JPS56154995A - Preparation of coenzyme q10 - Google Patents
Preparation of coenzyme q10Info
- Publication number
- JPS56154995A JPS56154995A JP5928580A JP5928580A JPS56154995A JP S56154995 A JPS56154995 A JP S56154995A JP 5928580 A JP5928580 A JP 5928580A JP 5928580 A JP5928580 A JP 5928580A JP S56154995 A JPS56154995 A JP S56154995A
- Authority
- JP
- Japan
- Prior art keywords
- agent
- coenzyme
- cultured
- vivo
- oxidation
- 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
- ACTIUHUUMQJHFO-UPTCCGCDSA-N coenzyme Q10 Chemical compound COC1=C(OC)C(=O)C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C)=C(C)C1=O ACTIUHUUMQJHFO-UPTCCGCDSA-N 0.000 title abstract 3
- 239000003795 chemical substances by application Substances 0.000 abstract 3
- 241000222120 Candida <Saccharomycetales> Species 0.000 abstract 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 230000008878 coupling Effects 0.000 abstract 2
- 238000010168 coupling process Methods 0.000 abstract 2
- 238000005859 coupling reaction Methods 0.000 abstract 2
- 238000001727 in vivo Methods 0.000 abstract 2
- 230000010627 oxidative phosphorylation Effects 0.000 abstract 2
- 238000006479 redox reaction Methods 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 abstract 1
- ZKHQWZAMYRWXGA-KQYNXXCUSA-J ATP(4-) Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-J 0.000 abstract 1
- ZKHQWZAMYRWXGA-UHFFFAOYSA-N Adenosine triphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C(O)C1O ZKHQWZAMYRWXGA-UHFFFAOYSA-N 0.000 abstract 1
- 229960000901 mepacrine Drugs 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 abstract 1
- GPKJTRJOBQGKQK-UHFFFAOYSA-N quinacrine Chemical compound C1=C(OC)C=C2C(NC(C)CCCN(CC)CC)=C(C=CC(Cl)=C3)C3=NC2=C1 GPKJTRJOBQGKQK-UHFFFAOYSA-N 0.000 abstract 1
- 235000011178 triphosphate Nutrition 0.000 abstract 1
- 239000001226 triphosphate Substances 0.000 abstract 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 abstract 1
Landscapes
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5928580A JPS56154995A (en) | 1980-05-02 | 1980-05-02 | Preparation of coenzyme q10 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5928580A JPS56154995A (en) | 1980-05-02 | 1980-05-02 | Preparation of coenzyme q10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56154995A true JPS56154995A (en) | 1981-11-30 |
| JPS6246154B2 JPS6246154B2 (enExample) | 1987-09-30 |
Family
ID=13108962
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5928580A Granted JPS56154995A (en) | 1980-05-02 | 1980-05-02 | Preparation of coenzyme q10 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS56154995A (enExample) |
-
1980
- 1980-05-02 JP JP5928580A patent/JPS56154995A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6246154B2 (enExample) | 1987-09-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS56154995A (en) | Preparation of coenzyme q10 | |
| JPS5731696A (en) | Anthracycline derivative | |
| JPS53121998A (en) | Preparation of maytansiol, maytansine and maytansinol propionate | |
| JPS5517A (en) | Production of adenosine triphosphate | |
| JPS53110800A (en) | Separation method of hydrogen isotope | |
| JPS56154996A (en) | Preparation of coenzyme q10 | |
| JPS5437888A (en) | Preparation of pullulan | |
| JPS5247990A (en) | Manufacture of co-enzyme q10 | |
| JPS5799199A (en) | Preparation of 8-adenosyl-l-methionine | |
| JPS543100A (en) | Extraction of ribonucleic acid | |
| JPS56169592A (en) | Preparation of coenzyme q10 | |
| JPS5244290A (en) | Method of producing coenzyme q10 | |
| JPS5227099A (en) | Separation method of boron and fluorine from acid solution containing both of boron and fluorine. | |
| JPS5369882A (en) | Preparation of l-isoleucine | |
| JPS54105291A (en) | Preparation of cholesterol oxydase | |
| JPS53118586A (en) | Preparation of microbial cells | |
| JPS56151493A (en) | Preparation of coenzyme q10 | |
| JPS5241293A (en) | Method of manufacturing glucose-1-phosphate and glucose-6-phosphate | |
| JPS5352689A (en) | Isolation of glutamic acid sodium salt | |
| JPS56127093A (en) | Preparation of mycophenolic acid | |
| JPS5432694A (en) | Preparation of 7beta-(4-carboxybutylamido)-7alpha-methoxy-delta3-cephem-4- carboxylic acid derivatives | |
| JPS52113924A (en) | Preparation of choline phosphates | |
| JPS5432689A (en) | Praparation of microorganism cells | |
| JPS533581A (en) | Cultivation of mould | |
| JPS5394088A (en) | Preparation of glutathione |