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PE20080856A1 - Inhibidores de metaloproteasas de matriz - Google Patents

Inhibidores de metaloproteasas de matriz

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Publication number
PE20080856A1
PE20080856A1 PE2007001347A PE2007001347A PE20080856A1 PE 20080856 A1 PE20080856 A1 PE 20080856A1 PE 2007001347 A PE2007001347 A PE 2007001347A PE 2007001347 A PE2007001347 A PE 2007001347A PE 20080856 A1 PE20080856 A1 PE 20080856A1
Authority
PE
Peru
Prior art keywords
phenyl
alkyl
hydroxy
inhibitors
propionamide
Prior art date
Application number
PE2007001347A
Other languages
English (en)
Inventor
Shyh-Ming Yang
Robert Scannevin
Kenneth Rhodes
Bharat Lagu
Lawrence J Wilson
Prabha Karnachi
William V Murray
Original Assignee
Janssen Pharmaceutica Nv
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of PE20080856A1 publication Critical patent/PE20080856A1/es

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    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/14Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/145Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/15Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • C07D211/14Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
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Abstract

SE REFIERE A COMPUESTOS HETEROCICLICOS DE FORMULA (I) DONDE R1 Y R2 SON CADA UNO H O CH3; R3 ES H, ALQUILO(C1-C3), FENILO O HETEROARILO DE 5 O 6 MIEMBROS; R4 ES UN COMPUESTO DE FORMULA (i), (ii), (iii), ENTRE OTROS, DONDE A=B ES -CH=CH- O S; Z ES S, O O NH; Ra ES H, Cl, F, OH, ENTRE OTROS; R5 ES ALQUILO(C1-C4), FENILO, -N(ALQUILO(C1-C4))2, ENTRE OTROS; R6 ES H, ALQUILO(C1-C4), ALILO, ALQUIL(C1-C3)-FENILO, ENTRE OTROS; R7 ES -OR8, -SR8, ENTRE OTROS, DONDE R8 ES H, ALQUILO(C1-C4), FENILO, INDOLILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: N-HIDROXI(2S)-2-HIDROXI-3-{N-[4-(4-CLOROFENOXI)FENIL],N-METANSULFONILAMINO}PROPIONAMIDA, N-HIDROXI(2S)-2-(2-PROPOXI)-3-{N-[4-(4-TRIFLUOROMETILFENOXI)FENIL],N-METANSULFONILAMINO}PROPIONAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LAS METALOPROTEINASAS DE MATRIZ (MMP) SIENDO UTILES EN EL TRATAMIENTO DE ACCIDENTE CEREBROVASCULAR, ENFERMEDAD DE PARKINSON, ENFERMEDAD DE ALZHEIMER, ANGIOPATIA AMILOIDE CEREBRAL
PE2007001347A 2006-10-06 2007-10-04 Inhibidores de metaloproteasas de matriz PE20080856A1 (es)

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US8242174B2 (en) * 2007-02-01 2012-08-14 Panthera Biopharma Llc Hydroxamic acid derivatives of aniline useful as therapeutic agents for treating anthrax poisoning
WO2010002976A2 (en) * 2008-07-03 2010-01-07 Bracco Imaging S.P.A. Enzyme-cleavable dye-containing fluor-quencher constructs
EP2334636A2 (en) 2008-09-19 2011-06-22 Pfizer Inc. Hydroxamic acid derivatives useful as antibacterial agents
FR2947270B1 (fr) 2009-06-30 2011-08-26 Galderma Res & Dev Nouveaux composes benzene-sulfonamides, leur procede de synthese et leur utilisation en medecine ainsi qu'en cosmetique
FR2947268B1 (fr) * 2009-06-30 2011-08-26 Galderma Res & Dev Nouveaux composes benzene-sulfonamides, leur procede de synthese et leur utilisation en medecine ainsi qu'en cosmetique
FR2950056B1 (fr) * 2009-09-17 2011-08-26 Galderma Res & Dev Nouveaux composes benzene-carboxylamides, leur procede de synthese et leur utilisation en medecine ainsi qu'en cosmetique
FR2950057B1 (fr) 2009-09-17 2011-08-26 Galderma Res & Dev Nouveaux composes benzene-carboxylamides, leur procede de synthese et leur utilisation en medecine ainsi qu'en cosmetique
US8664401B2 (en) 2009-12-16 2014-03-04 Pfizer Inc. N-linked hydroxamic acid derivatives useful as antibacterial agents
NZ603198A (en) * 2010-04-20 2013-10-25 Taisho Pharmaceutical Co Ltd Novel hydroxamic acid derivative
MA34963B1 (fr) 2011-03-07 2014-03-01 Pfizer Derives de fluoro-pyridinone utiles en tant qu'agents antibacteriens
CA2830866A1 (en) 2011-04-08 2012-10-11 Pfizer Inc. Imidazole, pyrazole, and triazole derivatives useful as antibacterial agents
JP2014510132A (ja) 2011-04-08 2014-04-24 ファイザー・インク 抗菌剤として有用なイソオキサゾール誘導体
CN102675595B (zh) * 2012-04-18 2014-07-02 上海维凯化学品有限公司 羟基酰胺型环氧树脂热潜在固化剂及其合成方法
US20140275108A1 (en) 2013-03-15 2014-09-18 Galderma Research & Development Novel benzenesulfonamide compounds, method for synthesizing same, and use thereof in medicine as well as in cosmetics
EP3199534B1 (en) 2016-02-01 2018-09-05 Galderma Research & Development Benzenesulfonamide compounds, method for synthesizing same, and use thereof in medicine and cosmetics

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US6506936B1 (en) * 1999-02-25 2003-01-14 Fibrogen, Inc. N-substituted arylsulfonylamino hydroxamic acids useful as inhibitors of c-proteinase and for treating or preventing disorders related to unregulated collagen production
AUPP982399A0 (en) * 1999-04-19 1999-05-13 Fujisawa Pharmaceutical Co., Ltd. Mmp inhibitor

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