MA32731B1 - Céphalosporine possédant un groupe catéchol - Google Patents
Céphalosporine possédant un groupe catécholInfo
- Publication number
- MA32731B1 MA32731B1 MA33798A MA33798A MA32731B1 MA 32731 B1 MA32731 B1 MA 32731B1 MA 33798 A MA33798 A MA 33798A MA 33798 A MA33798 A MA 33798A MA 32731 B1 MA32731 B1 MA 32731B1
- Authority
- MA
- Morocco
- Prior art keywords
- similar
- cepham compound
- protected
- ester
- substituted
- Prior art date
Links
Classifications
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- 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
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- 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
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- 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)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (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)
Abstract
L'INVENTION PORTE SUR UN COMPOSÉ DE CÉPHÈME REPRÉSENTÉ PAR LA FORMULE (I) [DANS LAQUELLE X REPRÉSENTE N, CH OU C-CL ; T REPRÉSENTE S OU SIMILAIRE ; A ET G REPRÉSENTENT INDÉPENDAMMENT UN ALKYLÈNE INFÉRIEUR OU SIMILAIRE ; B REPRÉSENTE UNE SIMPLE LIAISON OU SIMILAIRE ; D REPRÉSENTE UNE SIMPLE LIAISON, -NR7-CO-, -CO-NR7-, 'NR7-CO-NR7- OU SIMILAIRE ; E REPRÉSENTE UN ALKYLÈNE INFÉRIEUR QUI PEUT ÊTRE SUBSTITUÉ ; F REPRÉSENTE UNE SIMPLE LIAISON OU UN PHÉNYLÈNE QUI PEUT ÊTRE SUBSTITUÉ ; R3, R4, R5 ET R6 REPRÉSENTENT CHACUN INDÉPENDAMMENT UN HYDROGÈNE, UN HALOGÈNE, UN NITRILE OU 'OR8 ; R8 REPRÉSENTE UN HYDROGÈNE OU SIMILAIRE ; ET UN GROUPE REPRÉSENTÉ PAR LA FORMULE (II) REPRÉSENTE UN GROUPE AMMONIUM QUATERNAIRE MONOCYCLIQUE OU À CYCLES CONDENSÉS SATURÉ OU INSATURÉ QUI POSSÈDE AU MOINS UN ATOME N ET QUI PEUT ÊTRE SUBSTITUÉ, LA LIGNE TIRETÉE REPRÉSENTANT UNE LIAISON DANS LE CYCLE], UN ESTER DU COMPOSÉ DE CÉPHÈME, UN PRODUIT PROTÉGÉ DU COMPOSÉ DE CÉPHÈME DANS LEQUEL UN GROUPE AMINO, SITUÉ SUR LE NOYAU DANS LA CHAÎNE DU CÔTÉ DE LA POSITION 7, EST PROTÉGÉ, UN SEL PHARMACEUTIQUEMENT ACCEPTABLE DU COMPOSÉ DE CÉPHÈME, DE L'ESTER OU DU PRODUIT PROTÉGÉ, OU UN SOLVATE DU COMPOSÉ DE CÉPHÈME, DE L'ESTER, DU PRODUIT PROTÉGÉ OU DU SEL PHARMACEUTIQUEMENT ACCEPTABLE, QUI PRÉSENTE UN LARGE SPECTRE ANTIBACTÉRIEN ET EN PARTICULIER QUI PRÉSENTE UNE ACTIVITÉ ANTIBACTÉRIENNE PUISSANTE VIS-À-VIS DE BACTÉRIES À GRAM NÉGATIF PRODUISANT DE LA ß-LACTAMASE. L'INVENTION PORTE ÉGALEMENT SUR UNE COMPOSITION PHARMACEUTIQUE RENFERMANT LE COMPOSÉ DE CÉPHÈME, L'ESTER, LE PRODUIT PROTÉGÉ, LE SEL PHARMACEUTIQUEMENT ACCEPTABLE OU LE SOLVATE.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008280828 | 2008-10-31 | ||
| PCT/JP2009/068400 WO2010050468A1 (fr) | 2008-10-31 | 2009-10-27 | Céphalosporine possédant un groupe catéchol |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA32731B1 true MA32731B1 (fr) | 2011-10-02 |
Family
ID=42128829
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA33798A MA32731B1 (fr) | 2008-10-31 | 2011-04-29 | Céphalosporine possédant un groupe catéchol |
Country Status (38)
| Country | Link |
|---|---|
| US (1) | US9238657B2 (fr) |
| EP (2) | EP2341053B1 (fr) |
| JP (2) | JP5498393B2 (fr) |
| KR (1) | KR101655961B1 (fr) |
| CN (1) | CN102203100B (fr) |
| AU (1) | AU2009310959B2 (fr) |
| BR (1) | BRPI0921701B8 (fr) |
| CA (1) | CA2736953C (fr) |
| CL (1) | CL2011000939A1 (fr) |
| CO (1) | CO6331443A2 (fr) |
| CR (1) | CR20110144A (fr) |
| CY (2) | CY1118536T1 (fr) |
| DK (1) | DK2960244T3 (fr) |
| EA (1) | EA019520B1 (fr) |
| ES (2) | ES2564836T3 (fr) |
| FI (1) | FIC20200039I1 (fr) |
| FR (1) | FR20C1050I2 (fr) |
| HR (1) | HRP20161408T1 (fr) |
| HU (2) | HUE031802T2 (fr) |
| IL (1) | IL211720A (fr) |
| LT (2) | LT2960244T (fr) |
| MA (1) | MA32731B1 (fr) |
| ME (1) | ME02666B (fr) |
| MX (1) | MX2011004636A (fr) |
| MY (1) | MY155655A (fr) |
| NL (1) | NL301067I2 (fr) |
| NO (1) | NO2020035I1 (fr) |
| NZ (1) | NZ591728A (fr) |
| PE (1) | PE20120010A1 (fr) |
| PL (1) | PL2960244T3 (fr) |
| PT (1) | PT2960244T (fr) |
| RS (1) | RS55365B1 (fr) |
| SI (1) | SI2960244T1 (fr) |
| SM (1) | SMT201600397B (fr) |
| TW (1) | TWI535727B (fr) |
| UA (1) | UA105190C2 (fr) |
| WO (1) | WO2010050468A1 (fr) |
| ZA (1) | ZA201102024B (fr) |
Families Citing this family (43)
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|---|---|---|---|---|
| US8883772B2 (en) | 2007-10-09 | 2014-11-11 | Sopharmia, Inc. | Broad spectrum beta-lactamase inhibitors |
| BRPI0921701B8 (pt) * | 2008-10-31 | 2022-11-29 | Shionogi & Co | Cefarosporina tendo um grupo catecol, seu uso e composição farmacêutica que a compreende |
| US8883773B2 (en) | 2010-04-05 | 2014-11-11 | Shionogi & Co., Ltd. | Cephem compound having pseudo-catechol group |
| AU2011236933A1 (en) * | 2010-04-05 | 2013-05-02 | Shionogi & Co., Ltd. | Cephem compound having catechol group |
| JP5852562B2 (ja) * | 2010-04-28 | 2016-02-03 | 塩野義製薬株式会社 | 新規なセフェム誘導体 |
| EP2966061B1 (fr) | 2011-03-04 | 2017-05-03 | Life Technologies Corporation | Composés et procédés de conjugaison de biomolécules |
| KR101719556B1 (ko) * | 2011-03-30 | 2017-03-24 | 주식회사 레고켐 바이오사이언스 | 신규한 세파로스포린 유도체 및 이를 함유하는 의약 조성물 |
| CA2833121A1 (fr) | 2011-04-28 | 2012-11-01 | Shionogi & Co., Ltd. | Nouveau compose de cepheme ayant la structure du catechol ou une structure proche du catechol |
| 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 (fr) | 2011-10-04 | 2013-04-11 | 塩野義製薬株式会社 | Dérivé céphem ayant un groupe catéchol |
| UY35103A (es) * | 2012-10-29 | 2014-05-30 | Glaxo Group Ltd | Compuestos de cefem 2-sustituidos |
| CN104854113A (zh) | 2012-10-29 | 2015-08-19 | 盐野义制药株式会社 | 2-烷基头孢烯化合物的中间体的生产方法 |
| WO2014104148A1 (fr) * | 2012-12-26 | 2014-07-03 | 塩野義製薬株式会社 | Composé de céphem |
| ES2800603T3 (es) | 2013-09-09 | 2021-01-04 | Merck Sharp & Dohme | Tratamiento de infecciones con ceftolozano/tazobactam en sujetos con insuficiencia renal |
| WO2015148379A1 (fr) | 2014-03-24 | 2015-10-01 | Novartis Ag | Composés organiques monobactam pour le traitement d'infections bactériennes |
| 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 |
| RU2686740C2 (ru) | 2014-06-11 | 2019-04-30 | Венаторкс Фармасьютикалс, Инк. | Ингибиторы бета-лактамазы |
| PT3190115T (pt) | 2014-09-04 | 2021-10-19 | Shionogi & Co | Sal de derivado de cefalosporina, forma sólida cristalina do mesmo e método para produzir o mesmo |
| CN106661052B (zh) * | 2014-09-04 | 2021-05-11 | 盐野义制药株式会社 | 头孢菌素衍生物的中间体及其制造方法 |
| US9949982B2 (en) | 2014-09-04 | 2018-04-24 | Shionogi & Co., Ltd. | Preparation containing cephalosporin having a catechol moiety |
| JP2018521021A (ja) | 2015-06-11 | 2018-08-02 | バジリア・ファルマスーチカ・インターナショナル・アーゲーBasilea Pharmaceutica International Ag | 排出ポンプ阻害剤及びその治療的使用 |
| EA202092620A1 (ru) | 2015-09-23 | 2021-06-30 | Новартис Аг | Соли и твердые формы монобактамного антибиотика |
| US9751894B2 (en) * | 2015-12-10 | 2017-09-05 | Naeja-Rgm Pharmaceuticals Inc. | Cephem compounds, their production and use |
| ES2881776T3 (es) | 2016-03-08 | 2021-11-30 | Novartis Ag | Compuestos tricíclicos útiles para tratar las infecciones por ortomixovirus |
| EP3471724A1 (fr) * | 2016-06-17 | 2019-04-24 | Wockhardt Limited | Compositions anti-bactériennes |
| JOP20170169A1 (ar) | 2016-08-29 | 2019-01-30 | Novartis Ag | مركبات بيريدازين ثلاثية الحلقة مندمجة تفيد في علاج العدوى بفيروس أورثوميكسو |
| US11267826B2 (en) | 2017-05-26 | 2022-03-08 | VenatoRx Pharmaceuticals, Inc. | Penicillin-binding protein inhibitors |
| EP3634471A4 (fr) * | 2017-06-09 | 2021-02-24 | FOB Synthesis, Inc. | Composés de carbapenem et compositions pour le traitement d'infections bactériennes |
| AU2018311521B2 (en) | 2017-08-02 | 2022-03-03 | Novartis Ag | Process for preparing 1 -(((Z)-(1 -(2-aminothiazol-4-yl)-2-oxo-2-(((3S,4R)-2-oxo-4-((2-oxooxazolidin-3-y l)methyl)-1 -sulfoazetidin-3- yl)amino)ethylidene)amino)oxy)cyclopropane carboxylic acid |
| IL276901B2 (en) | 2018-02-28 | 2024-03-01 | Novartis Ag | 10-(di(phenyl)methyl)-4-hydroxy-8,9,9a,10-tetrahydro-7h-pyrrolo[1 ',2':4,5]pyrazino[1,2-b]pyridazine-3,5-dione derivatives and related compounds as inhibitors of the orthomyxovirus replication for treating influenza |
| US12173018B2 (en) | 2018-05-25 | 2024-12-24 | VenatoRx Pharmaceuticals, Inc. | Penicillin-binding protein inhibitors |
| WO2020184399A1 (fr) * | 2019-03-08 | 2020-09-17 | 塩野義製薬株式会社 | Composition pharmaceutique antibactérienne |
| US12371441B2 (en) | 2019-09-06 | 2025-07-29 | Ariva Med Gmbh | Siderophore cephalosporin conjugates and uses thereof |
| EP4095141A4 (fr) * | 2020-01-22 | 2023-06-28 | Shanghai Senhui Medicine Co., Ltd. | Composé céphalosporine antibactérien et son application pharmaceutique |
| 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 |
| CN116528874A (zh) * | 2021-01-12 | 2023-08-01 | 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 |
| WO2024245383A1 (fr) * | 2023-06-01 | 2024-12-05 | 江苏恒瑞医药股份有限公司 | Composition pharmaceutique comprenant un composé antibactérien céphalosporine |
| 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 |
| CN117088764B (zh) * | 2023-08-24 | 2026-01-30 | 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 |
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