JPS6034556B2 - 抗生物質c−15003 - Google Patents
抗生物質c−15003Info
- Publication number
- JPS6034556B2 JPS6034556B2 JP52037166A JP3716677A JPS6034556B2 JP S6034556 B2 JPS6034556 B2 JP S6034556B2 JP 52037166 A JP52037166 A JP 52037166A JP 3716677 A JP3716677 A JP 3716677A JP S6034556 B2 JPS6034556 B2 JP S6034556B2
- Authority
- JP
- Japan
- Prior art keywords
- antibiotic
- ethyl acetate
- culture
- medium
- water
- 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.)
- Expired
Links
- 230000003115 biocidal effect Effects 0.000 title claims description 40
- QAIPRVGONGVQAS-DUXPYHPUSA-N trans-caffeic acid Chemical compound OC(=O)\C=C\C1=CC=C(O)C(O)=C1 QAIPRVGONGVQAS-DUXPYHPUSA-N 0.000 claims description 30
- 239000002609 medium Substances 0.000 claims description 28
- 239000000126 substance Substances 0.000 claims description 19
- 241000894006 Bacteria Species 0.000 claims description 9
- 239000001963 growth medium Substances 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 241000187654 Nocardia Species 0.000 claims description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 117
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 45
- 239000000243 solution Substances 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- 238000000034 method Methods 0.000 description 23
- 230000002829 reductive effect Effects 0.000 description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 18
- 230000001580 bacterial effect Effects 0.000 description 18
- 210000004027 cell Anatomy 0.000 description 18
- 239000000741 silica gel Substances 0.000 description 18
- 229910002027 silica gel Inorganic materials 0.000 description 18
- 229920001817 Agar Polymers 0.000 description 17
- 239000008272 agar Substances 0.000 description 17
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- 239000007788 liquid Substances 0.000 description 14
- 239000002904 solvent Substances 0.000 description 14
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 13
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 12
- 244000005700 microbiome Species 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 229940041514 candida albicans extract Drugs 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 238000004809 thin layer chromatography Methods 0.000 description 10
- 239000012138 yeast extract Substances 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- -1 etc.) Substances 0.000 description 8
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- 238000010521 absorption reaction Methods 0.000 description 7
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 7
- 239000003208 petroleum Substances 0.000 description 7
- 238000000746 purification Methods 0.000 description 7
- 238000011218 seed culture Methods 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
- 238000012258 culturing Methods 0.000 description 6
- 239000000284 extract Substances 0.000 description 6
- 239000008103 glucose Substances 0.000 description 6
- 238000001179 sorption measurement Methods 0.000 description 6
- 229920002472 Starch Polymers 0.000 description 5
- 239000003463 adsorbent Substances 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 238000003556 assay Methods 0.000 description 5
- 239000012141 concentrate Substances 0.000 description 5
- 238000000605 extraction Methods 0.000 description 5
- 150000002576 ketones Chemical class 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 241000894007 species Species 0.000 description 5
- 235000019698 starch Nutrition 0.000 description 5
- 239000008107 starch Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000003242 anti bacterial agent Substances 0.000 description 4
- 229940088710 antibiotic agent Drugs 0.000 description 4
- 239000013058 crude material Substances 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- 238000010828 elution Methods 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- QWPXBEHQFHACTK-KZVYIGENSA-N (10e,12e)-86-chloro-12,14,4-trihydroxy-85,14-dimethoxy-33,2,7,10-tetramethyl-15,16-dihydro-14h-7-aza-1(6,4)-oxazina-3(2,3)-oxirana-8(1,3)-benzenacyclotetradecaphane-10,12-dien-6-one Chemical compound CN1C(=O)CC(O)C2(C)OC2C(C)C(OC(=O)N2)CC2(O)C(OC)\C=C\C=C(C)\CC2=CC(OC)=C(Cl)C1=C2 QWPXBEHQFHACTK-KZVYIGENSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 3
- QWPXBEHQFHACTK-UHFFFAOYSA-N Maytansinol Natural products CN1C(=O)CC(O)C2(C)OC2C(C)C(OC(=O)N2)CC2(O)C(OC)C=CC=C(C)CC2=CC(OC)=C(Cl)C1=C2 QWPXBEHQFHACTK-UHFFFAOYSA-N 0.000 description 3
- 241000699670 Mus sp. Species 0.000 description 3
- 229910002651 NO3 Inorganic materials 0.000 description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
- 238000005273 aeration Methods 0.000 description 3
- MQYZCKOGTWYJAZ-UHFFFAOYSA-N ansamitocin P1 Natural products CN1C(=O)CC(OC(C)=O)C2(C)OC2C(C)C(OC(=O)N2)CC2(O)C(OC)C=CC=C(C)CC2=CC(OC)=C(Cl)C1=C2 MQYZCKOGTWYJAZ-UHFFFAOYSA-N 0.000 description 3
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 235000013312 flour Nutrition 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 230000001766 physiological effect Effects 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000000638 solvent extraction Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 3
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical compound O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 description 2
- 241000186361 Actinobacteria <class> Species 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 description 2
- 240000004528 Catalpa ovata Species 0.000 description 2
- 235000010005 Catalpa ovata Nutrition 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- 239000004375 Dextrin Substances 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 2
- 241000699666 Mus <mouse, genus> Species 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000588769 Proteus <enterobacteria> Species 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241000248418 Tetrahymena pyriformis Species 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
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- 125000002252 acyl group Chemical group 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 230000000845 anti-microbial effect Effects 0.000 description 2
- 230000000259 anti-tumor effect Effects 0.000 description 2
- 239000003904 antiprotozoal agent Substances 0.000 description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 2
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
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- FDGQSTZJBFJUBT-UHFFFAOYSA-N hypoxanthine Chemical compound O=C1NC=NC2=C1NC=N2 FDGQSTZJBFJUBT-UHFFFAOYSA-N 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
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- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 2
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- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
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- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/18—Bridged 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
- A61P35/00—Antineoplastic agents
-
- 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
- C12P17/188—Heterocyclic compound containing in the condensed system at least one hetero ring having nitrogen atoms and oxygen atoms as the only ring heteroatoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Communicable Diseases (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Compounds Of Unknown Constitution (AREA)
Priority Applications (45)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP52037166A JPS6034556B2 (ja) | 1977-03-31 | 1977-03-31 | 抗生物質c−15003 |
US05/811,448 US4162940A (en) | 1977-03-31 | 1977-06-29 | Method for producing Antibiotic C-15003 by culturing nocardia |
AU29074/77A AU510499B2 (en) | 1977-03-31 | 1977-09-23 | Antibiotic 0-15003 |
AU29072/77A AU506415B2 (en) | 1977-03-31 | 1977-09-23 | Antibiotic c-15003 |
PH20297A PH13381A (en) | 1977-03-31 | 1977-10-04 | Antibiotic c-15003 |
FR7730339A FR2385714A1 (fr) | 1977-03-31 | 1977-10-07 | Nouvel antibiotique denomme c-15003, son procede de preparation et son application comme medicament |
SU772529301A SU741804A3 (ru) | 1977-03-31 | 1977-10-07 | Способ получени антибиотика |
GR54548A GR66051B (fr) | 1977-03-31 | 1977-10-11 | |
YU02453/77A YU245377A (en) | 1977-03-31 | 1977-10-12 | Process for producing antibiotics |
CS776678A CS214749B2 (en) | 1977-03-31 | 1977-10-13 | Means for treating the diseased plants and method of preparation of active substance |
SE7711542A SE442873B (sv) | 1977-03-31 | 1977-10-13 | Forfarande for framstellning av ett nytt antibiotikum c-15003 med angiven formel genom odling av nocardia no c-15003 (ifo 13726, ferm 3992, atcc 31281) |
NL7711272A NL7711272A (nl) | 1977-03-31 | 1977-10-13 | Werkwijze ter bereiding van farmaceutische pre- paraten, alsmede gevormde farmaceutische prepa- raten. |
HU77TA1459A HU178359B (en) | 1977-03-31 | 1977-10-13 | Process for preparing the antibiotic c-15003 |
HU802440A HU187372B (en) | 1977-03-31 | 1977-10-13 | Process for the preparation of c-15003 p-o antibiotic |
NLAANVRAGE7711274,A NL188102C (nl) | 1977-03-31 | 1977-10-13 | Werkwijze ter bereiding van antibiotica. |
GB42822/77A GB1586688A (en) | 1977-03-31 | 1977-10-14 | Antibiotic c-15003 |
DE19772746252 DE2746252A1 (de) | 1977-03-31 | 1977-10-14 | Antibiotikum c-15003 enthaltendes arzneimittel zur behandlung von tumore aufweisenden warmbluetern |
DE19772746209 DE2746209A1 (de) | 1977-03-31 | 1977-10-14 | Neues antibiotikum und verfahren zu dessen herstellung |
ES463207A ES463207A1 (es) | 1977-03-31 | 1977-10-14 | Un metodo para producir el antibiotico c-15003 |
DK458877A DK458877A (da) | 1977-03-31 | 1977-10-14 | Antibiotika |
GB42823/77A GB1592264A (en) | 1977-03-31 | 1977-10-14 | Treatment of tumor-carrying animal with antibiotic c-15003 |
IE2101/77A IE46064B1 (en) | 1977-03-31 | 1977-10-14 | Antibiotic c-15003 |
AT0736277A AT364081B (de) | 1977-03-31 | 1977-10-14 | Verfahren zur herstellung von neuen antibiotika |
CA288,731A CA1107212A (fr) | 1977-03-31 | 1977-10-14 | C-15003 antibiotique |
PL1977201541A PL122289B1 (en) | 1977-03-31 | 1977-10-15 | Process for preparing novel antibiotic |
PL1977221358A PL124349B1 (en) | 1977-03-31 | 1977-10-15 | Process for preparing maytansinol |
CH1260577A CH637137A5 (en) | 1977-03-31 | 1978-01-01 | Antibiotic and process for its preparation |
IT21818/78A IT1094308B (it) | 1977-03-31 | 1978-03-30 | Composizione antibiotica e relativo frocedimento di trattamento di animali affetti da tumori |
PT67854A PT67854B (en) | 1977-03-31 | 1978-03-30 | Antibiotic c-15003 |
IT21817/78A IT1094020B (it) | 1977-03-31 | 1978-03-30 | Antibioticc c-15003 e procedimento per la produzione di esso e dei relativi derivati |
ZA00781863A ZA781863B (en) | 1977-03-31 | 1978-03-31 | Treatment of tumor-carrying animal with antibiotic c-15003 |
BE186487A BE865590A (fr) | 1977-03-31 | 1978-03-31 | Compositions antibiotiques et leur utilisation |
ZA00781862A ZA781862B (en) | 1977-03-31 | 1978-03-31 | Antibiotic c-15003 |
BE186486A BE865589A (fr) | 1977-03-31 | 1978-03-31 | Antibiotiques et leur preparation |
SU782627804A SU890978A3 (ru) | 1977-03-31 | 1978-06-20 | Способ получени антибиотика с-1500зр-0 |
ES472230A ES472230A1 (es) | 1977-03-31 | 1978-07-31 | Metodo para producir el antibiotico c-15003 p-o. |
AT822678A AT362061B (de) | 1977-03-31 | 1978-11-17 | Verfahren zur herstellung eines neuen antibiotikums |
US05/972,492 US4225494A (en) | 1977-03-31 | 1978-12-22 | Maytansinol esters |
PH22216A PH15985A (en) | 1977-03-31 | 1979-02-20 | A method for producing maytansinol |
US06/131,787 US4320200A (en) | 1977-03-31 | 1980-03-19 | Antibiotic |
DK338880A DK148180B (da) | 1977-03-31 | 1980-08-06 | Fremgangsmaade til fremstilling af maytansinol |
CA000373582A CA1121814A (fr) | 1977-03-31 | 1981-03-20 | Antibiotique c-15003 |
US06/313,974 US4360462A (en) | 1977-03-31 | 1981-10-22 | Process for preparing maytansinol |
YU01785/82A YU178582A (en) | 1977-03-31 | 1982-08-17 | Process for obtaining antibiotics |
SE8302517A SE446004B (sv) | 1977-03-31 | 1983-05-03 | Forfarande for framstellning av antibiotikum c-15003 p-o (maytansinol) |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP52037166A JPS6034556B2 (ja) | 1977-03-31 | 1977-03-31 | 抗生物質c−15003 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS53130693A JPS53130693A (en) | 1978-11-14 |
JPS6034556B2 true JPS6034556B2 (ja) | 1985-08-09 |
Family
ID=12490004
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP52037166A Expired JPS6034556B2 (ja) | 1977-03-31 | 1977-03-31 | 抗生物質c−15003 |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS6034556B2 (fr) |
AT (1) | AT364081B (fr) |
BE (2) | BE865589A (fr) |
HU (1) | HU187372B (fr) |
SU (2) | SU741804A3 (fr) |
ZA (2) | ZA781863B (fr) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7432088B2 (en) * | 2003-05-08 | 2008-10-07 | Immunogen Inc. | Methods for the production of ansamitocins |
SI2900676T1 (sl) * | 2012-09-26 | 2019-04-30 | Immunogen, Inc. | Izboljšana metoda za aciliranje majtanzinola |
CN116421733B (zh) * | 2023-06-08 | 2023-09-12 | 金宇保灵生物药品有限公司 | 可用于猪多杀性巴氏杆菌病活疫苗的疫苗耐热保护剂 |
-
1977
- 1977-03-31 JP JP52037166A patent/JPS6034556B2/ja not_active Expired
- 1977-10-07 SU SU772529301A patent/SU741804A3/ru active
- 1977-10-13 HU HU802440A patent/HU187372B/hu unknown
- 1977-10-14 AT AT0736277A patent/AT364081B/de not_active IP Right Cessation
-
1978
- 1978-03-31 BE BE186486A patent/BE865589A/fr not_active IP Right Cessation
- 1978-03-31 ZA ZA00781863A patent/ZA781863B/xx unknown
- 1978-03-31 BE BE186487A patent/BE865590A/fr not_active IP Right Cessation
- 1978-03-31 ZA ZA00781862A patent/ZA781862B/xx unknown
- 1978-06-20 SU SU782627804A patent/SU890978A3/ru active
Also Published As
Publication number | Publication date |
---|---|
BE865589A (fr) | 1978-10-02 |
JPS53130693A (en) | 1978-11-14 |
HU187372B (en) | 1985-12-28 |
SU890978A3 (ru) | 1981-12-15 |
ZA781863B (en) | 1979-03-28 |
BE865590A (fr) | 1978-10-02 |
ZA781862B (en) | 1979-03-28 |
ATA736277A (de) | 1981-02-15 |
AT364081B (de) | 1981-09-25 |
SU741804A3 (ru) | 1980-06-15 |
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