SG150385A1 - Astaxanthin medium-chain fatty acid ester, production method of the same, and composition comprising the same - Google Patents
Astaxanthin medium-chain fatty acid ester, production method of the same, and composition comprising the sameInfo
- Publication number
- SG150385A1 SG150385A1 SG200607508-9A SG2006075089A SG150385A1 SG 150385 A1 SG150385 A1 SG 150385A1 SG 2006075089 A SG2006075089 A SG 2006075089A SG 150385 A1 SG150385 A1 SG 150385A1
- Authority
- SG
- Singapore
- Prior art keywords
- fatty acid
- chain fatty
- same
- acid ester
- composition
- Prior art date
Links
- 235000013793 astaxanthin Nutrition 0.000 title abstract 7
- JEBFVOLFMLUKLF-IFPLVEIFSA-N Astaxanthin Natural products CC(=C/C=C/C(=C/C=C/C1=C(C)C(=O)C(O)CC1(C)C)/C)C=CC=C(/C)C=CC=C(/C)C=CC2=C(C)C(=O)C(O)CC2(C)C JEBFVOLFMLUKLF-IFPLVEIFSA-N 0.000 title abstract 6
- -1 Astaxanthin medium-chain fatty acid ester Chemical class 0.000 title abstract 6
- 229940022405 astaxanthin Drugs 0.000 title abstract 6
- 239000001168 astaxanthin Substances 0.000 title abstract 6
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 239000002537 cosmetic Substances 0.000 abstract 2
- 150000005690 diesters Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 235000013305 food Nutrition 0.000 abstract 2
- 102000004882 Lipase Human genes 0.000 abstract 1
- 108090001060 Lipase Proteins 0.000 abstract 1
- 239000004367 Lipase Substances 0.000 abstract 1
- MQZIGYBFDRPAKN-ZWAPEEGVSA-N astaxanthin Chemical compound C([C@H](O)C(=O)C=1C)C(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)C(=O)[C@@H](O)CC1(C)C MQZIGYBFDRPAKN-ZWAPEEGVSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000007796 conventional method Methods 0.000 abstract 1
- 235000019621 digestibility Nutrition 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 235000019421 lipase Nutrition 0.000 abstract 1
- 150000002646 long chain fatty acid esters Chemical class 0.000 abstract 1
- 150000004667 medium chain fatty acids Chemical class 0.000 abstract 1
- 230000035515 penetration Effects 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/24—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by six-membered non-aromatic rings, e.g. beta-carotene
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/115—Fatty acids or derivatives thereof; Fats or oils
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
-
- 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
- C12P23/00—Preparation of compounds containing a cyclohexene ring having an unsaturated side chain containing at least ten carbon atoms bound by conjugated double bonds, e.g. carotenes
-
- 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
- C12P7/62—Carboxylic acid esters
-
- 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
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
-
- 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
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C12P7/6445—Glycerides
- C12P7/6454—Glycerides by esterification
-
- 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
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C12P7/6445—Glycerides
- C12P7/6458—Glycerides by transesterification, e.g. interesterification, ester interchange, alcoholysis or acidolysis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Food Science & Technology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Mycology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002128989 | 2002-04-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG150385A1 true SG150385A1 (en) | 2009-03-30 |
Family
ID=29397288
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG200607508-9A SG150385A1 (en) | 2002-04-30 | 2003-04-28 | Astaxanthin medium-chain fatty acid ester, production method of the same, and composition comprising the same |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20050228188A1 (fr) |
| EP (1) | EP1500645B1 (fr) |
| JP (1) | JP4410675B2 (fr) |
| KR (1) | KR100941899B1 (fr) |
| CN (1) | CN100374417C (fr) |
| AU (1) | AU2003234765B2 (fr) |
| CA (1) | CA2481704C (fr) |
| DE (1) | DE60328374D1 (fr) |
| IL (1) | IL164089A0 (fr) |
| MY (1) | MY137041A (fr) |
| SG (1) | SG150385A1 (fr) |
| WO (1) | WO2003093229A1 (fr) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101845009B (zh) * | 2002-07-29 | 2012-10-03 | 卡达克斯药物公司 | 用于抑制和改善疾病的类胡萝卜素结构类似物 |
| GB0501365D0 (en) * | 2005-01-21 | 2005-03-02 | Promar As | Compositions |
| US20070293568A1 (en) | 2006-06-16 | 2007-12-20 | Yamaha Hatsudoki Kabushiki Kaisha | Neurocyte Protective Agent |
| EP1952845A1 (fr) * | 2007-01-26 | 2008-08-06 | DSMIP Assets B.V. | Utilisation d'un dérivé d'astaxathine à des fins cosmétiques |
| CA2724463C (fr) * | 2008-05-15 | 2017-10-03 | Pronova Biopharma Norge As | Procede se rapportant a l'huile de krill |
| WO2010038964A2 (fr) * | 2008-09-30 | 2010-04-08 | 주식회사 유맥스 | Procédé d'extraction et de séparation de matières actives de krill, et produits associés |
| RU2693455C2 (ru) | 2014-05-20 | 2019-07-03 | Аста Фармасьютикалз Ко., Лтд. | Каротеноидное производное, его фармацевтически приемлемая соль и фармацевтическая композиция, содержащая его |
| CN104513844A (zh) * | 2014-12-17 | 2015-04-15 | 北京科技大学 | 一种利用脂肪酶催化合成虾青素琥珀酸酯的方法 |
| WO2016146803A1 (fr) * | 2015-03-19 | 2016-09-22 | Basf Se | Compositions d'astaxanthine (iii) |
| WO2016146804A1 (fr) * | 2015-03-19 | 2016-09-22 | Basf Se | Compositions d'astaxanthine (iv) |
| US20180110741A1 (en) * | 2015-03-19 | 2018-04-26 | Basf Se | Astaxanthin compositions (i) |
| CN105418472B (zh) * | 2015-11-21 | 2017-05-10 | 中国海洋大学 | 一种利用溶剂分级结晶分离虾青素单双酯的方法 |
| CN106278979B (zh) * | 2016-08-16 | 2017-12-05 | 集美大学 | 一种虾青素棕榈酸‑二十二碳二烯酸双酯的制备方法 |
| WO2018050793A1 (fr) * | 2016-09-16 | 2018-03-22 | Basf Se | Procédé de préparation d'esters de sel de phosphonium en tant que blocs de construction pour carotinoïdes |
| WO2018050794A1 (fr) | 2016-09-16 | 2018-03-22 | Basf Se | Procédé de préparation de mono-esters de caroténoïdes |
| WO2018050795A1 (fr) | 2016-09-16 | 2018-03-22 | Basf Se | Procédé de préparation de mono-esters de caroténoïdes |
| CN109251945B (zh) * | 2018-10-16 | 2021-08-20 | 云南爱尔康生物技术有限公司 | 一种制备虾青素中链脂肪酸单酯和虾青素中链脂肪酸双酯的方法 |
| WO2021085916A1 (fr) * | 2019-10-29 | 2021-05-06 | 주식회사 내추럴바이오트리 | Procédé de préparation d'un monoester d'astaxanthine par transestérification |
| KR102423643B1 (ko) * | 2019-10-29 | 2022-07-22 | 주식회사 내추럴바이오트리 | 에스테르 교환 반응을 통한 아스타잔틴 모노에스테르의 제조방법 |
| KR102423638B1 (ko) * | 2019-10-29 | 2022-07-22 | 주식회사 내추럴바이오트리 | 아스타잔틴 모노에스테르의 제조방법 |
| CN110940743A (zh) * | 2019-10-31 | 2020-03-31 | 厦门昶科生物工程有限公司 | 一种丁酸虾青素双酯的制备方法 |
| SG10201914033YA (en) * | 2019-12-31 | 2021-07-29 | Wilmar International Ltd | Polypeptides with Lipase Activity and Uses Thereof |
| CA3184353A1 (fr) * | 2020-05-29 | 2021-12-02 | Cerecin Inc. | Procedes pour le traitement de spasmes infantiles a l'aide de triglycerides a chaine moyenne |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3450819A (en) * | 1965-07-12 | 1969-06-17 | Drew Chem Corp | Synthetic therapeutic fat |
| JPH01202261A (ja) * | 1988-02-09 | 1989-08-15 | Kyowa Hakko Kogyo Co Ltd | 赤色魚用餌料と赤色魚の養殖方法 |
| JPH07300421A (ja) * | 1994-04-28 | 1995-11-14 | Itano Reitou Kk | 抗炎症剤 |
| JPH09124470A (ja) * | 1995-10-26 | 1997-05-13 | Suntory Ltd | 抗ストレス組成物 |
| US5916791A (en) * | 1995-11-24 | 1999-06-29 | Hirschberg; Joseph | Polynucleotide molecule from Haematococcus pluvialis encoding a polypeptide having a β--C--4--oxygenase activity for biotechnological production of (3S,3S)astaxanthin |
| JPH10421A (ja) * | 1996-06-18 | 1998-01-06 | Chugai Ro Co Ltd | ダイコータの塗布方法 |
| JPH11290094A (ja) * | 1998-04-06 | 1999-10-26 | Nof Corp | アスタキサンチン脂肪酸エステルの製造方法 |
| NO309386B1 (no) * | 1999-04-19 | 2001-01-22 | Norsk Hydro As | Pigment |
-
2003
- 2003-04-28 KR KR1020047016796A patent/KR100941899B1/ko not_active IP Right Cessation
- 2003-04-28 WO PCT/JP2003/005443 patent/WO2003093229A1/fr active Application Filing
- 2003-04-28 EP EP03728006A patent/EP1500645B1/fr not_active Expired - Lifetime
- 2003-04-28 AU AU2003234765A patent/AU2003234765B2/en not_active Ceased
- 2003-04-28 CN CNB038095327A patent/CN100374417C/zh not_active Expired - Fee Related
- 2003-04-28 CA CA2481704A patent/CA2481704C/fr not_active Expired - Fee Related
- 2003-04-28 JP JP2004501368A patent/JP4410675B2/ja not_active Expired - Fee Related
- 2003-04-28 US US10/511,829 patent/US20050228188A1/en not_active Abandoned
- 2003-04-28 SG SG200607508-9A patent/SG150385A1/en unknown
- 2003-04-28 DE DE60328374T patent/DE60328374D1/de not_active Expired - Lifetime
- 2003-04-28 IL IL16408903A patent/IL164089A0/xx unknown
- 2003-04-30 MY MYPI20031648A patent/MY137041A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2481704C (fr) | 2011-06-21 |
| AU2003234765A1 (en) | 2003-11-17 |
| CN1649839A (zh) | 2005-08-03 |
| KR20040103979A (ko) | 2004-12-09 |
| AU2003234765B2 (en) | 2009-09-17 |
| IL164089A0 (en) | 2005-12-18 |
| DE60328374D1 (de) | 2009-08-27 |
| EP1500645B1 (fr) | 2009-07-15 |
| CN100374417C (zh) | 2008-03-12 |
| US20050228188A1 (en) | 2005-10-13 |
| JPWO2003093229A1 (ja) | 2005-09-08 |
| WO2003093229A1 (fr) | 2003-11-13 |
| MY137041A (en) | 2008-12-31 |
| EP1500645A1 (fr) | 2005-01-26 |
| KR100941899B1 (ko) | 2010-02-11 |
| CA2481704A1 (fr) | 2003-11-13 |
| JP4410675B2 (ja) | 2010-02-03 |
| EP1500645A4 (fr) | 2005-06-08 |
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