HUP0401499A2 - Indolszármazékok, mint COX II inhibítorok - Google Patents

Indolszármazékok, mint COX II inhibítorok

Info

Publication number
HUP0401499A2
HUP0401499A2 HU0401499A HUP0401499A HUP0401499A2 HU P0401499 A2 HUP0401499 A2 HU P0401499A2 HU 0401499 A HU0401499 A HU 0401499A HU P0401499 A HUP0401499 A HU P0401499A HU P0401499 A2 HUP0401499 A2 HU P0401499A2
Authority
HU
Hungary
Prior art keywords
group
alkyl
nr5r6
hydrogen atom
cox
Prior art date
Application number
HU0401499A
Other languages
English (en)
Inventor
Chris Allen Broka
Jeffrey Allen Campbell
Original Assignee
F. Hoffmann-La Roche 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 F. Hoffmann-La Roche Ag filed Critical F. Hoffmann-La Roche Ag
Publication of HUP0401499A2 publication Critical patent/HUP0401499A2/hu
Publication of HUP0401499A3 publication Critical patent/HUP0401499A3/hu

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/06Antiabortive agents; Labour repressants
    • 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
    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32Oxygen atoms
    • C07D209/36Oxygen atoms in position 3, e.g. adrenochrome

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (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)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Rheumatology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Gynecology & Obstetrics (AREA)
  • Pregnancy & Childbirth (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Psychiatry (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)

Abstract

A találmány (I) általános képletű vegyületekre vonatkozik[melyképletben A jelentése -CH2-, -O-, -S- vagy -S(O)- ; Ar jelentése adottesetben helyettesített fenilcsoport vagy adott esetben helyettesítettnaftalenilcsoport; Rl jelentése hidrogénatom, alkil-, alkoxi-,hidroxi-, hidroxi-alkil-, alkil-tio-csoport, halogénatom,cianocsoport, -C(O)R5, -C(O)NR5R6, -NR5R6, -(CR'R'')0-3OC(O)R5-, -(CR'R'')0-3SO2R5, vagy -(CR'R'')0-3NSO2R5; ahol R5, R6, R' és R''jelentése egymástól függetlenül hidrogénatom vagy alkilcsoport, azzala feltétellel, hogy ha A jelentése -CH2-, úgy R1 -C(O)NR5R6 csoporttóleltérő jelentésű; R2 jelentése hidrogénatom, alkil-, alkoxi-,hidroxicsoport, halogénatom, halogén-alkil-, nitro-, ciano- vagy -NR5R6 csoport; ahol R5 és R6 jelentése a korábbiakban megadott; R3jelentése -SOR7, -SO2R7 vagy -SO2NR5R6; ahol R7 jelentése alkil-,hidroxi-alkil-, alkoxi-alkil- vagy alkoxikarbonil-alkil-csoport; és R5és R6 jelentése a korábbiakban megadott; R4 jelentése hidrogénatomvagy alkilcsoport]. A találmány szerinti vegyületek szelektív COX-IIinhibitorok és ezért COX-II által közvetített betegségek kezelésérealkalmazhatók. A találmány kiterjed a vegyületek előállítására és avegyületeket tartalmazó gyógyszerkészítményekre is. Ó
HU0401499A 2001-09-27 2002-09-20 Indole derivatives as cox ii inhibitors, process for their preparation and pharmaceutical compositions containing them HUP0401499A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US32538901P 2001-09-27 2001-09-27
PCT/EP2002/010557 WO2003029212A1 (en) 2001-09-27 2002-09-20 Indole derivatives as cox ii inhibitors

Publications (2)

Publication Number Publication Date
HUP0401499A2 true HUP0401499A2 (hu) 2004-12-28
HUP0401499A3 HUP0401499A3 (en) 2007-05-02

Family

ID=23267681

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0401499A HUP0401499A3 (en) 2001-09-27 2002-09-20 Indole derivatives as cox ii inhibitors, process for their preparation and pharmaceutical compositions containing them

Country Status (25)

Country Link
US (3) US6872744B2 (hu)
EP (1) EP1438289B1 (hu)
JP (1) JP4141954B2 (hu)
KR (1) KR20040047862A (hu)
CN (1) CN1261412C (hu)
AR (1) AR036624A1 (hu)
AT (1) ATE292115T1 (hu)
BR (1) BR0212925A (hu)
CA (1) CA2461670A1 (hu)
CO (1) CO5560557A2 (hu)
DE (1) DE60203529T2 (hu)
DK (1) DK1438289T3 (hu)
ES (1) ES2238616T3 (hu)
HR (1) HRPK20040271B3 (hu)
HU (1) HUP0401499A3 (hu)
IL (1) IL160752A0 (hu)
MX (1) MXPA04002824A (hu)
NO (1) NO20041237L (hu)
NZ (1) NZ531577A (hu)
PL (1) PL370342A1 (hu)
PT (1) PT1438289E (hu)
RU (1) RU2004113111A (hu)
SI (1) SI1438289T1 (hu)
WO (1) WO2003029212A1 (hu)
ZA (1) ZA200402360B (hu)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL370342A1 (en) * 2001-09-27 2005-05-16 F.Hoffmann-La Roche Ag Indole derivatives as cox ii inhibitors
SE0202241D0 (sv) * 2002-07-17 2002-07-17 Astrazeneca Ab Novel Compounds
US7365090B2 (en) * 2002-08-07 2008-04-29 Idenix Pharmaceuticals, Inc. Substituted phenylindoles for the treatment of HIV
US20050250794A1 (en) * 2003-12-19 2005-11-10 Andrew Napper Methods of treating a disorder
US7119214B2 (en) * 2004-04-13 2006-10-10 Cephalon France Thio-substituted tricyclic and bicyclic aromatic methanesulfinyl derivatives
EP1589016A1 (en) * 2004-04-13 2005-10-26 Cephalon France Thio-substituted tricyclic and bicyclic aromatic methanesulfinyl derivatives
US7423176B2 (en) 2004-04-13 2008-09-09 Cephalon, Inc. Bicyclic aromatic sulfinyl derivatives
BRPI0512252A (pt) 2004-06-18 2008-02-19 Biolipox Ab composto ou um sal farmaceuticamente aceitável do mesmo, formulação farmacêutica, uso de um composto, método de tratamento de uma doença, produto combinado, e, processo para a preparação de um composto
WO2006041961A1 (en) * 2004-10-05 2006-04-20 GOVERNMENT OF THE UNITED STATES OF AMERICA, as represented by THE SECRETARY, DEPARTMENT OF HEALTHAND HUMAN SERVICES Arylthioindole tubulin polymerization inhibitors and methods of treating or preventing cancer using same
KR20070114123A (ko) 2005-01-19 2007-11-29 바이올리폭스 에이비 염증 치료에 유용한 인돌
US7622495B2 (en) * 2006-10-03 2009-11-24 Neurim Pharmaceuticals (1991) Ltd. Substituted aryl-indole compounds and their kynurenine/kynuramine-like metabolites as therapeutic agents
CA2668959A1 (en) 2006-11-09 2008-05-15 F. Hoffmann-La Roche Ag Indole and benzofuran 2-carboxamide derivatives
WO2012024620A2 (en) 2010-08-20 2012-02-23 Amira Pharmaceuticals, Inc. Autotaxin inhibitors and uses thereof
WO2012166415A1 (en) 2011-05-27 2012-12-06 Amira Pharmaceuticals, Inc. Heterocyclic autotaxin inhibitors and uses thereof
US9714240B2 (en) 2013-09-17 2017-07-25 Pharmakea, Inc. Vinyl autotaxin inhibitor compounds
JP2016530210A (ja) 2013-09-17 2016-09-29 ファーマケア,インク. ヘテロ環式ビニルオートタキシン阻害剤化合物
EP3049405A4 (en) 2013-09-26 2017-03-08 Pharmakea Inc. Autotaxin inhibitor compounds
HUE055213T2 (hu) 2013-11-22 2021-11-29 Sabre Therapeutics Llc Autotaxin inhibitor vegyületek
JP6873919B2 (ja) 2015-05-27 2021-05-19 セイバー セラピューティクス エルエルシー オートタキシン阻害剤とその使用
KR102241064B1 (ko) 2019-07-30 2021-04-16 부산대학교 산학협력단 신규한 인돌 유도체 및 이를 포함하는 염증성 질환 예방 또는 치료용 조성물
CN113004187B (zh) * 2021-03-16 2022-09-20 沈阳药科大学 一种具有抑制有机阴离子转运体1活性的化合物及制备方法和应用

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4654360A (en) 1984-06-01 1987-03-31 Syntex (U.S.A.) Inc. 1,2,3-trisubstituted indoles for treatment of inflammation
JPH0347123A (ja) 1989-05-05 1991-02-28 G D Searle & Co インドール―2―カルボキシレート化合物類を含有するcns疾患治療用組成物
DE4338770A1 (de) 1993-11-12 1995-05-18 Matthias Dr Lehr Indol-2-alkansäuren und ihre Derivate als Hemmstoffe der Phospholipase A¶2¶
CA2264020A1 (en) 1996-08-26 1998-03-05 Jean Bemis Inhibitors of phospholipase enzymes
AU7237998A (en) * 1997-05-16 1998-12-08 Chugai Seiyaku Kabushiki Kaisha Indole derivatives and mono- and diazaindole derivatives
CN1298404A (zh) 1998-02-25 2001-06-06 遗传研究所有限公司 磷脂酶a2的抑制剂
MXPA00006605A (es) * 1999-07-02 2004-12-09 Pfizer Compuestos de carbonil-indol biciclicos como agentes antiinflamatorios/analgesicos.
US6306890B1 (en) * 1999-08-30 2001-10-23 Vanderbilt University Esters derived from indolealkanols and novel amides derived from indolealkylamides that are selective COX-2 inhibitors
US6376708B1 (en) * 2000-04-11 2002-04-23 Monsanto Technology Llc Process and catalyst for dehydrogenating primary alcohols to make carboxylic acid salts
PL370342A1 (en) * 2001-09-27 2005-05-16 F.Hoffmann-La Roche Ag Indole derivatives as cox ii inhibitors
TW200400177A (en) * 2002-06-04 2004-01-01 Wyeth Corp 1-(Aminoalkyl)-3-sulfonylindole and-indazole derivatives as 5-hydroxytryptamine-6 ligands

Also Published As

Publication number Publication date
NO20041237L (no) 2004-03-24
BR0212925A (pt) 2004-10-13
US20050176803A1 (en) 2005-08-11
CA2461670A1 (en) 2003-04-10
ATE292115T1 (de) 2005-04-15
US7074939B2 (en) 2006-07-11
DE60203529D1 (de) 2005-05-04
HRPK20040271B3 (en) 2006-02-28
RU2004113111A (ru) 2005-06-27
WO2003029212A1 (en) 2003-04-10
DE60203529T2 (de) 2006-03-16
AR036624A1 (es) 2004-09-22
JP2005510474A (ja) 2005-04-21
US6872744B2 (en) 2005-03-29
KR20040047862A (ko) 2004-06-05
IL160752A0 (en) 2004-08-31
HUP0401499A3 (en) 2007-05-02
PL370342A1 (en) 2005-05-16
MXPA04002824A (es) 2004-07-05
NZ531577A (en) 2005-09-30
CN1261412C (zh) 2006-06-28
ES2238616T3 (es) 2005-09-01
US7410994B2 (en) 2008-08-12
CO5560557A2 (es) 2005-09-30
CN1561334A (zh) 2005-01-05
ZA200402360B (en) 2005-04-26
EP1438289B1 (en) 2005-03-30
PT1438289E (pt) 2005-06-30
HRP20040271A2 (en) 2004-08-31
DK1438289T3 (da) 2005-08-08
JP4141954B2 (ja) 2008-08-27
US20060178420A1 (en) 2006-08-10
US20030130337A1 (en) 2003-07-10
SI1438289T1 (hu) 2005-08-31
EP1438289A1 (en) 2004-07-21

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