[go: up one dir, main page]

PE20091398A1 - Compuestos biciclicos conteniendo nitrogeno activos en condiciones de dolor cronicas - Google Patents

Compuestos biciclicos conteniendo nitrogeno activos en condiciones de dolor cronicas

Info

Publication number
PE20091398A1
PE20091398A1 PE2009000262A PE2009000262A PE20091398A1 PE 20091398 A1 PE20091398 A1 PE 20091398A1 PE 2009000262 A PE2009000262 A PE 2009000262A PE 2009000262 A PE2009000262 A PE 2009000262A PE 20091398 A1 PE20091398 A1 PE 20091398A1
Authority
PE
Peru
Prior art keywords
chronic pain
compounds containing
containing active
pain conditions
active nitrogen
Prior art date
Application number
PE2009000262A
Other languages
English (en)
Inventor
Carla Ghelardini
Marisa Martinelli
Carlo Parini
Silvano Ronzoni
Original Assignee
Neurotune Ag
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 Neurotune Ag filed Critical Neurotune Ag
Publication of PE20091398A1 publication Critical patent/PE20091398A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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 two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A61P29/02Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Pain & Pain Management (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

SE REFIERE A COMPUESTOS BICICLICOS QUE CONTIENEN N DE FORMULA (I) DONDE R ES H, ALQUILO(C1-C6), CF3 O ARILO; Y ES CH2 O C=O; X ES UN ENLACE, C=O, SO2 O C=N-CN; A ES UN HETEROCICLO O UN COMPUESTO DE FORMULA (i), EN DONDE R1, R2, R4 Y R5 SON CADA UNO H, HALOGENO, ALQUILO(C1-C6), ALCOXI(C1-C6), ENTRE OTROS; R3 ES H, CN, ALQUILO(C1-C6), HIDROXI, ENTRE OTROS; m Y n SON CADA UNO 0 O 1. SON COMPUESTOS PREFERIDOS: (S)-(-)2-(2-FLUOROFENILSULFONIL)HEXAHIDROPIRROLO[1,2-a]PIRAZIN-6(7H)-UNO, (S)-(-)2-(3-FLUOROFENILSULFONIL)HEXAHIDROPIRROLO[1,2-a]PIRAZIN-6(7H)-UNO, (R)-(+)-2-(3,4-DIFLUOROFENILSULFONIL)HEXAHIDROPIRROLO[1,2-a]PIRAZIN-6(7H)-UNO, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION. DICHOS COMPUESTOS SON UTILES PARA EL TRATAMIENTO DEL DOLOR CRONICO DE ORIGEN NEUROPATICO O INFLAMATORIO TALES COMO MIGRANA, FIBROMIALGIA
PE2009000262A 2008-02-22 2009-02-23 Compuestos biciclicos conteniendo nitrogeno activos en condiciones de dolor cronicas PE20091398A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP08101879.8A EP2098526B1 (en) 2008-02-22 2008-02-22 Nitrogen-containing bicyclic compounds active on chronic pain conditions

Publications (1)

Publication Number Publication Date
PE20091398A1 true PE20091398A1 (es) 2009-10-13

Family

ID=39472460

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2009000262A PE20091398A1 (es) 2008-02-22 2009-02-23 Compuestos biciclicos conteniendo nitrogeno activos en condiciones de dolor cronicas

Country Status (17)

Country Link
US (1) US8334286B2 (es)
EP (1) EP2098526B1 (es)
JP (1) JP5400804B2 (es)
CN (1) CN101945876B (es)
AR (1) AR070465A1 (es)
AU (1) AU2009217201B2 (es)
BR (1) BRPI0908495A2 (es)
CA (1) CA2716230C (es)
CL (1) CL2009000388A1 (es)
EA (1) EA017737B1 (es)
ES (1) ES2454366T3 (es)
IL (1) IL207669A (es)
MX (1) MX2010009228A (es)
PE (1) PE20091398A1 (es)
PL (1) PL2098526T3 (es)
WO (1) WO2009103176A1 (es)
ZA (1) ZA201005704B (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9125898B2 (en) 2008-11-14 2015-09-08 Neurotune Ag Acetam derivatives for pain relief
US8933132B2 (en) * 2011-01-19 2015-01-13 Convergence Pharmaceuticals Limited Tricyclic substituted benzenesulfonamide piperazine derivatives as CAV2.2 calcium channel blockers
WO2013049164A1 (en) 2011-09-29 2013-04-04 Abbvie Inc. SUBSTITUTED OCTAHYDROPYRROLO[1,2-a]PYRAZINES AS CALCIUM CHANNEL BLOCKERS
AR088064A1 (es) 2011-09-29 2014-05-07 Abbvie Inc Octahidropirrolo[1,2-a]pirazina sulfonamidas sustituidas como bloqueadores de canales de calcio
JP2016503007A (ja) 2012-12-12 2016-02-01 アッヴィ・インコーポレイテッド 疼痛治療におけるカルシウムチャネル遮断薬として有用なジアゼピン誘導体
CA2935811C (en) 2014-03-07 2018-09-18 F. Hoffmann-La Roche Ag 6-fused heteroaryldihydropyrimidines for the treatment and prophylaxis of hepatitis b virus infection
KR102139708B1 (ko) 2015-03-16 2020-07-31 에프. 호프만-라 로슈 아게 Tlr7 작용제 및 hbv 캡시드 조립 억제제를 사용하는 병용 치료
JP7101663B2 (ja) 2016-09-13 2022-07-15 エフ.ホフマン-ラ ロシュ アーゲー Tlr7アゴニストとhbvキャプシドアセンブリ阻害剤の併用療法
JOP20190251A1 (ar) 2017-05-31 2019-10-21 Metys Pharmaceuticals AG تركيبات تآزرية تشتمل على (r)-ديميراسيتام (1) و(s)-ديميراسيتام (2) بنسبة غير راسيمية
PL3890833T3 (pl) 2018-12-04 2023-09-18 Metys Pharmaceuticals AG Synergistyczne kompozycje zawierające (r)-2-(2-oksopirolidyn-1-ylo)butanoamid i (s)-2-(2-oksopirolidyn-1-ylo)butanoamid w stosunku nieracemicznym
MX2021006248A (es) * 2018-12-04 2021-08-11 Metys Pharmaceuticals AG Composiciones sinergicas que comprenden r-2-(sulfonil sustituido)-hexahidro-pirrolo[1,2-a]pirazin-6(2h)-onas y s-2-(sulfonil sustituido)-hexahidro-pirrolo[1,2-a]pirazin-6(2h)-on as en una proporcion no racemica.
EP3947383B1 (en) 2019-03-25 2024-10-02 F. Hoffmann-La Roche AG Solid forms of a compound of hbv core protein allosteric modifier

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3225077A (en) 1963-03-05 1965-12-21 American Cyanamid Co N-cyanoimidates and processes for preparing same
JP3058945B2 (ja) * 1990-10-26 2000-07-04 三共株式会社 N−(3,3−ジ置換アクリロイル)ピペラジン誘導体
US5925648A (en) 1997-07-29 1999-07-20 Schering Corporation Tricyclic N-cyanoimines useful as inhibitors of a farnesyl-protein transferase
EP1118612A1 (en) 2000-01-21 2001-07-25 Universita Degli Studi di Firenze Piperazine derivatives possesing nootropic activity
CN1984901B (zh) * 2004-05-18 2011-02-09 先灵公司 用作pde4抑制剂的取代的2-喹啉基-*唑
US7683056B2 (en) * 2005-09-09 2010-03-23 Glaxosmithkline Llc Pyridine derivatives and their use in the treatment of psychotic disorders
AR057828A1 (es) * 2005-09-29 2007-12-19 Astrazeneca Ab Compuestos derivados de azetidina, su preparacion y composicion farmaceuutica

Also Published As

Publication number Publication date
US8334286B2 (en) 2012-12-18
CA2716230A1 (en) 2009-08-27
BRPI0908495A2 (pt) 2019-09-24
EP2098526A1 (en) 2009-09-09
JP2011512365A (ja) 2011-04-21
EP2098526B1 (en) 2014-01-15
AU2009217201B2 (en) 2013-06-20
PL2098526T3 (pl) 2014-06-30
US20110015200A1 (en) 2011-01-20
CA2716230C (en) 2016-11-01
CL2009000388A1 (es) 2010-02-19
AU2009217201A1 (en) 2009-08-27
MX2010009228A (es) 2010-11-12
AR070465A1 (es) 2010-04-07
EA017737B1 (ru) 2013-02-28
CN101945876A (zh) 2011-01-12
ES2454366T3 (es) 2014-04-10
JP5400804B2 (ja) 2014-01-29
EA201001344A1 (ru) 2011-02-28
ZA201005704B (en) 2013-01-30
CN101945876B (zh) 2014-04-30
IL207669A0 (en) 2010-12-30
IL207669A (en) 2014-08-31
WO2009103176A1 (en) 2009-08-27

Similar Documents

Publication Publication Date Title
PE20091398A1 (es) Compuestos biciclicos conteniendo nitrogeno activos en condiciones de dolor cronicas
PE20090649A1 (es) DERIVADOS DE PIRAZOL COMO INHIBIDORES DE LA ENZIMA 11ßHSD1
PE20091724A1 (es) Derivados de indol como moduladores del receptor nicotinico de acetilcolina alfa 7
PE20091834A1 (es) Compuestos de 2-imino-3-metilpirrolopirimidinona tiofenilo-sustituida como inhibidores de bace-1 y composiciones que los contienen
PE20120505A1 (es) Derivados de 1-heterociclil-1,5-dihidro-pirazolo[3,4-d]pirimidin-4-ona como moduladores de pde9a
PE20081159A1 (es) Inhibidores de las quinasas y metodos para su utilizacion
PE20121182A1 (es) Derivados arilo y heteroarilcarbonilo de hexahidroindenopiridina y octahidrobenzoquinolina
PE20091427A1 (es) Derivados de amidas del acido 6,7-dihidro-5h-imidazo[1,2-alfa]imidazol-3-carboxilico
PE20070218A1 (es) COMPUESTOS DE CICLOALQUILO AMINO-HIDANTOINA Y USO DE ESTOS PARA LA MODULACION DE ß-SECRETASA
PE20091712A1 (es) Derivados de azetidina y ciclobutano como inhibidores de jak
PE20120629A1 (es) Compuesto triazolopiridina y su accion como inhibidor de prolil hidroxilasa e inductor de la produccion de eritropoyetina
PE20070367A1 (es) Compuestos de espiropiperidina como inhibidores de la enzima beta secretasa
CL2009001152A1 (es) Compuestos derivados de n-(4-(cicloalquilo nitrogenado-1-il)-1h-pirrolo[2,3-b]piridin-3-il)amida, inhibidores de cinasa; proceso de preparacion; composicion farmaceutica; y su uso para el tratamiento de una enfermedad proliferativa.
PE20091444A1 (es) Derivados de isoxazolo-pirazina
CL2009000127A1 (es) Compuestos derivados de [indol, azaindol]-2-carboxamida sustituidos con un grupo silanilo; procedimiento de preparacion; compuestos intermediarios; composicion farmaceutica; y su uso en el tratamiento del dolor, inflamacion, trastornos metabolicos, entre otras enfermedades mediadas por la modulacion del receptor trpv1.
PE20091833A1 (es) Derivados heterociclicos espiro biciclicos o heterociclicos biciclicos, puenteados, de pirazolo [1,5-a]pirimidinas como inhibidores de quinasas raf y metodos para su preparacion
PE20110328A1 (es) Compuestos heterociclicos fusionados como moduladores del receptor de la orexina
AR083058A1 (es) Compuestos de estructura de imidazotriazinona
PE20081345A1 (es) Compuestos heterociclicos que contienen nitrogeno como agonistas del receptor nicotinico
PE20060680A1 (es) Compuestos de morfolina sustituida como inhibidores de la recaptacion de norepinefrina
PE20121438A1 (es) Derivados de imidazopiridina o imidazopirimidina como inhibidores de fosfodiesterasa 10a
PE20120261A1 (es) Piperidina espiro pirrolidinona y piperidinonas sustitudos como moduladores de los receptores h3
AR075583A1 (es) Derivados de isoxazol/o-piridina con eslabon etilo o etenilo
AR068466A1 (es) Cianoisoquinolina
AR053092A1 (es) Compuestos derivados de acido fenoxiacetico y compuestos intermediarios de sintesis

Legal Events

Date Code Title Description
FD Application declared void or lapsed