DE1518328C3 - Verfahren zur Herstellung von in Wasser schwer löslichen Bacitracin-Schwermetallkomplexverbindungen - Google Patents
Verfahren zur Herstellung von in Wasser schwer löslichen Bacitracin-SchwermetallkomplexverbindungenInfo
- Publication number
- DE1518328C3 DE1518328C3 DE1518328A DE1518328A DE1518328C3 DE 1518328 C3 DE1518328 C3 DE 1518328C3 DE 1518328 A DE1518328 A DE 1518328A DE 1518328 A DE1518328 A DE 1518328A DE 1518328 C3 DE1518328 C3 DE 1518328C3
- Authority
- DE
- Germany
- Prior art keywords
- bacitracin
- water
- production
- heavy metal
- complex compounds
- 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
- CLKOFPXJLQSYAH-ABRJDSQDSA-N bacitracin A Chemical compound C1SC([C@@H](N)[C@@H](C)CC)=N[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]1C(=O)N[C@H](CCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2N=CNC=2)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)NCCCC1 CLKOFPXJLQSYAH-ABRJDSQDSA-N 0.000 title claims description 17
- 108010001478 Bacitracin Proteins 0.000 title claims description 15
- 229960003071 bacitracin Drugs 0.000 title claims description 15
- 229930184125 bacitracin Natural products 0.000 title claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 10
- 238000000034 method Methods 0.000 title claims description 7
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- -1 metal complex compounds Chemical class 0.000 title claims description 6
- 229910001385 heavy metal Inorganic materials 0.000 title claims description 5
- 150000003839 salts Chemical class 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 7
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
- 230000004071 biological effect Effects 0.000 description 4
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 3
- 229960001763 zinc sulfate Drugs 0.000 description 3
- 229910000368 zinc sulfate Inorganic materials 0.000 description 3
- ZETIVVHRRQLWFW-UHFFFAOYSA-N 3-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=CC(C=O)=C1 ZETIVVHRRQLWFW-UHFFFAOYSA-N 0.000 description 2
- SXINBFXPADXIEY-UHFFFAOYSA-N 5-Nitrofurfural Chemical compound [O-][N+](=O)C1=CC=C(C=O)O1 SXINBFXPADXIEY-UHFFFAOYSA-N 0.000 description 2
- 241000194108 Bacillus licheniformis Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003674 animal food additive Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000009918 complex formation Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/50—Cyclic peptides containing at least one abnormal peptide link
- C07K7/54—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring
- C07K7/56—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring the cyclisation not occurring through 2,4-diamino-butanoic acid
- C07K7/58—Bacitracins; Related peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Baking, Grill, Roasting (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS553064 | 1964-10-06 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE1518328A1 DE1518328A1 (de) | 1969-07-24 |
| DE1518328B2 DE1518328B2 (de) | 1973-11-15 |
| DE1518328C3 true DE1518328C3 (de) | 1974-06-27 |
Family
ID=5400361
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1518328A Expired DE1518328C3 (de) | 1964-10-06 | 1965-10-04 | Verfahren zur Herstellung von in Wasser schwer löslichen Bacitracin-Schwermetallkomplexverbindungen |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3481916A (OSRAM) |
| AT (1) | AT263214B (OSRAM) |
| BE (1) | BE670561A (OSRAM) |
| CH (1) | CH465770A (OSRAM) |
| DE (1) | DE1518328C3 (OSRAM) |
| DK (1) | DK111686B (OSRAM) |
| FI (1) | FI44454B (OSRAM) |
| GB (1) | GB1084878A (OSRAM) |
| NL (1) | NL147134B (OSRAM) |
| NO (1) | NO118708B (OSRAM) |
| SE (1) | SE326524B (OSRAM) |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2834711A (en) * | 1956-05-17 | 1958-05-13 | Commercial Solvents Corp | Production of bacitracin |
| US3228836A (en) * | 1962-10-09 | 1966-01-11 | Warner Lambert Pharmaceutical | Aldehyde complexes of colistin and polymyxin antibiotics |
| US3205137A (en) * | 1963-03-19 | 1965-09-07 | Warner Lambert Pharmaceutical | Bacitracin derivatives |
| CH476838A (de) * | 1964-06-26 | 1969-08-15 | Spofa Vereinigte Pharma Werke | Verfahren zur Isolierung von Bacitracin |
-
1965
- 1965-09-29 CH CH1343665A patent/CH465770A/de unknown
- 1965-10-01 NO NO159923A patent/NO118708B/no unknown
- 1965-10-01 DK DK505465AA patent/DK111686B/da unknown
- 1965-10-04 DE DE1518328A patent/DE1518328C3/de not_active Expired
- 1965-10-04 NL NL656512824A patent/NL147134B/xx unknown
- 1965-10-04 US US492895A patent/US3481916A/en not_active Expired - Lifetime
- 1965-10-05 AT AT900265A patent/AT263214B/de active
- 1965-10-05 FI FI2367/65A patent/FI44454B/fi active
- 1965-10-05 GB GB42206/65A patent/GB1084878A/en not_active Expired
- 1965-10-06 BE BE670561D patent/BE670561A/xx unknown
- 1965-10-06 SE SE12965/65A patent/SE326524B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE1518328A1 (de) | 1969-07-24 |
| CH465770A (de) | 1968-11-30 |
| NO118708B (OSRAM) | 1970-02-02 |
| DE1518328B2 (de) | 1973-11-15 |
| BE670561A (OSRAM) | 1966-01-31 |
| FI44454B (OSRAM) | 1971-08-02 |
| AT263214B (de) | 1968-07-10 |
| SE326524B (OSRAM) | 1970-07-27 |
| NL6512824A (OSRAM) | 1966-04-07 |
| GB1084878A (en) | 1967-09-27 |
| US3481916A (en) | 1969-12-02 |
| DK111686B (da) | 1968-09-30 |
| NL147134B (nl) | 1975-09-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2332878C2 (de) | Salze von Cephalosporinen mit Arginin und Lysin, ihre Herstellung und injizierbare pharmazeutische Zubereitungen | |
| CH648037A5 (de) | Imidazo-rifamycin-derivate mit antibakterieller wirksamkeit. | |
| DE1518328C3 (de) | Verfahren zur Herstellung von in Wasser schwer löslichen Bacitracin-Schwermetallkomplexverbindungen | |
| DE2954593C2 (OSRAM) | ||
| DE2121648A1 (de) | Monoacetylderivate der Antibiotika SF-837undSF-837-Atief2 | |
| DE1518314C3 (de) | Verfahren zur Isolierung von Bacitracin | |
| DE1493618A1 (de) | Cumarinderivate und ein Verfahren zu ihrer Herstellung | |
| CH371217A (de) | Verfahren zur Herstellung von Distamycin und Distacin | |
| DE1567046A1 (de) | Parasitizides,insbesondere fungizides Mittel | |
| DE2261832C3 (de) | 5-Dihydrocoriolin C und Verfahren zu seiner Gewinnung | |
| AT245169B (de) | Verfahren zur Herstellung des neuen Antibiotikums WG 696 | |
| AT234270B (de) | Verfahren zur Herstellung von α-Methylphenoxymethylpenicillin durch Fermentation | |
| CH378340A (de) | Verfahren zur Herstellung neuer Nitrofurane | |
| AT219196B (de) | Verfahren zur Rückgewinnung eines Tetracyclin-Antibiotikums | |
| DE446782C (de) | Verfahren zur Gewinnung des herzwirksamen Reinglykosids aus Bulbus Scillae | |
| AT247519B (de) | Verfahren zur Herstellung neuer Additionsverbindungen von Antibiotika | |
| AT347456B (de) | Verfahren zur herstellung von neuen 5-methyl-7- hydroxy-isoflavon-derivaten | |
| DE3129637C2 (OSRAM) | ||
| AT301030B (de) | Verfahren zur herstellung von neuen spiramycinderivaten | |
| DE937055C (de) | Verfahren zur Herstellung von 6ª‰, 17ª‡-Dioxyprogesteron | |
| DE1139843B (de) | Verfahren zur Herstellung von Derivate der 6-Aminopenicillansaeure enthaltenden Loesungen | |
| DE911135C (de) | Verfahren zur Herstellung von Pteridinen | |
| DE1194097B (de) | Herstellung von Derivaten des Chlortetracyclins und/oder Tetracyclins | |
| DE1094927B (de) | Verfahren zur Gewinnung von Cobalaminen | |
| DE1176147B (de) | Verfahren zur Herstellung von 7-Aminocephalosporansaeure |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| E77 | Valid patent as to the heymanns-index 1977 | ||
| EHJ | Ceased/non-payment of the annual fee |