AR046859A1 - Biaril sulfonamidas con actividad inhibitoria de metaloproteinasa, composiciones farmaceuticas que las contienen y su uso en el tratamiento de enfermedades asociadas a la degradacion del tejido conectivo. - Google Patents
Biaril sulfonamidas con actividad inhibitoria de metaloproteinasa, composiciones farmaceuticas que las contienen y su uso en el tratamiento de enfermedades asociadas a la degradacion del tejido conectivo.Info
- Publication number
- AR046859A1 AR046859A1 ARP040104461A ARP040104461A AR046859A1 AR 046859 A1 AR046859 A1 AR 046859A1 AR P040104461 A ARP040104461 A AR P040104461A AR P040104461 A ARP040104461 A AR P040104461A AR 046859 A1 AR046859 A1 AR 046859A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- independently
- methaloproteinase
- biaril
- sulfonamids
- Prior art date
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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Abstract
La presente se relaciona con biaril sulfonamidas y su uso como, por ejemplo, inhibidores de metaloproteinasas. Reivindicación 1: Un método para modular la actividad de una metaloproteinasa caracterizado porque comprende poner en contacto dicha metaloproteinasa con una cantidad efectiva de una biaril sulfonamida unida a un grupo heteroarilo. Reivindicación 47: Un compuesto caracterizado porque posee la fórmula (1), en donde: R1 y R2 son, independientemente, H, CH(OH)R4, fenilo, heteroarilo, o alquilo C1-6, con la provisión de que, cuando R1 o R2 es CH(OH)R4, entonces Z se sustituye con NR4SO2R5, SO2NR4R5, heterocicloalquilo, heteroarilo o cicloalquilo C3-6; R3 es H o alquilo C1-6; R4 y R5 son, independientemente en cada una de las ocurrencias, un enlace hacia el otro, H, alquilo C1-6, o fenilo; G y E son, independientemente, S, O, N(R4), C(R6)=C(R6), o N=C(R6); R6 es, independientemente en cada una de las ocurrencias, H, halógeno, NR4R5, N[(CH2)2]2O, N[(CH2)2]2NR4, NR4SO2R5, NR4C(=O)R5, NHC(=O)OR4, NO2, SO2NR4R5, SO2R4, OR4, C(=O)R4, COOR4, CONR4R5, CN, fenilo, heteroarilo, alquilo C1-6, alquenilo C2-6, o alquinilo C2-6; X es N(R3)C(=O), OC(=O), OS(O2), NHSO2, OCH2, CH2S(O), o CH2S(O)2; y Z es al menos un grupo heteroarilo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US52684003P | 2003-12-04 | 2003-12-04 | |
PCT/US2003/040835 WO2005061477A1 (en) | 2003-12-04 | 2003-12-22 | Biaryl sulfonamides as mmp inhibitors |
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AR046859A1 true AR046859A1 (es) | 2005-12-28 |
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Family Applications (1)
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ARP040104461A AR046859A1 (es) | 2003-12-04 | 2004-12-01 | Biaril sulfonamidas con actividad inhibitoria de metaloproteinasa, composiciones farmaceuticas que las contienen y su uso en el tratamiento de enfermedades asociadas a la degradacion del tejido conectivo. |
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US (2) | US7420001B2 (es) |
EP (1) | EP1692124B1 (es) |
JP (1) | JP2007524567A (es) |
KR (1) | KR20060093735A (es) |
CN (1) | CN1623537A (es) |
AR (1) | AR046859A1 (es) |
AT (1) | ATE411306T1 (es) |
AU (2) | AU2003299789A1 (es) |
BR (1) | BR0318640A (es) |
CA (1) | CA2548518A1 (es) |
CR (1) | CR8418A (es) |
DE (1) | DE60324208D1 (es) |
EC (1) | ECSP066637A (es) |
IL (1) | IL159679A0 (es) |
NO (1) | NO20062649L (es) |
PA (1) | PA8618901A1 (es) |
PE (1) | PE20050669A1 (es) |
RU (1) | RU2006123559A (es) |
TW (1) | TW200519100A (es) |
WO (1) | WO2005061477A1 (es) |
ZA (1) | ZA200604551B (es) |
Families Citing this family (26)
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JP2007525406A (ja) * | 2003-12-04 | 2007-09-06 | ワイス | ビアリールスルホンアミドおよびその使用方法 |
US20080119513A1 (en) * | 2004-09-06 | 2008-05-22 | Fumihiko Watanabe | Sulfonamide Derivative Selectively Inhibiting Mmp-13 |
CA2617055A1 (en) * | 2005-07-29 | 2007-02-08 | Bayer Healthcare Llc | Preparation and use of biphenyl amino acid derivatives for the treatment of obesity |
US7615363B2 (en) * | 2005-08-25 | 2009-11-10 | Wyeth | Aggrecanase structure |
US7625731B2 (en) * | 2005-08-25 | 2009-12-01 | Wyeth | Aggrecanase structure |
JP2009526048A (ja) * | 2006-02-08 | 2009-07-16 | ワイス | パラジウム媒介カップリング反応を介する7−アルケニル−3キノリンカルボニトリルの調製 |
DK2402317T3 (da) * | 2006-03-31 | 2013-10-07 | Novartis Ag | DGAT-inhibitor |
WO2008147763A1 (en) * | 2007-05-23 | 2008-12-04 | Array Biopharma Inc. | Mmp inhibitors and methods of use thereof |
EP2321268A2 (en) * | 2008-08-15 | 2011-05-18 | F. Hoffmann-La Roche AG | Bi-aryl aminotetralines |
WO2010059602A2 (en) * | 2008-11-19 | 2010-05-27 | Schering Corporation | Inhibitors of diacylglycerol acyltransferase |
US20120172369A1 (en) * | 2009-09-14 | 2012-07-05 | Ting Pauline C | Inhibitors of diacylglycerol acyltransferase |
US8530453B2 (en) * | 2009-09-28 | 2013-09-10 | Aquilus Pharmaceuticals, Inc. | Compounds and methods for the treatment of pain and other diseases |
EP2593226B1 (en) | 2010-07-16 | 2018-11-14 | AbbVie Ireland Unlimited Company | Phosphine ligands for catalytic reactions |
US9255074B2 (en) | 2010-07-16 | 2016-02-09 | Abbvie Inc. | Process for preparing antiviral compounds |
US8975443B2 (en) | 2010-07-16 | 2015-03-10 | Abbvie Inc. | Phosphine ligands for catalytic reactions |
CR20180412A (es) | 2010-07-16 | 2018-11-01 | Abbvie Ireland Unlimited Co | Proceso para preparar compuestos antivirales |
AU2011360973A1 (en) * | 2011-03-02 | 2013-09-19 | Aquilus Pharmaceuticals, Inc. | Compounds and methods for the treatment of pain and other disorders |
SG11201406311UA (en) | 2012-04-05 | 2014-11-27 | Chdi Foundation Inc | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
CN103333144B (zh) * | 2013-06-17 | 2014-12-10 | 温州大学 | 一种2-硫基-3-卤代苯并呋喃化合物及其合成方法和用途 |
US9884853B2 (en) | 2013-09-26 | 2018-02-06 | Chdi Foundation, Inc. | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
US9938252B2 (en) | 2013-09-26 | 2018-04-10 | Chdi Foundation, Inc. | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
KR20160066490A (ko) | 2014-12-02 | 2016-06-10 | 주식회사 씨앤드씨신약연구소 | 헤테로사이클 유도체 및 그의 용도 |
WO2017180723A1 (en) | 2016-04-12 | 2017-10-19 | Atrin Pharmaceuticals LLC | Ataxia telengiectasia and rad3-related (atr) inhibitors and methods of their use |
CN106905348B (zh) * | 2017-02-13 | 2018-12-04 | 牡丹江医学院 | 一种预防和治疗急性肾损伤的药物及其制备方法和用途 |
CN112480020B (zh) * | 2020-12-11 | 2023-10-10 | 东华理工大学 | 一种2-取代苯并恶唑化合物 |
CN113527152B (zh) * | 2021-08-09 | 2023-07-28 | 西北农林科技大学 | 一种联苯磺酰胺类化合物及其防治农作物害虫的方法 |
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CZ298814B6 (cs) * | 1996-01-23 | 2008-02-13 | Shionogi & Co., Ltd. | Sulfonované deriváty aminokyselin a metaloproteasové inhibitory obsahující tyto deriváty |
US6566381B1 (en) * | 1999-03-03 | 2003-05-20 | The Procter & Gamble Company | Hetero-substituted metalloprotease inhibitors |
EP1224171A1 (en) * | 1999-10-14 | 2002-07-24 | The Procter & Gamble Company | Beta disubstituted metalloprotease inhibitors |
JP2007525406A (ja) * | 2003-12-04 | 2007-09-06 | ワイス | ビアリールスルホンアミドおよびその使用方法 |
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- 2004-12-01 AR ARP040104461A patent/AR046859A1/es not_active Application Discontinuation
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- 2006-06-08 NO NO20062649A patent/NO20062649L/no not_active Application Discontinuation
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Also Published As
Publication number | Publication date |
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EP1692124B1 (en) | 2008-10-15 |
CN1623537A (zh) | 2005-06-08 |
ZA200604551B (en) | 2008-11-26 |
US7420001B2 (en) | 2008-09-02 |
KR20060093735A (ko) | 2006-08-25 |
ATE411306T1 (de) | 2008-10-15 |
DE60324208D1 (de) | 2008-11-27 |
IL159679A0 (en) | 2004-06-20 |
US20050143422A1 (en) | 2005-06-30 |
BR0318640A (pt) | 2006-11-28 |
PE20050669A1 (es) | 2005-11-02 |
US20100137298A1 (en) | 2010-06-03 |
WO2005061477A1 (en) | 2005-07-07 |
EP1692124A1 (en) | 2006-08-23 |
JP2007524567A (ja) | 2007-08-30 |
TW200519100A (en) | 2005-06-16 |
NO20062649L (no) | 2006-09-01 |
RU2006123559A (ru) | 2008-01-10 |
AU2003299789A1 (en) | 2005-07-14 |
CA2548518A1 (en) | 2005-07-07 |
PA8618901A1 (es) | 2005-11-25 |
CR8418A (es) | 2007-08-28 |
AU2004200247A1 (en) | 2005-06-23 |
ECSP066637A (es) | 2006-10-25 |
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