JPS55133394A - Novel aminosaccharide antibiotic g-367-1 and its preparation - Google Patents
Novel aminosaccharide antibiotic g-367-1 and its preparationInfo
- Publication number
- JPS55133394A JPS55133394A JP4127479A JP4127479A JPS55133394A JP S55133394 A JPS55133394 A JP S55133394A JP 4127479 A JP4127479 A JP 4127479A JP 4127479 A JP4127479 A JP 4127479A JP S55133394 A JPS55133394 A JP S55133394A
- Authority
- JP
- Japan
- Prior art keywords
- aminosaccharide
- antibiotic
- novel
- preparation
- negative
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- 230000003115 biocidal effect Effects 0.000 title abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-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
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 241000186361 Actinobacteria <class> Species 0.000 abstract 1
- 241000894006 Bacteria Species 0.000 abstract 1
- 241001495437 Dactylosporangium Species 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- 229940088710 antibiotic agent Drugs 0.000 abstract 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 238000004949 mass spectrometry Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000002844 melting Methods 0.000 abstract 1
- 230000008018 melting Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 abstract 1
- 231100000252 nontoxic Toxicity 0.000 abstract 1
- 230000003000 nontoxic effect Effects 0.000 abstract 1
- 239000012286 potassium permanganate Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000126 substance Substances 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
- C07H15/20—Carbocyclic rings
- C07H15/22—Cyclohexane rings, substituted by nitrogen atoms
- C07H15/222—Cyclohexane rings substituted by at least two nitrogen atoms
- C07H15/226—Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings
- C07H15/234—Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings attached to non-adjacent ring carbon atoms of the cyclohexane rings, e.g. kanamycins, tobramycin, nebramycin, gentamicin A2
-
- 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
-
- 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
- C07H15/20—Carbocyclic rings
- C07H15/22—Cyclohexane rings, substituted by nitrogen atoms
- C07H15/222—Cyclohexane rings substituted by at least two nitrogen atoms
- C07H15/226—Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings
- C07H15/234—Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings attached to non-adjacent ring carbon atoms of the cyclohexane rings, e.g. kanamycins, tobramycin, nebramycin, gentamicin A2
- C07H15/236—Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings attached to non-adjacent ring carbon atoms of the cyclohexane rings, e.g. kanamycins, tobramycin, nebramycin, gentamicin A2 a saccharide radical being substituted by an alkylamino radical in position 3 and by two substituents different from hydrogen in position 4, e.g. gentamicin complex, sisomicin, verdamycin
-
- 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
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/44—Preparation of O-glycosides, e.g. glucosides
- C12P19/46—Preparation of O-glycosides, e.g. glucosides having an oxygen atom of the saccharide radical bound to a cyclohexyl radical, e.g. kasugamycin
- C12P19/48—Preparation of O-glycosides, e.g. glucosides having an oxygen atom of the saccharide radical bound to a cyclohexyl radical, e.g. kasugamycin the cyclohexyl radical being substituted by two or more nitrogen atoms, e.g. destomycin, neamin
- C12P19/485—Having two saccharide radicals bound through only oxygen to non-adjacent ring carbons of the cyclohexyl radical, e.g. gentamycin, kanamycin, sisomycin, verdamycin, mutamycin, tobramycin, nebramycin, antibiotics 66-40B, 66-40D, XK-62-2, 66-40, G-418, G-52
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Wood Science & Technology (AREA)
- Biochemistry (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Biomedical Technology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
NEW MATERIAL:Aminosaccharide antibiotic G-367-1 (nontoxic acid addition salt) having the following physico-chemical properties: Melting point 130W133°C. [α]D24+188.9° (C=1.0, H2O). C, 50.14%; H, 7.60%; N, 14.42%. Molecular weight 475(mass spectrometry). Molecular formula C20H37N5O8. Soluble in water and methanol; insoluble in acetone, benzene, chloroform, etc. Positive to ninhydrin and KMnO4 decoloration reactions; negative to the biuret reaction. Basic.
USE: Antibacterials having a great activity particularly against Gram-negative bacteria.
PROCESS: G-367-1 producing actinomycetes, (FERM-P No. 4840), which belong to the genus Dactylosporangium, are incubated in a medium aerobically at 25W35°C for 100W200hr.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4127479A JPS55133394A (en) | 1979-04-04 | 1979-04-04 | Novel aminosaccharide antibiotic g-367-1 and its preparation |
US06/137,292 US4297486A (en) | 1979-04-04 | 1980-04-03 | Aminoglycoside antibiotic G-367-1 and method for the production thereof |
DE19803013210 DE3013210A1 (en) | 1979-04-04 | 1980-04-03 | NEW AMINOGLYCOSIDE ANTIBIOTICS AND METHOD FOR THEIR PRODUCTION |
FR8007574A FR2452932A1 (en) | 1979-04-04 | 1980-04-03 | NOVEL AMINOGLYCOSIDE ANTIBIOTICS AND THEIR PRODUCTION |
GB8011265A GB2053895B (en) | 1979-04-04 | 1980-04-03 | Aminoglycoside antibiotics and their production |
CA000349243A CA1140877A (en) | 1979-04-04 | 1980-04-03 | Aminoglycoside antibiotics and production thereof |
CH5618/80A CH648855A5 (en) | 1979-04-04 | 1980-07-23 | Aminoglycoside antibiotics and process for their preparation |
BE0/201867A BE884925A (en) | 1979-04-04 | 1980-08-26 | NOVEL AMINOGLYCOSIDE ANTIBIOTIC AND METHOD FOR THE PRODUCTION THEREOF. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4127479A JPS55133394A (en) | 1979-04-04 | 1979-04-04 | Novel aminosaccharide antibiotic g-367-1 and its preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS55133394A true JPS55133394A (en) | 1980-10-17 |
JPS6126914B2 JPS6126914B2 (en) | 1986-06-23 |
Family
ID=12603856
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4127479A Granted JPS55133394A (en) | 1979-04-04 | 1979-04-04 | Novel aminosaccharide antibiotic g-367-1 and its preparation |
Country Status (4)
Country | Link |
---|---|
JP (1) | JPS55133394A (en) |
BE (1) | BE884925A (en) |
CH (1) | CH648855A5 (en) |
DE (1) | DE3013210A1 (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3907771A (en) * | 1971-02-03 | 1975-09-23 | Schering Corp | Antibiotic 66-40 |
US3920628A (en) * | 1972-10-24 | 1975-11-18 | Schering Corp | 2{41 -Deoxyaminoglycosides and 2{41 -epi-amino-3{41 -desamino derivatives thereof, methods for their manufacture and novel intermediates useful therein |
EP0000473B1 (en) * | 1977-06-24 | 1981-03-11 | Scherico Ltd. | Process for preparing aminoglycoside derivatives, novel derivatives obtained and pharmaceutical compositions containing such derivatives |
-
1979
- 1979-04-04 JP JP4127479A patent/JPS55133394A/en active Granted
-
1980
- 1980-04-03 DE DE19803013210 patent/DE3013210A1/en not_active Ceased
- 1980-07-23 CH CH5618/80A patent/CH648855A5/en not_active IP Right Cessation
- 1980-08-26 BE BE0/201867A patent/BE884925A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JPS6126914B2 (en) | 1986-06-23 |
DE3013210A1 (en) | 1980-11-20 |
CH648855A5 (en) | 1985-04-15 |
BE884925A (en) | 1980-12-16 |
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