DK1100792T3 - Tricycliske sulfonamider og derivater deraf som inhibitorer af matrix-metalloproteinaser - Google Patents

Tricycliske sulfonamider og derivater deraf som inhibitorer af matrix-metalloproteinaser

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Publication number
DK1100792T3
DK1100792T3 DK99963141T DK99963141T DK1100792T3 DK 1100792 T3 DK1100792 T3 DK 1100792T3 DK 99963141 T DK99963141 T DK 99963141T DK 99963141 T DK99963141 T DK 99963141T DK 1100792 T3 DK1100792 T3 DK 1100792T3
Authority
DK
Denmark
Prior art keywords
inhibitors
derivatives
matrix metalloproteinases
tricyclic sulfonamides
sulfonamides
Prior art date
Application number
DK99963141T
Other languages
English (en)
Inventor
Patrick Michael O'brien
Joseph Armand Picard
Drago Robert Sliskovic
Original Assignee
Warner Lambert Co
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 Warner Lambert Co filed Critical Warner Lambert Co
Application granted granted Critical
Publication of DK1100792T3 publication Critical patent/DK1100792T3/da

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/91—Dibenzofurans; Hydrogenated dibenzofurans
    • 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
    • A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • 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
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • 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
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
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    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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    • A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
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    • 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
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • 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
    • C07D209/82—Carbazoles; Hydrogenated carbazoles
    • C07D209/88—Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D333/76—Dibenzothiophenes
    • 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
    • C07D405/04—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 directly linked by a ring-member-to-ring-member bond
    • H—ELECTRICITY
    • H04—ELECTRIC COMMUNICATION TECHNIQUE
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    • H04M—TELEPHONIC COMMUNICATION
    • H04M15/00—Arrangements for metering, time-control or time indication ; Metering, charging or billing arrangements for voice wireline or wireless communications, e.g. VoIP
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    • H04M15/30—Arrangements for metering, time-control or time indication ; Metering, charging or billing arrangements for voice wireline or wireless communications, e.g. VoIP with meter at substation or with calculation of charges at terminal the meter or calculation of charges not being controlled from an exchange
    • H—ELECTRICITY
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    • H04M2215/96—Distributed calculation of charges, e.g. in different nodes like for mobiles between HLR and VLR, or between the terminal and the billing function

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Computer Networks & Wireless Communication (AREA)
  • Signal Processing (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Cardiology (AREA)
  • Psychology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Pain & Pain Management (AREA)
  • Immunology (AREA)
  • Virology (AREA)
  • Urology & Nephrology (AREA)
  • AIDS & HIV (AREA)
  • Oncology (AREA)
  • Psychiatry (AREA)
  • Molecular Biology (AREA)
  • Dermatology (AREA)
  • Tropical Medicine & Parasitology (AREA)
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  • Ophthalmology & Optometry (AREA)
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DK99963141T 1998-07-30 1999-06-02 Tricycliske sulfonamider og derivater deraf som inhibitorer af matrix-metalloproteinaser DK1100792T3 (da)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US9500698P 1998-07-30 1998-07-30

Publications (1)

Publication Number Publication Date
DK1100792T3 true DK1100792T3 (da) 2004-07-05

Family

ID=22248526

Family Applications (1)

Application Number Title Priority Date Filing Date
DK99963141T DK1100792T3 (da) 1998-07-30 1999-06-02 Tricycliske sulfonamider og derivater deraf som inhibitorer af matrix-metalloproteinaser

Country Status (32)

Country Link
US (2) US6420408B1 (da)
EP (1) EP1100792B1 (da)
JP (1) JP2002521478A (da)
KR (1) KR20010072089A (da)
CN (1) CN1310716A (da)
AP (1) AP2001002037A0 (da)
AT (1) ATE261954T1 (da)
AU (1) AU758619B2 (da)
BG (1) BG105185A (da)
BR (1) BR9912600A (da)
CA (1) CA2335077A1 (da)
DE (1) DE69915634T2 (da)
DK (1) DK1100792T3 (da)
EA (1) EA200100158A1 (da)
EE (1) EE200100063A (da)
ES (1) ES2216614T3 (da)
GE (1) GEP20033052B (da)
HR (1) HRP20010078A2 (da)
HU (1) HUP0102714A3 (da)
ID (1) ID27192A (da)
IL (1) IL140746A0 (da)
IS (1) IS5810A (da)
NO (1) NO20010479D0 (da)
NZ (1) NZ509439A (da)
OA (1) OA11589A (da)
PL (1) PL345776A1 (da)
PT (1) PT1100792E (da)
SK (1) SK1192001A3 (da)
TR (1) TR200100239T2 (da)
WO (1) WO2000006561A1 (da)
YU (1) YU6701A (da)
ZA (1) ZA200100455B (da)

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US7354894B2 (en) 1998-08-18 2008-04-08 The Regents Of The University Of California Preventing airway mucus production by administration of EGF-R antagonists
MXPA01013171A (es) * 2001-02-14 2004-05-21 Warner Lambert Co Inhibidores triciclicos de sulfonamida de metaloproteinasa de matriz.
ATE515495T1 (de) * 2001-08-03 2011-07-15 Schering Corp Gamma sekretase inhibitoren
EP1438036A2 (en) * 2001-10-12 2004-07-21 Eli Lilly And Company Use of sulfonamide derivatives as pharmaceuticals compounds
RS51155B (sr) * 2001-12-20 2010-10-31 Bristol-Myers Squibb Company DERIVATI α -(N-SULFONAMIDO)ACETAMIDA KAO INHIBITORI β -AMILOIDA
AU2003237518B8 (en) * 2002-06-11 2009-03-12 Arqule, Inc. Substituted phenylsulfonamide inhibitors of beta amyloid production
CA2495432A1 (en) * 2002-07-17 2004-01-22 Warner-Lambert Company Llc Combination of an allosteric carboxylic inhibitor of matrix metalloproteinase-13 with celecoxib or valdecoxib
US20050095267A1 (en) * 2002-12-04 2005-05-05 Todd Campbell Nanoparticle-based controlled release polymer coatings for medical implants
AU2003300076C1 (en) 2002-12-30 2010-03-04 Angiotech International Ag Drug delivery from rapid gelling polymer composition
US7524938B2 (en) 2003-04-04 2009-04-28 Yeda Research And Development Co., Ltd. Antibodies and pharmaceutical compositions containing same useful for inhibiting activity of metalloproteins
ES2537514T3 (es) 2003-04-04 2015-06-09 Incyte Corporation Composiciones, métodos y kits relacionados con la escisión de HER-2
WO2005061448A1 (en) * 2003-12-24 2005-07-07 Monash University Compositions and methods for treating vascular conditions
US20060112494A1 (en) * 2004-12-01 2006-06-01 David Oppong Method of protecting an animal skin product from metalloproteinase activity
CA2678304A1 (en) 2007-02-23 2008-08-28 Yeda Research And Development Co. Ltd. Antibodies and pharmaceutical compositions containing same useful for inhibiting activity of metalloproteins
US8012947B2 (en) * 2007-03-15 2011-09-06 Hospital For Special Surgery Methods and compositions for promoting wound healing
US20090285840A1 (en) * 2008-04-29 2009-11-19 New York Society For The Ruptured And Crippled Maintaining The Hospital For Special Surgery Methods for treating pathological neovascularization
CA2676946A1 (en) 2009-08-28 2011-02-28 Lucie Peduto Adam12 inhibitors and their use against inflammation-induced fibrosis
CN103249719A (zh) 2010-09-24 2013-08-14 兰贝克赛实验室有限公司 基质金属蛋白酶抑制剂
WO2017134265A1 (en) 2016-02-05 2017-08-10 Institut Pasteur Use of inhibitors of adam12 as adjuvants in tumor therapies
CN114981251B (zh) * 2020-01-21 2023-11-21 深圳信立泰药业股份有限公司 一种二苯并呋喃类衍生物组织蛋白酶k抑制剂及其制备方法和医药用途

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JP2000516607A (ja) 1996-08-16 2000-12-12 ワーナー―ランバート・コンパニー 酪酸マトリックスメタロプロテイナーゼ阻害剤
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PL345776A1 (en) 2002-01-02
BG105185A (en) 2002-04-30
EE200100063A (et) 2002-06-17
OA11589A (en) 2004-07-30
TR200100239T2 (tr) 2001-05-21
YU6701A (sh) 2003-12-31
NZ509439A (en) 2002-10-25
AU4329299A (en) 2000-02-21
CN1310716A (zh) 2001-08-29
WO2000006561A1 (en) 2000-02-10
DE69915634T2 (de) 2004-08-12
EA200100158A1 (ru) 2001-08-27
GEP20033052B (en) 2003-08-25
JP2002521478A (ja) 2002-07-16
NO20010479L (no) 2001-01-29
ZA200100455B (en) 2002-01-16
US6420408B1 (en) 2002-07-16
ES2216614T3 (es) 2004-10-16
HUP0102714A3 (en) 2003-01-28
PT1100792E (pt) 2004-08-31
AU758619B2 (en) 2003-03-27
US20020169164A1 (en) 2002-11-14
ID27192A (id) 2001-03-08
DE69915634D1 (de) 2004-04-22
KR20010072089A (ko) 2001-07-31
ATE261954T1 (de) 2004-04-15
IL140746A0 (en) 2002-02-10
AP2001002037A0 (en) 2001-03-31
BR9912600A (pt) 2001-05-02
EP1100792A1 (en) 2001-05-23
IS5810A (is) 2001-01-12
HUP0102714A2 (hu) 2002-01-28
EP1100792B1 (en) 2004-03-17
HRP20010078A2 (en) 2002-02-28
SK1192001A3 (en) 2002-02-05
NO20010479D0 (no) 2001-01-29
CA2335077A1 (en) 2000-02-10
US6492422B2 (en) 2002-12-10

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