WO2000041473A3 - Utilisation de 3-isoxazolidinones et d'hydroxylaminoacides pour le traitement d'infections - Google Patents

Utilisation de 3-isoxazolidinones et d'hydroxylaminoacides pour le traitement d'infections Download PDF

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Publication number
WO2000041473A3
WO2000041473A3 PCT/EP2000/000165 EP0000165W WO0041473A3 WO 2000041473 A3 WO2000041473 A3 WO 2000041473A3 EP 0000165 W EP0000165 W EP 0000165W WO 0041473 A3 WO0041473 A3 WO 0041473A3
Authority
WO
WIPO (PCT)
Prior art keywords
infections
treatment
isoxazolidinones
hydroxylamine
acids
Prior art date
Application number
PCT/EP2000/000165
Other languages
German (de)
English (en)
Other versions
WO2000041473A2 (fr
Inventor
Hassan Jomaa
Original Assignee
Jomaa Pharmaka Gmbh
Hassan Jomaa
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 DE19903666A external-priority patent/DE19903666A1/de
Priority to EA200100768A priority Critical patent/EA200100768A1/ru
Priority to BR0007491-8A priority patent/BR0007491A/pt
Priority to EP00902582A priority patent/EP1143941A3/fr
Priority to IL14379500A priority patent/IL143795A0/xx
Priority to SK950-2001A priority patent/SK9502001A3/sk
Application filed by Jomaa Pharmaka Gmbh, Hassan Jomaa filed Critical Jomaa Pharmaka Gmbh
Priority to AU24366/00A priority patent/AU2436600A/en
Priority to CA002360366A priority patent/CA2360366A1/fr
Priority to JP2000593097A priority patent/JP2002534440A/ja
Publication of WO2000041473A2 publication Critical patent/WO2000041473A2/fr
Priority to NO20013464A priority patent/NO20013464L/no
Publication of WO2000041473A3 publication Critical patent/WO2000041473A3/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/164Amides, e.g. hydroxamic acids of a carboxylic acid with an aminoalcohol, e.g. ceramides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • A61P33/02Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • A61P33/06Antimalarials
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

L'invention concerne des médicaments contenant au moins un composé de formule générale (I), ainsi que leur utilisation pour le traitement thérapeutique et prophylactique d'infections chez l'homme et chez les animaux, provoquées par des bactéries, champignons et parasites.
PCT/EP2000/000165 1999-01-13 2000-01-12 Utilisation de 3-isoxazolidinones et d'hydroxylaminoacides pour le traitement d'infections WO2000041473A2 (fr)

Priority Applications (9)

Application Number Priority Date Filing Date Title
JP2000593097A JP2002534440A (ja) 1999-01-13 2000-01-12 感染症の治療のための3−イソキサゾリジノンおよびヒドロキシルアミン酸の使用
BR0007491-8A BR0007491A (pt) 1999-01-13 2000-01-12 Uso de 3-isoxazolidinonas e ácidos hidroxilâmicospara o tratamento de infecções
EP00902582A EP1143941A3 (fr) 1999-01-13 2000-01-12 Utilisation de 3-isoxazolidinones et d'hydroxylaminoacides pour le traitement d'infections
IL14379500A IL143795A0 (en) 1999-01-13 2000-01-12 Use of 3-isoxazolidinones and hydroxylamic acids for the treatment of infections
SK950-2001A SK9502001A3 (en) 1999-01-13 2000-01-12 Use of 3-isoxazolidinones and hydroxylamine acids for the treatment of infections
EA200100768A EA200100768A1 (ru) 1999-01-13 2000-01-12 Применение 3-изоксазолидинонов и гидроксиаминокислот для лечения инфекций
AU24366/00A AU2436600A (en) 1999-01-13 2000-01-12 Use of 3-isoxazolidinones and hydroxylamine acids for the treatment of infections
CA002360366A CA2360366A1 (fr) 1999-01-13 2000-01-12 Utilisation de 3-isoxazolidinones et d'hydroxylaminoacides pour le traitement d'infections
NO20013464A NO20013464L (no) 1999-01-13 2001-07-12 Anvendelse av 3-isoksazolidinoner og hydroksylaminsyrer for behandling av infeksjoner

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE19900907.4 1999-01-13
DE19900907 1999-01-13
DE19903666A DE19903666A1 (de) 1999-01-13 1999-01-30 Arzneimittel mit einem Gehalt an 3-Isoxazolidinonen und Hydroxylaminsäuren als Wirkstoff und ihre Verwendung
DE19903666.7 1999-01-30

Publications (2)

Publication Number Publication Date
WO2000041473A2 WO2000041473A2 (fr) 2000-07-20
WO2000041473A3 true WO2000041473A3 (fr) 2001-11-29

Family

ID=26051290

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2000/000165 WO2000041473A2 (fr) 1999-01-13 2000-01-12 Utilisation de 3-isoxazolidinones et d'hydroxylaminoacides pour le traitement d'infections

Country Status (14)

Country Link
EP (1) EP1143941A3 (fr)
JP (1) JP2002534440A (fr)
CN (1) CN1342078A (fr)
AU (1) AU2436600A (fr)
BR (1) BR0007491A (fr)
CA (1) CA2360366A1 (fr)
CZ (1) CZ20012380A3 (fr)
HU (1) HUP0105412A2 (fr)
IL (1) IL143795A0 (fr)
NO (1) NO20013464L (fr)
PL (1) PL350128A1 (fr)
SK (1) SK9502001A3 (fr)
TR (1) TR200102019T2 (fr)
WO (1) WO2000041473A2 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1443930A1 (fr) 2001-10-25 2004-08-11 AstraZeneca AB Derives d'isoxazoline utilises en tant qu'agents antimicrobiens
GB202209172D0 (en) * 2022-06-22 2022-08-10 Syngenta Crop Protection Ag Improvements in or relating to organic compounds

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3911007A (en) * 1974-08-08 1975-10-07 Searle & Co N-substituted N-benzyloxy-2-methyl-2-(4-halophenoxy)propionamides
FR2290442A1 (fr) * 1974-11-06 1976-06-04 Aries Robert Nouvelles rifamycines
GB1457950A (en) * 1973-08-10 1976-12-08 Merck & Co Inc Antibacterial compositions
WO1987004152A1 (fr) * 1985-12-30 1987-07-16 The Wellcome Foundation Ltd. Nouveaux derives aryles
JPS63119462A (ja) * 1986-11-05 1988-05-24 Takeda Chem Ind Ltd 五員環n−スルホ化合物
JPS63119476A (ja) * 1986-11-05 1988-05-24 Takeda Chem Ind Ltd イソキサゾリドン誘導体
US4851422A (en) * 1985-04-30 1989-07-25 Takeda Chemical Industries, Ltd. Antibiotic 2-(3-oxo-2-isoxazolidinyl)-5-oxo-2-tetrahydrofuran-carboxylates
US5288896A (en) * 1992-01-15 1994-02-22 Warner-Lambert Company 3,5-di-t-butyl-4-hydroxylphenylmethylhydroxylamines and their derivatives, pharmaceutical compositions, and methods of use therefor
WO1995006031A1 (fr) * 1993-08-23 1995-03-02 Immunex Corporation Inhibiteurs de la secretion de facteur alpha de necrose tumorale
WO1995019957A1 (fr) * 1994-01-21 1995-07-27 British Biotech Pharmaceuticals Limited Derives d'acide hydroxamique inhibiteurs de metalloproteinase
WO1996013263A2 (fr) * 1994-11-01 1996-05-09 Research Corporation Technologies, Inc. Methodes de traitement de maladies virales par des inhibiteurs de la biosynthese des sphingolipides
US5652262A (en) * 1993-03-16 1997-07-29 British Biotech Pharmaceutical, Ltd. Hydroxamic acid derivatives as metalloproteinase inhibitors
WO1998043959A1 (fr) * 1997-03-28 1998-10-08 Zeneca Limited Acides hydroxamiques substitues par des composes heterocycliques pouvant inhiber le facteur de necrose tumorale
WO1998055449A1 (fr) * 1997-06-06 1998-12-10 The University Of Queensland Composes d'acide hydroxamique ayant des proprietes anticancereuses et antiparasitaires
US5919790A (en) * 1996-10-11 1999-07-06 Warner-Lambert Company Hydroxamate inhibitors of interleukin-1β converting enzyme

Patent Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1457950A (en) * 1973-08-10 1976-12-08 Merck & Co Inc Antibacterial compositions
US3911007A (en) * 1974-08-08 1975-10-07 Searle & Co N-substituted N-benzyloxy-2-methyl-2-(4-halophenoxy)propionamides
FR2290442A1 (fr) * 1974-11-06 1976-06-04 Aries Robert Nouvelles rifamycines
US4851422A (en) * 1985-04-30 1989-07-25 Takeda Chemical Industries, Ltd. Antibiotic 2-(3-oxo-2-isoxazolidinyl)-5-oxo-2-tetrahydrofuran-carboxylates
WO1987004152A1 (fr) * 1985-12-30 1987-07-16 The Wellcome Foundation Ltd. Nouveaux derives aryles
JPS63119476A (ja) * 1986-11-05 1988-05-24 Takeda Chem Ind Ltd イソキサゾリドン誘導体
JPS63119462A (ja) * 1986-11-05 1988-05-24 Takeda Chem Ind Ltd 五員環n−スルホ化合物
US5288896A (en) * 1992-01-15 1994-02-22 Warner-Lambert Company 3,5-di-t-butyl-4-hydroxylphenylmethylhydroxylamines and their derivatives, pharmaceutical compositions, and methods of use therefor
US5652262A (en) * 1993-03-16 1997-07-29 British Biotech Pharmaceutical, Ltd. Hydroxamic acid derivatives as metalloproteinase inhibitors
WO1995006031A1 (fr) * 1993-08-23 1995-03-02 Immunex Corporation Inhibiteurs de la secretion de facteur alpha de necrose tumorale
WO1995019957A1 (fr) * 1994-01-21 1995-07-27 British Biotech Pharmaceuticals Limited Derives d'acide hydroxamique inhibiteurs de metalloproteinase
WO1996013263A2 (fr) * 1994-11-01 1996-05-09 Research Corporation Technologies, Inc. Methodes de traitement de maladies virales par des inhibiteurs de la biosynthese des sphingolipides
US5919790A (en) * 1996-10-11 1999-07-06 Warner-Lambert Company Hydroxamate inhibitors of interleukin-1β converting enzyme
WO1998043959A1 (fr) * 1997-03-28 1998-10-08 Zeneca Limited Acides hydroxamiques substitues par des composes heterocycliques pouvant inhiber le facteur de necrose tumorale
WO1998055449A1 (fr) * 1997-06-06 1998-12-10 The University Of Queensland Composes d'acide hydroxamique ayant des proprietes anticancereuses et antiparasitaires

Non-Patent Citations (16)

* Cited by examiner, † Cited by third party
Title
BALDWIN, JACK E. ET AL: "Synthesis of phenoxyacetyl-N-sulfonyl cycloserine", TETRAHEDRON LETT. (1987), 28(37), 4319-20, 1987, XP000990044 *
BALDWIN, JACK E. ET AL: "The synthesis of potential.gamma.-lactam antibiotics containing a cycloserine nucleus", TETRAHEDRON LETT. (1990), 31(15), 2211-12, 1990, XP000990045 *
GEARY, TIMOTHY G. ET AL: "Nutritional requirements of Plasmodium falciparum in culture. II. Effects of antimetabolites in a semi-defined medium", J. PROTOZOOL. (1985), 32(1), 65-9, 1985, XP000952017 *
GERARDIN, PHILIPPE ET AL: "Synthesis of potential.gamma.-lactam antibiotics", BIOORG. MED. CHEM. LETT. (1995), 5(14), 1467-70, 1995, XP004135426 *
KHALIL, ZARIF HALEEM ET AL: "Synthesis and application of some 1-[8-hydroxy-5(or 7)-quinolinyl]alkylidene-substituted heterocycles as bactericides, fungicides, and bioregulators", BULL. CHEM. SOC. JPN. (1988), 61(4), 1345-9, 1988, XP000990042 *
MITTENDORF, JOACHIM: "Enantioselective synthesis of (R)- and (S)-4-methylcycloserine by the bislactim ether method", LIEBIGS ANN. CHEM. (1988), (12), 1201-2, 1988, XP000990041 *
NICHTERLEIN, THOMAS ET AL: "Subinhibitory concentrations of.beta.-lactams and other cell-wall antibiotics inhibit listeriolysin production by Listeria monocytogenes", INT. J. ANTIMICROB. AGENTS (1996), 7(1), 75-81, 1996, XP000991436 *
O'GRADY, F.: "Cycloserine, amino acid analogs and oligopeptides", ANTIBIOT. CHEMOTHER. (7TH ED.) (1997), 344-345. EDITOR(S): O'GRADY, FRANCIS. PUBLISHER: CHURCHILL LIVINGSTONE, EDINBURGH, UK., 1997, XP000951569 *
OMAR, M. T.: "Synthesis of some new isoxazolidine-3,5-diones, pyrazolidine-3,5- diones, and barbituric acids of expected antimicrobial activity", EGYPT. J. PHARM. SCI. (1998), VOLUME DATE 1997, 38(4-6), 281-289, 1998, XP000991461 *
PATENT ABSTRACTS OF JAPAN vol. 012, no. 365 (C - 532) 29 September 1988 (1988-09-29) *
STAMMER, CHARLES H. ET AL: "5-Carboxamido-4-amino-3-isoxazolidone, an asparagine analog", J. MED. CHEM. (1978), 21(7), 709-12, 1978, XP000990040 *
TAMURA, NORIKAZU ET AL: "Synthesis and antibacterial activity of lactivicin derivatives", CHEM. PHARM. BULL. (1990), 38(1), 116-22, 1990, XP000990010 *
UEDA, Y. ET AL: "Synthesis of phenoxyacetyl-N-(hydroxydioxocyclobutenyl)cycloserines", TETRAHEDRON LETT. (1991), 32(31), 3767-70, 1991, XP000990046 *
VIGORITA, M. GABRIELLA ET AL: "Fluoro-containing D-cycloserines. Synthesis and in vitro evaluation of antimicrobial and antiviral activities", FARMACO (1992), 47(6), 907-18, 1992, XP000991416 *
WEWALKA, G. ET AL: "Sensitivity of bacteria causing urinary tract infections towards Terizidone", WIEN. KLIN. WOCHENSCHR. (1976), 88(11), 355-60, 1976, XP000991442 *
WISE, R. ET AL: "In vitro activity of fludalanine combined with pentizidone compared with those of other agents", ANTIMICROB. AGENTS CHEMOTHER. (1984), 25(5), 612-17, 1984, XP000991424 *

Also Published As

Publication number Publication date
CA2360366A1 (fr) 2000-07-20
NO20013464L (no) 2001-09-12
CN1342078A (zh) 2002-03-27
EP1143941A2 (fr) 2001-10-17
CZ20012380A3 (cs) 2002-01-16
HUP0105412A2 (hu) 2002-05-29
PL350128A1 (en) 2002-11-04
TR200102019T2 (tr) 2002-04-22
EP1143941A3 (fr) 2002-02-06
JP2002534440A (ja) 2002-10-15
BR0007491A (pt) 2001-11-20
AU2436600A (en) 2000-08-01
WO2000041473A2 (fr) 2000-07-20
SK9502001A3 (en) 2002-05-09
NO20013464D0 (no) 2001-07-12
IL143795A0 (en) 2002-04-21

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