[go: up one dir, main page]

AR008483A1 - Una sustancia cristalina de cefditoren pivoxil y la produccion de la misma. - Google Patents

Una sustancia cristalina de cefditoren pivoxil y la produccion de la misma.

Info

Publication number
AR008483A1
AR008483A1 ARP970104349A ARP970104349A AR008483A1 AR 008483 A1 AR008483 A1 AR 008483A1 AR P970104349 A ARP970104349 A AR P970104349A AR P970104349 A ARP970104349 A AR P970104349A AR 008483 A1 AR008483 A1 AR 008483A1
Authority
AR
Argentina
Prior art keywords
crystalline substance
cefditoren pivoxil
pivoxil
cefditoren
substance
Prior art date
Application number
ARP970104349A
Other languages
English (en)
Original Assignee
Meiji Seika Kaisha
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 Meiji Seika Kaisha filed Critical Meiji Seika Kaisha
Publication of AR008483A1 publication Critical patent/AR008483A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic 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
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic 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
    • 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

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)
  • Liquid Crystal Substances (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

Se revela una nueva sustancia cristalina de Cefditoren pivoxil, a saber, el pivaloilmetil éster del ácido 7-[(CZ)-2-(2-aminotiazol-4-ilo)-2metoxiiminoacetamido]-3-[(Z)-2-(4-metiltiazol-5-ilo)etenilo]-3-efem-4- carboxílico. Dicha sustancia cristalinade Cefditoren pivozil, de altapureza y estabilidad es de forma ortorombica y tiene un punto de fusion con descomposicion a una temperatura del rango de 206,2°C a 215,7°C como fueevaluado a partir del pico de absorcion térmica mostrand o en lacurva de flujo de calor de dicha sustancia determinada por medio de un calorímetrode escaneo diferencial, que un cristal unico de dicha sustancia cristalina tiene una densidad de 1,21 a 1,23 gm/cm3 y que contienen 4 moléculas deCe fditoren pivoxildentro de una unidad recticular del cristal unico, que dicha sustancia cristalina tiene una pureza del 97% al 98% para el componente deCefditoren pivoxil, tal como fue medido de una cromatografía líquida con la utilizacion de una fase reversade columna de gel de sílice y por medio dela deteccion de absorcion de rayos ultra-violeta, y que dicha sustancia cristalina tiene una más alta estabilidad térmica que la sustancia conocida deCefditoren pivoxil. Se describe a demás su procedimientode preparacion, que consiste esencialmente en disolver el Cefditoren pivoxil amorfo en un primersolvente orgánico anhidro, mezclar dicha solucion con un alcanol C1-C5 anhidro, concentrar a presion reducida, por deb ajo de 15°C, hastaunaconcentracion de 50 a 250 mg/ml de Cefditoren pivoxil y cristalizar completamente induciendo con agua y agitacion a temperatura igual, o pordebajo de, 10°C.
ARP970104349A 1996-09-20 1997-09-22 Una sustancia cristalina de cefditoren pivoxil y la produccion de la misma. AR008483A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24956196 1996-09-20

Publications (1)

Publication Number Publication Date
AR008483A1 true AR008483A1 (es) 2000-01-19

Family

ID=17194838

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP970104349A AR008483A1 (es) 1996-09-20 1997-09-22 Una sustancia cristalina de cefditoren pivoxil y la produccion de la misma.

Country Status (25)

Country Link
US (2) US6294669B1 (es)
EP (1) EP0937083B1 (es)
JP (1) JP3403206B2 (es)
KR (1) KR100441907B1 (es)
CN (1) CN1116299C (es)
AR (1) AR008483A1 (es)
AT (1) ATE238310T1 (es)
AU (1) AU714735B2 (es)
BR (1) BR9712072A (es)
CA (1) CA2265686C (es)
CZ (1) CZ295199B6 (es)
DE (1) DE69721290T2 (es)
EA (1) EA001526B1 (es)
ES (1) ES2198593T3 (es)
HU (1) HU224196B1 (es)
ID (1) ID22064A (es)
IL (1) IL129016A (es)
NZ (1) NZ334883A (es)
PL (1) PL189548B1 (es)
PT (1) PT937083E (es)
RO (1) RO120196B1 (es)
SK (1) SK284973B6 (es)
TR (1) TR199900614T2 (es)
UA (1) UA55426C2 (es)
WO (1) WO1998012200A1 (es)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR9712072A (pt) * 1996-09-20 1999-08-24 Meiji Seika Kaisha Subst-ncia cristalina de defditoren pivoxil e a produ-Æo da mesma
IL137004A0 (en) 1998-01-07 2001-06-14 Meiji Seika Kaisha Crystallographically stable amorphous cephalosporin compositions and process for producing the same
NZ517706A (en) * 1999-10-08 2004-01-30 Affinium Pharm Inc Fab I inhibitors
HU226640B1 (en) * 1999-10-18 2009-05-28 Egis Gyogyszergyar Nyilvanosan Process for producing amorphous atorvastatin calcium salt
JP2001131071A (ja) * 1999-10-29 2001-05-15 Meiji Seika Kaisha Ltd 非晶質および非晶質を含有する医薬組成物
DE60230934D1 (de) * 2001-04-06 2009-03-05 Affinium Pharm Inc Fab-i-inhibitoren
ATE499116T1 (de) * 2002-08-16 2011-03-15 Immunogen Inc Vernetzer mit hoher reaktivität und löslichkeit und ihre verwendung bei der herstellung von konjugaten für die gezielte abgabe von kleinmolekularen arzneimitteln
US8648065B2 (en) * 2002-10-02 2014-02-11 Meiji Seika Pharma Co., Ltd. Antibacterial medicinal composition of enhanced oral absorptivity
US7244842B2 (en) * 2002-11-15 2007-07-17 Orchid Chemicals & Pharmaceuticals Ltd. Amorphous hydrate of a cephalosporin antibiotic
ES2518316T3 (es) * 2002-12-06 2014-11-05 Debiopharm International Sa Compuestos heterocíclicos, métodos de fabricación de los mismos y su uso en terapia
ATE409485T1 (de) * 2003-03-17 2008-10-15 Affinium Pharm Inc Pharmazeutische zusammensetzungen inhibitoren von fab i und weitere antibiotika enthaltend
JP5230934B2 (ja) * 2003-03-27 2013-07-10 バジリア ファルマスーチカ アーゲー 結晶形態のセファロスポリン
US8088387B2 (en) * 2003-10-10 2012-01-03 Immunogen Inc. Method of targeting specific cell populations using cell-binding agent maytansinoid conjugates linked via a non-cleavable linker, said conjugates, and methods of making said conjugates
WO2005016936A2 (en) * 2003-08-14 2005-02-24 Ranbaxy Laboratories Limited Process for selective preparation of z-isomer of cefditoren and pharmaceutically acceptable salts and esters thereof
US20070053973A1 (en) * 2003-10-08 2007-03-08 Shigeru Chikase Amorphous antibiotic composition comprising cefditoren pivoxil
JP2007510709A (ja) * 2003-11-07 2007-04-26 ランバクシー ラボラトリーズ リミテッド 高純度3−(2−置換ビニル)セファロスポリンの製法
JP2005162696A (ja) * 2003-12-04 2005-06-23 Nichiko Pharmaceutical Co Ltd 溶出性に優れたセフジトレンピボキシル製剤
SI1828167T1 (sl) * 2004-06-04 2014-12-31 Debiopharm International Sa Forum "Apres-Demain" Akrilamidni derivati kot anitibiotična sredstva
WO2006024900A1 (en) * 2004-08-31 2006-03-09 Ranbaxy Laboratories Limited Highly pure cefditoren pivoxil
EP1973902A2 (en) * 2005-12-05 2008-10-01 Affinium Pharmaceuticals, Inc. 3-heterocyclylacrylamide compounds as fabi inhibitors and antibacterial agents
US20080069879A1 (en) * 2006-05-02 2008-03-20 Ravishekhar Bhiwgade Stable solid dosage form containing amorphous cefditoren pivoxil and process for preparation thereof
EP2687533B1 (en) 2006-07-20 2017-07-19 Debiopharm International SA Acrylamide derivatives as FAB I inhibitors
US8263613B2 (en) * 2007-02-16 2012-09-11 Affinium Pharmaceuticals, Inc. Salts, prodrugs and polymorphs of fab I inhibitors
EP2520578A1 (en) 2011-05-06 2012-11-07 Lupin Limited Process for purification of cephalosporins
CN103421025B (zh) * 2012-05-21 2016-05-11 上海医药工业研究院 制备7α-甲氧基头孢菌素C的方法
RS58898B1 (sr) 2012-06-19 2019-08-30 Debiopharm Int Sa Prolek derivati (e)-n-metil-n-((3-metilbenzofuran-2-il)metil)-3-(7-okso-5,6,7,8-tetrahidro-1,8-naftiridin-3-il)akrilamida
KR101561963B1 (ko) * 2013-05-23 2015-10-22 영진약품공업 주식회사 세프디토렌 피복실의 신규 결정 형태 및 이의 제조 방법
CN103665002B (zh) * 2013-12-18 2016-02-03 成都医路康医学技术服务有限公司 一种头孢妥仑匹酯的制备方法
WO2016114727A1 (en) 2015-01-16 2016-07-21 Öğün Yusuf Toktamiş Cefditoren pivoxil compositions with improved stability and production methods thereof
PT3419628T (pt) 2016-02-26 2021-01-05 Debiopharm Int Sa Medicamento para o tratamento de infeções do pé diabético
CA3129508A1 (en) 2019-02-14 2020-08-20 Debiopharm International S.A. Solid formulations of afabicin with histidine
CN113939306B (zh) 2019-06-14 2024-07-19 德彪药业国际股份公司 用于治疗涉及生物膜的细菌感染的药物及其用途

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE58487B1 (en) * 1984-09-07 1993-09-22 Kaisha Maiji Seika New cephalosporin compounds and the production thereof
DE69427365T2 (de) * 1993-09-29 2002-02-28 Meiji Seika Kaisha Ltd., Tokio/Tokyo Neue cephalosporinderivate
DK0658558T3 (da) * 1993-11-17 2001-04-17 Biochemie Gmbh Adskillelse af cephalosporinisomere
BR9712072A (pt) * 1996-09-20 1999-08-24 Meiji Seika Kaisha Subst-ncia cristalina de defditoren pivoxil e a produ-Æo da mesma

Also Published As

Publication number Publication date
TR199900614T2 (xx) 1999-06-21
HK1022912A1 (en) 2000-08-25
IL129016A (en) 2003-01-12
AU4222297A (en) 1998-04-14
BR9712072A (pt) 1999-08-24
ID22064A (id) 1999-08-26
EP0937083B1 (en) 2003-04-23
ATE238310T1 (de) 2003-05-15
JP2001500521A (ja) 2001-01-16
WO1998012200A1 (en) 1998-03-26
CZ295199B6 (cs) 2005-06-15
EP0937083A1 (en) 1999-08-25
CN1234036A (zh) 1999-11-03
US6294669B1 (en) 2001-09-25
AU714735B2 (en) 2000-01-13
HUP9903454A2 (hu) 2000-03-28
CN1116299C (zh) 2003-07-30
US6441162B2 (en) 2002-08-27
RO120196B1 (ro) 2005-10-28
CZ97599A3 (cs) 1999-08-11
IL129016A0 (en) 2000-02-17
HUP9903454A3 (en) 2001-04-28
EA001526B1 (ru) 2001-04-23
PL189548B1 (pl) 2005-08-31
HU224196B1 (hu) 2005-06-28
JP3403206B2 (ja) 2003-05-06
SK284973B6 (sk) 2006-03-02
SK35499A3 (en) 2000-03-13
UA55426C2 (uk) 2003-04-15
US20020002279A1 (en) 2002-01-03
DE69721290T2 (de) 2004-01-22
KR100441907B1 (ko) 2004-07-27
CA2265686A1 (en) 1998-03-26
CA2265686C (en) 2006-10-31
DE69721290D1 (de) 2003-05-28
ES2198593T3 (es) 2004-02-01
NZ334883A (en) 2000-09-29
PT937083E (pt) 2003-08-29
PL332314A1 (en) 1999-08-30
EA199900311A1 (ru) 1999-10-28
KR20000048496A (ko) 2000-07-25

Similar Documents

Publication Publication Date Title
AR008483A1 (es) Una sustancia cristalina de cefditoren pivoxil y la produccion de la misma.
Ikehara Purine 8-cyclonucleosides
ES2526671T3 (es) Compuestos de benzotriazoldiazepina inhibidores de bromodominios
ES2271280T3 (es) Anticolinergico cristalino, procedimiento para su preparacion y su uso para la produccion de un medicamento.
ES2701098T7 (es) Derivados de acilaminopirimidina para el tratamiento de infecciones víricas y otras enfermedades
AR036375A1 (es) Compuestos pirrolo [2,3-d] pirimidina -2- carbonitrilo, un proceso para su preparacion, una composicion farmaceutica y el uso de dichos compuestos para la preparacion de medicamentos
AR007960A1 (es) Nuevos derivados de imino, procedimiento para su preparacion, preparado farmaceutico que los contiene y su utilizacion
Sarkar et al. Effect of paracetamol in aqueous sodium malonate solutions with reference to volumetric and viscometric measurements
RU96121625A (ru) Стабильная кристаллическая соль тетрагидрофолиевой кислоты
ES2620660T3 (es) Método para la fabricación de naltrexona
PT94034B (pt) Processo para a preparacao de eteres (tio) morfolinilo e piperazinilo-alquilfenolico anti-rinovirais
ES2284029T3 (es) Preparacion de sales metalicas de acidos grasos de cadena media.
SE7901493L (sv) Nya amidderivat av 5-pyrimidin-karbonsyror och sett for deras framstellning och anvendning som lekemedel
ATE1101T1 (de) Anthracyclin-glycoside, verfahren zu ihrer herstellung und sie enthaltende pharmazeutische zusammensetzung.
ES2389376T3 (es) Composición farmacéutica que comprende ester de temozolomida
NO176276C (no) Flytende krystallinske trans-cykloheksankarboksylsyre-fenylpyrimidinestere med smektisk fase og anvendelse av esterne i flytende krystall-blandinger
ES2312650T3 (es) Nuevo derivado de triazolobenzazepina triciclica cristalina.
ES2553574T3 (es) Polimorfos de un principio activo farmacéutico
WO2025006693A1 (en) Cannabidiol-like compounds and methods for the selective preparation of the same
ES2267421T1 (es) Procedimiento para la preparacion de acido (6rs)-n(5)-formil-5,6,7,8-tetrahidrofolico cristalino.
Chernyak et al. Synthesis of carbohydrate-amino acid conjugates related to the capsular antigen K54 from Escherichia coli O6: K54: H10 and artificial antigens therefrom
JPH0459730A (ja) セフェム系抗生物質含有凍結乾燥製剤
JPS55151588A (en) Preparation of cephalosporin salt crystal
WO2009031202A1 (ja) 桂皮酸誘導体及びその紫外線吸収剤としての利用
Hedgley et al. Behavior of Esters in Liquid Hydrogen Fluoride. Some Glycitol Esters

Legal Events

Date Code Title Description
FG Grant, registration