PT97416A - Processo para a preparacao de novos compostos quinolona-tio-ureia antimicrobianos - Google Patents
Processo para a preparacao de novos compostos quinolona-tio-ureia antimicrobianosInfo
- Publication number
- PT97416A PT97416A PT97416A PT9741691A PT97416A PT 97416 A PT97416 A PT 97416A PT 97416 A PT97416 A PT 97416A PT 9741691 A PT9741691 A PT 9741691A PT 97416 A PT97416 A PT 97416A
- Authority
- PT
- Portugal
- Prior art keywords
- ureia
- tio
- compounds
- preparation
- new antimicrobial
- Prior art date
Links
- 230000000845 anti-microbial effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
- C07D215/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D455/00—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/03—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/04—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing a quinolizine ring system condensed with only one six-membered carbocyclic ring, e.g. julolidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D477/00—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
- C07D477/10—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D503/00—Heterocyclic compounds containing 4-oxa-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. oxapenicillins, clavulanic acid derivatives; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D505/00—Heterocyclic compounds containing 5-oxa-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. oxacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/513,368 US5328908A (en) | 1988-10-24 | 1990-04-20 | Antimicrobial quinolone thioureas |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PT97416A true PT97416A (pt) | 1992-01-31 |
| PT97416B PT97416B (pt) | 1998-08-31 |
Family
ID=24042972
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT97416A PT97416B (pt) | 1990-04-20 | 1991-04-19 | Processo para a preparacao de novos compostos quinolona-tio-ureia antimicrobianos |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US5328908A (pt) |
| EP (1) | EP0593457A1 (pt) |
| JP (1) | JP3046068B2 (pt) |
| KR (1) | KR100256457B1 (pt) |
| AU (1) | AU659996B2 (pt) |
| CA (1) | CA2077435A1 (pt) |
| EG (1) | EG19861A (pt) |
| FI (1) | FI102897B1 (pt) |
| IE (1) | IE911324A1 (pt) |
| IL (1) | IL97737A (pt) |
| MY (1) | MY111870A (pt) |
| NO (1) | NO179448C (pt) |
| NZ (1) | NZ237887A (pt) |
| PH (1) | PH30053A (pt) |
| PT (1) | PT97416B (pt) |
| SG (1) | SG68555A1 (pt) |
| WO (1) | WO1991016310A1 (pt) |
| ZA (1) | ZA912494B (pt) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5273973A (en) * | 1988-10-24 | 1993-12-28 | Norwich Eaton Pharmaceuticals, Inc. | Antimicrobial quinolonyl esters |
| EP0997466A1 (en) * | 1988-10-24 | 2000-05-03 | PROCTER & GAMBLE PHARMACEUTICALS, INC. | Novel antimicrobial lactam-quinolones |
| 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 |
| CA2001203C (en) * | 1988-10-24 | 2001-02-13 | Thomas P. Demuth, Jr. | Novel antimicrobial dithiocarbamoyl quinolones |
| US5491139A (en) * | 1988-10-24 | 1996-02-13 | The Procter & Gamble Company | Antimicrobial quinolonyl lactams |
| WO1991016327A1 (en) * | 1990-04-18 | 1991-10-31 | Norwich Eaton Pharmaceuticals, Inc. | Antimicrobial quinolonyl lactams |
| FR2675144B1 (fr) * | 1991-04-10 | 1995-06-16 | Bouchara Sa | Nouvelles quinolones difluorees - leur procede de preparation et les compositions pharmaceutiques en renfermant. |
| FR2692577B1 (fr) * | 1992-05-26 | 1996-02-02 | Bouchara Sa | Nouvelles quinolones fluorees, leur procede de preparation et les compositions pharmaceutiques en renfermant. |
| 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 |
| TW252107B (pt) * | 1993-08-27 | 1995-07-21 | Hokuriku Pharmacetical Co Ltd | |
| KR950018003A (ko) * | 1993-12-09 | 1995-07-22 | 스미스클라인 비참 피엘씨 | 신규한 퀴놀론 유도체 및 그의 제조 방법 |
| CN1159809A (zh) * | 1994-08-02 | 1997-09-17 | 普罗克特和甘保尔公司 | 喹诺酮基内酰胺抗微生物化合物和新型的中间体化合物的制备方法 |
| DE4427530A1 (de) * | 1994-08-04 | 1996-02-08 | Bayer Ag | Chinolon- und Naphthyridoncarbonsäure-Derivate |
| KR100299430B1 (ko) * | 1995-09-22 | 2001-09-06 | 기스케 와구나가, 구사이 요시히로 | 신규피리돈카르복실산유도체또는그염및이물질을유효성분으로하는항균제 |
| KR20000068711A (ko) | 1997-08-06 | 2000-11-25 | 도리이 신이치로 | Ⅳ형 포스포디에스테라제 억제제로서의 1-아릴-1,8-나프틸리딘-4-온 유도체 |
| JP4669607B2 (ja) * | 1997-09-15 | 2011-04-13 | ザ プロクター アンド ギャンブル カンパニー | 抗微生物キノロン類、その組成物およびその使用 |
| AU2002230891B2 (en) | 2000-12-14 | 2005-04-07 | The Procter & Gamble Company | Antimicrobial quinolones |
| WO2002048143A2 (en) | 2000-12-14 | 2002-06-20 | The Procter & Gamble Company | Antimicrobial 2-pyridones, their compositions and uses |
| IS7839A (is) * | 2002-11-22 | 2004-05-23 | Merck Frosst Canada Ltd. | 4-oxó-1-(3-setið fenýl-1,4-díhýdró-1,8-naftýridín-3-karboxamíð fosfódíesterasa-4 hindrar |
| BRPI0413528A (pt) * | 2003-08-12 | 2006-10-10 | Achillion Pharmaceuticals Inc | isotiazol quinolonas e compostos afins como agentes antiinfecciosos |
| DE10351448A1 (de) * | 2003-11-04 | 2005-06-09 | Bayer Healthcare Ag | Geschmackstoffhaltige Arzneimittelformulierungen mit verbesserten pharmazeutischen Eigenschaften |
| SG169238A1 (en) * | 2004-08-11 | 2011-03-30 | Williamsburg Holdings Llc | Noncardiotoxic pharmaceutical compounds |
| US20060100215A1 (en) * | 2004-11-11 | 2006-05-11 | Bradbury Barton J | 8A,9-dihydro-4aH-isothiazolo[5,4-b]quinoline-3,4-diones and related compounds as anti-infective agents |
| WO2006074317A1 (en) * | 2005-01-05 | 2006-07-13 | Achillion Pharmaceuticals, Inc. | 1-thia-2,4a-diaza-cyclopenta[b]naphthalene-3,4-diones and related compounds as anti-infective agents |
| US7199128B2 (en) | 2005-02-02 | 2007-04-03 | Achillion Pharmaceuticals, Inc. | 8-N-substituted-2H-isothiazolo[5,4-b]quinolizine-3,4-diones and related compounds as antiinfective agents |
| JP5142730B2 (ja) * | 2005-02-16 | 2013-02-13 | アキリオン ファーマシューティカルズ,インコーポレーテッド | 抗感染薬としての新規なイソチアゾロキノロンおよび関連化合物 |
| NZ566209A (en) * | 2005-07-27 | 2011-03-31 | Achillion Pharmaceuticals Inc | 8-methoxy-9H-isothiazolo[5,4-b]quinoline-3,4-diones and related compounds as anti-infective agents |
| HRP20110558T1 (hr) * | 2006-03-28 | 2011-09-30 | Warner Chilcott Company | Malatne soli i polimorfi od (3s, 5s)-7-[3-amino-5-metil-piperidinil]-1-ciklopropil-1, 4-dihidro-8-metoksi-4-okso-3-kinolinkarboksilne kiseline |
| US7456279B2 (en) * | 2006-03-28 | 2008-11-25 | The Procter & Gamble Company | Coupling process for preparing quinolone intermediates |
| MX2011010434A (es) * | 2009-04-03 | 2012-01-20 | Achillion Pharmaceuticals Inc | Hidroxitienoquinolonas y compuestos relacionados como agentes antiinfecciosos. |
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| YU33873B (en) * | 1968-08-08 | 1978-06-30 | Pliva Pharm & Chem Works | Process for the preparation of the novel 6-nalidixyl-penicillanic acid |
| JPS5219561Y2 (pt) * | 1971-03-05 | 1977-05-06 | ||
| AR204162A1 (es) * | 1972-05-08 | 1975-11-28 | Yamanouchi Pharma Co Ltd | Proceso para la preparacion de derivados de ampicilina |
| FR2191556A5 (en) * | 1972-06-29 | 1974-02-01 | Aries Robert | N-Acylampicillins - with broad-spectrum antibacterial activity prepd. by acylation with naphthyridine carboxylic acids |
| JPS4935392A (pt) * | 1972-08-02 | 1974-04-01 | ||
| JPS5023037A (pt) * | 1973-07-03 | 1975-03-12 | ||
| JPS5023036A (pt) * | 1973-07-06 | 1975-03-12 | ||
| FR2243940A1 (en) * | 1973-09-17 | 1975-04-11 | Aries Robert | Antibacterial nalidixamido cephems - prepd from 7-amino cephem (salt) and nalidixic acid deriv |
| DE2448966A1 (de) * | 1973-10-19 | 1975-04-30 | Yamanouchi Pharma Co Ltd | Penicillinderivate |
| GB1509074A (en) * | 1974-04-05 | 1978-04-26 | Yamanouchi Pharma Co Ltd | Cephalosporin derivatives |
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| JPS5573686A (en) * | 1978-11-28 | 1980-06-03 | Mitsui Toatsu Chem Inc | Novel penicillin |
| JPS5732290A (en) * | 1980-08-06 | 1982-02-20 | Fujimoto Seiyaku Kk | Novel penicillin derivative and its preparation |
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| GB8816519D0 (en) * | 1987-07-23 | 1988-08-17 | Ici Plc | Antibiotic compounds |
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| EP0341990B1 (en) * | 1988-05-10 | 1994-11-09 | Imperial Chemical Industries Plc | Cephalosporins, process for their preparation and pharmaceutical compositions |
| SG67307A1 (en) * | 1988-10-24 | 1999-09-21 | Procter & Gamble Pharma | Novel antimicrobial quinolonyl lactam esters |
| EP0997466A1 (en) * | 1988-10-24 | 2000-05-03 | PROCTER & GAMBLE PHARMACEUTICALS, INC. | Novel antimicrobial lactam-quinolones |
| US5328908A (en) * | 1988-10-24 | 1994-07-12 | Procter & Gamble Pharmaceuticals, Inc. | Antimicrobial quinolone thioureas |
| EP0366193A3 (en) * | 1988-10-24 | 1992-01-08 | Norwich Eaton Pharmaceuticals, Inc. | Novel antimicrobial quinolonyl lactams |
| CA2001203C (en) * | 1988-10-24 | 2001-02-13 | Thomas P. Demuth, Jr. | Novel antimicrobial dithiocarbamoyl quinolones |
| SG54293A1 (en) * | 1988-10-24 | 1998-11-16 | Procter & Gamble Pharma | Novel antimicrobial fluoroquinolonyl cephems |
| ZA912279B (en) * | 1990-04-09 | 1992-02-26 | Hoffmann La Roche | Carbapenem compounds |
| WO1991016327A1 (en) * | 1990-04-18 | 1991-10-31 | Norwich Eaton Pharmaceuticals, Inc. | Antimicrobial quinolonyl lactams |
| US5066800A (en) * | 1990-04-27 | 1991-11-19 | Hoffmann-La Roche Inc. | Qunoline intermediates useful therein for synthesizing antibacterial compounds |
| US5112967A (en) * | 1990-04-27 | 1992-05-12 | Hoffmann-La Roches Inc. | Process for synthesizing antibacterial cephalosporin compounds |
-
1990
- 1990-04-20 US US07/513,368 patent/US5328908A/en not_active Expired - Fee Related
-
1991
- 1991-03-31 IL IL9773791A patent/IL97737A/en not_active IP Right Cessation
- 1991-04-01 JP JP3507992A patent/JP3046068B2/ja not_active Expired - Lifetime
- 1991-04-01 KR KR1019920702587A patent/KR100256457B1/ko not_active Expired - Fee Related
- 1991-04-01 PH PH42230A patent/PH30053A/en unknown
- 1991-04-01 EP EP91908276A patent/EP0593457A1/en not_active Ceased
- 1991-04-01 SG SG1996003367A patent/SG68555A1/en unknown
- 1991-04-01 CA CA002077435A patent/CA2077435A1/en not_active Abandoned
- 1991-04-01 WO PCT/US1991/002203 patent/WO1991016310A1/en not_active Ceased
- 1991-04-01 AU AU77415/91A patent/AU659996B2/en not_active Ceased
- 1991-04-02 MY MYPI91000547A patent/MY111870A/en unknown
- 1991-04-04 ZA ZA912494A patent/ZA912494B/xx unknown
- 1991-04-14 EG EG22191A patent/EG19861A/xx active
- 1991-04-19 NZ NZ237887A patent/NZ237887A/en unknown
- 1991-04-19 IE IE132491A patent/IE911324A1/en unknown
- 1991-04-19 PT PT97416A patent/PT97416B/pt not_active IP Right Cessation
-
1992
- 1992-10-15 FI FI924672A patent/FI102897B1/fi active
- 1992-10-15 NO NO924000A patent/NO179448C/no not_active IP Right Cessation
-
1994
- 1994-04-08 US US08/225,123 patent/US5631256A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| IL97737A (en) | 1995-12-08 |
| NO179448C (no) | 1996-10-09 |
| FI924672A7 (fi) | 1992-10-15 |
| FI924672A0 (fi) | 1992-10-15 |
| SG68555A1 (en) | 1999-11-16 |
| PT97416B (pt) | 1998-08-31 |
| WO1991016310A1 (en) | 1991-10-31 |
| CA2077435A1 (en) | 1991-10-21 |
| KR930700450A (ko) | 1993-03-15 |
| US5631256A (en) | 1997-05-20 |
| NO179448B (no) | 1996-07-01 |
| NO924000L (no) | 1992-12-16 |
| EP0593457A4 (en) | 1993-01-15 |
| US5328908A (en) | 1994-07-12 |
| AU659996B2 (en) | 1995-06-08 |
| MY111870A (en) | 2001-02-28 |
| FI102897B (fi) | 1999-03-15 |
| PH30053A (en) | 1996-11-08 |
| EG19861A (en) | 1996-03-31 |
| FI102897B1 (fi) | 1999-03-15 |
| AU7741591A (en) | 1991-11-11 |
| NZ237887A (en) | 1996-10-28 |
| EP0593457A1 (en) | 1994-04-27 |
| KR100256457B1 (ko) | 2001-04-02 |
| JP3046068B2 (ja) | 2000-05-29 |
| IL97737A0 (en) | 1992-06-21 |
| ZA912494B (en) | 1992-01-29 |
| IE911324A1 (en) | 1991-10-23 |
| NO924000D0 (no) | 1992-10-15 |
| JPH05506032A (ja) | 1993-09-02 |
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Effective date: 19910912 |
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| FG3A | Patent granted, date of granting |
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| MM3A | Annulment or lapse |
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