ES2172690T3 - Compuestos de mercaptoalquilpeptidil con un sustituyente de imidazol y su utilizacion como inhibidores de metaloproteinasas de matriz (mmp) y/o del factor de necrosis tumoral (tnf). - Google Patents

Compuestos de mercaptoalquilpeptidil con un sustituyente de imidazol y su utilizacion como inhibidores de metaloproteinasas de matriz (mmp) y/o del factor de necrosis tumoral (tnf).

Info

Publication number
ES2172690T3
ES2172690T3 ES96939208T ES96939208T ES2172690T3 ES 2172690 T3 ES2172690 T3 ES 2172690T3 ES 96939208 T ES96939208 T ES 96939208T ES 96939208 T ES96939208 T ES 96939208T ES 2172690 T3 ES2172690 T3 ES 2172690T3
Authority
ES
Spain
Prior art keywords
rent
heteroarilo
arilo
imidazol
substitute
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
ES96939208T
Other languages
English (en)
Inventor
Andrew Douglas Baxter
John Gary Montana
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.)
Darwin Discovery Ltd
Original Assignee
Darwin Discovery 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
Priority claimed from GBGB9523828.3A external-priority patent/GB9523828D0/en
Priority claimed from GBGB9607121.2A external-priority patent/GB9607121D0/en
Application filed by Darwin Discovery Ltd filed Critical Darwin Discovery Ltd
Application granted granted Critical
Publication of ES2172690T3 publication Critical patent/ES2172690T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/12Heterocyclic 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 chain containing hetero atoms as chain links
    • 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
    • A61P35/00Antineoplastic agents
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S530/00Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof
    • Y10S530/868Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof involving autoimmunity, allergy, immediate hypersensitivity, delayed hypersensitivity, immunosuppression, or immunotolerance

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Vascular Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Urology & Nephrology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

COMPUESTOS DE PEPTIDILO QUE LLEVAN UN SUSTITUYENTE DE IMIDAZOL DE FORMULA GENERAL (I), EN DONDE R 1 ES ALQUILO DE C 16 , ALQUENILO DE C 2-6 , ALQUIL-ARILO (EL ALQUILO DE C 16 ), ARILO, ALQUIL-HETEROARILO (EL ALQUILO DE C 1-6 ), HETEROARILO O ALQUIL-AR 9 (EL ALQUILO DE C 1-6 , DONDE A ES O, NR 9 O S(O) M , SIENDO M = 0-2, Y R SUP,9 ES H, ALQUILO DE C 1-4 , ARILO, HETEROARILO, ALQUIL-AR ILO (EL ALQUILO DE C 1-4 ) O ALQUIL-HETEROARILO (EL ALQUILO DE C 1-4 ); SI A = NR 9 EL GRUPO R 9 PUEDE SER EL MISMO O DIFERENTE; R 2 ES HIDROGENO O UN GRUPO ALQUILO DE C 1-6 ; R 3 ES UN GRUPO [ALQ] N R 6 EN DONDE ALQ ES UN ALQUILO DE C 1-6 O ALQUENILO DE C 2-6 Y N ES CERO O 1; X ES NR 9 , O O S; Y ES N O CR 4 ; R SUP,4 Y R 5 SON IGUALES O DIFERENTES Y SON R 9 , COR 13 ALQUIL - R 13 (EL ALQUILO DE C 1-3 ) O ALQUILCOR 13 (EL ALQUILO DE C 1-3 ); R 7 ES HIDROGENO O R 10 CO, EN DONDE R 10 ES ALQUILO DE C 1-4 , ALQUILARILO (EL ALQUILO DE C 1-4 , ALQUIL-HETEROARILO (EL AL QUILO DE C 1-4 , CICLOALQUILO DE C 3-6 , ALQUIL-CICLOALQUILO (EL PRIMER ALQUILO DE C 1-4 , EL CICLOALQUILO DE C SUB,3-6 , ALQUENILO DE C 2-6 , ALQUENIL-ARILO DE C 2-6, ARILO O HETEROARILO; R 8 ES ARILO (OPCIONALMENTE SUSTI TUIDO CON R 11 ), HETEROARILO (OPCIONALMENTE SUSTITUIDO CON R 11 ), ALQUILO DE C 1-4 (OPCIONALMENTE SUSTITUIDO CON R 11 , ETC; TIENEN UNA UTILIDAD TERAPEUTICA MEDIANTE SU EFECTO INHIBIDOR SOBRE LAS METALOPROTEINASAS Y SOBRE EL FACTOR DE NECROSIS TUMORAL.
ES96939208T 1995-11-22 1996-11-22 Compuestos de mercaptoalquilpeptidil con un sustituyente de imidazol y su utilizacion como inhibidores de metaloproteinasas de matriz (mmp) y/o del factor de necrosis tumoral (tnf). Expired - Lifetime ES2172690T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9523828.3A GB9523828D0 (en) 1995-11-22 1995-11-22 Compounds
GBGB9607121.2A GB9607121D0 (en) 1996-04-04 1996-04-04 Compounds

Publications (1)

Publication Number Publication Date
ES2172690T3 true ES2172690T3 (es) 2002-10-01

Family

ID=26308152

Family Applications (1)

Application Number Title Priority Date Filing Date
ES96939208T Expired - Lifetime ES2172690T3 (es) 1995-11-22 1996-11-22 Compuestos de mercaptoalquilpeptidil con un sustituyente de imidazol y su utilizacion como inhibidores de metaloproteinasas de matriz (mmp) y/o del factor de necrosis tumoral (tnf).

Country Status (19)

Country Link
US (1) US6048841A (es)
EP (1) EP0874842B1 (es)
JP (1) JP2000500482A (es)
KR (1) KR19990067687A (es)
CN (1) CN1072667C (es)
AT (1) ATE215946T1 (es)
AU (1) AU711907B2 (es)
BR (1) BR9611636A (es)
CA (1) CA2229438C (es)
CZ (1) CZ291337B6 (es)
DE (1) DE69620639T2 (es)
ES (1) ES2172690T3 (es)
HU (1) HUP9904131A3 (es)
IL (1) IL123431A (es)
MX (1) MX9804052A (es)
NO (1) NO982290D0 (es)
NZ (1) NZ322565A (es)
PL (1) PL326710A1 (es)
WO (1) WO1997019075A1 (es)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6673927B2 (en) 1996-02-16 2004-01-06 Societe De Conseils De Recherches Et D'applications Scientifiques, S.A.S. Farnesyl transferase inhibitors
US6953788B1 (en) 1996-09-19 2005-10-11 Aventis Pharmaceuticals Inc. 3-mercaptoacetylamino-1,5-substituted-2-oxo-azepan derivatives useful as inhibitors of matrix metalloproteinase
RU2201931C2 (ru) 1996-11-20 2003-04-10 Биомежер Инкорпорэйтед Ингибиторы фарнезилтрансферазы и способы ингибирования фарнезилтрансферазы
CA2876779A1 (en) 2000-05-12 2001-11-22 Genzyme Corporation Modulators of tnf-.alpha. signaling
ES2208595T3 (es) 2000-05-15 2004-06-16 Darwin Discovery Limited Derivados del acido hidroxamico.
SE0100903D0 (sv) * 2001-03-15 2001-03-15 Astrazeneca Ab Compounds
SE0100902D0 (sv) * 2001-03-15 2001-03-15 Astrazeneca Ab Compounds
SE0103710D0 (sv) * 2001-11-07 2001-11-07 Astrazeneca Ab Compounds
CN100503608C (zh) * 2002-01-07 2009-06-24 卫材R&D管理株式会社 脱氮嘌呤及其用途
SE0202539D0 (sv) 2002-08-27 2002-08-27 Astrazeneca Ab Compounds
GB0221246D0 (en) * 2002-09-13 2002-10-23 Astrazeneca Ab Compounds
ES2363914T3 (es) * 2002-11-21 2011-08-19 Genzyme Corporation Utilización de un derivado de diamida para inhibir el rechazo crónico de un transplante.
US7217718B2 (en) * 2002-11-21 2007-05-15 Genzyme Corporation Induction of immune tolerance
US20040259744A1 (en) * 2003-12-19 2004-12-23 Meidong Yang Skin and hair cleansers containing sulfur
US7648992B2 (en) 2004-07-05 2010-01-19 Astrazeneca Ab Hydantoin derivatives for the treatment of obstructive airway diseases
SE0401762D0 (sv) * 2004-07-05 2004-07-05 Astrazeneca Ab Novel compounds
SE0403086D0 (sv) * 2004-12-17 2004-12-17 Astrazeneca Ab Compounds
SE0403085D0 (sv) * 2004-12-17 2004-12-17 Astrazeneca Ab Novel componds
TW200831488A (en) * 2006-11-29 2008-08-01 Astrazeneca Ab Novel compounds
PL227790B1 (pl) 2015-08-13 2018-01-31 Slaski Univ Medyczny W Katowicach Fosfoniany acetylenowych pochodnych betuliny o działaniu przeciwnowotworowym, sposób ich wytwarzania i zastosowanie.

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE150452T1 (de) * 1992-04-07 1997-04-15 British Biotech Pharm Hydroxamsäure enthaltende collagenase-inhibitoren und cytokinaktivitätsinhibitoren
GB9215665D0 (en) * 1992-07-23 1992-09-09 British Bio Technology Compounds
GB9323165D0 (en) * 1993-11-10 1994-01-05 Chiros Ltd Compounds
GB9404046D0 (en) * 1994-03-03 1994-04-20 Smithkline Beecham Corp Novel compounds
CN1193978A (zh) * 1994-10-05 1998-09-23 奇罗斯恩有限公司 肽基化合物和它们作为金属蛋白酶抑制剂的医疗用途

Also Published As

Publication number Publication date
IL123431A0 (en) 1998-09-24
NO982290L (no) 1998-05-20
HUP9904131A3 (en) 2002-04-29
NO982290D0 (no) 1998-05-20
NZ322565A (en) 1999-11-29
WO1997019075A1 (en) 1997-05-29
AU711907B2 (en) 1999-10-21
DE69620639T2 (de) 2002-10-17
JP2000500482A (ja) 2000-01-18
CN1202895A (zh) 1998-12-23
MX9804052A (es) 1998-09-30
CZ291337B6 (cs) 2003-02-12
KR19990067687A (ko) 1999-08-25
CN1072667C (zh) 2001-10-10
CA2229438A1 (en) 1997-05-29
DE69620639D1 (de) 2002-05-16
EP0874842B1 (en) 2002-04-10
PL326710A1 (en) 1998-10-26
CZ145598A3 (cs) 1998-08-12
US6048841A (en) 2000-04-11
HUP9904131A2 (hu) 2000-06-28
AU7634396A (en) 1997-06-11
CA2229438C (en) 2006-01-17
ATE215946T1 (de) 2002-04-15
BR9611636A (pt) 1999-12-28
IL123431A (en) 2001-05-20
EP0874842A1 (en) 1998-11-04

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