ES2141904T3 - Derivados (tia)-cicloalquil-(b)-indoles como inhibidores de la 5-lipoxigenasa. - Google Patents

Derivados (tia)-cicloalquil-(b)-indoles como inhibidores de la 5-lipoxigenasa.

Info

Publication number
ES2141904T3
ES2141904T3 ES95401536T ES95401536T ES2141904T3 ES 2141904 T3 ES2141904 T3 ES 2141904T3 ES 95401536 T ES95401536 T ES 95401536T ES 95401536 T ES95401536 T ES 95401536T ES 2141904 T3 ES2141904 T3 ES 2141904T3
Authority
ES
Spain
Prior art keywords
sub
compounds
ozyzyl
alkilo
inhibition
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES95401536T
Other languages
English (en)
Inventor
Paul Caubere
Brigitte Jamart-Gregoire
Catherine Caubere
Dominique Manechez
Pierre Renard
Gerard Adam
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ADIR SARL
Original Assignee
ADIR SARL
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 ADIR SARL filed Critical ADIR SARL
Application granted granted Critical
Publication of ES2141904T3 publication Critical patent/ES2141904T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • 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
    • A61P37/08—Antiallergic agents
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • 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
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/80—[b, c]- or [b, d]-condensed
    • C07D209/94—[b, c]- or [b, d]-condensed containing carbocyclic rings other than six-membered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Cardiology (AREA)
  • Endocrinology (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Vascular Medicine (AREA)
  • Reproductive Health (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

COMPUESTOS DE FORMULA (I) EN LA QUE R 1 REPRESENTA UN GRUPO AR-{(CH{SUB,2})}{SUB,N}-O- CON N REPRESENTANDO CERO O UN ENTERO DE 1 A 4, SIENDO AR UN RADICAL ELEGIDO ENTRE FENILO, NAFTILO, TIENILO, FURILO, PIROLILO, IMIDAZOLILO, PIROZOLILO, TIAZOLILO, ISOTIAZOLILO, OXAZOLILO,ISOZAXOLILO, TIADIAZOLILO, OXADIAZOL, PIRIDILO,QUINOLILO, IOSQUINOLILO, INDOLILO, BENZOFUILO Y BENZOTIENILO; PUDIENDO AR ESTAR SUSTIDUIO O SUSTITUIDO POR UNO O VARIOS RADICALES ELEGIDOS ENTRE HALOGENO, ALKILO, ALCOXI, HIDROXI Y TRIFLUORMETILO, - R{SUB,2} REPRESENTA UN ATOMO DE HIDROGENO O UN RADICAL ELEGIDO ENTRE HALOGENO, ALILO, ALCOXI Y TRIFULORMETILO, -R{SUB,3} REPRESENTA UN RADICAL ELEGIDO ENTRE HIDROGENO, ALKILO, CARBOXIALKIL Y ALCOXICERBONIALKILO, - A REPRESENTA UNA CADENA ALKILENO {(CH{SUB,2})}{SUB,M} CON M COMPRENDIDO ENTRE 3 Y 6 O UN GRUPO DE FORMULA {(AL EN EL QUE P ESTA COMPRENDIDO ENTRE 1 Y 4. LA ACTIVIDAD ANTIINFLAMATORIA DE LOS COMPUESTOS DE LA INVENCION PERMITE AL PERSONAL CLINICO DISPOSNER DE AGENTES TERAPEUTICOS UTILES PARA IBNHIBIR CIERTOS PROCESOS (Y PARTICUALRMENTE LA ACTIVACION DE LA 5-LIPOXIGENASA) IMPLICADOS EN VARIAS PATOLOGIAS DE COMPONENTE ANTIIMFLAMATORIA (COMO LA ARTRITIS, LA COITIS Y LA SORIASIS) SIN AFECTAR A LA VIA DE LA CICLOOXIGENASA. LOS COMPUESTOS DELA INVENCION PERMITEN PARTICULARMENTE UNA INHIBICION DE LA 5-LIPO-OXIGENASA POR UN MECANISMO ANTI-FLAP ("FIVE LIPOXIGENASE ACTIVATORY PROTEIN"), INHIBICION QUE ES MUCHO MAS ELEVADA QUE LA DE LOS INHIBIDORES REDOX O DE LOS QUELANTES DE HIERRO.
ES95401536T 1994-06-28 1995-06-28 Derivados (tia)-cicloalquil-(b)-indoles como inhibidores de la 5-lipoxigenasa. Expired - Lifetime ES2141904T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9407888A FR2721610B1 (fr) 1994-06-28 1994-06-28 Nouveaux dérivés (thia)cycloalkyl [b] indoles, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.

Publications (1)

Publication Number Publication Date
ES2141904T3 true ES2141904T3 (es) 2000-04-01

Family

ID=9464699

Family Applications (1)

Application Number Title Priority Date Filing Date
ES95401536T Expired - Lifetime ES2141904T3 (es) 1994-06-28 1995-06-28 Derivados (tia)-cicloalquil-(b)-indoles como inhibidores de la 5-lipoxigenasa.

Country Status (16)

Country Link
US (1) US5635516A (es)
EP (1) EP0690050B1 (es)
JP (1) JP3004566B2 (es)
CN (1) CN1054374C (es)
AT (1) ATE186722T1 (es)
AU (1) AU686800B2 (es)
CA (1) CA2152725A1 (es)
DE (1) DE69513332T2 (es)
DK (1) DK0690050T3 (es)
ES (1) ES2141904T3 (es)
FI (1) FI953193L (es)
FR (1) FR2721610B1 (es)
GR (1) GR3032172T3 (es)
NO (1) NO305022B1 (es)
NZ (1) NZ272447A (es)
ZA (1) ZA955355B (es)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2128283A1 (fr) * 1993-07-20 1995-01-21 Paul Caubere (thia)cycloalkyl¬b|indoles, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
AU2002322720B2 (en) 2001-07-25 2008-11-13 Raptor Pharmaceutical Inc. Compositions and methods for modulating blood-brain barrier transport
CA2789262C (en) 2005-04-28 2016-10-04 Proteus Digital Health, Inc. Pharma-informatics system
US20070225285A1 (en) * 2005-11-04 2007-09-27 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein (flap) inhibitors
US20070219206A1 (en) * 2005-11-04 2007-09-20 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein (flap) inhibitors
US7977359B2 (en) 2005-11-04 2011-07-12 Amira Pharmaceuticals, Inc. 5-lipdxygenase-activating protein (FLAP) inhibitors
GB2431927B (en) * 2005-11-04 2010-03-17 Amira Pharmaceuticals Inc 5-Lipoxygenase-activating protein (FLAP) inhibitors
US8399666B2 (en) * 2005-11-04 2013-03-19 Panmira Pharmaceuticals, Llc 5-lipoxygenase-activating protein (FLAP) inhibitors
US20070244128A1 (en) * 2005-11-04 2007-10-18 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein (flap) inhibitors
EP2063905B1 (en) 2006-09-18 2014-07-30 Raptor Pharmaceutical Inc Treatment of liver disorders by administration of receptor-associated protein (rap)-conjugates
US7925075B2 (en) * 2007-05-07 2011-04-12 General Electric Company Inspection system and methods with autocompensation for edge break gauging orientation
TW200920369A (en) * 2007-10-26 2009-05-16 Amira Pharmaceuticals Inc 5-lipoxygenase activating protein (flap) inhibitor
MX2010012814A (es) * 2008-05-23 2010-12-20 Amira Pharmaceuticals Inc Inhibidor de proteina activadora de 5-lipoxigenasa.
US8546431B2 (en) 2008-10-01 2013-10-01 Panmira Pharmaceuticals, Llc 5-lipoxygenase-activating protein (FLAP) inhibitors
TR201908314T4 (tr) 2009-02-20 2019-06-21 2 Bbb Medicines B V Glutatyon bazlı ilaç dağıtım sistemi.
KR101909711B1 (ko) 2009-05-06 2018-12-19 라보라토리 스킨 케어, 인크. 활성제-칼슘 포스페이트 입자 복합체를 포함하는 피부 전달 조성물 및 이들을 이용하는 방법
US20120077778A1 (en) 2010-09-29 2012-03-29 Andrea Bourdelais Ladder-Frame Polyether Conjugates
US11633379B2 (en) 2017-01-04 2023-04-25 Trustees Of Dartmouth College Methods of inhibiting PCSK9
CN108558905B (zh) * 2018-05-21 2021-03-12 华南农业大学 一种噻喃[4,3-b]吲哚类化合物及其制备方法和应用

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2243574A1 (de) 1972-09-05 1974-03-14 Boehringer Mannheim Gmbh Aryloxy-essigsaeure-derivate und verfahren zur herstellung derselben
GB1432649A (es) * 1973-09-07 1976-04-22 Ici Ltd
CA1326030C (en) * 1987-07-21 1994-01-11 John W. Gillard Cyclohept[b]indolealkanoic acids
PT95692A (pt) * 1989-10-27 1991-09-13 American Home Prod Processo para a preparacao de derivados de acidos indole-,indeno-,piranoindole- e tetra-hidrocarbazole-alcanoicos, ou quais sao uteis como inibidores de pla2 e da lipoxigenase
US5221678A (en) * 1990-07-26 1993-06-22 Merck Frosst Canada, Inc. (quinolin-2-ylmethoxy)tetrahydrocarbazoles as inhibitors of the biosynthesis of leukotrienes
WO1993009774A1 (en) * 1991-11-18 1993-05-27 G.D. Searle & Co. 2-(4-substituted)phenylmethylene derivatives and methods of use
US5288751A (en) * 1992-11-06 1994-02-22 Abbott Laboratories [(Substituted) phenyalkyl]furylalkynyl-and [substituted) phenyalkyl] thienylalkynyl-N-hydroxyurea inhibitors or leukotriene biosynthesis
US5314900A (en) * 1992-11-19 1994-05-24 Merck Frosst Canada, Inc. Aryl thiopyrano[2,3,4-C,D]indoles as inhibitors of leukotriene biosynthesis
ES2062943B1 (es) * 1993-03-23 1995-11-16 Uriach & Cia Sa J Nuevos derivados de la (2-metil-3-piridil) cianometilpiperazinas.
CA2128283A1 (fr) * 1993-07-20 1995-01-21 Paul Caubere (thia)cycloalkyl¬b|indoles, leur procede de preparation et les compositions pharmaceutiques qui les contiennent

Also Published As

Publication number Publication date
DK0690050T3 (da) 2000-04-17
NO305022B1 (no) 1999-03-22
FR2721610B1 (fr) 1996-08-23
NZ272447A (en) 1996-02-27
AU686800B2 (en) 1998-02-12
FI953193A0 (fi) 1995-06-28
ATE186722T1 (de) 1999-12-15
ZA955355B (en) 1996-02-12
CN1114957A (zh) 1996-01-17
JP3004566B2 (ja) 2000-01-31
FR2721610A1 (fr) 1995-12-29
EP0690050A1 (fr) 1996-01-03
FI953193A7 (fi) 1995-12-29
EP0690050B1 (fr) 1999-11-17
CA2152725A1 (fr) 1995-12-29
NO952579L (no) 1995-12-29
FI953193L (fi) 1995-12-29
JPH0812649A (ja) 1996-01-16
AU2327495A (en) 1996-01-11
DE69513332T2 (de) 2000-07-27
NO952579D0 (no) 1995-06-27
DE69513332D1 (de) 1999-12-23
CN1054374C (zh) 2000-07-12
US5635516A (en) 1997-06-03
GR3032172T3 (en) 2000-04-27

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