BRPI0413791A - composto, método para o tratamento de um indivìduo humano ou animal que sofre de, ou que é suscetìvel a um distúrbio auto-imune ou uma condição inflamatória, uso de um composto, composição farmacêutica, e, processo para a prearação de compostos - Google Patents

composto, método para o tratamento de um indivìduo humano ou animal que sofre de, ou que é suscetìvel a um distúrbio auto-imune ou uma condição inflamatória, uso de um composto, composição farmacêutica, e, processo para a prearação de compostos

Info

Publication number
BRPI0413791A
BRPI0413791A BRPI0413791-4A BRPI0413791A BRPI0413791A BR PI0413791 A BRPI0413791 A BR PI0413791A BR PI0413791 A BRPI0413791 A BR PI0413791A BR PI0413791 A BRPI0413791 A BR PI0413791A
Authority
BR
Brazil
Prior art keywords
alkyl
alkylaryl
compound
cor
optionally substituted
Prior art date
Application number
BRPI0413791-4A
Other languages
English (en)
Inventor
Simon Gaines
Ian Peter Holmes
Stephen Lewis Martin
Stephen Paul Watson
Original Assignee
Glaxo Group Ltd
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 Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of BRPI0413791A publication Critical patent/BRPI0413791A/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44—Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/4035—Isoindoles, e.g. phthalimide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52—Two oxygen atoms
    • C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Anti-Oxidant Or Stabilizer Compositions (AREA)
  • Soft Magnetic Materials (AREA)
  • Lubricants (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

"COMPOSTO, MéTODO PARA O TRATAMENTO DE UM INDIVìDUO HUMANO OU ANIMAL QUE SOFRE DE, OU QUE é SUSCETìVEL A UM DISTúRBIO AUTO-IMUNE OU UMA CONDIçãO INFLAMATóRIA, USO DE UM COMPOSTO, COMPOSIçãO FARMACêUTICA, E, PROCESSO PARA A PREPARAçãO DE COMPOSTOS". Descreve-se compostos de fórmula (I): sendo que: A representa uma ligação, C~ 1-6~alquila ou CH=CHC~ 1-4~alquila; B representa ligação, O, S, SO, SO~ 2~, CO, CR¬ 7¬R¬ 8¬, CO¬ 2¬R¬ 14¬, CONR¬ 14¬R¬ 15¬, N(COR¬ 14¬)(COR¬ 15¬), N(SO¬ 2¬R¬ 14¬)(COR¬ 15¬) ou NR¬ 14¬R¬ 15¬; D representa ligação, ou C~ 1-6~ alquila; E representa arila substituído ou heteroarila substituído ou não substituído; Q representa um anel heteroarila ou arila com 5 ou 6 membros opcionalmente substituído; X representa O, S, SO, SO~ 2~, CO, CNRS, CNOR¬ 5¬, CNNR¬ 5¬R¬ 6¬, NR¬ 11¬ ou CR¬ 7¬R¬ 8¬; Y representa CR¬ 5¬OR¬ 11¬, CR¬ 5¬SR¬ 11¬, NOR¬ 5¬, CR¬ 5¬NR¬ 6¬R¬ 11¬, SO, SO~ 2~, CO, CNR¬ 5¬, CNOR¬ 5¬ ou CS; R¬ 1¬ e R¬ 1¬<39>, sendo que cada um representa independentemente H, C~ 1-6~alquila ou C~ 1-4~alquilarila; R¬ 2¬; representa CO~ 2~R¬ 12¬, CH~ 2~OR¬ 12¬ ou CONR¬ 12¬R¬ 13¬, CONR¬ 12¬OR¬ 13¬, NR¬ 12¬COR¬ 13¬, SR¬ 12¬, PO(OH)~ 2~, PONHR¬ 12¬ ou SONHR¬ 12¬; R¬ 3¬ representa H, C~ 1-6~alquila ou C~ 1-4~alquilarila; R¬ 4¬ representa heteroarila ou arila opcionalmente substituído; Z representa uma ligação. CH~ 2~, O, S, SO, SO~ 2~, NR¬ 5¬, OCR¬ 5¬R¬ 6¬, CR¬ 9¬R¬ 10¬O ou Z, R¬ 4¬ e Q em conjunto, formam um grupo tricíclico fundido opcionalmente substituído; R¬ 5¬ e R¬ 6¬ representam, cada um, independentemente, H, C~ 1-6~ alquila ou C~ 1-4~ alquilarila; R¬ 7¬ e R¬ 8¬, sendo que cada um representa independentemente H, halo, C~ 1-6~ alquila ou C~ 1-4~ alquilarila; R¬ 9¬ e R¬ 10¬ representam, cada um, independentemente, H, C~ 1-6~ alquila opcionalmente substituído por halo, ciano, OR¬ 11¬ ou NR¬ 6¬R¬ 11¬, C~ 1-4~ alquilarila opcionalmente substituído por halo, ciano, OR¬ 11¬ ou NR¬ 6¬R¬ 11¬, OR¬ 11¬ ou, em conjunto com o N a que estão ligados, R¬ 9¬ e R¬ 10¬ formam um grupo heterocíclico: R¬ 11¬ representa H, C~ 1-6~ alquila, C~ 1-4~ alquilarila ou COR¬ 5¬; R¬ 12¬ e R¬ 13¬, cada um, independentemente, representam H, C~ 1-3~ alquila, C~ 1-3~ alquilarila ou C~ 1-3~ alquil-heteroarila ou, em conjunto com a funcionalidade a que estão ligados, R¬ 12¬ e R¬ 13¬ formam um grupo heterocíclico: R¬ 14¬ e R¬ 15¬, cada um, independentemente, representa H, C~ 1-6~ alquila, C~ 1-4~ alquilarila ou C~ 1-4~ alquil-heteroarila ou, em conjunto com a funcionalidade a que estão ligados, R¬ 14¬ e R¬ 15¬ formam um heterocíclico ou grupo heterocíclico fundido: e derivados fisiologicamente funcionais dos mesmos, processos para sua preparação, formulações farmacêuticas contendo os mesmos, e seu uso como inibidores de enzimas de metaloproteinase de matriz (MMPs).
BRPI0413791-4A 2003-09-13 2004-09-10 composto, método para o tratamento de um indivìduo humano ou animal que sofre de, ou que é suscetìvel a um distúrbio auto-imune ou uma condição inflamatória, uso de um composto, composição farmacêutica, e, processo para a prearação de compostos BRPI0413791A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0321538.1A GB0321538D0 (en) 2003-09-13 2003-09-13 Therapeutically useful compounds
PCT/EP2004/010319 WO2005026120A1 (en) 2003-09-13 2004-09-10 Matrix metalloproteinase inhibitors

Publications (1)

Publication Number Publication Date
BRPI0413791A true BRPI0413791A (pt) 2006-11-07

Family

ID=29227079

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0413791-4A BRPI0413791A (pt) 2003-09-13 2004-09-10 composto, método para o tratamento de um indivìduo humano ou animal que sofre de, ou que é suscetìvel a um distúrbio auto-imune ou uma condição inflamatória, uso de um composto, composição farmacêutica, e, processo para a prearação de compostos

Country Status (29)

Country Link
US (3) US7601729B2 (pt)
EP (3) EP2295408A1 (pt)
JP (3) JP2007505081A (pt)
KR (3) KR20120007566A (pt)
CN (1) CN1849306B (pt)
AT (2) ATE502922T1 (pt)
AU (1) AU2004272280C1 (pt)
BR (1) BRPI0413791A (pt)
CA (1) CA2538315C (pt)
CY (1) CY1109400T1 (pt)
DE (2) DE602004031991D1 (pt)
DK (1) DK1663970T3 (pt)
ES (2) ES2362954T3 (pt)
GB (1) GB0321538D0 (pt)
HK (1) HK1092141A1 (pt)
HR (1) HRP20080668T3 (pt)
IL (1) IL173305A (pt)
IS (2) IS2622B (pt)
MA (1) MA28039A1 (pt)
MX (1) MXPA06002458A (pt)
NO (1) NO20060540L (pt)
NZ (2) NZ573479A (pt)
PL (1) PL1663970T3 (pt)
PT (1) PT1663970E (pt)
RU (2) RU2370488C2 (pt)
SG (1) SG145685A1 (pt)
SI (1) SI1663970T1 (pt)
WO (1) WO2005026120A1 (pt)
ZA (1) ZA200602070B (pt)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0321538D0 (en) * 2003-09-13 2003-10-15 Glaxo Group Ltd Therapeutically useful compounds
EP1856063B1 (en) * 2005-02-22 2012-01-25 Ranbaxy Laboratories Limited 5-phenyl-pentanoic acid derivatives as matrix metalloproteinase inhibitors for the treatment of asthma and other diseases
ES2397284T3 (es) 2006-08-22 2013-03-06 Ranbaxy Laboratories Limited Proceso para preparar inhibidores de la metaloproteinasa de la matriz y auxiliares quirales para los mismos
AU2013200728B2 (en) * 2006-08-22 2014-12-18 Sun Pharmaceutical Industries Limited Matrix metalloproteinase inhibitors
MX2009013332A (es) 2007-06-08 2010-01-25 Mannkind Corp Inhibidores de ire-1 alfa.
FR2949463B1 (fr) * 2009-08-26 2011-09-16 Commissariat Energie Atomique Inhibiteurs de mmp
CN103119030A (zh) 2010-07-30 2013-05-22 兰贝克赛实验室有限公司 基质金属蛋白酶抑制剂
CN103228634A (zh) 2010-09-24 2013-07-31 兰贝克赛实验室有限公司 基质金属蛋白酶抑制剂
EP2926808A1 (en) 2012-11-28 2015-10-07 Administración General De La Communidad Autónoma De Euskadi Use of metalloprotease inhibitors for the treatment of polycystic liver diseases
AR107592A1 (es) 2016-02-12 2018-05-16 Astellas Pharma Inc Derivados de tetrahidroisoquinolina
CN110769866B (zh) * 2017-06-13 2022-07-29 爱惜康有限责任公司 具有可控愈合的外科缝合器

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MXPA03009361A (es) * 2001-04-13 2004-01-29 Boehringer Ingelheim Pharma Compuestos de urea utilies como agentes anti-inflamatorios.
AU2003261319A1 (en) * 2002-08-01 2004-02-23 Bristol-Myers Squibb Company Hydantoin derivatives as inhibitors of matrix metalloproteinases and/or tnf-alpha converting enzyme
ATE455096T1 (de) * 2002-11-19 2010-01-15 Galderma Res & Dev Biaromatische verbindungen die ppar-gamma rezeptoren aktivieren und deren anwendungen in kosmetischen oder pharmazeutischen zusammensetzungen
GB0312654D0 (en) * 2003-06-03 2003-07-09 Glaxo Group Ltd Therapeutically useful compounds
GB0314488D0 (en) * 2003-06-20 2003-07-23 Glaxo Group Ltd Therapeutically useful compounds
GB0319069D0 (en) * 2003-08-14 2003-09-17 Glaxo Group Ltd Therapeutically useful compounds
GB0321538D0 (en) 2003-09-13 2003-10-15 Glaxo Group Ltd Therapeutically useful compounds
EP1856063B1 (en) 2005-02-22 2012-01-25 Ranbaxy Laboratories Limited 5-phenyl-pentanoic acid derivatives as matrix metalloproteinase inhibitors for the treatment of asthma and other diseases
ES2397284T3 (es) 2006-08-22 2013-03-06 Ranbaxy Laboratories Limited Proceso para preparar inhibidores de la metaloproteinasa de la matriz y auxiliares quirales para los mismos

Also Published As

Publication number Publication date
RU2008146479A (ru) 2010-06-20
KR20060120648A (ko) 2006-11-27
US20060293353A1 (en) 2006-12-28
CA2538315A1 (en) 2005-03-24
IL173305A (en) 2011-01-31
ES2362954T3 (es) 2011-07-15
DE602004017622D1 (de) 2008-12-18
MA28039A1 (fr) 2006-07-03
EP2295408A1 (en) 2011-03-16
IS8268A (is) 2006-01-26
JP2011231118A (ja) 2011-11-17
DK1663970T3 (da) 2009-01-12
GB0321538D0 (en) 2003-10-15
PT1663970E (pt) 2009-01-09
US20100029699A1 (en) 2010-02-04
EP1663970B1 (en) 2008-11-05
AU2004272280A1 (en) 2005-03-24
IS2622B (is) 2010-05-15
JP2007505081A (ja) 2007-03-08
US8263602B2 (en) 2012-09-11
US8343986B2 (en) 2013-01-01
MXPA06002458A (es) 2006-06-20
RU2370488C2 (ru) 2009-10-20
EP1663970A1 (en) 2006-06-07
ZA200602070B (en) 2007-05-30
ES2314436T3 (es) 2009-03-16
US7601729B2 (en) 2009-10-13
KR20130079628A (ko) 2013-07-10
IS8843A (is) 2009-08-19
ATE502922T1 (de) 2011-04-15
IL173305A0 (en) 2006-06-11
ATE413384T1 (de) 2008-11-15
KR20120007566A (ko) 2012-01-20
AU2004272280B2 (en) 2011-04-21
PL1663970T3 (pl) 2009-04-30
JP2012107031A (ja) 2012-06-07
CN1849306B (zh) 2014-01-29
CN1849306A (zh) 2006-10-18
SI1663970T1 (sl) 2009-04-30
SG145685A1 (en) 2008-09-29
WO2005026120A1 (en) 2005-03-24
NO20060540L (no) 2006-04-04
EP2042488A1 (en) 2009-04-01
HK1092141A1 (en) 2007-02-02
CY1109400T1 (el) 2014-07-02
NZ545211A (en) 2009-01-31
CA2538315C (en) 2014-04-08
HRP20080668T3 (en) 2009-02-28
EP2042488B1 (en) 2011-03-23
AU2004272280C1 (en) 2011-10-27
NZ573479A (en) 2010-09-30
US20090082377A1 (en) 2009-03-26
DE602004031991D1 (de) 2011-05-05
RU2006106850A (ru) 2007-10-20

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