NO783545L - Fremgangsmaate til fremstilling av deoksynarasinantibiotisk kompleks - Google Patents
Fremgangsmaate til fremstilling av deoksynarasinantibiotisk kompleksInfo
- Publication number
- NO783545L NO783545L NO783545A NO783545A NO783545L NO 783545 L NO783545 L NO 783545L NO 783545 A NO783545 A NO 783545A NO 783545 A NO783545 A NO 783545A NO 783545 L NO783545 L NO 783545L
- Authority
- NO
- Norway
- Prior art keywords
- deoxynarazine
- deoxy
- antibiotic
- narazine
- epi
- Prior art date
Links
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- 238000011161 development Methods 0.000 description 1
- ZJULYDCRWUEPTK-UHFFFAOYSA-N dichloromethyl Chemical compound Cl[CH]Cl ZJULYDCRWUEPTK-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
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- 229940043279 diisopropylamine Drugs 0.000 description 1
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- 239000012895 dilution Substances 0.000 description 1
- AIUDWMLXCFRVDR-UHFFFAOYSA-N dimethyl 2-(3-ethyl-3-methylpentyl)propanedioate Chemical class CCC(C)(CC)CCC(C(=O)OC)C(=O)OC AIUDWMLXCFRVDR-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
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- 235000021323 fish oil Nutrition 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004459 forage Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
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- 238000001990 intravenous administration Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 210000002311 liver mitochondria Anatomy 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
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- 239000012528 membrane Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- 231100000219 mutagenic Toxicity 0.000 description 1
- 239000003471 mutagenic agent Substances 0.000 description 1
- 230000003505 mutagenic effect Effects 0.000 description 1
- 208000010125 myocardial infarction Diseases 0.000 description 1
- 229960002748 norepinephrine Drugs 0.000 description 1
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000004816 paper chromatography Methods 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 229940066779 peptones Drugs 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 201000006509 pleuropneumonia Diseases 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000002460 polyether antibiotic agent Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000002980 postoperative effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012746 preparative thin layer chromatography Methods 0.000 description 1
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- 238000011160 research Methods 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000025033 vasoconstriction Effects 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/10—Spiro-condensed systems
-
- 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
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/01—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing oxygen
-
- 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
- C12P17/18—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
- C12P17/181—Heterocyclic compounds containing oxygen atoms as the only ring heteroatoms in the condensed system, e.g. Salinomycin, Septamycin
-
- 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
- C12R2001/465—Streptomyces
- C12R2001/485—Streptomyces aureofaciens
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/886—Streptomyces
- Y10S435/889—Streptomyces aureofaciens
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Microbiology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Tropical Medicine & Parasitology (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Feed For Specific Animals (AREA)
- Fodder In General (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/844,087 US4141907A (en) | 1977-10-20 | 1977-10-20 | Deoxynarasin antibiotics |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO783545L true NO783545L (no) | 1979-04-23 |
Family
ID=25291778
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO783545A NO783545L (no) | 1977-10-20 | 1978-10-19 | Fremgangsmaate til fremstilling av deoksynarasinantibiotisk kompleks |
Country Status (33)
| Country | Link |
|---|---|
| US (1) | US4141907A (xx) |
| EP (1) | EP0001709B1 (xx) |
| JP (1) | JPS5470276A (xx) |
| AR (1) | AR217869A1 (xx) |
| AT (1) | AT362499B (xx) |
| AU (1) | AU519966B2 (xx) |
| BE (1) | BE871274A (xx) |
| CA (1) | CA1119541A (xx) |
| CH (1) | CH636903A5 (xx) |
| CS (1) | CS204037B2 (xx) |
| DD (1) | DD139520A5 (xx) |
| DE (1) | DE2861882D1 (xx) |
| DK (1) | DK465978A (xx) |
| ES (1) | ES474327A1 (xx) |
| FI (1) | FI58791C (xx) |
| FR (1) | FR2406639A1 (xx) |
| GB (1) | GB2006774B (xx) |
| GR (1) | GR71734B (xx) |
| HU (1) | HU179463B (xx) |
| IE (1) | IE47665B1 (xx) |
| IL (1) | IL55738A (xx) |
| IT (1) | IT1101615B (xx) |
| MX (1) | MX5603E (xx) |
| MY (1) | MY8500595A (xx) |
| NO (1) | NO783545L (xx) |
| NZ (1) | NZ188670A (xx) |
| PH (1) | PH14339A (xx) |
| PL (1) | PL117570B1 (xx) |
| PT (1) | PT68661A (xx) |
| RO (1) | RO77417A (xx) |
| SU (1) | SU818492A3 (xx) |
| YU (1) | YU241578A (xx) |
| ZA (1) | ZA785804B (xx) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2024806B (en) * | 1978-03-16 | 1982-05-06 | Taisho Pharmaceutical Co Ltd | Onomycin derivatives |
| IE49936B1 (en) * | 1979-07-11 | 1986-01-08 | Int Minerals & Chem Corp | Zinc-containing antibiotic agents |
| US4309504A (en) * | 1980-01-28 | 1982-01-05 | Eli Lilly And Company | Process for preparing narasin |
| US4394377A (en) * | 1981-07-31 | 1983-07-19 | Syntex (U.S.A.) Inc. | Ruminant animal performance by co-administering choline and propionate enchancers |
| US4625041A (en) * | 1984-02-17 | 1986-11-25 | Pfizer Inc. | Acidic polycyclic ether antibiotic |
| US4613503A (en) * | 1984-10-11 | 1986-09-23 | The Dow Chemical Company | Antibiotic A26201-1 and antibiotic A26201-2 produced by a novel strain of actinoplanes |
| US4859599A (en) * | 1984-10-11 | 1989-08-22 | The Dow Chemical Company | Antibiotic A26201-1 and antibiotic A26201-2 produced by a novel strain of actinoplanes |
| US5047338A (en) * | 1986-05-29 | 1991-09-10 | International Minerals & Chemical Corp. | Polyester Antibiotic preparation |
| US5049495A (en) * | 1986-05-29 | 1991-09-17 | International Minerals & Chemical Corp. | Fermentation method for producing polyether antibiotics |
| US5041374A (en) * | 1986-05-29 | 1991-08-20 | International Minerals & Chemical Corp. | Polyether antibiotic recovery and purification |
| US20080161324A1 (en) * | 2006-09-14 | 2008-07-03 | Johansen Lisa M | Compositions and methods for treatment of viral diseases |
| CN108743905A (zh) * | 2018-08-24 | 2018-11-06 | 河南科技大学第附属医院 | 一种治疗感冒的中药配方及其制备方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3753887A (en) | 1969-06-04 | 1973-08-21 | Hydronautics | Alkali metal specific measuring electrode |
| US3947586A (en) | 1974-05-20 | 1976-03-30 | Hoffmann-La Roche Inc. | Method of combatting swine dysentery |
| US4038384A (en) * | 1974-06-10 | 1977-07-26 | Eli Lilly And Company | Antibiotic a-28086 and process for production thereof |
| US3985893A (en) | 1974-10-29 | 1976-10-12 | Eli Lilly And Company | Method for treating cardiac insufficiency with antibiotic A-23187 |
| US4009262A (en) | 1975-04-21 | 1977-02-22 | Eli Lilly And Company | Antibiotic a-28086 recovery process |
| US4035481A (en) | 1975-04-21 | 1977-07-12 | Eli Lilly And Company | Antibiotic A-28086 and process for production thereof |
-
1977
- 1977-10-20 US US05/844,087 patent/US4141907A/en not_active Expired - Lifetime
-
1978
- 1978-10-15 IL IL55738A patent/IL55738A/xx unknown
- 1978-10-16 ZA ZA785804A patent/ZA785804B/xx unknown
- 1978-10-16 FR FR7829423A patent/FR2406639A1/fr active Granted
- 1978-10-16 RO RO7895412A patent/RO77417A/ro unknown
- 1978-10-16 PH PH21709A patent/PH14339A/en unknown
- 1978-10-16 AR AR274094A patent/AR217869A1/es active
- 1978-10-16 BE BE1009097A patent/BE871274A/xx not_active IP Right Cessation
- 1978-10-16 YU YU02415/78A patent/YU241578A/xx unknown
- 1978-10-16 PT PT68661A patent/PT68661A/pt unknown
- 1978-10-16 NZ NZ188670A patent/NZ188670A/xx unknown
- 1978-10-17 DE DE7878300514T patent/DE2861882D1/de not_active Expired
- 1978-10-17 AU AU40776/78A patent/AU519966B2/en not_active Expired
- 1978-10-17 CA CA000313589A patent/CA1119541A/en not_active Expired
- 1978-10-17 GB GB7840888A patent/GB2006774B/en not_active Expired
- 1978-10-17 EP EP78300514A patent/EP0001709B1/en not_active Expired
- 1978-10-18 GR GR57458A patent/GR71734B/el unknown
- 1978-10-18 FI FI783174A patent/FI58791C/fi not_active IP Right Cessation
- 1978-10-18 ES ES474327A patent/ES474327A1/es not_active Expired
- 1978-10-18 CS CS786777A patent/CS204037B2/cs unknown
- 1978-10-19 SU SU782676001A patent/SU818492A3/ru active
- 1978-10-19 JP JP12940478A patent/JPS5470276A/ja active Granted
- 1978-10-19 CH CH1083778A patent/CH636903A5/fr not_active IP Right Cessation
- 1978-10-19 IE IE2078/78A patent/IE47665B1/en not_active IP Right Cessation
- 1978-10-19 IT IT28926/78A patent/IT1101615B/it active
- 1978-10-19 AT AT750778A patent/AT362499B/de not_active IP Right Cessation
- 1978-10-19 DK DK465978A patent/DK465978A/da unknown
- 1978-10-19 NO NO783545A patent/NO783545L/no unknown
- 1978-10-19 MX MX787479U patent/MX5603E/es unknown
- 1978-10-19 HU HU78EI817A patent/HU179463B/hu unknown
- 1978-10-20 PL PL1978210410A patent/PL117570B1/pl unknown
- 1978-10-20 DD DD78208586A patent/DD139520A5/de unknown
-
1985
- 1985-12-30 MY MY595/85A patent/MY8500595A/xx unknown
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