KR890016180A - 사키오미신 e 및 이의 유도체, 이의 제조방법 및 용도 - Google Patents

사키오미신 e 및 이의 유도체, 이의 제조방법 및 용도 Download PDF

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KR890016180A
KR890016180A KR1019890004410A KR890004410A KR890016180A KR 890016180 A KR890016180 A KR 890016180A KR 1019890004410 A KR1019890004410 A KR 1019890004410A KR 890004410 A KR890004410 A KR 890004410A KR 890016180 A KR890016180 A KR 890016180A
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compound
carried out
culturing
hydrogen
sakiomicin
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KR1019890004410A
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페터 크래머 한스
로벨 루쯔
미카엘 쉬베넨 루드거
Original Assignee
필립스타인, 헤리베르트 부그
베링베르케 아크티엔게젤샤프트
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Publication of KR890016180A publication Critical patent/KR890016180A/ko

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/10—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00—Preparation of compounds containing saccharide radicals
    • C12P19/02—Monosaccharides
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20—Bacteria; Culture media therefor
    • C12N1/205—Bacterial isolates
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02—Oxygen as only ring hetero atoms
    • C12P17/06—Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
    • C12R2001/00—Microorganisms ; Processes using microorganisms
    • C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
    • C12R2001/03—Actinomadura

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Tropical Medicine & Parasitology (AREA)
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  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Communicable Diseases (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
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Abstract

내용 없음

Description

사키오미신 E 및 이의 유도체, 이의 제조방법 및 용도
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제 1 도는 사키오미신 E의 IR스펙드럼(KBr디스크)을 도시한 것이다. 제 2 도는 메탄올중 사키오미신 E의 UV스펙트럼을 도시한 것이다. 제 3 도는 사키오미신 E의1H NMR스펙트럼(200MHz, CDC13)을 도시한 것이다.

Claims (10)

  1. 일반식(I)의 화합물.
    상기식에서, R1내지 R2는 서로 독립적으로 수소 또는 (C1-C18)-아실 그룹이다.
  2. 제 1 항에 있어서, R1내지 R3가 서로 독립적으로 수소 또는 아세틸이고 최소한 하나의 R이 아세틸인 화합물.
  3. a) 악티노마두라(Actinomadura) 종 DSM 4249를 배양하고, b)R1내지 R2가 수소인 일반식(I)의 화합물을 분리하고, 경우에 따라, c) 이 화합물 아실화함을 특징으로 하는, 제 1 항에 청구한 일반식(I) 화합물을 제조하는 방법.
  4. 제 3 항에 있어서, 배양을 2%글루코즈, 1%대두펩톤, 0.2%탄산칼슘 및 0.0001%염화코발트를 함유하는 영양용액에서 수행하는 방법.
  5. 제 3 항에 있어서, 배양을 15 내지 38℃의 온도 범위에서 수행하는 방법.
  6. 제 3 항에 있어서, 배양을 25 내지 30℃의 온도범위에서 수행하는 방법.
  7. 제 3 항에 있어서, 배양을 40 내지 80시간 동안 수행하는 방법.
  8. 제 3 항에 있어서, 배양을 65 내지 70시간 동안 수행하는 방법.
  9. 의약제로서의 제 1 항에서 청구한 화합물.
  10. 악티노마두라(Actinomadura) 종 DSM 4249.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890004410A 1988-04-06 1989-04-04 사키오미신 e 및 이의 유도체, 이의 제조방법 및 용도 KR890016180A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP3811463.1 1988-04-06
DE3811463A DE3811463A1 (de) 1988-04-06 1988-04-06 Sakyomicin e und dessen derivate, verfahren zu ihrer herstellung und ihre verwendung

Publications (1)

Publication Number Publication Date
KR890016180A true KR890016180A (ko) 1989-11-28

Family

ID=6351440

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019890004410A KR890016180A (ko) 1988-04-06 1989-04-04 사키오미신 e 및 이의 유도체, 이의 제조방법 및 용도

Country Status (9)

Country Link
US (1) US4975531A (ko)
EP (1) EP0336349A3 (ko)
JP (1) JPH01291788A (ko)
KR (1) KR890016180A (ko)
AU (1) AU616132B2 (ko)
DE (1) DE3811463A1 (ko)
DK (1) DK163589A (ko)
FI (1) FI891603A (ko)
PT (1) PT90202A (ko)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61167679A (ja) * 1985-01-22 1986-07-29 Kirin Brewery Co Ltd 新規物質ａ３２
DE3629274A1 (de) * 1986-08-28 1988-03-10 Hoechst Ag Urdamycin g und dessen derivate, verfahren zu ihrer herstellung und ihre verwendung
EP0300474A3 (en) * 1987-07-23 1991-09-04 Takeda Chemical Industries, Ltd. Seikosaponin derivatives, their production and use
US4847245A (en) * 1988-04-18 1989-07-11 Pfizer Inc. N-demethylefrotomycin

Also Published As

Publication number Publication date
US4975531A (en) 1990-12-04
JPH01291788A (ja) 1989-11-24
EP0336349A2 (de) 1989-10-11
DK163589D0 (da) 1989-04-05
FI891603A0 (fi) 1989-04-04
EP0336349A3 (de) 1990-03-21
DK163589A (da) 1989-10-07
DE3811463A1 (de) 1989-10-19
FI891603A (fi) 1989-10-07
PT90202A (pt) 1989-11-10
AU3244589A (en) 1989-10-12
AU616132B2 (en) 1991-10-17

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