ES250767A1 - Procedimiento quimico para la obtenciën de quinona - Google Patents
Procedimiento quimico para la obtenciën de quinonaInfo
- Publication number
- ES250767A1 ES250767A1 ES0250767A ES250767A ES250767A1 ES 250767 A1 ES250767 A1 ES 250767A1 ES 0250767 A ES0250767 A ES 0250767A ES 250767 A ES250767 A ES 250767A ES 250767 A1 ES250767 A1 ES 250767A1
- Authority
- ES
- Spain
- Prior art keywords
- formula
- yeast
- solution
- quinone
- bakers
- 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
- 150000004059 quinone derivatives Chemical class 0.000 title 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 3
- 240000004808 Saccharomyces cerevisiae Species 0.000 abstract 3
- 125000002252 acyl group Chemical group 0.000 abstract 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 abstract 2
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 abstract 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract 2
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical group CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- 241000006364 Torula Species 0.000 abstract 2
- 235000015278 beef Nutrition 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 abstract 2
- 210000004536 heart mitochondria Anatomy 0.000 abstract 2
- 150000002430 hydrocarbons Chemical group 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 abstract 2
- 150000004053 quinones Chemical class 0.000 abstract 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- 241000589151 Azotobacter Species 0.000 abstract 1
- 241000589149 Azotobacter vinelandii Species 0.000 abstract 1
- 241000272201 Columbiformes Species 0.000 abstract 1
- 241000221961 Neurospora crassa Species 0.000 abstract 1
- 229910000564 Raney nickel Inorganic materials 0.000 abstract 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 abstract 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
- 235000021336 beef liver Nutrition 0.000 abstract 1
- 210000000481 breast Anatomy 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 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 abstract 1
- 235000017471 coenzyme Q10 Nutrition 0.000 abstract 1
- 238000002425 crystallisation Methods 0.000 abstract 1
- 230000008025 crystallization Effects 0.000 abstract 1
- 238000000605 extraction Methods 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 210000002311 liver mitochondria Anatomy 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 210000003205 muscle Anatomy 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 229940079877 pyrogallol Drugs 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 229910001923 silver oxide Inorganic materials 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/12—Ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C50/00—Quinones
- C07C50/26—Quinones containing groups having oxygen atoms singly bound to carbon atoms
- C07C50/28—Quinones containing groups having oxygen atoms singly bound to carbon atoms with monocyclic quinoid structure
-
- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/66—Preparation of oxygen-containing organic compounds containing the quinoid structure
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Microbiology (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74678758A | 1958-07-07 | 1958-07-07 | |
| US758838A US3162654A (en) | 1958-09-03 | 1958-09-03 | Tetra-substituted benzoquinones and derivatives of the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES250767A1 true ES250767A1 (es) | 1960-03-01 |
Family
ID=27114647
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0250767A Expired ES250767A1 (es) | 1958-07-07 | 1959-07-04 | Procedimiento quimico para la obtenciën de quinona |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE580391A (de) |
| CH (1) | CH401028A (de) |
| ES (1) | ES250767A1 (de) |
| GB (1) | GB925581A (de) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3426125A (en) * | 1965-04-07 | 1969-02-04 | Yukio Shigeta | Method of treating diabetes mellitus |
| US4525350A (en) * | 1975-02-20 | 1985-06-25 | The New England Institute, Inc. | Methods of stimulating host defense system with coenzymes Q4 to Q.sub.1 |
| IT1284873B1 (it) * | 1996-07-26 | 1998-05-22 | Idi Farmaceutici Spa | Derivati stabili di ubichinolo procedimenti per la loro produzione e loro impiego farmaceutico |
-
1959
- 1959-07-01 GB GB2262759A patent/GB925581A/en not_active Expired
- 1959-07-04 ES ES0250767A patent/ES250767A1/es not_active Expired
- 1959-07-06 BE BE580391A patent/BE580391A/fr unknown
- 1959-07-07 CH CH7542359A patent/CH401028A/de unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BE580391A (fr) | 1960-01-06 |
| GB925581A (en) | 1963-05-08 |
| CH401028A (de) | 1965-10-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Sharpless et al. | One-step synthesis of 1, 5-dienes involving reductive coupling of allyl alcohols | |
| Naya et al. | The structural elucidation of sesquiterpene lactones from Petasites japonicus Maxim | |
| Dubeck et al. | CYCLOPENTADIENYL-3-CYCLOPENTENYLNICKEL (II) | |
| Henbest et al. | 960. Aspects of stereochemistry. Part IX. The formation of fluorohydrins from the cholesterol 5: 6-epoxides and boron trifluoride–ether complex | |
| Kupchan et al. | Tumor inhibitors. LXVII. Eupacunin, a novel antileukemic sesquiterpene lactone from Eupatorium cuneifolium | |
| ES250767A1 (es) | Procedimiento quimico para la obtenciën de quinona | |
| GB1286031A (en) | Production of buten-2-ol-4 compounds | |
| US3068295A (en) | diether groups | |
| Ogawa et al. | Studies on the constituents of enkianthus nudipes. V. A new lignan xyloside from the stems | |
| GB1154424A (en) | New Derivatives of Steroids and a method of preparation thereof | |
| GB1146991A (en) | Improvements in or relating to novel steroids and the manufacture thereof | |
| US3564025A (en) | 2-methoxy-6-multiprenyl-1,4-benzoquinones and a process of making | |
| Caglioti et al. | Hydroboration—IV: Hydroboration of 7-dehydrocholesterol | |
| GB1206873A (en) | 7alpha-METHYL-ANDROSTENE COMPOUNDS | |
| KASAI et al. | Constituents of Chinese Crude Drug" Wujiapi". VI. Studies on the Aglycones of Steroidal Glycosides of Bei-Wujiapi (2) | |
| GB1308127A (en) | Octa-and deca-hydro-2-naphthalones and 2-hydroxy naphthalenes and their use as odorants and flavourants | |
| GB1368545A (en) | Preparation of dihydrocoumarin and of alkyl derivatives thereof | |
| GB932325A (en) | Estrane derivatives | |
| GB853012A (en) | 1:6-dimethyl aromatic steroids and the preparation thereof | |
| GB965713A (en) | Processes for the production of fused polycyclic hydrocarbon derivatives,and the compounds thus produced | |
| US3507873A (en) | -8-aza-19-norpregn-4-en-3,20-diones | |
| Wicha et al. | Transformations of steroidal neopentyl systems—VI: Intramolecular claisen condensation of 19R-acetoxy-19A-methyl-3-ones of the (5α) series | |
| GB1049034A (en) | New compounds of the coenzyme q type | |
| GB1490047A (en) | Process for the preparation of 4-exo-hydroxy-endo-tricyclo(5.2.2.02,6)undec-8-ene | |
| GB928161A (en) | Substituted benzoquinones and hydroquinones and their preparation |