KR880007528A - [3s(z)]-2[[[1-(2-아미노-4-티아졸릴)-2-[[2,2-디메틸-4-옥소-1-(술포옥시)-3-아제티디닐]아미노]-2-옥소에틸리덴]아미노]옥시]아세트산의 결정질 염류 - Google Patents

[3s(z)]-2[[[1-(2-아미노-4-티아졸릴)-2-[[2,2-디메틸-4-옥소-1-(술포옥시)-3-아제티디닐]아미노]-2-옥소에틸리덴]아미노]옥시]아세트산의 결정질 염류 Download PDF

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Publication number
KR880007528A
KR880007528A KR870014447A KR870014447A KR880007528A KR 880007528 A KR880007528 A KR 880007528A KR 870014447 A KR870014447 A KR 870014447A KR 870014447 A KR870014447 A KR 870014447A KR 880007528 A KR880007528 A KR 880007528A
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South Korea
Prior art keywords
amino
compound
oxoethylidene
sulfooxy
thiazolyl
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KR870014447A
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KR960007534B1 (ko
Inventor
로렌스 파커 윌리암
몰톤 코헨 에드워드
헨리 코스터 윌리암
Original Assignee
니콜라스 피.말라테스티닉
이이. 아르. 스퀴부 앤드 산즈 인코오포레이티드
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Publication of KR880007528A publication Critical patent/KR880007528A/ko
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H17/00Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
    • C07H17/04Heterocyclic radicals containing only oxygen as ring hetero atoms
    • C07H17/08Hetero rings containing eight or more ring members, e.g. erythromycins

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Communicable Diseases (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

내용 없음.

Description

[3S(Z)]-2[[[1-(2-아미노-4-티아졸릴)-2-[[2,2-디메틸-4-옥소-1-(술포옥시)-3-아제티디닐]아미노]-2-옥소에틸리덴]아미노]옥시]아세트산의 결정질 염류
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (4)

  1. 화합물 [3S(Z)]-2[[[1-(2-아미노-4-티아졸릴)-2-[[2,2-디메틸-4-옥소-1-(술포옥시)-3-아제티디닐]아미노]-2-옥소에틸리덴]아미노]옥시]아세트산의 이에리트로마이신염 및 이콜린염.
  2. 제1항에 있어서, 결정형 화합물.
  3. 화합물 [3S(Z)]-2[[[1-(2-아미노-4-티아졸릴)-2-[[2,2-디메틸-4-옥소-1-(술포옥시)-3-아제티디닐]아미노]-2-옥소에틸리덴]아미노]옥시]아세트산의 이에리트로마이신염 또는 이콜린염 유효량을 필요로 하는 포유동물에 투여하는 것으로 되는, 포유 동물의 세균 감염 치료 방법.
  4. 하기 구조식(Ⅰ)로 표시되는 화합물의 유리산(여기에서 M=H)을 용매 존재 하에 에리트로마이신 또는 콜린과 반응시켜서 일반식(Ⅰ) 화합물의 이에리트로 마이신염 또는 이콜린염을 얻는 것으로 되는, M가 에리트로마이신 또는 콜린인 하기 구조식(Ⅰ)을 갖는 화합물의 제조방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019870014447A 1986-12-19 1987-12-18 [3에스(지)]-2[[[1-(2-아미노-4-티아졸릴)-2-[[2,2-디메틸-4-옥소-1-(술포옥시)-3-아제티디닐]아미노]-2-옥소에틸리덴]아미노]옥시]아세트산의 결정질 염류 KR960007534B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US06/944,283 US4751220A (en) 1986-12-19 1986-12-19 Crystalline salts of [3S(Z)]-2[[[1-(2-amino-4-thiazolyl)-2-[[2,2-dimethyl-4-oxo-1-(sulfooxy)-3-azetidinyl]amino]-2-oxoethylidene]-amino]oxy]acetic acid
US944283 1986-12-19
US944,283 1997-10-06

Publications (2)

Publication Number Publication Date
KR880007528A true KR880007528A (ko) 1988-08-27
KR960007534B1 KR960007534B1 (ko) 1996-06-05

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019870014447A KR960007534B1 (ko) 1986-12-19 1987-12-18 [3에스(지)]-2[[[1-(2-아미노-4-티아졸릴)-2-[[2,2-디메틸-4-옥소-1-(술포옥시)-3-아제티디닐]아미노]-2-옥소에틸리덴]아미노]옥시]아세트산의 결정질 염류

Country Status (25)

Country Link
US (1) US4751220A (ko)
JP (1) JP2511083B2 (ko)
KR (1) KR960007534B1 (ko)
AU (1) AU600536B2 (ko)
BE (1) BE1000625A3 (ko)
CA (1) CA1296717C (ko)
CH (1) CH674009A5 (ko)
DE (1) DE3743111C2 (ko)
DK (1) DK671487A (ko)
ES (1) ES2007766A6 (ko)
FI (1) FI91757C (ko)
FR (1) FR2610627B1 (ko)
GB (1) GB2199033B (ko)
GR (1) GR871937B (ko)
HU (1) HU197568B (ko)
IE (1) IE61325B1 (ko)
IL (1) IL84521A (ko)
IT (1) IT1233457B (ko)
LU (1) LU87076A1 (ko)
NL (1) NL193639C (ko)
NZ (1) NZ222599A (ko)
PH (1) PH23170A (ko)
PT (1) PT86403B (ko)
SE (1) SE467782B (ko)
ZA (1) ZA879031B (ko)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5567592A (en) * 1994-02-02 1996-10-22 Regents Of The University Of California Screening method for the identification of bioenhancers through the inhibition of P-glycoprotein transport in the gut of a mammal
US7041650B2 (en) * 2001-07-09 2006-05-09 Ortho-Mcneil Pharmaceutical, Inc. Anticonvulsant derivative salts
AU2002359721A1 (en) * 2001-12-19 2003-07-09 Bristol-Myers Squibb Company Pichia pastoris formate dehydrogenase and uses therefor
CN101724000B (zh) * 2008-10-29 2012-05-30 广东东阳光药业有限公司 一种红霉素的结晶方法
CN113754651B (zh) * 2020-06-02 2023-04-18 中国医学科学院医药生物技术研究所 一种β-内酰胺化合物、其用途及其制备方法
CN115463219A (zh) * 2021-11-09 2022-12-13 中国医学科学院医药生物技术研究所 包含β-内酰胺类化合物的药物组合物及其用途

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES376380A1 (es) * 1970-01-30 1972-04-16 Roger Lab Procedimiento de obtencion de un nuevo derivado de eritro- micina.
AU8364875A (en) * 1974-08-21 1977-02-10 Hoffmann La Roche Choline and n-methyl-d-glucamine salts of amoxycillin
US4337197A (en) * 1980-10-31 1982-06-29 E. R. Squibb & Sons, Inc. O-sulfated β-lactam hydroxamic acids and intermediates
US4533660A (en) * 1980-10-31 1985-08-06 E. R. Squibb & Sons, Inc. Antibacterial O-sulfated β-lactam hydroxamic acids
US4638061A (en) * 1985-01-28 1987-01-20 E. R. Squibb & Sons, Inc. [3S(Z)]-2-[[[1-(2-amino-4-thiazolyl)-2-[[2,2-dimethyl-4-oxo-1-(sulfooxy)-3-azetidinyl]amino]-2-oxoethylidene]-amino]oxy] acetic acid and intermediate

Also Published As

Publication number Publication date
LU87076A1 (fr) 1988-07-14
FI91757C (fi) 1994-08-10
BE1000625A3 (fr) 1989-02-21
FI875159A0 (fi) 1987-11-23
IE61325B1 (en) 1994-11-02
PT86403A (en) 1988-01-01
PT86403B (pt) 1990-11-20
DE3743111A1 (de) 1988-06-30
AU8185787A (en) 1988-06-23
SE467782B (sv) 1992-09-14
HU197568B (en) 1989-04-28
HUT45998A (en) 1988-09-28
FR2610627A1 (fr) 1988-08-12
NL8703047A (nl) 1988-07-18
IT1233457B (it) 1992-04-02
IL84521A0 (en) 1988-04-29
IT8722908A0 (it) 1987-12-07
US4751220A (en) 1988-06-14
NL193639B (nl) 2000-01-03
GB8727048D0 (en) 1987-12-23
AU600536B2 (en) 1990-08-16
FI875159A (fi) 1988-06-20
KR960007534B1 (ko) 1996-06-05
SE8705068L (sv) 1988-06-20
FR2610627B1 (fr) 1989-12-01
JP2511083B2 (ja) 1996-06-26
DK671487A (da) 1988-06-20
FI91757B (fi) 1994-04-29
IE873447L (en) 1988-06-19
GR871937B (en) 1988-04-26
NL193639C (nl) 2000-05-04
PH23170A (en) 1989-05-19
ZA879031B (ko) 1988-05-27
ES2007766A6 (es) 1989-07-01
NZ222599A (en) 1989-09-27
CA1296717C (en) 1992-03-03
GB2199033B (en) 1990-10-24
CH674009A5 (ko) 1990-04-30
SE8705068D0 (sv) 1987-12-18
JPS63165381A (ja) 1988-07-08
DK671487D0 (da) 1987-12-18
IL84521A (en) 1992-02-16
GB2199033A (en) 1988-06-29
DE3743111C2 (de) 1996-04-04

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