DK2344256T3 - Skin treatments containing carboxylic acid-substituted idebenone derivatives and methods of preparation and use thereof - Google Patents
Skin treatments containing carboxylic acid-substituted idebenone derivatives and methods of preparation and use thereof Download PDFInfo
- Publication number
- DK2344256T3 DK2344256T3 DK09807729.0T DK09807729T DK2344256T3 DK 2344256 T3 DK2344256 T3 DK 2344256T3 DK 09807729 T DK09807729 T DK 09807729T DK 2344256 T3 DK2344256 T3 DK 2344256T3
- Authority
- DK
- Denmark
- Prior art keywords
- acid
- idebenone
- skin
- derivatives
- compound
- Prior art date
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- JGPMMRGNQUBGND-UHFFFAOYSA-N idebenone Chemical class COC1=C(OC)C(=O)C(CCCCCCCCCCO)=C(C)C1=O JGPMMRGNQUBGND-UHFFFAOYSA-N 0.000 title claims description 148
- 238000000034 method Methods 0.000 title claims description 26
- 238000002360 preparation method Methods 0.000 title claims description 7
- 238000011282 treatment Methods 0.000 title description 7
- 239000000203 mixture Substances 0.000 claims description 109
- 229960004135 idebenone Drugs 0.000 claims description 85
- -1 dipalmitoyl glycerate Chemical compound 0.000 claims description 58
- 150000001875 compounds Chemical class 0.000 claims description 50
- 239000002537 cosmetic Substances 0.000 claims description 44
- RBNPOMFGQQGHHO-UWTATZPHSA-N D-glyceric acid Chemical compound OC[C@@H](O)C(O)=O RBNPOMFGQQGHHO-UWTATZPHSA-N 0.000 claims description 37
- 239000002253 acid Substances 0.000 claims description 37
- 239000003963 antioxidant agent Substances 0.000 claims description 27
- PORPENFLTBBHSG-MGBGTMOVSA-N 1,2-dihexadecanoyl-sn-glycerol-3-phosphate Chemical group CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCC PORPENFLTBBHSG-MGBGTMOVSA-N 0.000 claims description 25
- 235000000346 sugar Nutrition 0.000 claims description 24
- 239000000194 fatty acid Substances 0.000 claims description 22
- 239000000126 substance Substances 0.000 claims description 22
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 17
- 229930195729 fatty acid Natural products 0.000 claims description 17
- 150000004665 fatty acids Chemical class 0.000 claims description 17
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- 239000000463 material Substances 0.000 claims description 14
- 230000008569 process Effects 0.000 claims description 14
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 150000001735 carboxylic acids Chemical class 0.000 claims description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
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- 230000008859 change Effects 0.000 claims description 9
- 239000004094 surface-active agent Substances 0.000 claims description 9
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 claims description 8
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- 239000002562 thickening agent Substances 0.000 claims description 7
- YCNPPBWOGAQFGQ-UHFFFAOYSA-N (2-hexadecanoyloxy-3-oxo-3-phenylmethoxypropyl) hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC)C(=O)OCC1=CC=CC=C1 YCNPPBWOGAQFGQ-UHFFFAOYSA-N 0.000 claims description 6
- YNDKVGFDHKZHQI-UHFFFAOYSA-N 2,3-di(hexadecanoyloxy)propanoic acid Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(C(O)=O)OC(=O)CCCCCCCCCCCCCCC YNDKVGFDHKZHQI-UHFFFAOYSA-N 0.000 claims description 6
- RDONDBREQKWFBL-UHFFFAOYSA-N benzyl 2,3-dihydroxypropanoate Chemical compound OCC(O)C(=O)OCC1=CC=CC=C1 RDONDBREQKWFBL-UHFFFAOYSA-N 0.000 claims description 6
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- ARBOVOVUTSQWSS-UHFFFAOYSA-N hexadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCC(Cl)=O ARBOVOVUTSQWSS-UHFFFAOYSA-N 0.000 claims description 4
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- 239000003109 Disodium ethylene diamine tetraacetate Substances 0.000 description 7
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 7
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- ODBLHEXUDAPZAU-UHFFFAOYSA-N threo-D-isocitric acid Natural products OC(=O)C(O)C(C(O)=O)CC(O)=O ODBLHEXUDAPZAU-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000002640 tocopherol group Chemical class 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- ZCIHMQAPACOQHT-ZGMPDRQDSA-N trans-isorenieratene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/c1c(C)ccc(C)c1C)C=CC=C(/C)C=Cc2c(C)ccc(C)c2C ZCIHMQAPACOQHT-ZGMPDRQDSA-N 0.000 description 1
- LOIYMIARKYCTBW-OWOJBTEDSA-N trans-urocanic acid Chemical compound OC(=O)\C=C\C1=CNC=N1 LOIYMIARKYCTBW-OWOJBTEDSA-N 0.000 description 1
- LOIYMIARKYCTBW-UHFFFAOYSA-N trans-urocanic acid Natural products OC(=O)C=CC1=CNC=N1 LOIYMIARKYCTBW-UHFFFAOYSA-N 0.000 description 1
- 229960001727 tretinoin Drugs 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- HTJNEBVCZXHBNJ-XCTPRCOBSA-H trimagnesium;(2r)-2-[(1s)-1,2-dihydroxyethyl]-3,4-dihydroxy-2h-furan-5-one;diphosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.OC[C@H](O)[C@H]1OC(=O)C(O)=C1O HTJNEBVCZXHBNJ-XCTPRCOBSA-H 0.000 description 1
- LINXHFKHZLOLEI-UHFFFAOYSA-N trimethyl-[phenyl-bis(trimethylsilyloxy)silyl]oxysilane Chemical compound C[Si](C)(C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C1=CC=CC=C1 LINXHFKHZLOLEI-UHFFFAOYSA-N 0.000 description 1
- BYGOPQKDHGXNCD-UHFFFAOYSA-N tripotassium;iron(3+);hexacyanide Chemical compound [K+].[K+].[K+].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] BYGOPQKDHGXNCD-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 229940040064 ubiquinol Drugs 0.000 description 1
- QNTNKSLOFHEFPK-UPTCCGCDSA-N ubiquinol-10 Chemical compound COC1=C(O)C(C)=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(O)=C1OC QNTNKSLOFHEFPK-UPTCCGCDSA-N 0.000 description 1
- 229940035936 ubiquinone Drugs 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 230000000280 vitalizing effect Effects 0.000 description 1
- 235000019156 vitamin B Nutrition 0.000 description 1
- 239000011720 vitamin B Substances 0.000 description 1
- 230000037373 wrinkle formation Effects 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 229960001296 zinc oxide Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Classifications
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- 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
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- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
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- A—HUMAN NECESSITIES
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
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- A61K8/673—Vitamin B group
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
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- A61K8/67—Vitamins
- A61K8/678—Tocopherol, i.e. vitamin E
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- A—HUMAN NECESSITIES
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- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/16—Emollients or protectives, e.g. against radiation
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/004—Aftersun preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/007—Preparations for dry skin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/02—Preparations for care of the skin for chemically bleaching or whitening the skin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/06—Preparations for care of the skin for countering cellulitis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
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- A61Q19/08—Anti-ageing preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q90/00—Cosmetics or similar toiletry preparations for specific uses not provided for in other groups of this subclass
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/14—Preparation of carboxylic acid esters from carboxylic acid halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/28—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/31—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/95—Esters of quinone carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Gerontology & Geriatric Medicine (AREA)
- Toxicology (AREA)
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Biotechnology (AREA)
- Botany (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Medicinal Preparation (AREA)
- Saccharide Compounds (AREA)
Claims (16)
1. Forbindelse med den almene formel I:
hvor R1 er en lige eller forgrenet C2-22-sukkersyre, og hvor to eller flere hy-droxygrupper på sukkersyren hver især uafhængigt er substitueret med en C-i-22-carboxylsyre.
2. Forbindelse ifølge krav 1, hvor en eller flere carboxylsyrer er en fedtsyre.
3. Forbindelse ifølge krav 2, hvor en eller flere fedtsyrer er en konjugeret fedtsyre.
4. Forbindelse ifølge krav 1, hvor forbindelsen med den almene formel I er idebenondipalmitoylglycerat.
5. Fremgangsmåde til fremstilling af en forbindelse med formel I:
hvor R1 er en lige eller forgrenet C2-22-sukkersyre, og hvor to eller flere hy-droxygrupper på sukkersyren hver især uafhængigt er substitueret med en C-i-22-carboxylsyre; hvor fremgangsmåden omfatter et trin, hvor en tilsvarende di-, tri- eller polycarboxylsyre funktionaliseret sukkersyre forbindes med idebenon.
6. Fremgangsmåde ifølge krav 5, hvor en eller flere carboxylsyrer er en fedtsyre.
7. Fremgangsmåde ifølge krav 6, hvor en eller flere fedtsyrer er en konjugeret fedtsyre.
8. Fremgangsmåde ifølge krav 5 til fremstilling af idebenondipalmitoylglycerat omfattende følgende trin: (a) at underkaste benzylacrylat en dihydroxyleringsreaktion for at danne ben-zyl-2,3-dihydroxypropanoat; (b) at reagere benzyl-2,3-dihydroxypropanoatet med palmitoylchlorid for at danne 3-(benzyloxy)-3-oxopropan-1,2-diyldipalmitat; (c) at reagere 3-(benzyloxy)-3-oxopropan-1,2-diyldipalmitat med ethylacetat for at danne 2,3-bis(palmitoyloxy)propansyre; og (d) at reagere 2,3-bis(palmitoyloxy)propansyre med idebenon for at danne dipalmitoylglycerat.
9. Sammensætning omfattende en forbindelse med den almene formel I:
hvor R1 er en lige eller forgrenet C2-22-sukkersyre, og hvor to eller flere hy-droxygrupper på sukkersyren hver især uafhængigt er substitueret med en C-i-22-carboxylsyre; og mindst et additiv.
10. Sammensætning ifølge krav 9, hvor forbindelsen med den almene formel I er:
11. Forbindelse ifølge krav 9, hvor sammensætningen er tilvejebragt i en form udvalgt blandt cremer, lotions, opløsninger, sera, vandfrie præparater, emulsioner, mikro-emulsioner, multiple emulsioner, geler, faste stifter, salver og aerosoler.
12. Forbindelse ifølge krav 9, hvor det mindst ene additiv er udvalgt blandt overfladeaktive stoffer, kosmetiske hjælpemidler, pigmenter, UVA-filtre, UVB-filtre, drivmidler, fortykningsmidler, emulgatorer, opløsningsmidler, vand, an-tioxidanter, parfumer, farvestoffer, deodoranter, antimikrobielle materialer, back-fatting-midler, komplekserings- og sekvestreringsmidler, perlemorsstoffer, planteekstrakter, vitaminer og kombinationer deraf.
13. Kosmetisk anvendelse af en virksom mængde af en forbindelse ifølge et af kravene 1-4 i en topisk kosmetisk sammensætning til behandling af en hudforandring hos et individ med behov herfor, hvor hudforandringen er ældning af huden.
14. Anvendelse ifølge krav 13, hvor den virksomme mængde er 0,0001 vægt-% til 30 vægt-%, baseret på sammensætningens samlede vægt.
15. Forbindelse ifølge et af kravene 1-4 til anvendelse i en topisk sammensætning til behandling, i en terapeutisk virksom mængde, af en hudforandring hos et individ med behov herfor, hvor hudforandringen er hyperpigmentering eller er forårsaget af UV-skade eller omfatter erythematøse symptomer eller er cellulitis.
16. Forbindelse ifølge krav 15, hvor den terapeutisk virksomme mængde er 0,0001 vægt-% til 30 vægt-%, baseret på sammensætningens samlede vægt.
Applications Claiming Priority (2)
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US10304308P | 2008-10-06 | 2008-10-06 | |
PCT/US2009/059673 WO2010051138A2 (en) | 2008-10-06 | 2009-10-06 | Skin treatments containing carboxylic acid-substituted idebenone derivatives and methods of preparation and use thereof |
Publications (1)
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DK2344256T3 true DK2344256T3 (da) | 2017-07-17 |
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DK09807729.0T DK2344256T3 (da) | 2008-10-06 | 2009-10-06 | Skin treatments containing carboxylic acid-substituted idebenone derivatives and methods of preparation and use thereof |
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US (4) | US8173703B2 (da) |
EP (1) | EP2344256B1 (da) |
JP (1) | JP5739335B2 (da) |
KR (1) | KR101630240B1 (da) |
CN (1) | CN102231996B (da) |
AU (1) | AU2009309056B2 (da) |
BR (1) | BRPI0920020B1 (da) |
CA (1) | CA2739974C (da) |
DK (1) | DK2344256T3 (da) |
ES (1) | ES2634423T3 (da) |
HK (1) | HK1162996A1 (da) |
IL (1) | IL211844A (da) |
MX (1) | MX2011003361A (da) |
NZ (1) | NZ592663A (da) |
RU (1) | RU2537299C2 (da) |
SG (1) | SG194410A1 (da) |
WO (1) | WO2010051138A2 (da) |
ZA (1) | ZA201101965B (da) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7872047B2 (en) * | 2008-02-08 | 2011-01-18 | Eastman Chemical Company | Esters of long-chain alcohols and preparation thereof |
WO2014043230A2 (en) * | 2012-09-14 | 2014-03-20 | Elizabeth Arden, Inc. | Formulations comprising idebenone, n-acetyl-s-farnesyl-l-cysteine and ergothioneine and uses thereof |
WO2016153938A1 (en) * | 2015-03-25 | 2016-09-29 | Biosynthetic Technologies, Llc | Ester compounds including triesters having terminal vicinal acyl groups |
IT201600111315A1 (it) * | 2016-11-04 | 2018-05-04 | Laura Castoldi | Composizione cosmetica anti-età. |
FR3091176B1 (fr) * | 2018-12-26 | 2021-04-16 | Oreal | Composition cosmétique comprenant des filtres UV hydrosolubles |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4144325A (en) | 1976-11-10 | 1979-03-13 | Voyt Walter F | Method of and composition for preventing sunburn while affording tanning |
US4248861A (en) | 1979-02-21 | 1981-02-03 | Schutt Steven R | Skin treatment methods |
JPS6143132A (ja) * | 1984-08-06 | 1986-03-01 | Takeda Chem Ind Ltd | キノン誘導体,その製造法およびそれを含んでなる医薬組成物 |
FR2765881B1 (fr) * | 1997-07-09 | 1999-08-13 | Michelin & Cie | Composition de caoutchouc vulcanisable au soufre contenant de la silice |
DE19932197A1 (de) * | 1999-07-09 | 2001-01-18 | Neudecker Birgit | Topisch anzuwendendes Mittel mit schützender und regenerativer Wirkung |
US20050281853A1 (en) * | 2002-02-15 | 2005-12-22 | Fox Charles A | Skin compatible cosmetic compositions and delivery methods therefor |
AU2004266988B2 (en) * | 2003-08-22 | 2011-05-26 | Antipodean Pharmaceuticals, Inc. | Mitoquinone derivatives used as mitochondrially targeted antioxidants |
AR055453A1 (es) * | 2004-01-06 | 2007-08-22 | Creactivar S A | Uso de la idebenona en una composicion destinada a ser aplicada sobre la piel y composicion que la comprende |
KR101312422B1 (ko) * | 2004-12-22 | 2013-09-30 | 시바 홀딩 인코포레이티드 | 항라디칼제 |
US7872047B2 (en) * | 2008-02-08 | 2011-01-18 | Eastman Chemical Company | Esters of long-chain alcohols and preparation thereof |
CN102238983B (zh) * | 2008-06-25 | 2016-08-24 | 巴斯夫欧洲公司 | 苯并环庚三烯酚酮衍生物作为uv吸收剂和抗氧化剂的用途及其在防晒剂和/或化妆品组合物中的用途 |
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2009
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- 2009-10-06 US US12/574,135 patent/US8173703B2/en active Active
- 2009-10-06 DK DK09807729.0T patent/DK2344256T3/da active
- 2009-10-06 BR BRPI0920020A patent/BRPI0920020B1/pt active IP Right Grant
- 2009-10-06 RU RU2011112707/04A patent/RU2537299C2/ru active
- 2009-10-06 EP EP09807729.0A patent/EP2344256B1/en active Active
- 2009-10-06 CA CA2739974A patent/CA2739974C/en active Active
-
2011
- 2011-03-15 ZA ZA2011/01965A patent/ZA201101965B/en unknown
- 2011-03-22 IL IL211844A patent/IL211844A/en active IP Right Grant
-
2012
- 2012-01-13 US US13/349,651 patent/US8354550B2/en active Active
- 2012-04-09 HK HK12103450.3A patent/HK1162996A1/xx unknown
- 2012-12-13 US US13/714,136 patent/US9290436B2/en active Active
-
2016
- 2016-02-08 US US15/018,259 patent/US20160151260A1/en not_active Abandoned
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