ES338725A1 - Procedimiento para preparar kalamicina. - Google Patents
Procedimiento para preparar kalamicina.Info
- Publication number
- ES338725A1 ES338725A1 ES338725A ES338725A ES338725A1 ES 338725 A1 ES338725 A1 ES 338725A1 ES 338725 A ES338725 A ES 338725A ES 338725 A ES338725 A ES 338725A ES 338725 A1 ES338725 A1 ES 338725A1
- Authority
- ES
- Spain
- Prior art keywords
- salts
- fish
- kalamycin
- treating
- roosts
- 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
- XUWPJKDMEZSVTP-LTYMHZPRSA-N kalafungina Chemical compound O=C1C2=C(O)C=CC=C2C(=O)C2=C1[C@@H](C)O[C@H]1[C@@H]2OC(=O)C1 XUWPJKDMEZSVTP-LTYMHZPRSA-N 0.000 title abstract 2
- 150000003839 salts Chemical class 0.000 abstract 3
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 abstract 2
- 241000251468 Actinopterygii Species 0.000 abstract 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 abstract 2
- UCTWMZQNUQWSLP-UHFFFAOYSA-N adrenaline Chemical compound CNCC(O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-UHFFFAOYSA-N 0.000 abstract 2
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 abstract 2
- YAPQBXQYLJRXSA-UHFFFAOYSA-N theobromine Chemical compound CN1C(=O)NC(=O)C2=C1N=CN2C YAPQBXQYLJRXSA-UHFFFAOYSA-N 0.000 abstract 2
- 241000213004 Alternaria solani Species 0.000 abstract 1
- 244000144730 Amygdalus persica Species 0.000 abstract 1
- 241000255789 Bombyx mori Species 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- 241000272201 Columbiformes Species 0.000 abstract 1
- 241000588694 Erwinia amylovora Species 0.000 abstract 1
- 241000879841 Fusarium oxysporum f. cubense Species 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 abstract 1
- 244000141359 Malus pumila Species 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 240000008790 Musa x paradisiaca Species 0.000 abstract 1
- 244000046052 Phaseolus vulgaris Species 0.000 abstract 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- 244000018633 Prunus armeniaca Species 0.000 abstract 1
- 235000009827 Prunus armeniaca Nutrition 0.000 abstract 1
- 235000006040 Prunus persica var persica Nutrition 0.000 abstract 1
- 241000589613 Pseudomonas savastanoi pv. phaseolicola Species 0.000 abstract 1
- 241000220324 Pyrus Species 0.000 abstract 1
- 235000004789 Rosa xanthina Nutrition 0.000 abstract 1
- 241000109329 Rosa xanthina Species 0.000 abstract 1
- 244000061456 Solanum tuberosum Species 0.000 abstract 1
- 235000002595 Solanum tuberosum Nutrition 0.000 abstract 1
- 241000985670 Xanthomonas arboricola pv. pruni Species 0.000 abstract 1
- -1 amine salts Chemical class 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- 230000000843 anti-fungal effect Effects 0.000 abstract 1
- 229940125715 antihistaminic agent Drugs 0.000 abstract 1
- 239000000739 antihistaminic agent Substances 0.000 abstract 1
- 235000021016 apples Nutrition 0.000 abstract 1
- 235000021015 bananas Nutrition 0.000 abstract 1
- 230000003115 biocidal effect Effects 0.000 abstract 1
- 229960001948 caffeine Drugs 0.000 abstract 1
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 abstract 1
- 229960001231 choline Drugs 0.000 abstract 1
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 abstract 1
- 239000000645 desinfectant Substances 0.000 abstract 1
- 229960002179 ephedrine Drugs 0.000 abstract 1
- QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 235000005152 nicotinamide Nutrition 0.000 abstract 1
- 239000011570 nicotinamide Substances 0.000 abstract 1
- 235000021017 pears Nutrition 0.000 abstract 1
- 235000021018 plums Nutrition 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 235000012015 potatoes Nutrition 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 229960004559 theobromine Drugs 0.000 abstract 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 abstract 1
- 229960000278 theophylline Drugs 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 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
- C07D493/04—Ortho-condensed systems
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Compounds Of Unknown Constitution (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Fodder In General (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US539465A US3300382A (en) | 1966-04-01 | 1966-04-01 | Kalamycin and method for preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES338725A1 true ES338725A1 (es) | 1968-04-01 |
Family
ID=24151326
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES338725A Expired ES338725A1 (es) | 1966-04-01 | 1967-03-31 | Procedimiento para preparar kalamicina. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US3300382A (OSRAM) |
| BE (1) | BE696413A (OSRAM) |
| CH (1) | CH485849A (OSRAM) |
| DE (1) | DE1617915A1 (OSRAM) |
| ES (1) | ES338725A1 (OSRAM) |
| FR (2) | FR1517342A (OSRAM) |
| GB (1) | GB1159231A (OSRAM) |
| GR (1) | GR35043B (OSRAM) |
| NL (1) | NL150510B (OSRAM) |
| SE (1) | SE327179B (OSRAM) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3367833A (en) * | 1967-02-14 | 1968-02-06 | Upjohn Co | Antibiotic erizomycin and process for making same |
| US3524868A (en) * | 1967-11-09 | 1970-08-18 | Upjohn Co | Kalamycinic acid and derivatives and their production |
| US4196266A (en) * | 1976-04-28 | 1980-04-01 | The Kitasato Institute (Kitasato Kenkyuosho) | Production of nanaomycin A and derivatives thereof |
| CN101317836B (zh) * | 2008-06-27 | 2010-11-24 | 中国科学院海洋研究所 | (3aR,5R,11bR)-3,3a,5,11b-四氢-7-羟基-5-甲基-2H-呋[3,2-b]萘并[2,3-d]吡喃-2,6,11-三酮的应用 |
-
1966
- 1966-04-01 US US539465A patent/US3300382A/en not_active Expired - Lifetime
-
1967
- 1967-03-04 GR GR670135043A patent/GR35043B/el unknown
- 1967-03-13 GB GB11697/67A patent/GB1159231A/en not_active Expired
- 1967-03-29 CH CH442767A patent/CH485849A/de not_active IP Right Cessation
- 1967-03-30 NL NL676704567A patent/NL150510B/xx unknown
- 1967-03-31 SE SE04511/67A patent/SE327179B/xx unknown
- 1967-03-31 DE DE19671617915 patent/DE1617915A1/de active Pending
- 1967-03-31 FR FR101010A patent/FR1517342A/fr not_active Expired
- 1967-03-31 BE BE696413D patent/BE696413A/xx unknown
- 1967-03-31 ES ES338725A patent/ES338725A1/es not_active Expired
- 1967-06-30 FR FR112668A patent/FR7227M/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GR35043B (el) | 1968-07-31 |
| GB1159231A (en) | 1969-07-23 |
| SE327179B (OSRAM) | 1970-08-17 |
| FR7227M (OSRAM) | 1969-09-01 |
| FR1517342A (fr) | 1968-03-15 |
| US3300382A (en) | 1967-01-24 |
| NL6704567A (OSRAM) | 1967-10-02 |
| DE1617915A1 (de) | 1971-04-08 |
| CH485849A (de) | 1970-02-15 |
| BE696413A (OSRAM) | 1967-10-02 |
| NL150510B (nl) | 1976-08-16 |
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