
| CN105348263B (zh) * | 2015-12-15 | 2018-03-23 | 乐普药业股份有限公司 | 一种达比加群酯中间体的制备方法 |
| CN113620981A (zh) * | 2016-10-05 | 2021-11-09 | 结核病药物开发全球联盟公司 | 用于治疗分枝杆菌感染的杂芳基三氟硼酸盐化合物 |
| WO2018170199A1 (en) | 2017-03-16 | 2018-09-20 | Celgene Car Llc | Forms and compositions of a mk2 inhibitor |
| EP3596084A4 (en) | 2017-03-16 | 2020-12-23 | Celgene CAR LLC | 9,10,11,12-TETRAHYDRO-8H- [1,4] DIAZEPINO [5 ', 6': 4,5] THIÉNO [3,2-F] QUINOLIN-8-ONE COMPOUNDS AND THEIR USES |
| WO2018170200A1 (en) | 2017-03-16 | 2018-09-20 | Celgene Car Llc | Heteroaryl compounds useful as mk2 inhibitors |
| EP3596086A4 (en) | 2017-03-16 | 2020-12-16 | Celgene CAR LLC | MK2 INHIBITORS, THEIR SYNTHESIS AND THEIR INTERMEDIARIES |
| WO2018170201A1 (en) | 2017-03-16 | 2018-09-20 | Celgene Car Llc | Deuterated analogs of mk2 inhibitors and uses thereof |
| CN107383026B (zh) * | 2017-06-29 | 2019-04-30 | 武汉药明康德新药开发有限公司 | 一种7-羟甲基-2,5-二氮杂螺[3,4]辛烷-2-甲酸叔丁酯的合成方法 |
| CN109336890B (zh) * | 2018-11-17 | 2020-03-20 | 重庆文理学院 | 一种吲唑类衍生物的合成方法及抗肿瘤应用 |
| CN109678879A (zh) * | 2019-02-27 | 2019-04-26 | 陕西科技大学 | 一种苯并噻吩并吡喃酮类化合物及其合成方法 |
| CN109678878A (zh) * | 2019-02-27 | 2019-04-26 | 陕西科技大学 | 一种苯并噻吩并香豆素类化合物及其合成方法 |
| CN110563726A (zh) * | 2019-07-23 | 2019-12-13 | 上海合全药业股份有限公司 | 叔丁基-7,9-二氧亚基-2,6-二氮杂螺[4.5]癸烷-2-甲酸基酯的制备方法 |
| EP4284805A1 (en) | 2021-02-01 | 2023-12-06 | Celgene Corporation | Mk2 inhibitors, the synthesis thereof, and intermediates thereto |
| TW202328141A (zh) * | 2021-08-27 | 2023-07-16 | 大陸商瑞石生物醫藥有限公司 | 喹啉并呋喃衍生物及其用途 |
| EP4661875A1 (en) * | 2023-02-07 | 2025-12-17 | Celgene Corporation | Compounds and compositions useful as degraders of mk2 kinase |
| WO2025096869A1 (en) * | 2023-11-01 | 2025-05-08 | Matchpoint Therapeutics Inc. | Pyrrolo-isoquinoline compounds and their use in therapy |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005529850A (ja) * | 2002-02-19 | 2005-10-06 | ファルマシア・イタリア・エス・ピー・エー | 三環系ピラゾール誘導体、その製造方法および抗腫瘍剤としてのその使用 |
| AU2003297431A1 (en) * | 2002-12-20 | 2004-07-22 | Pharmacia Corporation | Mitogen activated protein kinase-activated protein kinase-2 inhibiting compounds |
-
2008
- 2008-07-14 AU AU2008277676A patent/AU2008277676A1/en not_active Abandoned
- 2008-07-14 CN CN200880022905A patent/CN101687869A/zh active Pending
- 2008-07-14 WO PCT/EP2008/059158 patent/WO2009010488A1/en not_active Ceased
- 2008-07-14 EA EA201000100A patent/EA201000100A1/ru unknown
- 2008-07-14 KR KR1020107001022A patent/KR20100031619A/ko not_active Withdrawn
- 2008-07-14 EP EP08786115A patent/EP2178874A1/en not_active Withdrawn
- 2008-07-14 AR ARP080103021A patent/AR067535A1/es unknown
- 2008-07-14 BR BRPI0814426-5A2A patent/BRPI0814426A2/pt not_active Application Discontinuation
- 2008-07-14 JP JP2010516479A patent/JP2010533674A/ja active Pending
- 2008-07-14 MX MX2009014247A patent/MX2009014247A/es not_active Application Discontinuation
- 2008-07-14 PE PE2008001178A patent/PE20090480A1/es not_active Application Discontinuation
- 2008-07-14 CA CA2693904A patent/CA2693904A1/en not_active Abandoned
- 2008-07-15 CL CL2008002073A patent/CL2008002073A1/es unknown
- 2008-07-15 TW TW097126806A patent/TW200904818A/zh unknown
- 2008-07-16 US US12/174,324 patent/US7838674B2/en not_active Expired - Fee Related
-
2010
- 2010-09-13 US US12/880,473 patent/US20120022030A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20090098218A1 (en) | 2009-04-16 |
| TW200904818A (en) | 2009-02-01 |
| US7838674B2 (en) | 2010-11-23 |
| AU2008277676A1 (en) | 2009-01-22 |
| EA201000100A1 (ru) | 2010-08-30 |
| CN101687869A (zh) | 2010-03-31 |
| KR20100031619A (ko) | 2010-03-23 |
| EP2178874A1 (en) | 2010-04-28 |
| JP2010533674A (ja) | 2010-10-28 |
| CA2693904A1 (en) | 2009-01-22 |
| BRPI0814426A2 (pt) | 2015-01-06 |
| AR067535A1 (es) | 2009-10-14 |
| MX2009014247A (es) | 2010-01-28 |
| PE20090480A1 (es) | 2009-05-24 |
| US20120022030A1 (en) | 2012-01-26 |
| WO2009010488A1 (en) | 2009-01-22 |
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