BRPI0415500A - hidroxamatos cìclicos substituìdos como inibidores de metaloproteinases de matriz - Google Patents
hidroxamatos cìclicos substituìdos como inibidores de metaloproteinases de matrizInfo
- Publication number
- BRPI0415500A BRPI0415500A BRPI0415500-9A BRPI0415500A BRPI0415500A BR PI0415500 A BRPI0415500 A BR PI0415500A BR PI0415500 A BRPI0415500 A BR PI0415500A BR PI0415500 A BRPI0415500 A BR PI0415500A
- Authority
- BR
- Brazil
- Prior art keywords
- inhibitors
- substituted
- matrix metalloproteinase
- metalloproteinase inhibitors
- formula
- Prior art date
Links
- 125000004122 cyclic group Chemical group 0.000 title 1
- 239000003771 matrix metalloproteinase inhibitor Substances 0.000 title 1
- 229940121386 matrix metalloproteinase inhibitor Drugs 0.000 title 1
- 201000010099 disease Diseases 0.000 abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 102000005741 Metalloproteases Human genes 0.000 abstract 2
- 108010006035 Metalloproteases Proteins 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 206010020751 Hypersensitivity Diseases 0.000 abstract 1
- 102000002274 Matrix Metalloproteinases Human genes 0.000 abstract 1
- 108010000684 Matrix Metalloproteinases Proteins 0.000 abstract 1
- 201000004681 Psoriasis Diseases 0.000 abstract 1
- 230000007815 allergy Effects 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000011159 matrix material Substances 0.000 abstract 1
- 239000002207 metabolite Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000001613 neoplastic effect Effects 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
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- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- 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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- 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
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- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
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Abstract
"HIDROXAMATOS CìCLICOS SUBSTITUìDOS COMO INIBIDORES DE METALOPROTEINASES DE MATRIZ". A presente invenção fornece compostos de fórmula I: seus enantiómeros, diastereómeros, misturas racêmicas desses, pró-medicamentos, formas cristalinas, formas não cristalinas, formas amorfas desses, solvatos desses, metabólitos desses, e sais farmaceuticamente aceitáveis, onde os grupo substituintes de anel A são totalmente definidos na revelação a seguir. os compostos de fórmula I são inibidores de metaloproteases como metaloproteases de matriz e sheddases, e são úteis no tratamento de doenças como artrite reumatóide, psoríase, doenças neoplásicas, alergias e todas aquelas doenças onde a inibição de MMPs é desejável.
Applications Claiming Priority (4)
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| US51201603P | 2003-10-17 | 2003-10-17 | |
| US51535203P | 2003-10-28 | 2003-10-28 | |
| US58664604P | 2004-07-12 | 2004-07-12 | |
| PCT/US2004/033945 WO2005037826A1 (en) | 2003-10-17 | 2004-10-15 | Substituted cyclic hydroxamates as inhibitors of matrix metalloproteinases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0415500A true BRPI0415500A (pt) | 2007-04-10 |
Family
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| AU (1) | AU2004282189B2 (pt) |
| BR (1) | BRPI0415500A (pt) |
| CA (1) | CA2541509C (pt) |
| MX (1) | MXPA06004191A (pt) |
| WO (1) | WO2005037826A1 (pt) |
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| SI1511472T1 (sl) * | 2002-05-29 | 2009-08-31 | Merck & Co Inc | Spojine uporabne pri zdravljenju antraksa in inhibiranju letalnega faktorja |
| EP1613269B1 (en) | 2003-04-04 | 2015-02-25 | Incyte Corporation | Compositions, methods and kits relating to her-2 cleavage |
| CN101880277A (zh) | 2003-04-24 | 2010-11-10 | 因塞特公司 | 作为金属蛋白酶抑制剂的氮杂螺烷衍生物 |
| BRPI0415500A (pt) | 2003-10-17 | 2007-04-10 | Incyte Corp | hidroxamatos cìclicos substituìdos como inibidores de metaloproteinases de matriz |
| BRPI0506948B1 (pt) * | 2004-01-30 | 2018-09-18 | Medivir Ab | inibidores de serina protease ns-3 de hcv |
| WO2005118529A2 (en) * | 2004-05-11 | 2005-12-15 | Merck & Co., Inc. | Process for making n-sulfonated-amino acid derivatives |
| US20100003276A1 (en) * | 2004-12-07 | 2010-01-07 | Hermes Jeffery D | Methods for treating anthrax and inhibiting lethal factor |
| JP2008530123A (ja) * | 2005-02-09 | 2008-08-07 | ジェネンテック・インコーポレーテッド | マトリックスメタロプロテアーゼアンタゴニストを用いたher2のシェディングの阻害 |
| EP1888562B1 (en) * | 2005-04-22 | 2014-06-18 | Alantos Pharmaceuticals Holding, Inc. | Dipeptidyl peptidase-iv inhibitors |
| WO2007021803A1 (en) * | 2005-08-12 | 2007-02-22 | Schering Corporation | Compounds for the treatment of inflammatory disorders |
| WO2007062093A2 (en) * | 2005-11-22 | 2007-05-31 | Incyte Corporation | Combination therapy for the treatment of cancer comprising a metalloprotease inhibitor |
| CA2651663A1 (en) | 2006-05-30 | 2007-12-06 | Astrazeneca Ab | Chemical compounds |
| US7910108B2 (en) * | 2006-06-05 | 2011-03-22 | Incyte Corporation | Sheddase inhibitors combined with CD30-binding immunotherapeutics for the treatment of CD30 positive diseases |
| US8486979B2 (en) * | 2006-12-12 | 2013-07-16 | Abbvie Inc. | 1,2,4 oxadiazole compounds and methods of use thereof |
| CN101932562B (zh) | 2007-12-20 | 2013-06-12 | 阿斯利康(瑞典)有限公司 | 作为dgat1抑制剂190的氨基甲酰基化合物 |
| US20090312470A1 (en) * | 2008-06-11 | 2009-12-17 | Ferro Corporation | Asymmetric Cyclic Diester Compounds |
| WO2010146395A1 (en) | 2009-06-19 | 2010-12-23 | Astrazeneca Ab | Pyrazine carboxamides as inhibitors of dgat1 |
| CN101914051B (zh) * | 2010-07-30 | 2013-03-13 | 嘉兴宜博生物医药科技有限公司 | 光学异构纯的3-苯基吡咯啉衍生物的合成方法 |
| TWI565706B (zh) * | 2011-06-17 | 2017-01-11 | 阿斯特捷利康公司 | 用於製備包括反-7-酮基-6-(磺酸氧基)-1,6-二氮雜雙環[3,2,1]辛烷-2-甲醯胺之雜環化合物及其鹽類之方法 |
| WO2013134079A1 (en) | 2012-03-05 | 2013-09-12 | Amgen Inc. | Oxazolidinone compounds and derivatives thereof |
| CN104418866B (zh) | 2013-08-23 | 2018-10-16 | 青岛黄海制药有限责任公司 | Dgat1抑制剂及其制备方法和用途 |
| WO2017117130A1 (en) | 2015-12-28 | 2017-07-06 | The United States Of America, As Represented By The Secretary, Department Of Health & Human Services | Methods for inhibiting human immunodeficiency virus (hiv) release from infected cells |
| AU2017275657B2 (en) | 2016-06-02 | 2021-08-19 | Novartis Ag | Potassium channel modulators |
| UA123810C2 (uk) | 2017-01-23 | 2021-06-02 | Цадент Терапеутікс, Інк. | Модулятори калієвих каналів |
| CA3099610A1 (en) | 2018-05-09 | 2019-11-14 | Bayer Animal Health Gmbh | New quinoline derivatives |
| MX2021004647A (es) | 2018-10-22 | 2021-08-16 | Novartis Ag | Formas cristalinas de moduladores de los canales de potasio. |
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| WO1993021942A2 (en) | 1992-05-01 | 1993-11-11 | British Biotech Pharmaceuticals Limited | Use of mmp inhibitors |
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| US6084226A (en) * | 1998-04-21 | 2000-07-04 | Cem Corporation | Use of continuously variable power in microwave assisted chemistry |
| AU4074799A (en) | 1998-05-14 | 1999-11-29 | Du Pont Pharmaceuticals Company | Substituted aryl hydroxamic acids as metalloproteinase inhibitors |
| JP2002514647A (ja) * | 1998-05-14 | 2002-05-21 | デュポン ファーマシューティカルズ カンパニー | メタロプロテイナーゼ阻害薬としての新規な置換アリールヒドロキサム酸 |
| CA2333554A1 (en) * | 1998-06-17 | 1999-12-23 | Chu-Baio Xue | Cyclic hydroxamic acids as metalloproteinase inhibitors |
| IL144850A0 (en) | 1999-03-22 | 2002-06-30 | Pfizer | Resorcinol derivatives |
| SK13072002A3 (sk) | 2000-03-17 | 2003-08-05 | Bristol-Myers Squibb Pharma Company | Deriváty cyklických beta-aminokyselín ako inhibítory matrixových metaloproteáz a TNF-alfa |
| CA2434044A1 (en) * | 2001-01-11 | 2002-07-18 | Bristol-Myers Squibb Pharma Company | 1,2-disubstituted cyclic inhibitors of matrix metallorproteases and tnf-alpha |
| US7135575B2 (en) * | 2003-03-03 | 2006-11-14 | Array Biopharma, Inc. | P38 inhibitors and methods of use thereof |
| KR20050109969A (ko) | 2003-03-06 | 2005-11-22 | 보툴리늄 톡신 리서치 어쏘시에이츠, 인크. | 보툴리눔 톡신으로 부비동염 관련 만성 안면통 및 두통을치료하는 방법 |
| EP1613269B1 (en) * | 2003-04-04 | 2015-02-25 | Incyte Corporation | Compositions, methods and kits relating to her-2 cleavage |
| CN101880277A (zh) | 2003-04-24 | 2010-11-10 | 因塞特公司 | 作为金属蛋白酶抑制剂的氮杂螺烷衍生物 |
| BRPI0415500A (pt) | 2003-10-17 | 2007-04-10 | Incyte Corp | hidroxamatos cìclicos substituìdos como inibidores de metaloproteinases de matriz |
| WO2005117882A2 (en) | 2004-04-20 | 2005-12-15 | Incyte Corporation | Hydroxamic acid derivatives as metalloprotease inhibitors |
| WO2007062093A2 (en) | 2005-11-22 | 2007-05-31 | Incyte Corporation | Combination therapy for the treatment of cancer comprising a metalloprotease inhibitor |
| US7910108B2 (en) | 2006-06-05 | 2011-03-22 | Incyte Corporation | Sheddase inhibitors combined with CD30-binding immunotherapeutics for the treatment of CD30 positive diseases |
-
2004
- 2004-10-15 BR BRPI0415500-9A patent/BRPI0415500A/pt not_active IP Right Cessation
- 2004-10-15 EP EP04795145A patent/EP1678167A1/en not_active Withdrawn
- 2004-10-15 JP JP2006535665A patent/JP4956191B2/ja not_active Expired - Lifetime
- 2004-10-15 AU AU2004282189A patent/AU2004282189B2/en not_active Expired
- 2004-10-15 WO PCT/US2004/033945 patent/WO2005037826A1/en not_active Ceased
- 2004-10-15 CA CA2541509A patent/CA2541509C/en not_active Expired - Lifetime
- 2004-10-15 MX MXPA06004191A patent/MXPA06004191A/es active IP Right Grant
- 2004-10-15 EP EP10182170A patent/EP2264030A1/en not_active Withdrawn
- 2004-10-15 US US10/965,215 patent/US7491724B2/en active Active
- 2004-10-15 KR KR1020067009625A patent/KR20060101488A/ko not_active Ceased
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2008
- 2008-02-15 US US12/070,310 patent/US7973041B2/en not_active Expired - Lifetime
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2011
- 2011-05-19 US US13/111,426 patent/US8853243B2/en not_active Expired - Lifetime
- 2011-08-25 JP JP2011183395A patent/JP2012046517A/ja not_active Withdrawn
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2014
- 2014-10-03 US US14/506,333 patent/US9440958B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AU2004282189A1 (en) | 2005-04-28 |
| KR20060101488A (ko) | 2006-09-25 |
| JP4956191B2 (ja) | 2012-06-20 |
| JP2007509075A (ja) | 2007-04-12 |
| JP2012046517A (ja) | 2012-03-08 |
| US7973041B2 (en) | 2011-07-05 |
| AU2004282189B2 (en) | 2011-11-17 |
| MXPA06004191A (es) | 2007-01-19 |
| CA2541509A1 (en) | 2005-04-28 |
| US7491724B2 (en) | 2009-02-17 |
| WO2005037826A1 (en) | 2005-04-28 |
| EP1678167A1 (en) | 2006-07-12 |
| CA2541509C (en) | 2014-06-10 |
| US8853243B2 (en) | 2014-10-07 |
| US20080167288A1 (en) | 2008-07-10 |
| US20150025056A1 (en) | 2015-01-22 |
| US20050113344A1 (en) | 2005-05-26 |
| US20110224189A1 (en) | 2011-09-15 |
| US9440958B2 (en) | 2016-09-13 |
| EP2264030A1 (en) | 2010-12-22 |
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