ATE82982T1 - Neue mittel dc-92b und dc-92d, sowie deren verfahren zur herstellung. - Google Patents

Neue mittel dc-92b und dc-92d, sowie deren verfahren zur herstellung.

Info

Publication number: ATE82982T1
Authority: AT; Austria
Prior art keywords: manufacture; well; actinomadura; pref; antibiotics
Prior art date: 1986-07-21

Application number

AT87904737T

Other languages

English (en)

Inventor

Hirofumi Nakano

Isami Takahashi

Fusao Tomita

Kozo Asano

Toru Yasuzawa

Tadashi Ashizawa

Keiichi Takahashi

Original Assignee

Kyowa Hakko Kogyo Kk

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.)

1986-07-21

Filing date

1987-07-17

Publication date

1992-12-15

1987-07-17 Application filed by Kyowa Hakko Kogyo Kk filed Critical Kyowa Hakko Kogyo Kk

1992-12-15 Application granted granted Critical

1992-12-15 Publication of ATE82982T1 publication Critical patent/ATE82982T1/de

Links

SCWWNJYIUMBQKK-UHFFFAOYSA-N 10-[4-(dimethylamino)-5,6-dihydroxy-4,6-dimethyloxan-2-yl]-8-[4-(dimethylamino)-5-hydroxy-6-methyloxan-2-yl]-2-[3-(3,3-dimethyloxiran-2-yl)-2-methyloxiran-2-yl]-11-hydroxy-5-methylnaphtho[2,3-h]chromene-4,7,12-trione Chemical compound C1C(N(C)C)C(O)C(C)OC1C1=CC(C2OC(C)(O)C(O)C(C)(C2)N(C)C)=C(O)C2=C1C(=O)C(C=C(C)C=1C(C=C(OC3=1)C1(C)C(O1)C1C(O1)(C)C)=O)=C3C2=O SCWWNJYIUMBQKK-UHFFFAOYSA-N 0.000 title abstract 2
VNZXPSFYMLCKIO-UHFFFAOYSA-N 10-[3-(dimethylamino)-4,6-dihydroxy-3,6-dimethyloxan-2-yl]-8-[4-(dimethylamino)-3-hydroxy-2-methyl-3,4-dihydro-2h-pyran-6-yl]-2-[3-(3,3-dimethyloxiran-2-yl)-2-methyloxiran-2-yl]-11-hydroxy-5-methylnaphtho[2,3-h]chromene-4,7,12-trione Chemical compound CN(C)C1C(O)C(C)OC(C=2C=3C(=O)C4=C(C5=C(C(C=C(O5)C5(C)C(O5)C5C(O5)(C)C)=O)C(C)=C4)C(=O)C=3C(O)=C(C3C(C(O)CC(C)(O)O3)(C)N(C)C)C=2)=C1 VNZXPSFYMLCKIO-UHFFFAOYSA-N 0.000 title 1
238000004519 manufacturing process Methods 0.000 title 1
238000000034 method Methods 0.000 title 1
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
239000003242 anti bacterial agent Substances 0.000 abstract 2
229940088710 antibiotic agent Drugs 0.000 abstract 2
FXAAZACNORIIQX-UHFFFAOYSA-N 12bh-naphtho[2,3-h]chromene Chemical compound C1=CC=C2C=C(C3OC=CC=C3C=C3)C3=CC2=C1 FXAAZACNORIIQX-UHFFFAOYSA-N 0.000 abstract 1
241000187362 Actinomadura Species 0.000 abstract 1
241000187361 Actinomadura sp. Species 0.000 abstract 1
AZGNTCXZZGTRLQ-UHFFFAOYSA-N Antibiotic DC 92D Natural products CN(C)C1C(O)C(C)OC(C=2C=3C(=O)C4=C(C5=C(C(C=C(O5)C5(C)C(O5)C5C(O5)(C)C)=O)C(C)=C4)C(=O)C=3C(O)=C(C3OC(C)(O)C(O)C(C)(C3)N(C)C)C=2)=C1 AZGNTCXZZGTRLQ-UHFFFAOYSA-N 0.000 abstract 1
230000003115 biocidal effect Effects 0.000 abstract 1
229940093499 ethyl acetate Drugs 0.000 abstract 1
235000019439 ethyl acetate Nutrition 0.000 abstract 1
239000007787 solid Substances 0.000 abstract 1
230000003595 spectral effect Effects 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/12—Acyclic radicals, not substituted by cyclic structures attached to a nitrogen atom of the saccharide radical
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero 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
- C12P19/26—Preparation of nitrogen-containing carbohydrates
- 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
- C12P19/44—Preparation of O-glycosides, e.g. glucosides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Health & Medical Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Biotechnology (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Molecular Biology (AREA)
General Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Microbiology (AREA)
Bioinformatics & Cheminformatics (AREA)
Crystallography & Structural Chemistry (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Saccharide Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

AT87904737T 1986-07-21 1987-07-17 Neue mittel dc-92b und dc-92d, sowie deren verfahren zur herstellung. ATE82982T1 (de)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
JP17140386		1986-07-21
EP87904737A EP0274545B1 (de)	1986-07-21	1987-07-17	Neue mittel dc-92b und dc-92d, sowie deren verfahren zur herstellung
PCT/JP1987/000524 WO1988000591A1 (fr)	1986-07-21	1987-07-17	Nouvelles substances dc-92b et dc-92d, et procede de preparation desdites substances

Publications (1)

Publication Number	Publication Date
ATE82982T1 true ATE82982T1 (de)	1992-12-15

Family

ID=15922504

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
AT87904737T ATE82982T1 (de)	1986-07-21	1987-07-17	Neue mittel dc-92b und dc-92d, sowie deren verfahren zur herstellung.

Country Status (6)

Country	Link
US (1)	US4847387A (de)
EP (1)	EP0274545B1 (de)
JP (1)	JPH0819148B2 (de)
AT (1)	ATE82982T1 (de)
DE (1)	DE3782930T2 (de)
WO (1)	WO1988000591A1 (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH01193265A (ja) *	1988-01-28	1989-08-03	Meiji Seika Kaisha Ltd	新規抗腫瘍性抗生物質ｓｆ２５８７物質及びその製造法
JP2766351B2 (ja) *	1989-11-13	1998-06-18	協和醗酵工業株式会社	新規物質ｄｃ１１４―ｃ
US5254357A (en) *	1991-06-28	1993-10-19	Langner Bruce J	Process for making a fiber beverage
US5178896A (en) *	1991-06-28	1993-01-12	Langner Bruce J	Fiber beverage and method of manufacture
EP1125944A1 (de) *	2000-02-18	2001-08-22	Aventis Pharma Deutschland GmbH	Pluraflavine und Derivate davon, Verfahren zu ihrer Herstellung und Verwendung derselben
KR101911767B1 (ko) *	2017-08-10	2018-10-25	가톨릭대학교 산학협력단	키다마이신 유도체 l1-95-1 및 이를 유효성분으로 함유하는 암 예방 또는 치료용 조성물
CN115650913B (zh) *	2022-10-12	2024-03-01	北京中医药大学	醌式喹啉类化合物及其制备方法和用途

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3334016A (en) *	1966-10-24	1967-08-01	Bristol Myers Co	Hedamycin and process for its production
JPS61274693A (ja) *	1985-05-29	1986-12-04	Ss Pharmaceut Co Ltd	新規抗生物質ｓｓ２１０２０ｃおよびその製造法

1987
- 1987-07-17 AT AT87904737T patent/ATE82982T1/de active
- 1987-07-17 WO PCT/JP1987/000524 patent/WO1988000591A1/ja not_active Ceased
- 1987-07-17 JP JP62-504380A patent/JPH0819148B2/ja not_active Expired - Lifetime
- 1987-07-17 DE DE8787904737T patent/DE3782930T2/de not_active Expired - Fee Related
- 1987-07-17 US US07/199,043 patent/US4847387A/en not_active Expired - Lifetime
- 1987-07-17 EP EP87904737A patent/EP0274545B1/de not_active Expired

Also Published As

Publication number	Publication date
JPH0819148B2 (ja)	1996-02-28
EP0274545B1 (de)	1992-12-02
JPH0819148B1 (de)	1996-02-28
US4847387A (en)	1989-07-11
DE3782930T2 (de)	1993-04-29
EP0274545A1 (de)	1988-07-20
DE3782930D1 (de)	1993-01-14
WO1988000591A1 (fr)	1988-01-28
EP0274545A4 (en)	1991-04-17

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