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 same

Info

Publication number: SG150385A1
Authority: SG; Singapore
Prior art keywords: fatty acid; chain fatty; same; acid ester; composition
Prior art date: 2002-04-30

Application number

SG200607508-9A

Other languages

English (en)

Inventor

Motoo Sumida

Masahiro Nakao

Namino Tomimori

Koshi Namikawa

Harukazu Fukami

Original Assignee

Suntory Ltd

Priority date (The priority date 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 date listed.)

2002-04-30

Filing date

2003-04-28

Publication date

2009-03-30

2003-04-28 Application filed by Suntory Ltd filed Critical Suntory Ltd

2009-03-30 Publication of SG150385A1 publication Critical patent/SG150385A1/en

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 OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- 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 OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- 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)
Zoology (AREA)
Wood Science & Technology (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Bioinformatics & Cheminformatics (AREA)
Microbiology (AREA)
Genetics & Genomics (AREA)
General Engineering & Computer Science (AREA)
Biochemistry (AREA)
Biotechnology (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Mycology (AREA)
Nutrition Science (AREA)
Polymers & Plastics (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Food Science & Technology (AREA)
Animal Behavior & Ethology (AREA)
Emergency Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Cosmetics (AREA)

SG200607508-9A 2002-04-30 2003-04-28 Astaxanthin medium-chain fatty acid ester, production method of the same, and composition comprising the same SG150385A1 (en)

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 (de)
EP (1)	EP1500645B1 (de)
JP (1)	JP4410675B2 (de)
KR (1)	KR100941899B1 (de)
CN (1)	CN100374417C (de)
AU (1)	AU2003234765B2 (de)
CA (1)	CA2481704C (de)
DE (1)	DE60328374D1 (de)
IL (1)	IL164089A0 (de)
MY (1)	MY137041A (de)
SG (1)	SG150385A1 (de)
WO (1)	WO2003093229A1 (de)

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US7145025B2 (en) *	2002-07-29	2006-12-05	Hawaii Biotech, Inc.	Structural carotenoid analogs for the inhibition and amelioration of disease
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 (de) *	2007-01-26	2008-08-06	DSMIP Assets B.V.	Verwendung eines Astaxathinderivats für kosmetische Zwecke
KR20110021886A (ko) *	2008-05-15	2011-03-04	프로노바 바이오파마 노르지 에이에스	크릴 오일 처리 방법
WO2010038964A2 (ko) *	2008-09-30	2010-04-08	주식회사 유맥스	크릴로부터 유용성분 추출분리방법 및 관련 제품
SG11201609405VA (en)	2014-05-20	2016-12-29	Fuji Chem Ind Co Ltd	Carotenoid derivative, pharmaceutically acceptable salt thereof, and pharmaceutically acceptable ester or amide thereof
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 (de) *	2015-03-19	2016-09-22	Basf Se	Astaxanthinzusammensetzungen (iii)
EP3270910B1 (de) *	2015-03-19	2019-05-22	Basf Se	Astaxanthinzusammensetzungen (iv)
BR112017019831A2 (pt) *	2015-03-19	2018-05-29	Basf Se	uso de composições de astaxantina, composição, e, processo para preparação de alimento ou alimento animal
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
WO2018050795A1 (en)	2016-09-16	2018-03-22	Basf Se	Process for preparing of carotenoid mono-esters
CN109715605B (zh) *	2016-09-16	2022-04-12	巴斯夫欧洲公司	制备类胡萝卜素单酯的方法
WO2018050793A1 (en) *	2016-09-16	2018-03-22	Basf Se	Process for preparing phosphonium salt esters as building blocks for carotenoides
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 (ko) *	2019-10-29	2021-05-06	주식회사 내추럴바이오트리	에스테르 교환 반응을 통한 아스타잔틴 모노에스테르의 제조방법
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
EP4157250A4 (de) *	2020-05-29	2024-06-19	Cerecin Inc.	Verfahren zur behandlung von kindlichen spasmen mit mittelkettigen triglyceriden
WO2022140580A1 (en)	2020-12-24	2022-06-30	Orn Almarsson	Xanthophyll derivatives
JP7809395B1 (ja) *	2025-02-12	2026-02-02	株式会社八代	薄膜蒸留に使用するための抽出溶媒組成物、ならびにそれを用いた抽出対象成分の分取方法および分取システム

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2003
- 2003-04-28 JP JP2004501368A patent/JP4410675B2/ja not_active Expired - Fee Related
- 2003-04-28 DE DE60328374T patent/DE60328374D1/de not_active Expired - Lifetime
- 2003-04-28 IL IL16408903A patent/IL164089A0/xx unknown
- 2003-04-28 EP EP03728006A patent/EP1500645B1/de not_active Expired - Lifetime
- 2003-04-28 AU AU2003234765A patent/AU2003234765B2/en not_active Ceased
- 2003-04-28 KR KR1020047016796A patent/KR100941899B1/ko not_active Expired - Fee Related
- 2003-04-28 CN CNB038095327A patent/CN100374417C/zh not_active Expired - Fee Related
- 2003-04-28 SG SG200607508-9A patent/SG150385A1/en unknown
- 2003-04-28 US US10/511,829 patent/US20050228188A1/en not_active Abandoned
- 2003-04-28 WO PCT/JP2003/005443 patent/WO2003093229A1/ja not_active Ceased
- 2003-04-28 CA CA2481704A patent/CA2481704C/en not_active Expired - Fee Related
- 2003-04-30 MY MYPI20031648A patent/MY137041A/en unknown

Also Published As

Publication number	Publication date
KR20040103979A (ko)	2004-12-09
CA2481704C (en)	2011-06-21
EP1500645A1 (de)	2005-01-26
JP4410675B2 (ja)	2010-02-03
CN1649839A (zh)	2005-08-03
AU2003234765B2 (en)	2009-09-17
CN100374417C (zh)	2008-03-12
DE60328374D1 (de)	2009-08-27
AU2003234765A1 (en)	2003-11-17
MY137041A (en)	2008-12-31
IL164089A0 (en)	2005-12-18
EP1500645B1 (de)	2009-07-15
CA2481704A1 (en)	2003-11-13
JPWO2003093229A1 (ja)	2005-09-08
WO2003093229A1 (en)	2003-11-13
US20050228188A1 (en)	2005-10-13
KR100941899B1 (ko)	2010-02-11
EP1500645A4 (de)	2005-06-08

Publication	Publication Date	Title
MY137041A (en)	2008-12-31	Astaxanthin medium-chain fatty acid ester, production method of the same, and composition comprising the same
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Xue et al.	2002	Molecular species composition of glycolipids from Sprirulina platensis
WO2009019893A1 (ja)	2009-02-12	ジアシルグリセロール高含有油脂の製造方法
CA2417484A1 (en)	2002-01-31	Elongase genes and uses thereof
EA201000400A1 (ru)	2010-10-29	Твердые жировые композиции, содержащие полиненасыщенные жирные кислоты, и способы их получения и использования
WO2000066750A3 (en)	2001-08-30	Methods for producing plants with elevated oleic acid content
WO2004029186A3 (en)	2004-08-05	Conjugated linoleic acid compositions
AR022224A1 (es)	2002-09-04	Gen de la desaturasa humana y usos del mismo
WO1998046776A3 (en)	2000-04-06	Plant fatty acid synthases and use in improved methods for production of medium-chain fatty acids
EA200600776A1 (ru)	2007-02-27	Способ получения моноэфиров жирных кислот
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ATE352984T1 (de)	2007-02-15	Gefrorene geschäumte produkte und verfahren zu ihrer herstellung
AU5402900A (en)	2000-12-28	The combined use of triglycerides containing medium chain fatty acids and exogenous lipolytic enzymes as feed supplements
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ES2057106T3 (es)	1994-10-16	Compuestos tensioactivos y un procedimiento para su preparacion.
DE50309376D1 (de)	2008-04-24	Um- und veresterung von fetts uren und triglycerid herstellung von fettsäuremethylestern
MY144300A (en)	2011-08-29	Method for the transesterification of fats and oils of biological origin by means of alcoholysis using specific carbonates
TW200503634A (en)	2005-02-01	Method for the production of fatty acids having a low trans-fatty acid content
DE69708338D1 (de)	2001-12-20	Verfahren zur herstullung natürlicher 1,3 diol derivate und korrespondierende natürliche 1,3 dioxan derivate
Karmee	2011	The synthesis, properties, and applications of ascorbyl esters