JP2006524234A - アスコルビン酸の安定化誘導体 - Google Patents
アスコルビン酸の安定化誘導体 Download PDFInfo
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- JP2006524234A JP2006524234A JP2006507614A JP2006507614A JP2006524234A JP 2006524234 A JP2006524234 A JP 2006524234A JP 2006507614 A JP2006507614 A JP 2006507614A JP 2006507614 A JP2006507614 A JP 2006507614A JP 2006524234 A JP2006524234 A JP 2006524234A
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- Prior art keywords
- acid
- compound
- ascorbic acid
- composition according
- vitamin
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- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000002858 neurotransmitter agent Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 229940127234 oral contraceptive Drugs 0.000 description 1
- 239000003539 oral contraceptive agent Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003791 organic solvent mixture Substances 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000037368 penetrate the skin Effects 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 230000000865 phosphorylative effect Effects 0.000 description 1
- 230000003711 photoprotective effect Effects 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229940068968 polysorbate 80 Drugs 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229940017794 potassium ascorbate Drugs 0.000 description 1
- 235000019275 potassium ascorbate Nutrition 0.000 description 1
- CONVKSGEGAVTMB-RXSVEWSESA-M potassium-L-ascorbate Chemical compound [K+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] CONVKSGEGAVTMB-RXSVEWSESA-M 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 235000004252 protein component Nutrition 0.000 description 1
- 239000006100 radiation absorber Substances 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000004007 reversed phase HPLC Methods 0.000 description 1
- 239000012898 sample dilution Substances 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 230000037394 skin elasticity Effects 0.000 description 1
- 210000001626 skin fibroblast Anatomy 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 230000005808 skin problem Effects 0.000 description 1
- 230000036555 skin type Effects 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 1
- 235000010378 sodium ascorbate Nutrition 0.000 description 1
- 229960005055 sodium ascorbate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 210000000434 stratum corneum Anatomy 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 235000019364 tetracycline Nutrition 0.000 description 1
- 150000003522 tetracyclines Chemical class 0.000 description 1
- 229940040944 tetracyclines Drugs 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- FGMPLJWBKKVCDB-UHFFFAOYSA-N trans-L-hydroxy-proline Natural products ON1CCCC1C(O)=O FGMPLJWBKKVCDB-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
- 230000037373 wrinkle formation Effects 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/62—Three oxygen atoms, e.g. ascorbic acid
-
- 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
- A23L33/15—Vitamins
-
- 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
- A61K8/67—Vitamins
- A61K8/676—Ascorbic acid, i.e. vitamin C
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/18—Antioxidants, e.g. antiradicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/02—Nutrients, e.g. vitamins, minerals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- 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
-
- 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
-
- 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
- A61Q19/08—Anti-ageing preparations
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dermatology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Gerontology & Geriatric Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Mycology (AREA)
- Obesity (AREA)
- Toxicology (AREA)
- Hematology (AREA)
- Biochemistry (AREA)
- Diabetes (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US46409703P | 2003-04-21 | 2003-04-21 | |
| PCT/IL2004/000343 WO2004094369A2 (en) | 2003-04-21 | 2004-04-21 | Stabilized derivatives of ascorbic acid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006524234A true JP2006524234A (ja) | 2006-10-26 |
| JP2006524234A5 JP2006524234A5 (https=) | 2007-04-05 |
Family
ID=33310853
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006507614A Pending JP2006524234A (ja) | 2003-04-21 | 2004-04-21 | アスコルビン酸の安定化誘導体 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20070167517A1 (https=) |
| EP (1) | EP1620419A4 (https=) |
| JP (1) | JP2006524234A (https=) |
| KR (1) | KR20060008913A (https=) |
| CN (1) | CN1805948A (https=) |
| AU (1) | AU2004232556A1 (https=) |
| BR (1) | BRPI0409628A (https=) |
| CA (1) | CA2523042A1 (https=) |
| MX (1) | MXPA05011269A (https=) |
| WO (1) | WO2004094369A2 (https=) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050266064A1 (en) * | 2004-05-29 | 2005-12-01 | Mccarthy Kathryn J | Cosmetic compositions and methods |
| KR100691540B1 (ko) * | 2006-06-22 | 2007-03-12 | 주식회사 펩트론 | 펩타이드가 결합된 안정화된 비타민 ｃ 유도체, 이의제조방법 및 이를 함유하는 조성물 |
| FR2904549B1 (fr) * | 2006-08-03 | 2012-12-14 | Sederma Sa | Composition comprenant de la sarsasapogenine |
| DE102006037724A1 (de) * | 2006-08-11 | 2008-02-14 | Merck Patent Gmbh | Verwendung von Ascorbinsäurederivaten zur Funktionalisierung von Matrices |
| WO2008036238A2 (en) * | 2006-09-19 | 2008-03-27 | Wyeth | Use of lxr modulators for the prevention and treatment of skin aging |
| US20080095757A1 (en) * | 2006-10-23 | 2008-04-24 | Now Health Group, Inc. | Vitamin c compositions |
| FR2913686B1 (fr) * | 2007-03-14 | 2009-05-01 | Oreal | Nouveaux composes carbamates de vitamine c, compositions les comprenant, et utilisations |
| KR101056037B1 (ko) * | 2007-07-20 | 2011-08-10 | (주)바이오제닉스 | 알파-리포일기 함유 아스코르브산 유도체 및 그의 제조방법 |
| FR2946252B1 (fr) * | 2009-06-08 | 2011-07-29 | Fabre Pierre Dermo Cosmetique | Bis esters d'acide gras insature sur l'acide ascorbique et leurs utilisations cosmetiques |
| DE102009060543B4 (de) * | 2009-12-23 | 2014-02-06 | Axel Muntermann | Verfahren zur kosmetischen Hautglättung |
| US9387194B2 (en) * | 2012-01-18 | 2016-07-12 | Human Matrix Sciences, Llc | Sodium ascorbate stimulation of elastogenesis |
| EP3092220B1 (en) * | 2013-09-25 | 2021-01-20 | University of Florida Research Foundation, Inc. | Vitamin c prodrugs and uses thereof |
| CN103655223B (zh) * | 2013-11-14 | 2016-06-29 | 陕西东大生化科技有限责任公司 | 一种具有预防和治疗痤疮功效的制剂及其应用 |
| CN103896891A (zh) * | 2014-03-25 | 2014-07-02 | 李玉成 | 抗坏血酸锂及其制备方法 |
| CN113825786B (zh) * | 2019-01-11 | 2025-02-07 | 庆北大学校产学协力团 | 合成透明质酸纳米粒子的方法、以及通过该方法制备的透明质酸纳米粒子 |
| CN110467689A (zh) * | 2019-09-09 | 2019-11-19 | 山东众山生物科技有限公司 | 一种透明质酸衍生物及其制备方法 |
| CN113527537B (zh) * | 2021-07-14 | 2022-04-08 | 润辉生物技术（威海）有限公司 | 一种左旋维生素c透明质酸酯衍生物及其制备方法和应用 |
| CN120172937B (zh) * | 2025-03-18 | 2026-02-17 | 上海珈凯生物股份有限公司 | 一种维生素c乙基醚的合成工艺 |
Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61263969A (ja) * | 1985-05-17 | 1986-11-21 | Takeda Chem Ind Ltd | アスコルビン酸誘導体含有製剤 |
| WO1994007883A1 (fr) * | 1992-10-02 | 1994-04-14 | Tsumura & Co. | Sel de lithium d'acide 2-o-alkylascorbique |
| JPH07300469A (ja) * | 1994-01-20 | 1995-11-14 | L'oreal Sa | 桂皮酸またはその誘導体の１つとビタミンｃとのモノエステルまたはジエステル、その製造方法および、それを酸化防止剤として含む化粧品、医薬または栄養の組成物 |
| JPH07309753A (ja) * | 1994-03-01 | 1995-11-28 | Scotia Holdings Plc | 脂肪酸誘導体およびそれを含有する薬剤 |
| JPH11217380A (ja) * | 1997-11-14 | 1999-08-10 | Basf Ag | アスコルビルソルベート、その製造方法及びその使用 |
| JPH11236332A (ja) * | 1997-11-14 | 1999-08-31 | Basf Ag | 化粧用および医薬調剤のためのアスコルビン酸誘導体の使用、このような製剤、アスコルビン酸誘導体およびその製造方法 |
| JPH11286497A (ja) * | 1998-03-31 | 1999-10-19 | Hayashibara Biochem Lab Inc | グリコシル−ｌ−アスコルビン酸のアシル化誘導体 |
| JP2001316261A (ja) * | 2000-04-10 | 2001-11-13 | L'oreal Sa | 表皮セラミド類の合成を増大させるためのアスコルビン酸誘導体の用途 |
| WO2003010173A1 (en) * | 2001-07-26 | 2003-02-06 | Tagra Biotechnologies Ltd. | Stabilized derivatives of ascorbic acid -3-phosphate |
| WO2003018568A2 (en) * | 2001-08-24 | 2003-03-06 | Matthias Rath | Ascorbic acid derivatives, methods of synthesis and pharmaceutical use thereof |
| JP2004051535A (ja) * | 2002-07-19 | 2004-02-19 | Lion Corp | 口腔用組成物 |
-
2004
- 2004-04-21 CN CNA2004800165028A patent/CN1805948A/zh active Pending
- 2004-04-21 BR BRPI0409628-2A patent/BRPI0409628A/pt not_active IP Right Cessation
- 2004-04-21 WO PCT/IL2004/000343 patent/WO2004094369A2/en not_active Ceased
- 2004-04-21 EP EP04728625A patent/EP1620419A4/en not_active Withdrawn
- 2004-04-21 CA CA002523042A patent/CA2523042A1/en not_active Abandoned
- 2004-04-21 MX MXPA05011269A patent/MXPA05011269A/es unknown
- 2004-04-21 KR KR1020057020056A patent/KR20060008913A/ko not_active Withdrawn
- 2004-04-21 AU AU2004232556A patent/AU2004232556A1/en not_active Abandoned
- 2004-04-21 JP JP2006507614A patent/JP2006524234A/ja active Pending
- 2004-04-21 US US10/553,757 patent/US20070167517A1/en not_active Abandoned
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61263969A (ja) * | 1985-05-17 | 1986-11-21 | Takeda Chem Ind Ltd | アスコルビン酸誘導体含有製剤 |
| WO1994007883A1 (fr) * | 1992-10-02 | 1994-04-14 | Tsumura & Co. | Sel de lithium d'acide 2-o-alkylascorbique |
| JPH07300469A (ja) * | 1994-01-20 | 1995-11-14 | L'oreal Sa | 桂皮酸またはその誘導体の１つとビタミンｃとのモノエステルまたはジエステル、その製造方法および、それを酸化防止剤として含む化粧品、医薬または栄養の組成物 |
| JPH07309753A (ja) * | 1994-03-01 | 1995-11-28 | Scotia Holdings Plc | 脂肪酸誘導体およびそれを含有する薬剤 |
| JPH11217380A (ja) * | 1997-11-14 | 1999-08-10 | Basf Ag | アスコルビルソルベート、その製造方法及びその使用 |
| JPH11236332A (ja) * | 1997-11-14 | 1999-08-31 | Basf Ag | 化粧用および医薬調剤のためのアスコルビン酸誘導体の使用、このような製剤、アスコルビン酸誘導体およびその製造方法 |
| JPH11286497A (ja) * | 1998-03-31 | 1999-10-19 | Hayashibara Biochem Lab Inc | グリコシル−ｌ−アスコルビン酸のアシル化誘導体 |
| JP2001316261A (ja) * | 2000-04-10 | 2001-11-13 | L'oreal Sa | 表皮セラミド類の合成を増大させるためのアスコルビン酸誘導体の用途 |
| WO2003010173A1 (en) * | 2001-07-26 | 2003-02-06 | Tagra Biotechnologies Ltd. | Stabilized derivatives of ascorbic acid -3-phosphate |
| WO2003018568A2 (en) * | 2001-08-24 | 2003-03-06 | Matthias Rath | Ascorbic acid derivatives, methods of synthesis and pharmaceutical use thereof |
| JP2004051535A (ja) * | 2002-07-19 | 2004-02-19 | Lion Corp | 口腔用組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2004232556A1 (en) | 2004-11-04 |
| US20070167517A1 (en) | 2007-07-19 |
| CN1805948A (zh) | 2006-07-19 |
| MXPA05011269A (es) | 2006-01-24 |
| KR20060008913A (ko) | 2006-01-27 |
| BRPI0409628A (pt) | 2006-04-25 |
| WO2004094369A3 (en) | 2005-02-03 |
| WO2004094369A2 (en) | 2004-11-04 |
| EP1620419A2 (en) | 2006-02-01 |
| EP1620419A4 (en) | 2008-07-23 |
| CA2523042A1 (en) | 2004-11-04 |
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