ME02666B - Cefalosporin sa kateholskom grupom - Google Patents
Cefalosporin sa kateholskom grupomInfo
- Publication number
- ME02666B ME02666B MEP-2016-246A MEP24616A ME02666B ME 02666 B ME02666 B ME 02666B ME P24616 A MEP24616 A ME P24616A ME 02666 B ME02666 B ME 02666B
- Authority
- ME
- Montenegro
- Prior art keywords
- compound
- cephalosporin
- solvate
- ester
- pharmaceutically acceptable
- Prior art date
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
- 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
-
- 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
- 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
- C07D505/10—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 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
- C07D505/12—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 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 substituted in position 7
- C07D505/14—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 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 substituted in position 7 with hetero atoms directly attached in position 7
- C07D505/16—Nitrogen atoms
- C07D505/18—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof
- C07D505/20—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof with the acylating radicals further substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D505/24—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof with the acylating radicals further substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen further substituted by doubly-bound nitrogen atoms
-
- 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
- C07D519/06—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 containing at least one condensed beta-lactam ring system, provided for by groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00, e.g. a penem or a cepham system
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Claims (1)
- Jedinjenje formule:ili njegov estar, zaštićeno jedinjenje na amino grupi u prstenu u bočnom nizu u položaju 7, njegova farmaceutski prihvatljiva so ili solvat.Farmaceutska smeša naznačena time što sadrži jedinjenje ili njegov estar, zaštićeno jedinjenje na amino grupi u prstenu u bočnom nizu u položaju 7, njegova farmaceutski prihvatljiva so ili solvat, prema patentnom zahtevu 1.Farmaceutska smeša prema patentnom zahtevu 2, naznačena time što je za upotrebu u lečenju antimikrobne infekcije.Jedinjenje ili njegov estar, zaštićeno jedinjenje na amino grupi u prstenu u bočnom nizu u položaju 7, njegova farmaceutski prihvatljiva so ili solvat, prema patentnom zahtevu 1 , naznačeno time što je za upotrebu u lečenju zarazne bolesti.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008280828 | 2008-10-31 | ||
| EP15175084.1A EP2960244B1 (en) | 2008-10-31 | 2009-10-27 | Cephalosporin having catechol group |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ME02666B true ME02666B (me) | 2017-06-20 |
Family
ID=42128829
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2016-246A ME02666B (me) | 2008-10-31 | 2009-10-27 | Cefalosporin sa kateholskom grupom |
Country Status (38)
| Country | Link |
|---|---|
| US (1) | US9238657B2 (me) |
| EP (2) | EP2960244B1 (me) |
| JP (2) | JP5498393B2 (me) |
| KR (1) | KR101655961B1 (me) |
| CN (1) | CN102203100B (me) |
| AU (1) | AU2009310959B2 (me) |
| BR (1) | BRPI0921701B8 (me) |
| CA (1) | CA2736953C (me) |
| CL (1) | CL2011000939A1 (me) |
| CO (1) | CO6331443A2 (me) |
| CR (1) | CR20110144A (me) |
| CY (2) | CY1118536T1 (me) |
| DK (1) | DK2960244T3 (me) |
| EA (1) | EA019520B1 (me) |
| ES (2) | ES2564836T3 (me) |
| FI (1) | FIC20200039I1 (me) |
| FR (1) | FR20C1050I2 (me) |
| HR (1) | HRP20161408T1 (me) |
| HU (2) | HUE031802T2 (me) |
| IL (1) | IL211720A (me) |
| LT (2) | LT2960244T (me) |
| MA (1) | MA32731B1 (me) |
| ME (1) | ME02666B (me) |
| MX (1) | MX2011004636A (me) |
| MY (1) | MY155655A (me) |
| NL (1) | NL301067I2 (me) |
| NO (1) | NO2020035I1 (me) |
| NZ (1) | NZ591728A (me) |
| PE (1) | PE20120010A1 (me) |
| PL (1) | PL2960244T3 (me) |
| PT (1) | PT2960244T (me) |
| RS (1) | RS55365B1 (me) |
| SI (1) | SI2960244T1 (me) |
| SM (1) | SMT201600397B (me) |
| TW (1) | TWI535727B (me) |
| UA (1) | UA105190C2 (me) |
| WO (1) | WO2010050468A1 (me) |
| ZA (1) | ZA201102024B (me) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2702257C (en) | 2007-10-09 | 2016-07-12 | Sopharmia, Inc. | Broad spectrum beta-lactamase inhibitors |
| ME02666B (me) | 2008-10-31 | 2017-06-20 | Shionogi & Co | Cefalosporin sa kateholskom grupom |
| AU2011236933A1 (en) * | 2010-04-05 | 2013-05-02 | Shionogi & Co., Ltd. | Cephem compound having catechol group |
| WO2011125966A1 (ja) * | 2010-04-05 | 2011-10-13 | 塩野義製薬株式会社 | 擬似カテコール基を有するセフェム化合物 |
| US9085589B2 (en) | 2010-04-28 | 2015-07-21 | Shionogi & Co., Ltd. | Cephem derivative |
| WO2012121973A1 (en) * | 2011-03-04 | 2012-09-13 | Life Technologies Corporation | Compounds and methods for conjugation of biomolecules |
| KR101719556B1 (ko) * | 2011-03-30 | 2017-03-24 | 주식회사 레고켐 바이오사이언스 | 신규한 세파로스포린 유도체 및 이를 함유하는 의약 조성물 |
| EP2703406A4 (en) * | 2011-04-28 | 2015-08-05 | Shionogi & Co | NOVEL CEPHEM COMPOUND HAVING THE CATÉCHOL STRUCTURE OR A STRUCTURE CLOSE TO CATÉCHOL |
| US9242999B2 (en) | 2011-06-27 | 2016-01-26 | Shionogi & Co., Ltd. | Cephem compound having pyridinium group |
| TWI547496B (zh) | 2011-10-04 | 2016-09-01 | 葛蘭素集團公司 | 抗菌化合物 |
| WO2013051597A1 (ja) | 2011-10-04 | 2013-04-11 | 塩野義製薬株式会社 | カテコール基を有するセフェム誘導体 |
| UY35103A (es) * | 2012-10-29 | 2014-05-30 | Glaxo Group Ltd | Compuestos de cefem 2-sustituidos |
| RU2015120084A (ru) | 2012-10-29 | 2016-12-27 | Сионоги Энд Ко., Лтд. | Способы получения промежуточных соединений для 2-алкилцефемовых соединений |
| WO2014104148A1 (ja) * | 2012-12-26 | 2014-07-03 | 塩野義製薬株式会社 | セフェム化合物 |
| EP3043797B1 (en) | 2013-09-09 | 2020-04-08 | Merck Sharp & Dohme Corp. | Treating infections with ceftolozane/tazobactam in subjects having impaired renal function |
| UA121383C2 (uk) | 2014-03-24 | 2020-05-25 | Новартіс Аг | Органічні сполуки, що є монобактамами, для лікування бактеріальних інфекцій |
| JP6377570B2 (ja) * | 2014-04-28 | 2018-08-22 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | 2−置換セフェム化合物を含有する医薬組成物 |
| CA2950917C (en) | 2014-06-11 | 2022-08-23 | VenatoRx Pharmaceuticals, Inc. | Beta-lactamase inhibitors |
| WO2016035847A1 (ja) * | 2014-09-04 | 2016-03-10 | 塩野義製薬株式会社 | セファロスポリン誘導体の中間体およびその製造方法 |
| WO2016035846A1 (ja) * | 2014-09-04 | 2016-03-10 | 塩野義製薬株式会社 | カテコール基を有するセファロスポリン類を含有する製剤 |
| MY178017A (en) * | 2014-09-04 | 2020-09-29 | Shionogi & Co | A salt of cephalosporin derivative, its crystalline solid and a method of manufacturing thereof |
| KR20180011843A (ko) | 2015-06-11 | 2018-02-02 | 바실리어 파마슈티카 인터내셔널 리미티드 | 유출-펌프 억제제 및 이의 치료적 용도 |
| CN108137573B (zh) | 2015-09-23 | 2021-06-11 | 诺华股份有限公司 | 单环内酰胺抗生素的盐和固体形式 |
| EA039648B1 (ru) * | 2015-12-10 | 2022-02-21 | НАЕДЖА-АрДжиЭм ФАРМАСЬЮТИКАЛЗ ЮЭлСи | Соединения цефема, их получение и применение |
| ES2881776T3 (es) | 2016-03-08 | 2021-11-30 | Novartis Ag | Compuestos tricíclicos útiles para tratar las infecciones por ortomixovirus |
| US20200316083A1 (en) * | 2016-06-17 | 2020-10-08 | Wockhardt Limited | Antibacterial compositions |
| JOP20170169A1 (ar) | 2016-08-29 | 2019-01-30 | Novartis Ag | مركبات بيريدازين ثلاثية الحلقة مندمجة تفيد في علاج العدوى بفيروس أورثوميكسو |
| WO2018218154A1 (en) | 2017-05-26 | 2018-11-29 | VenatoRx Pharmaceuticals, Inc. | Penicillin-binding protein inhibitors |
| US10933051B2 (en) * | 2017-06-09 | 2021-03-02 | Fob Synthesis, Inc. | Carbapenem compounds and compositions for the treatment of bacterial infections |
| CA3063649A1 (en) | 2017-08-02 | 2019-02-07 | Novartis Ag | Chemical process for manufacturing monobactam antibiotic and intermediates thereof |
| CR20200372A (es) | 2018-02-28 | 2020-10-26 | Novartis Ag | Derivados de 10-(di(fenil)metil)-4-hidroxi8,9,9a,10-tetrahidro-7h-pirrolo (1`, 2`:4-5) pirazino (1,2-b) piridazina-3, 5-diona y compuestos relacionados como inhibidores de la replicación del ortomixo virus para el tratamiento de la influenza |
| US12173018B2 (en) | 2018-05-25 | 2024-12-24 | VenatoRx Pharmaceuticals, Inc. | Penicillin-binding protein inhibitors |
| WO2020184399A1 (ja) * | 2019-03-08 | 2020-09-17 | 塩野義製薬株式会社 | 抗菌用医薬組成物 |
| CA3147354A1 (en) | 2019-09-06 | 2021-03-11 | Rosemarie Riedl | Siderophore cephalosporin conjugates and uses thereof |
| US20230121689A1 (en) * | 2020-01-22 | 2023-04-20 | Shanghai Senhui Medicine Co., Ltd. | Cephalosporin antibacterial compound and pharmaceutical application thereof |
| TW202220663A (zh) | 2020-07-28 | 2022-06-01 | 日商鹽野義製藥股份有限公司 | 含有具有鄰苯二酚基之頭孢菌素類的凍結乾燥製劑及其製造方法 |
| WO2022152146A1 (zh) | 2021-01-12 | 2022-07-21 | 上海森辉医药有限公司 | 一种头孢类抗菌化合物及其制备方法 |
| CN113698365A (zh) * | 2021-08-30 | 2021-11-26 | 成都大学 | 一种头孢地尔侧链的制备方法 |
| TW202448477A (zh) * | 2023-06-01 | 2024-12-16 | 大陸商江蘇恆瑞醫藥股份有限公司 | 一種包含頭孢類抗菌化合物的醫藥組成物 |
| CN117024377B (zh) * | 2023-08-15 | 2025-04-29 | 济南大学 | 一种2-氯-3,4-二对甲氧苯甲氧基-n-(2-(1-吡咯烷)乙基)苯甲酰胺的制备方法 |
| CN117069638A (zh) * | 2023-08-17 | 2023-11-17 | 济南大学 | 一种头孢地尔中间体的制备方法 |
| CN117088764A (zh) * | 2023-08-24 | 2023-11-21 | 济南大学 | 一种头孢地尔关键中间体的合成和后处理方法 |
| US12225906B1 (en) | 2024-09-26 | 2025-02-18 | Terry Earl Brady | Pathogenic affinity pathway of infectious or parasitic organisms for nanogram and picogram dosimetry prophylaxis or cure |
Family Cites Families (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL47168A (en) | 1974-05-09 | 1979-07-25 | Toyama Chemical Co Ltd | Mono or dioxo piperazino(thio)carbonylamino derivatives ofpenicillins and cephalosporins and process for producing the same |
| JPS57118588A (en) | 1981-11-26 | 1982-07-23 | Toyama Chem Co Ltd | Novel cephalosporin |
| DE3207840A1 (de) | 1982-03-04 | 1983-09-15 | Hoechst Ag, 6230 Frankfurt | "cephalosporinderivate und verfahren zu ihrer herstellung" |
| AU2361184A (en) | 1983-01-21 | 1984-07-26 | Beecham Group Plc | Disubstituted 6-penicillins and 7-cephalosporins |
| NO165842C (no) | 1984-04-23 | 1991-04-17 | Takeda Chemical Industries Ltd | Analogifremgangsmaate for fremstilling av terapeutisk aktive cefem-forbindelser. |
| EP0168177A3 (en) | 1984-06-28 | 1987-04-01 | Pfizer Limited | Cephalosporin antibiotics |
| DE3688477T2 (de) | 1985-03-01 | 1993-09-16 | Takeda Chemical Industries Ltd | Antibakterielle verbindungen, ihre herstellung und verwendung. |
| JPH068300B2 (ja) * | 1985-08-02 | 1994-02-02 | 萬有製薬株式会社 | 新規セフアロスポリン誘導体 |
| EP0211656A3 (en) | 1985-08-10 | 1988-03-09 | Beecham Group Plc | Cephalosporin derivatives, process for their preparation and pharmaceutical compositions containing them |
| DE3687200T2 (de) * | 1985-09-03 | 1993-05-27 | Otsuka Kagaku Kk | Cephalosporinderivate. |
| JPH07107069B2 (ja) * | 1985-09-03 | 1995-11-15 | 大塚化学株式会社 | セフアロスポリン化合物の新規誘導体、その製造法及び該誘導体を含有する医薬組成物 |
| JPS62158291A (ja) * | 1986-01-07 | 1987-07-14 | Sagami Chem Res Center | セフアロスポリン誘導体 |
| DE3750411T2 (de) | 1986-04-14 | 1995-03-16 | Banyu Pharma Co Ltd | Cephalosporinderivate, Verfahren zu ihrer Herstellung und antibakterielle Präparate. |
| US5084453A (en) * | 1986-04-14 | 1992-01-28 | Banyu Pharmaceutical Co., Ltd. | 1-carboxy-1-vinyloxyimino aminothiazole cephalosporin derivatives |
| IE61679B1 (en) | 1987-08-10 | 1994-11-16 | Fujisawa Pharmaceutical Co | Water-soluble antibiotic composition and water-soluble salts of new cephem compounds |
| GB8719875D0 (en) | 1987-08-22 | 1987-09-30 | Beecham Group Plc | Compounds |
| JPH0228185A (ja) | 1988-04-14 | 1990-01-30 | Tanabe Seiyaku Co Ltd | セファロスポリン化合物及びその合成中間体 |
| GB8811055D0 (en) | 1988-05-10 | 1988-06-15 | Ici Plc | Antibiotic compounds |
| US5149803A (en) * | 1988-05-10 | 1992-09-22 | Imperial Chemical Industries Plc | Intermediates for cephalosporin compounds |
| US5244890A (en) | 1988-06-06 | 1993-09-14 | Fujisawa Pharmaceutical Co., Ltd. | Cephem compounds |
| PH25965A (en) | 1988-06-06 | 1992-01-13 | Fujisawa Pharmaceutical Co | New cephem compounds which have antimicrobial activities |
| GB8813945D0 (en) | 1988-06-13 | 1988-07-20 | Fujisawa Pharmaceutical Co | New cephem compounds & process for preparation thereof |
| GB8817653D0 (en) | 1988-07-25 | 1988-09-01 | Fujisawa Pharmaceutical Co | New cephem compounds & processes for preparation thereof |
| JPH02275886A (ja) | 1988-12-29 | 1990-11-09 | Tanabe Seiyaku Co Ltd | セファロスポリン化合物及びその製法 |
| CA2005787A1 (en) | 1988-12-29 | 1990-06-29 | Masao Wada | Cephalosporin compounds |
| US5143910A (en) | 1989-09-07 | 1992-09-01 | Shionogi & Co., Ltd. | Piperaziniocephalosporins |
| GB9005246D0 (en) | 1990-03-08 | 1990-05-02 | Fujisawa Pharmaceutical Co | New cephem compounds and processes for preparation thereof |
| 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 |
| US5126336A (en) * | 1990-08-23 | 1992-06-30 | Bristol-Myers Squibb Company | Antibiotic c-3 catechol-substituted cephalosporin compounds, compositions and method of use thereof |
| US5095012A (en) | 1990-08-23 | 1992-03-10 | Bristol-Myers Squibb Company | Antibiotic c-7 catechol-substituted cephalosporin compounds, compositions, and method of use thereof |
| US5194433A (en) * | 1990-11-13 | 1993-03-16 | Bristol-Myers Squibb Company | Antibiotic c-3 catechol-substituted cephalosporin compounds, compositions and method of use thereof |
| GB9111406D0 (en) | 1991-05-28 | 1991-07-17 | Fujisawa Pharmaceutical Co | New cephem compounds and processes for preparation thereof |
| GB9118672D0 (en) | 1991-08-30 | 1991-10-16 | Fujisawa Pharmaceutical Co | New cephem compounds and processes for preparation thereof |
| EP0628562A1 (fr) | 1993-06-10 | 1994-12-14 | Roussel Uclaf | Céphalosporines comportant en position 7 un radical oxymino substitué, leurs intermédiaires, leurs procédé de préparation et leur application comme médicaments |
| AU1694099A (en) | 1997-12-26 | 1999-07-19 | Cheil Jedang Corporation | Cephem derivatives and a method for producing the compounds and an antibacterialcomposition containing the compounds |
| MXPA03008639A (es) | 2001-03-27 | 2005-03-07 | Actelion Pharmaceuticals Ltd | Derivados de 1,2,3,4-tetrahidroisoquinolinas. |
| JP2003078440A (ja) | 2001-08-30 | 2003-03-14 | Kyocera Corp | 高周波スイッチ回路 |
| TW200305422A (en) | 2002-03-18 | 2003-11-01 | Shionogi & Co | Broad spectrum cefem compounds |
| US6713625B2 (en) | 2002-05-23 | 2004-03-30 | Orchid Chemicals & Pharmaceuticals Ltd. | Process for the preparation of cefditoren using the thioester of thiazolylacetic acid |
| JP4892926B2 (ja) | 2005-10-25 | 2012-03-07 | 宇部興産株式会社 | スルホン化芳香族ブロック共重合体の製造方法 |
| TW200637559A (en) | 2005-03-29 | 2006-11-01 | Shionogi & Co | 3-propenylcefem derivative |
| JP4557859B2 (ja) | 2005-09-29 | 2010-10-06 | 富士通株式会社 | 周波数分割多重送受信装置及び送受信方法 |
| WO2007096740A2 (en) | 2006-02-20 | 2007-08-30 | Orchid Research Laboratories Limited | Novel cephalosporins |
| JP2009530228A (ja) * | 2006-03-16 | 2009-08-27 | アステラス製薬株式会社 | セフェム化合物および抗菌薬としての利用 |
| ME02666B (me) | 2008-10-31 | 2017-06-20 | Shionogi & Co | Cefalosporin sa kateholskom grupom |
| WO2011125966A1 (ja) | 2010-04-05 | 2011-10-13 | 塩野義製薬株式会社 | 擬似カテコール基を有するセフェム化合物 |
| AU2011236933A1 (en) | 2010-04-05 | 2013-05-02 | Shionogi & Co., Ltd. | Cephem compound having catechol group |
| US9085589B2 (en) | 2010-04-28 | 2015-07-21 | Shionogi & Co., Ltd. | Cephem derivative |
-
2009
- 2009-10-27 ME MEP-2016-246A patent/ME02666B/me unknown
- 2009-10-27 EA EA201170632A patent/EA019520B1/ru unknown
- 2009-10-27 JP JP2010535799A patent/JP5498393B2/ja active Active
- 2009-10-27 MY MYPI2011001201A patent/MY155655A/en unknown
- 2009-10-27 PT PT151750841T patent/PT2960244T/pt unknown
- 2009-10-27 EP EP15175084.1A patent/EP2960244B1/en active Active
- 2009-10-27 PL PL15175084T patent/PL2960244T3/pl unknown
- 2009-10-27 HU HUE15175084A patent/HUE031802T2/en unknown
- 2009-10-27 SI SI200931549A patent/SI2960244T1/sl unknown
- 2009-10-27 CA CA2736953A patent/CA2736953C/en active Active
- 2009-10-27 BR BRPI0921701A patent/BRPI0921701B8/pt active IP Right Grant
- 2009-10-27 RS RS20160919A patent/RS55365B1/sr unknown
- 2009-10-27 NZ NZ591728A patent/NZ591728A/xx unknown
- 2009-10-27 DK DK15175084.1T patent/DK2960244T3/en active
- 2009-10-27 AU AU2009310959A patent/AU2009310959B2/en active Active
- 2009-10-27 MX MX2011004636A patent/MX2011004636A/es active IP Right Grant
- 2009-10-27 LT LTEP15175084.1T patent/LT2960244T/lt unknown
- 2009-10-27 CN CN200980143827.5A patent/CN102203100B/zh active Active
- 2009-10-27 UA UAA201106802A patent/UA105190C2/ru unknown
- 2009-10-27 EP EP09823578.1A patent/EP2341053B1/en active Active
- 2009-10-27 PE PE2011000941A patent/PE20120010A1/es active IP Right Grant
- 2009-10-27 WO PCT/JP2009/068400 patent/WO2010050468A1/ja not_active Ceased
- 2009-10-27 ES ES09823578.1T patent/ES2564836T3/es active Active
- 2009-10-27 ES ES15175084.1T patent/ES2602969T3/es active Active
- 2009-10-27 KR KR1020117012300A patent/KR101655961B1/ko active Active
- 2009-10-27 US US13/063,878 patent/US9238657B2/en active Active
- 2009-10-30 TW TW098136792A patent/TWI535727B/zh active
-
2011
- 2011-03-14 IL IL211720A patent/IL211720A/en active IP Right Grant
- 2011-03-17 ZA ZA2011/02024A patent/ZA201102024B/en unknown
- 2011-03-18 CR CR20110144A patent/CR20110144A/es unknown
- 2011-04-27 CL CL2011000939A patent/CL2011000939A1/es unknown
- 2011-04-29 MA MA33798A patent/MA32731B1/fr unknown
- 2011-05-02 CO CO11053320A patent/CO6331443A2/es active IP Right Grant
-
2013
- 2013-12-16 JP JP2013259499A patent/JP2014065732A/ja active Pending
-
2016
- 2016-10-27 HR HRP20161408TT patent/HRP20161408T1/hr unknown
- 2016-11-07 SM SM201600397T patent/SMT201600397B/it unknown
- 2016-11-16 CY CY20161101180T patent/CY1118536T1/el unknown
-
2020
- 2020-10-13 NL NL301067C patent/NL301067I2/nl unknown
- 2020-10-15 FR FR20C1050C patent/FR20C1050I2/fr active Active
- 2020-10-15 LT LTPA2020530C patent/LTC2960244I2/lt unknown
- 2020-10-16 CY CY2020034C patent/CY2020034I2/el unknown
- 2020-10-19 FI FIC20200039C patent/FIC20200039I1/fi unknown
- 2020-10-21 HU HUS2000042C patent/HUS2000042I1/hu unknown
- 2020-10-21 NO NO2020035C patent/NO2020035I1/no unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ME02666B (me) | Cefalosporin sa kateholskom grupom | |
| FI4219508T3 (fi) | Substituoitu polysyklinen pyridonijohdannainen ja sen aihiolääke | |
| HRP20171512T1 (hr) | Derivati betulina | |
| ME02558B (me) | Inhibitori replikacije virusa gripa | |
| HRP20151000T1 (hr) | Antivirusni spojevi | |
| HRP20171175T1 (hr) | Novi triciklički spojevi | |
| HRP20250119T1 (hr) | Kdm1a inhibitor i njegova primjena u terapiji | |
| HRP20161103T1 (hr) | Kemijski spojevi | |
| HRP20130976T1 (hr) | Karbonilaminopirolopirazoli, potentni inhibitori kinaza | |
| CL2007001427A1 (es) | Sal de maleato de 5-amino-3-(2',3'-di-o-acetil-beta-d-ribofuranosil)-3h-tiazolo[4,5-d]pirimidin-2-ona; procedimiento de preparacion; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento de una infeccion po | |
| HRP20171648T1 (hr) | Supstituirani piperidil-etil-pirimidin kao inhibitor grelin-o-acil-transferaze | |
| AR062392A1 (es) | Uso de compuestos y derivados de 2,5 dihidroxibenceno para el tratamiento de rosacea | |
| CR11208A (es) | Derivados de pirimidina utiles para el tratamiento de condiciones inflamatorias o alergicas | |
| BRPI0607545A2 (pt) | composto, uso de um composto de fórmula i ou um sal farmaceuticamente aceitável do mesmo, e, composição farmacêutica | |
| UA109421C2 (uk) | Фармацевтична композиція, яка містить ліганди сигма-рецептора | |
| EA201391325A1 (ru) | Новые производные цефалоспорина и их фармацевтические композиции | |
| EP2639229A3 (en) | Thiazole Derivative and use thereof as VAP-1 Inhibitor | |
| BR112012013252A2 (pt) | composição farmacêutica tópica, preservativo, composto, e, uso do mesmo | |
| JP2011527299A5 (me) | ||
| WO2010129057A3 (en) | Tetracycline compounds | |
| WO2008143649A3 (en) | Novel oxazolidinone compounds as antiinfective agents | |
| WO2011025982A3 (en) | Tetracycline compounds | |
| AR062390A1 (es) | Uso de derivados del 2,5-dihidroxibenceno para el tratamiento de hemangiomas o hemangioblastomas | |
| BR112015004523A2 (pt) | compostos de tetraciclina | |
| ME02405B (me) | Spojevi pirazola као inhibitori sglt1 |