FI803200L - Cefalosporinsolvat - Google Patents

Cefalosporinsolvat

Info

Publication number
FI803200L
FI803200L FI803200A FI803200A FI803200L FI 803200 L FI803200 L FI 803200L FI 803200 A FI803200 A FI 803200A FI 803200 A FI803200 A FI 803200A FI 803200 L FI803200 L FI 803200L
Authority
FI
Finland
Prior art keywords
cefalosporinsolvat
Prior art date
Application number
FI803200A
Other languages
English (en)
Finnish (fi)
Inventor
Billy Grinnell Jackson
Donna Nezich Gardner
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of FI803200L publication Critical patent/FI803200L/fi

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
    • C07D501/02Preparation
    • C07D501/12Separation; Purification
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/545Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
    • 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
    • C07D501/26Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
    • C07D501/34Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by carboxylic acids containing hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
FI803200A 1979-10-09 1980-10-09 Cefalosporinsolvat FI803200L (fi)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/082,822 US4252951A (en) 1979-10-09 1979-10-09 Isolation of syn-7-(2-amino-4-thiazolyl)-(methoxyimino)acetamido-3-acetoxymethyl-3-cephem-4-carboxylic acid

Publications (1)

Publication Number Publication Date
FI803200L true FI803200L (fi) 1981-04-10

Family

ID=22173679

Family Applications (1)

Application Number Title Priority Date Filing Date
FI803200A FI803200L (fi) 1979-10-09 1980-10-09 Cefalosporinsolvat

Country Status (27)

Country Link
US (1) US4252951A (fr)
EP (1) EP0027050B1 (fr)
JP (1) JPS5661388A (fr)
KR (1) KR840000866B1 (fr)
AT (1) AT369008B (fr)
AU (1) AU6306180A (fr)
BE (1) BE885569A (fr)
CA (1) CA1146539A (fr)
CH (1) CH647523A5 (fr)
CS (1) CS215142B2 (fr)
DD (1) DD153375A5 (fr)
DE (1) DE3065181D1 (fr)
DK (1) DK424680A (fr)
ES (1) ES8201166A1 (fr)
FI (1) FI803200L (fr)
FR (1) FR2467211A1 (fr)
GB (1) GB2059966B (fr)
GR (1) GR70219B (fr)
HU (1) HU183230B (fr)
IE (1) IE50390B1 (fr)
IL (1) IL61227A (fr)
IT (1) IT1132926B (fr)
PH (1) PH15023A (fr)
PT (1) PT71886B (fr)
RO (1) RO80664B (fr)
YU (1) YU256480A (fr)
ZA (1) ZA806192B (fr)

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JPS588086A (ja) * 1981-07-07 1983-01-18 Takeda Chem Ind Ltd セフアロスポリン溶媒和物およびその製造法
JPH07116200B2 (ja) * 1985-09-20 1995-12-13 富山化学工業株式会社 セファロスポリンの製造方法
JPH08831B2 (ja) * 1985-09-20 1996-01-10 富山化学工業株式会社 セファロスポリンの精製法
CZ20013607A3 (cs) * 1999-04-06 2002-06-12 Sepracor Inc. Farmaceutický prostředek
EP1219607B1 (fr) * 1999-09-02 2011-04-06 Shionogi & Co., Ltd. Inhibiteur d'integrase contenant des derives heterocycliques aromatiques
CA2284459C (fr) 1999-10-04 2012-12-11 Neokimia Inc. Synthese combinatoire de bibliotheques de composes macrocycliques utiles pour la decouverte de medicaments
EP1246792B1 (fr) * 2000-01-13 2014-08-13 Emisphere Technologies, Inc. Composes et compositions permettant d'administrer des principes actifs
KR100902171B1 (ko) * 2001-03-08 2009-06-10 더 트러스티스 오브 더 유니버시티 오브 펜실베니아 항-감염제로서의 표면적 친양쪽성 중합체
EP1435972B1 (fr) * 2001-08-29 2016-03-09 Seneb Biosciences Inc. Nouveaux dérivés synthétiques de ganglioside et compositions contenant ceux-ci
JP4571497B2 (ja) * 2002-09-19 2010-10-27 杏林製薬株式会社 アミノアルコール誘導体とその付加塩及び免疫抑制剤
US7056916B2 (en) * 2002-11-15 2006-06-06 Boehringer Ingelheim Pharma Gmbh & Co. Kg Medicaments for the treatment of chronic obstructive pulmonary disease
EP1608313A4 (fr) * 2003-03-17 2009-05-06 Univ Pennsylvania Polymeres et oligomeres a surface amphiphile et leurs utilisations
US7321065B2 (en) * 2003-04-18 2008-01-22 The Regents Of The University Of California Thyronamine derivatives and analogs and methods of use thereof
US20050203184A1 (en) 2003-09-10 2005-09-15 Petasis Nicos A. Benzo lipoxin analogues
EP1711455A4 (fr) 2004-01-23 2007-11-07 Univ Pennsylvania Polymeres et oligomeres de polyaryle et de polyarylalkynyle amphiphiles au niveau facial
EP1742904B1 (fr) * 2004-05-06 2012-10-31 The Regents of The University of California Enaminones substitues, leurs derives et leur utilisation
US20050255050A1 (en) * 2004-05-14 2005-11-17 Boehringer Ingelheim International Gmbh Powder formulations for inhalation, comprising enantiomerically pure beta agonists
US7220742B2 (en) * 2004-05-14 2007-05-22 Boehringer Ingelheim International Gmbh Enantiomerically pure beta agonists, process for the manufacture thereof and use thereof as medicaments
TWI403334B (zh) * 2004-12-23 2013-08-01 Merck Sharp & Dohme 包含生物素殘基之抗血栓雙重抑制劑
CA2599205A1 (fr) * 2005-02-25 2006-09-08 The Trustees Of The University Of Pennsylvania Polymeres et oligomeres a faces amphiphiles, composition a base de ceux-ci et, leur utilisation dans des procedes de traitement du cancer
EP2418191A1 (fr) * 2005-02-28 2012-02-15 Meiji Co., Ltd. Dérivés à longue chaîne de triméthoxyphénylalcanols et produits pharmaceutiques les comprenant
RU2008108632A (ru) * 2005-08-10 2009-09-20 Джонс Хопкинс Юниверсити (Us) Полиамины, используемые при противопаразитарных и противораковых терапиях и в качестве ингибиторов лизин-специфической деметилазы
CA2619402C (fr) * 2005-08-15 2015-02-03 Boehringer Ingelheim International Gmbh Procede de production de betamimetiques
WO2007053343A2 (fr) * 2005-10-28 2007-05-10 Irm Llc Composes et compositions utilises comme inhibiteurs des kinases des proteines
WO2007063286A2 (fr) * 2005-11-29 2007-06-07 Hammersmith Imanet Limited Composes d'imagerie in vivo
ES2288107B1 (es) * 2006-01-27 2008-11-01 Fundacion Imabis Instituto Mediterraneo Para El Avance De La Biotecnologia Y La Investigacion Sanita Derivados aciclicos saturados e insaturados de cadena larga de sulfamidas como activadores especificos de receptores ppar-alfa.
FR2902999B1 (fr) * 2006-07-03 2012-09-28 Oreal Utilisation de derives c-glycoside a titre d'actif prodesquamant
FR2903004B1 (fr) * 2006-07-03 2009-07-10 Oreal Utilisation en cosmetique d'un derive c-glycoside en association avec de l'acide ascorbique
US20090075935A1 (en) * 2006-07-03 2009-03-19 L'oreal Composition comprising at least one c-glycoside derivative and at least one hyaluronic acid and its cosmetic use
FR2902996B1 (fr) * 2006-07-03 2008-09-26 Oreal Compositions cosmetiques associant un derive c-glycoside et un derive n-acylaminoamide
NZ577460A (en) * 2006-12-14 2012-01-12 Teva Pharma Crystalline solid rasagiline base
WO2008138200A1 (fr) * 2007-05-11 2008-11-20 Hong Kong University Of Science & Technology Antagonistes des récepteurs de nmda et de mc présentant une activité de neuroprotection et d'amélioration de la mémoire
US7696383B2 (en) * 2007-06-26 2010-04-13 Solvay Pharmaceuticals B.V. N-oxides of venlafaxine and o-desmethylvenlafaxine as prodrugs
FR2920000B1 (fr) * 2007-08-13 2010-01-29 Oreal Composition cosmetique ou pharmaceutique contenant de l'acide hyaluronique, et procede cosmetique pour diminuer les signes du vieilissement
KR101618068B1 (ko) * 2007-10-19 2016-05-04 얀센 파마슈티카 엔.브이. γ-세크레타아제의 탄소 결합된 조절제
EP2212277B1 (fr) * 2007-10-19 2016-08-31 Janssen Pharmaceutica, N.V. Modulateurs de la g-secrétase liés à une amine
EP2212287B1 (fr) * 2007-10-19 2012-02-01 Janssen Pharmaceutica, N.V. MODULATEUR DE PIPÉRIDINYL ET DE PIPÉRAZINYL DE LA y-SECRÉTASE
EP2093207A1 (fr) * 2008-02-06 2009-08-26 Julius-Maximilians-Universität Würzburg Composés anti-infectieux et anti-tumoraux isolés de lianes tropicales
US8063249B1 (en) * 2008-04-25 2011-11-22 Olema Pharmaceuticals, Inc. Substituted triphenyl butenes
US20100056475A1 (en) * 2008-08-06 2010-03-04 Alexander Chucholowski Cyclodextrin conjugates
EA201100654A1 (ru) * 2008-10-22 2012-01-30 Акусела, Инк. Соединения для лечения офтальмологических заболеваний и расстройств
FR2940610B1 (fr) * 2008-12-30 2011-05-06 Oreal Association de monosaccharides avec des derives c-glycosides et son utilisation en cosmetique
US20120035120A1 (en) 2009-03-25 2012-02-09 Seneb Biosciences, Inc. Glycolipids as treatment for disease
RU2562245C2 (ru) 2009-05-14 2015-09-10 Милленниум Фармасьютикалз, Инк. ГИДРОХЛОРИД (1S,2S,4R)-4-{ 4-[(1S)-2,3-ДИГИДРО-1Н-ИНДЕН-1-ИЛАМИНО]-7Н-ПИРРОЛО [2,3-d]ПИРИМИДИН-7-ИЛ} -2-ГИДРОКСИЦИКЛОПЕНТИЛ)МЕТИЛ СУЛЬФАМАТА
US8962639B2 (en) * 2009-05-29 2015-02-24 Abbvie Inc. Potassium channel modulators
US8288592B2 (en) * 2009-09-22 2012-10-16 Actavis Group Ptc Ehf Solid state forms of tapentadol salts
US8609674B2 (en) 2010-11-16 2013-12-17 Abbvie Inc. Potassium channel modulators
EA029151B1 (ru) * 2011-09-06 2018-02-28 Курна, Инк. ЛЕЧЕНИЕ ЗАБОЛЕВАНИЙ, СВЯЗАННЫХ С АЛЬФА-СУБЪЕДИНИЦАМИ ПОТЕНЦИАЛЗАВИСИМЫХ НАТРИЕВЫХ КАНАЛОВ (SCNxA), С ПОМОЩЬЮ МАЛЫХ МОЛЕКУЛ
US8377946B1 (en) * 2011-12-30 2013-02-19 Pharmacyclics, Inc. Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3925372A (en) * 1973-02-23 1975-12-09 Lilly Co Eli Alpha-aminoacyl-3-halo cephalosporins
DK154939C (da) * 1974-12-19 1989-06-12 Takeda Chemical Industries Ltd Analogifremgangsmaade til fremstilling af thiazolylacetamido-cephemforbindelser eller farmaceutisk acceptable salte eller estere deraf
DE2760123C2 (de) * 1976-01-23 1986-04-30 Roussel-Uclaf, Paris 7-Aminothiazolyl-syn-oxyiminoacetamidocephalosporansäuren, ihre Herstellung und sie enthaltende pharmazeutische Zusammensetzungen
US4166115A (en) * 1976-04-12 1979-08-28 Fujisawa Pharmaceutical Co., Ltd. Syn 7-oxoimino substituted derivatives of cephalosporanic acid

Also Published As

Publication number Publication date
YU256480A (en) 1983-02-28
RO80664B (ro) 1983-02-28
HU183230B (en) 1984-04-28
EP0027050B1 (fr) 1983-10-05
IE50390B1 (en) 1986-04-16
DD153375A5 (de) 1982-01-06
BE885569A (fr) 1981-04-08
CS215142B2 (en) 1982-07-30
FR2467211B1 (fr) 1983-06-10
IT1132926B (it) 1986-07-09
DK424680A (da) 1981-04-10
DE3065181D1 (en) 1983-11-10
ES495753A0 (es) 1981-12-01
ES8201166A1 (es) 1981-12-01
GR70219B (fr) 1982-08-31
IE802086L (en) 1981-04-09
PH15023A (en) 1982-05-13
GB2059966A (en) 1981-04-29
KR840000866B1 (ko) 1984-06-20
CA1146539A (fr) 1983-05-17
RO80664A (fr) 1983-02-15
ATA498080A (de) 1982-04-15
AU6306180A (en) 1981-04-16
US4252951A (en) 1981-02-24
IL61227A0 (en) 1980-12-31
PT71886A (en) 1980-11-01
CH647523A5 (fr) 1985-01-31
PT71886B (en) 1981-08-13
FR2467211A1 (fr) 1981-04-17
IT8025200A0 (it) 1980-10-08
JPS5661388A (en) 1981-05-26
KR830004314A (ko) 1983-07-09
EP0027050A1 (fr) 1981-04-15
AT369008B (de) 1982-11-25
GB2059966B (en) 1983-09-01
IL61227A (en) 1983-07-31
ZA806192B (en) 1982-05-26

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Legal Events

Date Code Title Description
FD Application lapsed

Owner name: ELI LILLY AND COMPANY