PT946176E - Utilizacao de derivados de acido 7-(2-oxa-5,8-diazabiciclo¬4.3.0|non-8-il)-quinolonacarboxilico e -naftiridonacarboxilico para terapia de infeccoes por helicobacter pylori e das doencas gastroduodenais a elas associadas - Google Patents

Utilizacao de derivados de acido 7-(2-oxa-5,8-diazabiciclo¬4.3.0|non-8-il)-quinolonacarboxilico e -naftiridonacarboxilico para terapia de infeccoes por helicobacter pylori e das doencas gastroduodenais a elas associadas

Info

Publication number
PT946176E
PT946176E PT97954354T PT97954354T PT946176E PT 946176 E PT946176 E PT 946176E PT 97954354 T PT97954354 T PT 97954354T PT 97954354 T PT97954354 T PT 97954354T PT 946176 E PT946176 E PT 946176E
Authority
PT
Portugal
Prior art keywords
oxa
diazabicyclo
therapy
acid derivatives
helicobacter pylori
Prior art date
Application number
PT97954354T
Other languages
English (en)
Inventor
Thomas Schenke
Klaus Schaller
Michael Matzke
Thomas Himmler
Bartel Dr Stephan
Jaetsch Dr Thomas
Bernd Baasner
Harald Labischinski
Petersen Dr Uwe
Hans-Otto Werling
Original Assignee
Bayer 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 Bayer Ag filed Critical Bayer Ag
Publication of PT946176E publication Critical patent/PT946176E/pt

Links

Classifications

    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • 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
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines having two or more nitrogen atoms in the same ring, e.g. oxadiazines
    • 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
    • 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
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
PT97954354T 1996-12-16 1997-12-04 Utilizacao de derivados de acido 7-(2-oxa-5,8-diazabiciclo¬4.3.0|non-8-il)-quinolonacarboxilico e -naftiridonacarboxilico para terapia de infeccoes por helicobacter pylori e das doencas gastroduodenais a elas associadas PT946176E (pt)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19652239A DE19652239A1 (de) 1996-12-16 1996-12-16 Verwendung von 7-(2-Oxa-5,8-diazabicyclo[4.3.0]non-8-yl)-chinolon- und -naphthyridoncarbonsäure-Derivaten zur Therapie von Helicobacter-pylori-Infektionen und den damit assoziierten gastroduodenalen Erkrankungen

Publications (1)

Publication Number Publication Date
PT946176E true PT946176E (pt) 2002-08-30

Family

ID=7814837

Family Applications (1)

Application Number Title Priority Date Filing Date
PT97954354T PT946176E (pt) 1996-12-16 1997-12-04 Utilizacao de derivados de acido 7-(2-oxa-5,8-diazabiciclo¬4.3.0|non-8-il)-quinolonacarboxilico e -naftiridonacarboxilico para terapia de infeccoes por helicobacter pylori e das doencas gastroduodenais a elas associadas

Country Status (28)

Country Link
US (2) US6133260A (pt)
EP (1) EP0946176B1 (pt)
JP (3) JP3463939B2 (pt)
KR (1) KR100536153B1 (pt)
CN (1) CN100335054C (pt)
AT (1) ATE214929T1 (pt)
AU (1) AU717751B2 (pt)
BG (1) BG64615B1 (pt)
BR (1) BR9714032A (pt)
CA (1) CA2274894C (pt)
CZ (2) CZ297363B6 (pt)
DE (2) DE19652239A1 (pt)
DK (1) DK0946176T3 (pt)
EA (1) EA002477B1 (pt)
EE (1) EE04090B1 (pt)
ES (1) ES2175519T3 (pt)
HK (1) HK1025517A1 (pt)
HU (1) HU226523B1 (pt)
IL (1) IL130311A (pt)
NO (1) NO325617B1 (pt)
NZ (2) NZ336228A (pt)
PL (1) PL191193B1 (pt)
PT (1) PT946176E (pt)
RS (1) RS49684B (pt)
SK (2) SK283224B6 (pt)
TR (1) TR199901754T2 (pt)
UA (1) UA57055C2 (pt)
WO (1) WO1998026779A1 (pt)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19633805A1 (de) * 1996-02-23 1997-08-28 Bayer Ag Gegenenenfalls substituierte 8-Cyan-l-cyclopropyl-7-(2,8-diazabicyclo-[4.3.0]-nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chinolincarbonsäuren und ihre Derivate
WO2000029369A1 (fr) * 1998-11-18 2000-05-25 Asahi Glass Company Ltd. Derives d'acide aminoacrylique et procede de production correspondant
DE19917617A1 (de) * 1999-04-19 2000-10-26 Bayer Ag -(-)Enantiomeres des 2-[2-(1-Chlor-cyclopropyl)-3-(2-chlorphenyl) 2-hydroxy-propyl]-2,4-dihydro-[1,2,4]-triazol-3-thions
AU766014B2 (en) * 1999-07-01 2003-10-09 Wakunaga Pharmaceutical Co., Ltd Quinolinecarboxylic acid derivative or salts thereof
IL148820A0 (en) * 1999-10-08 2002-09-12 Smithkline Beecham Corp Fab i inhibitors
AU2002367773A1 (en) * 2001-04-06 2003-11-03 Affinium Pharmaceuticals, Inc. Fab i inhibitors
US7790709B2 (en) 2002-12-06 2010-09-07 Affinium Pharmaceuticals, Inc. Heterocyclic compounds, methods of making them and their use in therapy
WO2004082586A2 (en) 2003-03-17 2004-09-30 Affinium Pharmaceuticals, Inc. Phamaceutical compositions comprising inhibitors of fab i and further antibiotics
EP1669354B1 (en) 2003-09-29 2013-03-20 Daiichi Sankyo Company, Limited 8-cyanoquinolonecarboxylic acid derivative
CN1244582C (zh) * 2004-04-21 2006-03-08 中国医学科学院医药生物技术研究所 喹诺酮羧酸类化合物及其制备方法和医药用途
US7759362B2 (en) 2004-04-21 2010-07-20 Institut Of Medicinal Biotechnology Chinese Academy Of Medical Sciences Quinolonecarboxylic acid compounds, preparation methods and pharmaceutical uses thereof
PT1828167E (pt) * 2004-06-04 2014-10-08 Debiopharm Int Sa Derivados de acrilamida como agentes antibióticos
WO2007067416A2 (en) * 2005-12-05 2007-06-14 Affinium Pharmaceuticals, Inc. Heterocyclylacrylamide compounds as fabi inhibitors and antibacterial agents
EP2687533B1 (en) 2006-07-20 2017-07-19 Debiopharm International SA Acrylamide derivatives as FAB I inhibitors
EP2125802A4 (en) 2007-02-16 2014-08-20 Debiopharm Int Sa SALTS, PRODRUGS AND POLYMORPHES OF FAB I INHIBITORS
RU2570731C2 (ru) 2009-07-02 2015-12-10 Алькон Рисерч, Лтд. Композиции, включающие финафлоксации, и способы лечения офтальмологических, ушных или назальных инфекций
RU2449805C1 (ru) 2011-01-27 2012-05-10 Общество С Ограниченной Ответственностью "Гармония" Пептидная фармацевтическая композиция, средство на ее основе для лечения гастродуоденальных заболеваний, вызываемых helicobacter pylori, и способ его использования
RS58898B1 (sr) 2012-06-19 2019-08-30 Debiopharm Int Sa Prolek derivati (e)-n-metil-n-((3-metilbenzofuran-2-il)metil)-3-(7-okso-5,6,7,8-tetrahidro-1,8-naftiridin-3-il)akrilamida
US9504691B2 (en) * 2012-12-06 2016-11-29 Alcon Research, Ltd. Finafloxacin suspension compositions
MX2016001912A (es) 2013-08-12 2016-06-02 Novartis Ag Metodos para tratar infecciones oticas luego de la colocacion de un tubo de timpanostomia.
DE102014115951A1 (de) 2014-11-03 2016-05-04 Merlion Pharmaceuticals Pte Ltd. Zusammensetzungen, die Finafloxacin und Tris enthalten
DE102015100068A1 (de) 2015-01-06 2016-07-07 Merlion Pharmaceuticals Pte Ltd. Finafloxacin zur verwendung bei der behandlung von harnwegsinfektionen
LT3419628T (lt) 2016-02-26 2021-01-25 Debiopharm International Sa Medikamentas diabetinėms pėdų infekcijoms gydyti
CN107987074B (zh) * 2017-10-27 2020-12-29 浙江美诺华药物化学有限公司 一种普拉沙星的合成方法
DK3784656T3 (da) * 2018-04-25 2023-09-18 Elanco Animal Health Gmbh Fremgangsmåde til hydrolyse af quinoloncarboxylestere

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4822801A (en) * 1984-07-20 1989-04-18 Warner-Lambert Company 4-oxo-1,4-dihydroquinoline-3-carboxylic acid derivative as antibacterial agents
JPS62205060A (ja) * 1986-03-04 1987-09-09 Kyorin Pharmaceut Co Ltd ８位置換キノロンカルボン酸誘導体
DE3702393A1 (de) * 1987-01-28 1988-08-11 Bayer Ag 8-cyano-1-cyclopropyl-1,4-dihydro-4-oxo- 3-chinolincarbonsaeuren, verfahren zu ihrer herstellung und diese enthaltende antibakterielle mittel
US5563138A (en) * 1987-04-16 1996-10-08 Otsuka Pharmaceutical Company, Limited Benzoheterocyclic compounds
US4889857A (en) * 1987-10-12 1989-12-26 Yoshitomi Pharmaceutical Industries, Ltd. Quinolonecarboxylic acid compounds and pharmaceutical use thereof
WO1989005643A1 (en) * 1987-12-18 1989-06-29 Pfizer Inc. Heterocyclic-substituted quinoline-carboxylic acids
JP2844079B2 (ja) * 1988-05-23 1999-01-06 塩野義製薬株式会社 ピリドンカルボン酸系抗菌剤
DE3906365A1 (de) * 1988-07-15 1990-01-18 Bayer Ag 7-(1-pyrrolidinyl)-3-chinolon- und -naphthyridoncarbonsaeure-derivate, verfahren sowie substituierte (oxa)diazabicyclooctane und -nonane als zwischenprodukte zu ihrer herstellung, und sie enthaltende antibakterielle mittel und futterzusatzstoffe
US5147873A (en) * 1988-08-23 1992-09-15 Pfizer Inc. Amino-substituted bridged azabicyclic quinolone carboxylic acids and esters
CA2001203C (en) * 1988-10-24 2001-02-13 Thomas P. Demuth, Jr. Novel antimicrobial dithiocarbamoyl quinolones
US5262417A (en) * 1988-12-06 1993-11-16 The Upjohn Company Antibacterial quinolone compounds
US5407932A (en) * 1989-03-31 1995-04-18 Wakunaga Seiyaku Kabushiki Kaisha Quinolone derivatives and antibacterial agents containing the same
DE3910663A1 (de) * 1989-04-03 1990-10-04 Bayer Ag 5-alkylchinoloncarbonsaeuren
US5252734A (en) * 1989-04-03 1993-10-12 Bayer Aktiengesellschaft Antibacterial 5-alkylquinolonecarboxylic acids
US5140033A (en) * 1989-04-03 1992-08-18 Bayer Aktiengesellschaft Antibacterial 5-alkylquinolonecarboxylic acids
US5164402A (en) * 1989-08-16 1992-11-17 Pfizer Inc Azabicyclo quinolone and naphthyridinone carboxylic acids
KR910009330B1 (ko) * 1989-10-23 1991-11-11 재단법인 한국화학연구소 항균작용을 갖는 퀴놀린계 화합물과 그의 제조방법
TW209865B (pt) * 1992-01-10 1993-07-21 Bayer Ag
DE4200415A1 (de) 1992-01-10 1993-07-15 Bayer Ag Enantiomerenreine 2-oxa-5,8-diazabicyclo(4.3.0)nonane sowie verfahren zu ihrer herstellung
NO301165B1 (no) * 1992-12-25 1997-09-22 Daiichi Seiyaku Co Bicykliske aminderivater og antibakterielle midler inneholdende disse
DE4309964A1 (de) 1993-03-26 1994-09-29 Bayer Ag Verfahren zur Herstellung enantiomerenreiner trans-2-Oxa-5,8-diazabicyclo[4.3.0]nonane
AU4272793A (en) * 1993-04-24 1994-11-21 Korea Research Institute Of Chemical Technology Novel quinolone carboxylic acid derivatives and process for preparing the same
US5532239A (en) * 1993-08-02 1996-07-02 Assistance Publique - Hopitaux De Paris Therapeutic application of fluoroquinolone derivatives
DE4329600A1 (de) * 1993-09-02 1995-03-09 Bayer Ag Pyrido [1,2,3-d,e] [1,3,4] benzoxadiazinderivate
DK0676199T3 (da) * 1994-04-07 1999-02-08 Pfizer Anvendelse af trovafloxacin eller derivater deraf til fremstilling af et medikament til behandling af H. pylori-infektione
GB2289674A (en) * 1994-05-23 1995-11-29 Pfizer Antibacterial naphthyridine
JPH0848629A (ja) * 1994-08-08 1996-02-20 Dainippon Pharmaceut Co Ltd ピリドンカルボン酸誘導体およびそれを有効成分とする抗ピロリ菌剤

Also Published As

Publication number Publication date
EP0946176B1 (de) 2002-03-27
HUP0000450A2 (hu) 2000-10-28
ES2175519T3 (es) 2002-11-16
JP2000514825A (ja) 2000-11-07
SK79599A3 (en) 2001-01-18
NZ506162A (en) 2001-06-29
DK0946176T3 (da) 2002-06-10
JP5112395B2 (ja) 2013-01-09
IL130311A0 (en) 2000-06-01
EP0946176A1 (de) 1999-10-06
DE59706808D1 (de) 2002-05-02
IL130311A (en) 2004-01-04
CZ216899A3 (cs) 2000-02-16
PL191193B1 (pl) 2006-03-31
RS49684B (sr) 2007-11-15
TR199901754T2 (xx) 1999-09-21
HK1025517A1 (en) 2000-11-17
BG103474A (en) 2000-01-31
CA2274894A1 (en) 1998-06-25
US6432948B1 (en) 2002-08-13
NZ336228A (en) 2000-12-22
US6133260A (en) 2000-10-17
EE9900248A (et) 1999-12-15
CN1245428A (zh) 2000-02-23
EA002477B1 (ru) 2002-06-27
SK283224B6 (sk) 2003-03-04
EE04090B1 (et) 2003-08-15
JP3463939B2 (ja) 2003-11-05
EA199900526A1 (ru) 2000-08-28
JP4463380B2 (ja) 2010-05-19
WO1998026779A1 (de) 1998-06-25
JP2009235106A (ja) 2009-10-15
CZ297364B6 (cs) 2006-11-15
SK283223B6 (sk) 2003-03-04
CZ297363B6 (cs) 2006-11-15
HUP0000450A3 (en) 2001-02-28
UA57055C2 (uk) 2003-06-16
KR100536153B1 (ko) 2005-12-14
BG64615B1 (bg) 2005-09-30
BR9714032A (pt) 2000-05-09
HU226523B1 (en) 2009-03-30
PL333928A1 (en) 2000-01-31
NO325617B1 (no) 2008-06-30
CN100335054C (zh) 2007-09-05
SK14962000A3 (sk) 2003-01-09
KR20000069483A (ko) 2000-11-25
AU717751B2 (en) 2000-03-30
NO992903L (no) 1999-06-14
NO992903D0 (no) 1999-06-14
DE19652239A1 (de) 1998-06-18
CA2274894C (en) 2009-04-07
YU27499A (sh) 2002-10-18
JP2000351781A (ja) 2000-12-19
ATE214929T1 (de) 2002-04-15
AU5854198A (en) 1998-07-15

Similar Documents

Publication Publication Date Title
PT946176E (pt) Utilizacao de derivados de acido 7-(2-oxa-5,8-diazabiciclo¬4.3.0|non-8-il)-quinolonacarboxilico e -naftiridonacarboxilico para terapia de infeccoes por helicobacter pylori e das doencas gastroduodenais a elas associadas
AR006012A1 (es) Tabletas que contienen antibioticos de beta-lactamas y un metodo para obtenerlas
HK1080284A1 (en) Pharmaceutical composition for treatment of rhinitis
ES2135046T3 (es) 2-isoxazolinas e isoxazoles 3,5-disustituidos y 3,4,5-trisustituidos, procedimiento para su preparacion y su empleo como medicamentos.
NO984330L (no) Benzopyranderivater som har leukotrien-antagonistisk virkning
SE8500996D0 (sv) Method of treatment
BR0309009A (pt) Método para o tratamento de hipersecreção de muco
ES2034678T3 (es) Procedimiento para aumentar la productividad de los cerdos.
IT1289154B1 (it) Derivati di isoflavone loro preparazione e loro impiego terapeutico
DK0767783T3 (da) Substituerede alkyldiaminderivater og deres anvendelse som tachykinin-antagonister
ATE290374T1 (de) Iga produktionsinhibitoren
ES542583A0 (es) Procedimiento para la preparacion de nuevos derivados de triazolopirimidina.
BR9810031A (pt) Derivados de ácido pirrolidina carboxìlico como antagonistas á endotelina
AU7436098A (en) Use of mizolastine for preparing a medicine for treating inflammation
NO20012328L (no) Fluorerte 3,4-dihydrokinolinderivater anvendt som NOS- inhibitorer