FI883439A - Antibiotikumkompositioner. - Google Patents

Antibiotikumkompositioner. Download PDF

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Publication number
FI883439A
FI883439A FI883439A FI883439A FI883439A FI 883439 A FI883439 A FI 883439A FI 883439 A FI883439 A FI 883439A FI 883439 A FI883439 A FI 883439A FI 883439 A FI883439 A FI 883439A
Authority
FI
Finland
Prior art keywords
het
ring
group
chem
hydroxy
Prior art date
Application number
FI883439A
Other languages
English (en)
Finnish (fi)
Other versions
FI883439A0 (fi
Inventor
Jean Claude Arnould
Dominique Boucherot
Frederick Henri Jung
David Huw Davies
Colin John Strawson
Original Assignee
Ici Plc
Ici Pharma
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 Ici Plc, Ici Pharma filed Critical Ici Plc
Publication of FI883439A0 publication Critical patent/FI883439A0/fi
Publication of FI883439A publication Critical patent/FI883439A/fi

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/38—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/38—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
    • C07D501/46—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • 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
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/38—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
    • C07D501/40—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by an aliphatic carboxylic acid, which is substituted by hetero atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Communicable Diseases (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Revetment (AREA)
  • Pit Excavations, Shoring, Fill Or Stabilisation Of Slopes (AREA)
  • Threshing Machine Elements (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Saccharide Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
FI883439A 1987-07-23 1988-07-20 Antibiotikumkompositioner. FI883439A (fi)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP87401718 1987-07-23

Publications (2)

Publication Number Publication Date
FI883439A0 FI883439A0 (fi) 1988-07-20
FI883439A true FI883439A (fi) 1989-01-24

Family

ID=8198237

Family Applications (1)

Application Number Title Priority Date Filing Date
FI883439A FI883439A (fi) 1987-07-23 1988-07-20 Antibiotikumkompositioner.

Country Status (16)

Country Link
US (1) US5019570A (fr)
EP (1) EP0304158B1 (fr)
JP (1) JPH0193592A (fr)
KR (1) KR890002186A (fr)
CN (1) CN1031378A (fr)
AT (1) ATE107651T1 (fr)
AU (1) AU1976288A (fr)
DE (1) DE3850321T2 (fr)
DK (1) DK414888A (fr)
FI (1) FI883439A (fr)
GB (1) GB8816519D0 (fr)
HU (1) HU201949B (fr)
NO (1) NO883275L (fr)
NZ (1) NZ225533A (fr)
PT (1) PT88070B (fr)
ZA (1) ZA885271B (fr)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5232918A (en) * 1987-07-23 1993-08-03 Imperial Chemical Industries Plc Cephalosporin derivatives
US5149803A (en) * 1988-05-10 1992-09-22 Imperial Chemical Industries Plc Intermediates for cephalosporin compounds
DE68919273T2 (de) * 1988-05-10 1995-03-23 Ici Pharma Cephalosporine, Verfahren zu ihrer Herstellung und pharmazeutische Präparate.
GB8811056D0 (en) * 1988-05-10 1988-06-15 Ici Plc Antibiotic compounds
GB8811055D0 (en) * 1988-05-10 1988-06-15 Ici Plc Antibiotic compounds
US4904775A (en) * 1988-05-16 1990-02-27 E. R. Squibb & Sons, Inc. Heteroaroylhydrazide derivatives of monocyclic beta-lactam antibiotics
EP0366189A3 (fr) * 1988-10-24 1992-01-02 Norwich Eaton Pharmaceuticals, Inc. Lactames-quinolones antimicrobiennes
US5273973A (en) * 1988-10-24 1993-12-28 Norwich Eaton Pharmaceuticals, Inc. Antimicrobial quinolonyl esters
US5328908A (en) * 1988-10-24 1994-07-12 Procter & Gamble Pharmaceuticals, Inc. Antimicrobial quinolone thioureas
US5180719A (en) * 1988-10-24 1993-01-19 Norwich Eaton Pharmaceuticals, Inc. Antimicrobial quinolonyl lactam esters
EP0366193A3 (fr) * 1988-10-24 1992-01-08 Norwich Eaton Pharmaceuticals, Inc. Quinolonyl-lactames antimicrobiennes
US5491139A (en) * 1988-10-24 1996-02-13 The Procter & Gamble Company Antimicrobial quinolonyl lactams
CA2001203C (fr) * 1988-10-24 2001-02-13 Thomas P. Demuth, Jr. Dithiocarbamoyl quinolones antimicrobiens
CA2024282A1 (fr) * 1989-09-21 1991-03-22 Peter H. Ermann Derives hydrazide heterocycliques de beta-lactam monocyclique antibiotique
SG47533A1 (en) 1990-04-18 1998-04-17 Procter & Gamble Pharma Antimicrobial quinolonyl lactams
US5234920A (en) * 1990-08-23 1993-08-10 Bristol-Myers Squibb Company Antibiotic C-7 catechol-substituted cephalosporin compounds, compositions, and method of use thereof
ZA918014B (en) * 1990-11-05 1992-07-29 Squibb & Sons Inc Heteroaroyl derivatives of monocyclic beta-lactam antibiotics
US5250691A (en) * 1991-09-09 1993-10-05 E. R. Squibb & Sons, Inc. Heteroaryl derivatives of monocyclic beta-lactam antibiotics
ATE179422T1 (de) * 1994-02-25 1999-05-15 Aranda Lab Sa De Cv Chinolonylcarboxamidocephalosporin-derivate und diese enthaltende arzneimittel
CA2309882A1 (fr) * 1997-12-22 1999-07-01 Pharmacia & Upjohn Company 4-hydroxyquinoline-3-carboxamides et hydrazides utilises comme agents antiviraux
FI20001593A (fi) 2000-07-03 2002-01-04 Orion Yhtymo Oyj Comt-entsyymiõ inhiboivaa aktiivisuutta omaavia kumariinijohdannaisia
ES2389907T3 (es) 2004-04-30 2012-11-02 Takeda Pharmaceutical Company Limited Compuesto de amida heterocíclica y uso del mismo como un inhibidor de MMP-13
CA2572442A1 (fr) * 2004-07-30 2006-03-09 Palumed S.A. Molecules hybrides qa ou q est une aminoquinoleine et a est un residu antibiotique, leur synthese et leurs utilisations en tant qu'agent antibacterien
FR2873695A1 (fr) * 2004-07-30 2006-02-03 Palumed Sa Molecules hybrides qa ou q est une aminoquinoleine et a est un antibiotique ou un inhibiteur de resistance), leur synthese et leurs utilisations en tant qu'agent antibacterien
FR2874922A1 (fr) * 2004-07-30 2006-03-10 Palumed Sa Molecules hybrides qa ou q est une aminoquinoleine et a est un residu antibiotique, leur synthese et leurs utilisations en tant qu'agent antibacterien
WO2009100250A1 (fr) 2008-02-05 2009-08-13 Fibrogen, Inc. Dérivés de chromène et leur utilisation en tant qu'inhibiteurs de l'activité de l'hydroxylase hif
EP2370422B1 (fr) 2008-11-14 2019-06-05 Fibrogen, Inc. Dérivés de thiochromène utiles en tant qu'inhibiteurs de l'hydroxylase hif
US20130065922A1 (en) * 2010-05-21 2013-03-14 Syngenta Crop Protection Llc Novel amides as fungicides
TWI547496B (zh) * 2011-10-04 2016-09-01 葛蘭素集團公司 抗菌化合物
UY35103A (es) 2012-10-29 2014-05-30 Glaxo Group Ltd Compuestos de cefem 2-sustituidos
MX2015008036A (es) 2012-12-21 2015-10-29 Janssen Sciences Ireland Uc Compuestos antibacterianos.

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5718689A (en) * 1980-07-08 1982-01-30 Eisai Co Ltd 7alpha-methoxycephem derivative
NZ198350A (en) * 1980-09-25 1985-02-28 Toyama Chemical Co Ltd Cephalosporins and intermediates;pharmaceutical compositions
JPS57165389A (en) * 1981-04-02 1982-10-12 Eisai Co Ltd Novel penicillin and cephalosporin compound
GB8413152D0 (en) * 1983-06-03 1984-06-27 Ici Pharma Cephalosporin derivatives
US4552891A (en) * 1983-09-13 1985-11-12 Eli Lilly And Company Benzothiophene derivatives
JPS6064986A (ja) * 1983-09-20 1985-04-13 Toyama Chem Co Ltd セファロスポリン類の製造法
FI851934L (fi) * 1984-05-30 1985-12-01 Ici Plc Kefalosporinderivat.
DE3581891D1 (de) * 1984-11-12 1991-04-04 Banyu Pharma Co Ltd Cephalosporinderivate.
EP0187456A1 (fr) * 1984-11-29 1986-07-16 Ici Pharma Dérivés de céphalosporine
EP0186187B1 (fr) * 1984-12-27 1992-02-26 Banyu Pharmaceutical Co., Ltd. Dérivés de céphalosporine
JPS6251688A (ja) * 1985-08-30 1987-03-06 Taito Pfizer Kk 新規なセフアロスポリン化合物
JPS62209082A (ja) * 1986-03-11 1987-09-14 Banyu Pharmaceut Co Ltd セフアロスポリン誘導体
DE3775798D1 (de) * 1986-03-19 1992-02-20 Banyu Pharma Co Ltd Cephalosporinverbindungen, verfahren zu ihrer herstellung und antibakterielle mittel.
EP0241901B1 (fr) * 1986-04-14 1994-08-24 Banyu Pharmaceutical Co., Ltd. Dérivés de céphalosporine, leurs procédés de préparation et agents antibactériens
EP0265185A3 (fr) * 1986-10-21 1990-03-28 Beecham Group Plc Céphalosporines, leurs procédés de préparation et compositions pharmaceutiques les contenant

Also Published As

Publication number Publication date
NO883275D0 (no) 1988-07-22
NZ225533A (en) 1990-12-21
DE3850321T2 (de) 1994-10-06
AU1976288A (en) 1989-01-27
HUT47942A (en) 1989-04-28
CN1031378A (zh) 1989-03-01
ATE107651T1 (de) 1994-07-15
ZA885271B (en) 1989-03-29
HU201949B (en) 1991-01-28
EP0304158B1 (fr) 1994-06-22
DK414888D0 (da) 1988-07-22
PT88070B (pt) 1995-03-01
NO883275L (no) 1989-01-24
FI883439A0 (fi) 1988-07-20
GB8816519D0 (en) 1988-08-17
EP0304158A1 (fr) 1989-02-22
DE3850321D1 (de) 1994-07-28
DK414888A (da) 1989-01-24
KR890002186A (ko) 1989-04-08
JPH0193592A (ja) 1989-04-12
US5019570A (en) 1991-05-28
PT88070A (pt) 1989-06-30

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Legal Events

Date Code Title Description
FD Application lapsed
FD Application lapsed

Owner name: I.C.I PHARMA

Owner name: IMPERIAL CHEMICAL INDUSTRIES PLC