JP2016175983A5 - - Google Patents
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- Publication number
- JP2016175983A5 JP2016175983A5 JP2015056511A JP2015056511A JP2016175983A5 JP 2016175983 A5 JP2016175983 A5 JP 2016175983A5 JP 2015056511 A JP2015056511 A JP 2015056511A JP 2015056511 A JP2015056511 A JP 2015056511A JP 2016175983 A5 JP2016175983 A5 JP 2016175983A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- compound
- oxidation inhibitor
- group
- carbonyl
- 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
- 150000001875 compounds Chemical class 0.000 claims 8
- 239000003112 inhibitor Substances 0.000 claims 8
- 230000003647 oxidation Effects 0.000 claims 8
- 238000007254 oxidation reaction Methods 0.000 claims 8
- 150000001728 carbonyl compounds Chemical class 0.000 claims 5
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 claims 4
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 claims 3
- NDFKTBCGKNOHPJ-UHFFFAOYSA-N hex-2-enal Natural products CCCCC=CC=O NDFKTBCGKNOHPJ-UHFFFAOYSA-N 0.000 claims 3
- GXANMBISFKBPEX-ONEGZZNKSA-N (e)-hex-3-enal Chemical compound CC\C=C\CC=O GXANMBISFKBPEX-ONEGZZNKSA-N 0.000 claims 2
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 claims 2
- NWZIYQNUCXUJJJ-UHFFFAOYSA-N 2-butylfuran Chemical compound CCCCC1=CC=CO1 NWZIYQNUCXUJJJ-UHFFFAOYSA-N 0.000 claims 2
- MBDOYVRWFFCFHM-UHFFFAOYSA-N 2-hexenal Chemical compound CCCC=CC=O MBDOYVRWFFCFHM-UHFFFAOYSA-N 0.000 claims 2
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 claims 2
- JMLYDLZRFNYHHO-UHFFFAOYSA-N Methyl 9-oxononanoate Chemical compound COC(=O)CCCCCCCC=O JMLYDLZRFNYHHO-UHFFFAOYSA-N 0.000 claims 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 claims 2
- -1 aminocarbonyl compound Chemical class 0.000 claims 2
- 239000003925 fat Substances 0.000 claims 2
- FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 claims 2
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 claims 2
- IJXHLVMUNBOGRR-UHFFFAOYSA-N methyl nonanoate Chemical compound CCCCCCCCC(=O)OC IJXHLVMUNBOGRR-UHFFFAOYSA-N 0.000 claims 2
- JGHZJRVDZXSNKQ-UHFFFAOYSA-N methyl octanoate Chemical compound CCCCCCCC(=O)OC JGHZJRVDZXSNKQ-UHFFFAOYSA-N 0.000 claims 2
- VKCYHJWLYTUGCC-UHFFFAOYSA-N nonan-2-one Chemical compound CCCCCCCC(C)=O VKCYHJWLYTUGCC-UHFFFAOYSA-N 0.000 claims 2
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 claims 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims 2
- 239000003921 oil Substances 0.000 claims 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 claims 2
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N pentanal Chemical compound CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 claims 2
- 125000002657 sphingoid group Chemical group 0.000 claims 2
- WWUZIQQURGPMPG-UHFFFAOYSA-N (-)-D-erythro-Sphingosine Natural products CCCCCCCCCCCCCC=CC(O)C(N)CO WWUZIQQURGPMPG-UHFFFAOYSA-N 0.000 claims 1
- DTCCTIQRPGSLPT-ONEGZZNKSA-N (E)-2-pentenal Chemical compound CC\C=C\C=O DTCCTIQRPGSLPT-ONEGZZNKSA-N 0.000 claims 1
- 239000001764 (E)-oct-3-en-2-one Substances 0.000 claims 1
- SATICYYAWWYRAM-VNKDHWASSA-N (E,E)-hepta-2,4-dienal Chemical compound CC\C=C\C=C\C=O SATICYYAWWYRAM-VNKDHWASSA-N 0.000 claims 1
- FAHUKNBUIVOJJR-UHFFFAOYSA-N 1-(4-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine Chemical compound C1=CC(F)=CC=C1C1C2=CC=CN2CCN1 FAHUKNBUIVOJJR-UHFFFAOYSA-N 0.000 claims 1
- KEXCNWISTVJVBV-SIRUGEDZSA-N 2,4,7-decatrienal Chemical compound CC\C=C\C\C=C\C=C\C=O KEXCNWISTVJVBV-SIRUGEDZSA-N 0.000 claims 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims 1
- MBDOYVRWFFCFHM-SNAWJCMRSA-N 2-Hexenal Natural products CCC\C=C\C=O MBDOYVRWFFCFHM-SNAWJCMRSA-N 0.000 claims 1
- YVBAUDVGOFCUSG-UHFFFAOYSA-N 2-Pentylfuran Natural products CCCCCC1=CC=CO1 YVBAUDVGOFCUSG-UHFFFAOYSA-N 0.000 claims 1
- FIDBXHOCOXRPRO-CWWKMNTPSA-N 3,6-Nonadienal Chemical compound CC\C=C/C\C=C/CC=O FIDBXHOCOXRPRO-CWWKMNTPSA-N 0.000 claims 1
- ZCFOBLITZWHNNC-VOTSOKGWSA-N 3-Octen-2-one Chemical compound CCCC\C=C\C(C)=O ZCFOBLITZWHNNC-VOTSOKGWSA-N 0.000 claims 1
- ZCFOBLITZWHNNC-UHFFFAOYSA-N 3-Octen-2-one Natural products CCCCC=CC(C)=O ZCFOBLITZWHNNC-UHFFFAOYSA-N 0.000 claims 1
- AWQSAIIDOMEEOD-UHFFFAOYSA-N 5,5-Dimethyl-4-(3-oxobutyl)dihydro-2(3H)-furanone Chemical compound CC(=O)CCC1CC(=O)OC1(C)C AWQSAIIDOMEEOD-UHFFFAOYSA-N 0.000 claims 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims 1
- AERBNCYCJBRYDG-UHFFFAOYSA-N D-ribo-phytosphingosine Natural products CCCCCCCCCCCCCCC(O)C(O)C(N)CO AERBNCYCJBRYDG-UHFFFAOYSA-N 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- 239000005641 Methyl octanoate Substances 0.000 claims 1
- OTKJDMGTUTTYMP-ROUUACIJSA-N Safingol ( L-threo-sphinganine) Chemical group CCCCCCCCCCCCCCC[C@H](O)[C@@H](N)CO OTKJDMGTUTTYMP-ROUUACIJSA-N 0.000 claims 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- DTCCTIQRPGSLPT-UHFFFAOYSA-N beta-Aethyl-acrolein Natural products CCC=CC=O DTCCTIQRPGSLPT-UHFFFAOYSA-N 0.000 claims 1
- 235000013361 beverage Nutrition 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 238000013329 compounding Methods 0.000 claims 1
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 claims 1
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- OTKJDMGTUTTYMP-UHFFFAOYSA-N dihydrosphingosine Natural products CCCCCCCCCCCCCCCC(O)C(N)CO OTKJDMGTUTTYMP-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 235000013305 food Nutrition 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- MRYISIMMTIXZMC-UHFFFAOYSA-N methyl 10-oxodec-8-enoate Chemical compound COC(=O)CCCCCCC=CC=O MRYISIMMTIXZMC-UHFFFAOYSA-N 0.000 claims 1
- LVPNLDGNIRVDRF-UHFFFAOYSA-N methyl 10-oxodecanoate Chemical compound COC(=O)CCCCCCCCC=O LVPNLDGNIRVDRF-UHFFFAOYSA-N 0.000 claims 1
- KKONPTBIPYXILW-UHFFFAOYSA-N methyl 13-oxotrideca-9,11-dienoate Chemical compound COC(=O)CCCCCCCC=CC=CC=O KKONPTBIPYXILW-UHFFFAOYSA-N 0.000 claims 1
- HVAXGLYKECRETN-UHFFFAOYSA-N methyl 8-oxooctanoate Chemical compound COC(=O)CCCCCCC=O HVAXGLYKECRETN-UHFFFAOYSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- YRXOQXUDKDCXME-QWKHPXNBSA-N n,n-dimethylsphingosine Chemical compound CCCCCCCCCCCCC\C=C\[C@H](O)[C@@H](CO)N(C)C YRXOQXUDKDCXME-QWKHPXNBSA-N 0.000 claims 1
- 235000014593 oils and fats Nutrition 0.000 claims 1
- AERBNCYCJBRYDG-KSZLIROESA-N phytosphingosine Chemical compound CCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@@H](N)CO AERBNCYCJBRYDG-KSZLIROESA-N 0.000 claims 1
- 229940033329 phytosphingosine Drugs 0.000 claims 1
- WWUZIQQURGPMPG-KRWOKUGFSA-N sphingosine Chemical compound CCCCCCCCCCCCC\C=C\[C@@H](O)[C@@H](N)CO WWUZIQQURGPMPG-KRWOKUGFSA-N 0.000 claims 1
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2015056511A JP6232008B2 (ja) | 2015-03-19 | 2015-03-19 | 酸化抑制剤及びこれを用いた油脂含有飲食品 |
| EP16765067.0A EP3272835A4 (en) | 2015-03-19 | 2016-03-17 | Oxidation inhibitor, and food and drink containing fats and oils using same |
| PCT/JP2016/058502 WO2016148238A1 (ja) | 2015-03-19 | 2016-03-17 | 酸化抑制剤及びこれを用いた油脂含有飲食品 |
| US15/558,826 US11252974B2 (en) | 2015-03-19 | 2016-03-17 | Oxidation inhibitor, and food and drink containing fats and oils using same |
| TW105108389A TWI711600B (zh) | 2015-03-19 | 2016-03-18 | 抗氧化劑及採用該抗氧化劑的含油脂飲食品 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2015056511A JP6232008B2 (ja) | 2015-03-19 | 2015-03-19 | 酸化抑制剤及びこれを用いた油脂含有飲食品 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016175983A JP2016175983A (ja) | 2016-10-06 |
| JP2016175983A5 true JP2016175983A5 (cg-RX-API-DMAC7.html) | 2017-08-31 |
| JP6232008B2 JP6232008B2 (ja) | 2017-11-15 |
Family
ID=56919066
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015056511A Active JP6232008B2 (ja) | 2015-03-19 | 2015-03-19 | 酸化抑制剤及びこれを用いた油脂含有飲食品 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US11252974B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3272835A4 (cg-RX-API-DMAC7.html) |
| JP (1) | JP6232008B2 (cg-RX-API-DMAC7.html) |
| TW (1) | TWI711600B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2016148238A1 (cg-RX-API-DMAC7.html) |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2343273A (en) * | 1938-07-20 | 1944-03-07 | Marchant Calculating Machine | Calculating machine |
| JPH05320048A (ja) * | 1992-05-19 | 1993-12-03 | Shiseido Co Ltd | 抗酸化剤 |
| JP3813197B2 (ja) * | 1995-03-23 | 2006-08-23 | 雪印乳業株式会社 | 酸化防止剤及びこれを用いた油脂の酸化防止方法 |
| AU1556201A (en) * | 1999-12-06 | 2001-06-18 | Akihiko Niina | Stabilizer for unsaturated compounds or stuff containing the compounds and method of stabilization |
| EP1585508B1 (en) * | 2003-01-20 | 2009-04-01 | Nederlandse Organisatie voor toegepast-natuurwetenschappelijk Onderzoek TNO | Use of sphingolipids for reducing plasma cholesterol and triacylglycerol levels |
| CA2572310A1 (en) * | 2004-06-29 | 2006-01-12 | Jadolabs Gmbh | Sphingolipid-derived pharmaceutical compositions |
| EP2343273A4 (en) * | 2008-09-30 | 2014-04-23 | Kaneka Corp | NOVEL TYPE 1 CERAMIC DERIVATIVE AND MANUFACTURING METHOD THEREFOR |
| WO2010093615A2 (en) * | 2009-02-10 | 2010-08-19 | Tulane University | Compounds, their syntheses, compositions, and methods to treat cancer |
| JP5825672B2 (ja) * | 2011-12-22 | 2015-12-02 | 高砂香料工業株式会社 | 高純度セラミド類の製造方法 |
| JP2013147636A (ja) * | 2011-12-22 | 2013-08-01 | Snow Brand Milk Products Co Ltd | 酸化抑制剤およびこれを用いた油脂含有飲食品 |
-
2015
- 2015-03-19 JP JP2015056511A patent/JP6232008B2/ja active Active
-
2016
- 2016-03-17 US US15/558,826 patent/US11252974B2/en not_active Expired - Fee Related
- 2016-03-17 WO PCT/JP2016/058502 patent/WO2016148238A1/ja not_active Ceased
- 2016-03-17 EP EP16765067.0A patent/EP3272835A4/en not_active Withdrawn
- 2016-03-18 TW TW105108389A patent/TWI711600B/zh not_active IP Right Cessation
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