WO2006132033A1 - 新規トリテルペン酸誘導体及びそれを含有してなる皮膚外用剤 - Google Patents
新規トリテルペン酸誘導体及びそれを含有してなる皮膚外用剤 Download PDFInfo
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- WO2006132033A1 WO2006132033A1 PCT/JP2006/307818 JP2006307818W WO2006132033A1 WO 2006132033 A1 WO2006132033 A1 WO 2006132033A1 JP 2006307818 W JP2006307818 W JP 2006307818W WO 2006132033 A1 WO2006132033 A1 WO 2006132033A1
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- Prior art keywords
- acid
- skin
- salt
- triterpenic
- external preparation
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J63/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
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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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
- A61K31/661—Phosphorus acids or esters thereof not having P—C bonds, e.g. fosfosal, dichlorvos, malathion or mevinphos
-
- 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
- A61K8/55—Phosphorus compounds
-
- 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
- A61K8/63—Steroids; Derivatives thereof
-
- 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
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- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
Definitions
- the present invention relates to a novel triterpenic acid derivative and an external preparation for skin containing the same.
- Triterpenic acids such as ursolic acid are known to have a variety of physiological actions such as anti-acidic action, anti-inflammatory action, and melanin production-suppressing action, and techniques for incorporating them into skin external preparations such as cosmetics are already known.
- these components have problems such as the precipitation of triterpenic acid under long-term storage of a preparation that is not sufficiently soluble in oily components and in aqueous components. Further, since the solubility is not sufficient, there is a concern that the physiological activity of triterpenic acid is reduced and the physiological action is not sufficiently exhibited.
- Patent Document 1 Japanese Patent Application Laid-Open No. 08-165231
- Patent Document 2 Japanese Patent Laid-Open No. 08-208424
- Patent Document 3 No. 01Z072265 gazette
- Patent Document 4 JP-A-11-012122
- Patent Document 5 JP 2000-302659 A
- Patent Document 6 Japanese Patent Application Laid-Open No. 2004-331593
- Patent Document 7 JP-A-11 158197
- Patent Document 8 Japanese Patent Laid-Open No. 2001-354513
- the present invention has been made under such circumstances, and a technique for improving the solubility of triterpenic acids such as ursolic acid, which are known for various physiological activities, without impairing the physiological activities.
- the issue is to provide.
- the present inventors have proposed a technique for improving the solubility of triterpenic acid having a hydroxyl group such as ursolic acid, which is known for various physiological activities, without impairing the physiological activity.
- phosphoric acid-triterpenic acid power has such properties by phosphorylating at least one hydroxyl group of triterpenic acid, and completes the invention. It came to. That is, the present invention is as follows.
- Phosphoric acid triterpenic acid and Z or a salt thereof obtained by phosphorylating at least one of the hydroxyl groups of triterpenic acid having a hydroxyl group.
- Urso-monophosphate [0008] (3) A skin external preparation containing the phosphorylated triterpenic acid according to (1) or (2) and Z or a salt thereof.
- the compound of the present invention is phosphoric acid-triterpenic acid obtained by phosphoric acid-containing at least one of the hydroxyl groups of a triterpenic acid having a hydroxyl group (hereinafter sometimes simply referred to as triterpenic acid).
- the triterpenic acid having a hydroxyl group can be applied without particular limitation as long as it is used in the field of skin external preparations such as cosmetics.
- ursolic acid for example, ursolic acid, oleanolenoic acid, belinic acid, asiatic acid (Asiatic acid, (2 ⁇ , 3 ⁇ , 4 ⁇ ) ⁇ 2, 3, 2 3 Trihydroxy-12 ene-ursolic acid ((2, 3 ⁇ , 4 ⁇ )-2, 3, 23- Trihydr oxyurs -12-en-28-oic acid))
- asiatic acid Asiatic acid, (2 ⁇ , 3 ⁇ , 4 ⁇ ) ⁇ 2, 3, 2 3 Trihydroxy-12 ene-ursolic acid ((2, 3 ⁇ , 4 ⁇ )-2, 3, 23- Trihydr oxyurs -12-en-28-oic acid)
- ursolic acid can be particularly preferably exemplified. This is because it is already on the market as a reagent and is easily available and the physiological activity as a skin external preparation is particularly remarkable.
- triterpenic acid into a phosphoric acid ester may be performed in accordance with a generally known phosphorylation method.
- triterpenic acid is treated with 1 to 3 equivalents of jetyl-N, N jetyl phosphoramidate in the presence of tetrazole, reacted with t-butyl hydride peroxide, and formed with methyl phosphate of triterpenic acid, and It can be produced by reacting bromotrimethylsilane.
- the ursolic acid phosphate obtained by treating ursolic acid by such a method has the structure shown above.
- the phosphoric acid triterpenic acid thus obtained can be converted into a salt by reacting with an alkali usually used in pharmaceuticals and cosmetics.
- alkali metal salts such as sodium salt and potassium salt
- alkaline earth metal salts such as calcium and magnesium
- organic amines such as ammonium salt, triethanolamine salt, and triethylamine salt.
- Preferred examples include basic amino acid salts such as salts, lysine salts and arginine salts. Can show.
- the thus obtained phosphoric acid-triterpenic acid or a salt thereof exhibits remarkable solubility in an aqueous carrier, and its drug activity is significantly improved as compared with the original triterpenic acid.
- the phosphorylated triterpenic acid of the present invention is contained in an external preparation for skin, etc.
- the content is suitably 0.001 to 0.1% by mass with respect to the total amount of the external preparation for skin. This is because if the amount is too small, there is a case where the drug activity does not appear, and if it is too much, the drug activity may reach a peak.
- the external preparation for skin of the present invention contains the phosphoric acid triterpenic acid of the present invention and Z or a salt thereof.
- the external preparation for skin of the present invention include cosmetics and external preparations for skin. Among these, cosmetics can be preferably exemplified. Moreover, it is suitable for quasi-drugs among cosmetics.
- a quasi-drug means a product that has been confirmed to have a specific effect and effect according to the Japanese Pharmaceutical Affairs Law, and that exhibits a milder effect than a pharmaceutical product. In the present invention, it refers to cosmetics intended to prevent or improve specific symptoms as well as beauty. The concept is similar to quasi drugs in Japan and includes cosmetics used for similar purposes. Examples of such cosmetics include cosmetics such as medicinal cosmetics in Korea and drug-containing cosmetics in China.
- the external preparation for skin of the present invention has the anti-inflammatory effect and the melanin production-suppressing action because the essential components of phosphoric acid triterpenic acid and Z or a salt thereof have an anti-inflammatory effect and a melanin production-suppressing action. It is preferable to use a skin external preparation for whitening. Of these, it is preferable to use quasi-drugs for anti-inflammatory diseases and quasi-drugs for inhibiting melanin production. A form that displays the presence of this is preferable. This is because, by taking such a form, it is possible to clearly indicate the mode of use and encourage the user to use it appropriately.
- the external preparation for skin of the present invention includes various components generally used in pharmaceuticals, cosmetics and the like, that is, an aqueous component, an oily component, a powder component, a surfactant, and a moisturizer. , Thickener, colorant, fragrance, antioxidant, pH adjuster, chelating agent, preservative, or UV protection agent, anti-inflammatory agent, wound healing agent, metabolism promoter, whitening agent, etc. Or more can be mix
- Examples of the aqueous component include water, lower alcohols (ethanol, propanol, isopropanol V-) and the like.
- oils component examples include higher fatty acids (stearic acid, palmitic acid, myristic acid, lauric acid, and esters thereof), higher alcohols (cetanol, lanolin alcohol, stearyl alcohol, cetostearyl alcohol, etc.) and Waxes (solid paraffin, microcrystalline wax, ceresin wax, polyethylene wax, beeswax, wood wax, carnauba wax, candelillaro, etc.), natural or synthetic oils (squalane, liquid paraffin, lanolin or derivatives thereof, olive oil, straw oil, Cottonseed oil, oleyl alcohol, castor oil, petrolatum, adipic acid diethoxyethyl ester, silicone oil, hydrofluoric hydrocarbon, etc.).
- higher fatty acids stearic acid, palmitic acid, myristic acid, lauric acid, and esters thereof
- alcohols cetanol, lanolin alcohol, stearyl alcohol, cetostearyl alcohol, etc.
- Waxes solid paraffin,
- Examples of the powder component include aluminum oxide, titanium dioxide, zinc oxide, bengara, yellow iron oxide, ultramarine, bitumen, acrylic resin powder, silica, talc, sericite, my strength, titanium mica, and the like. Can be mentioned.
- Surfactants include, for example, fatty acid soaps (sodium laurate, sodium palmitate, etc.), key-on surfactants such as potassium lauryl sulfate, alkyl sulfate triethanolamine ether; Cationic surfactants such as hum, salt, benzalkonium and laurylamine oxide; imidazoline amphoteric surfactants (2-cocoyl 2-imidazolium-um hydroxide 1 carboxyethyloxy 2 sodium salt, etc.) Betaine surfactants (alkyl betaines, amide betaines, sulfobetaines, etc.), amphoteric surfactants such as isylmethyltaurine; sorbitan fatty acid esters (sorbitan monostearate, sorbitan sesquioleate, etc.), glycerin fatty acids (Glycerol monostearate, etc. , Propylene glycol fatty acid esters (Monosuteari phosphate propylene
- OE sorbitan fatty acid esters POE sorbitan monooleate, polyoxyethylene sorbitan monostearate, etc.
- POE sorbite fatty acid esters POE sorbitan monolaurate, etc.
- POE glycerin fatty acid esters POE glycerin monoisostearate
- POE fatty acid esters polyethylene glycol monooleate, POE distearate, etc.
- POE alkyl ethers POE2-Otachidodecyl ether, etc.
- PO E alkylphenol ethers POE norphenyl ether, etc.
- pull mouth nicks registered trademark
- POE ⁇ POP alkyl ethers POE ⁇ POP2-decyltetradecyl ether, etc.
- Tetronic registered trademark
- humectant examples include glycerin, propylene glycol, 1,3 butylene glycol, dipropylene glycol, ethylene glycol nore, 1,4-butylene glycol nole, diglycerin, triglycerin, sorbit or a derivative thereof, polyethylene glycol Polyols such as Gnore course, Manoletos, Manolecithonole, Sucrose, Funolectus, Slate mononole, Erythritol, Sorbit, Starch-degrading sugar, Hyaluronic acid, Chondroitin sulfate, Hydrolyzed collagen, Hydrolyzed elastin, Carboxymethylchitin, Casein soda , Mucins, glycosphingolipids, etc., and blended in the range of 0.1 to 30% by weight based on the whole
- Examples of the thickener include carboxyvinyl polymer, CP jelly, carboxymethylcellulose, carrageenan, sodium alginate, bentonite, beegum, synthetic hectite and the like.
- antioxidants examples include dibutylated hydroxytoluene (BHT), butylated hydroxy-sol (BHA), tocopherol sodium pyrosulfite, sodium bisulfate, tocofurol acetate and the like.
- Examples of the pH adjuster include citrate, lactic acid, tartaric acid, phosphoric acid and the like.
- Examples of the chelating agent include EDTA (ethylenediaminetetraacetic acid).
- preservatives include p-oxybenzoic acid methyl, ethyl, propyl, butyl ester, phenoxyethanol, o-phenol, dehydroacetic acid or a salt thereof, ⁇ -cresol, m-cresol, o chloro m —Xylenol and the like can be mentioned.
- UV protection agents include urocanic acid or derivatives thereof, isoferulic acid or salts thereof, oxybenzone or derivatives thereof, paminobenzoic acid or derivatives thereof, dibenzoylmethane or derivatives thereof, p-methoxycinnamic acid or derivatives thereof. It is blended in the range of 0.01 to 30% by weight with respect to the whole.
- Examples of the anti-inflammatory agent include glycyrrhetinic acid or a derivative of glycyrrhetinic acid such as stearyl glycyrrhetinate, glycyrrhizic acid or a salt thereof, a Maronnier extract, an aloe extract, and the like. It is blended in the range of 5% by weight.
- wound healing agent examples include royal jelly extract, toki extract, rosemary extract, and oral zumarinic acid, and are blended in the range of 0.01 to 5% by weight.
- Examples of the metabolism promoter include placenta extract, ⁇ oryzanol, amino acids or derivatives thereof, vitamin koji or derivatives thereof, and the like, and is blended in the range of 0.01 to 5% by weight.
- Examples of the whitening agent include pantethine S-sulfonic acid, ascorbic acid or its magnesium phosphate salt, arbutin, kojic acid, linoleic acid, tranexamic acid, esculin and the like.
- an effective ingredient for anti-inflammation particularly for an anti-inflammatory quasi drug Preferred examples of such an active ingredient include stearyl glycyrrhetinate and dipotassium glycyrrhizinate. Further, the content of such an active ingredient is preferably 0.01 to 5% by mass.
- an active ingredient for melanin production suppression and whitening especially for a quasi-drug for melanin production suppression.
- active ingredients include ascorbic acid and its salt, ascorbic acid phosphate and its salt, ascorbic acid dalcoside and its salt, arbutin and its salt, ellagic acid and its salt, tranexamic acid and its salt, 4-methoxysalicylic Examples thereof include acids and salts thereof. Further, the content of such an active ingredient is preferably 0.01 to 5% by mass.
- the external preparation for skin of the present invention can be produced by treating the essential components and optional components according to a conventional method.
- Ursolic acid 48. lg, 0.105 mol
- dimethyl-N, N jetyl phosphoramide After heating a mixture of diethyl N, N-diethylphosphoramidate (34.82g, 0.211mol) and dry tetrahydrofuran (1250ml) to 35 ° C to make a clear solution, 1H- at an internal temperature of 27 ° C Tetrazole (44.25g, 0.632mol) was added in one portion and stirred at room temperature (22 ° C) for 1 hour.
- the reaction solution was cooled with acetone'dry ice, and 70% t-butylhydride peroxide aqueous solution (84 mL, 0.607 mol) was added dropwise at 20 ° C. The temperature was gradually returned to room temperature except for the cooling bath. After confirming disappearance of dimethyl phosphite and formation of dimethyl phosphate by TLC, the reaction was stopped at 0 ° C with 10% aqueous sodium hydrogen sulfite solution (300 ml). Ethyl acetate (1250 mL) was added to the reaction solution, and the organic layer was separated.
- the organic layer was washed successively with 10% aqueous sodium hydrogen sulfite solution (lOOml X 3), 5% aqueous sodium hydrogen carbonate solution (200 ml X 3) and saturated brine, and then dried over anhydrous magnesium sulfate.
- silica gel 400 mL was added to the organic layer and concentrated to dryness under reduced pressure. Silica gel adsorbing this organic layer was packed in a column and packed with hexane. Further, the column was filled with hexane to elute non-adsorbed substances, and then developed with hexane Z ethyl acetate (2: 1).
- the fraction having a single composition was concentrated to obtain 35 g of the title compound as a gel powder.
- absorption of the dichloromethane used for washing with ethyl acetate was recognized by NMR.
- 6 g was obtained as a fraction containing slightly impurities.
- Ursolic acid 3-methyl phosphate (35 g, 62 mmol) synthesized in this manner was dissolved in dry dichloromethane (350 ml), and bromotrimethylsilane (25 mL, 186 mmol) was added under a stream of anoregone at room temperature. The reaction was performed for 1 hour.
- the solubility of the ursolic acid phosphate ester thus obtained was compared with that of ursolic acid as a control.
- Ursolic acid phosphate ester or 20 mg of ursolic acid was placed in a 2 mL glass container, the solvent shown in Table 1 was added, and the mixture was stirred for 16 hours, and then passed through a 0.45 / z m filter. Thereafter, the concentration was measured by HPLC. The results are shown in Table 1.
- the ursolic acid phosphate of the present invention has improved solubility compared to ursolic acid!
- a guinea pig 'maximization test (Guineapig Maximization Test) was conducted using 10 white tray guinea pigs. Emulsions of the same volume of distilled water and Freund's adjuvant complete adjuvant (FCA), test substance (olive oil solution, 5%), and the same volume of test substance and FCA mixture are placed in the skin of 5 guinea pigs. ImL was injected at two locations. On the next day, the site of intradermal injection was shaved, and 10% sodium lauryl sulfate ' ⁇ serine mixture was applied.
- FCA Freund's adjuvant complete adjuvant
- test substance olive oil solution, 5%
- an anti-inflammatory lotion which is an external preparation for skin of the present invention, was prepared. That is, the formulation components were heated to 80 ° C., mixed well, and then stirred and cooled to obtain Lotion 1. Comparative Example 1 in which the ursolic acid phosphate was replaced with ursolic acid was also prepared in the same manner. Lotion 1 was clear and stable even after 3 months storage at 5 ° C, 20 ° C and 40 ° C, but Comparative Example 1 was already cloudy immediately after production.
- Panelists who suffer from rough skin are divided into two groups of 10 people, each group is given lotion 1 and the other group is given comparative example 1 for 2 weeks of continuous use to investigate changes in rough skin conditions.
- the condition of rough skin was judged by scoring an image of the buttock enlarged with a video microscope, with a score according to the following criteria.
- people who feel abnormal skin during use test The test was stopped at the time when the patient felt an abnormality, and the case was dropped.
- the results are shown in Table 2. This shows that the quasi-drug of the present invention has an anti-inflammatory effect equivalent to or better than that containing ursolic acid. In Lotion 1, there was a dropout case. In Comparative Example 1, there was one dropout.
- an anti-inflammatory lotion which is an external preparation for skin of the invention.
- the prescription ingredients were heated to 80 ° C and mixed well, and then the mixture was neutralized by adding mouth) to b), emulsified with vigorous stirring under vigorous stirring, and stirred and cooled to emulsion.
- a comparative example 2 in which the ursolic acid phosphate was replaced with ursolic acid was also prepared. When these were stored at 5 ° C, 20 ° C, and 40 ° C for 1 month, the force that did not change at all was observed in Emulsion 1. In Comparative Example 2, insoluble “collapse” precipitation was observed at all temperature conditions. It was done.
- a mouth preparation for suppressing melanin production which is an external preparation for skin of the present invention, was prepared. That is, the prescription ingredients were heated to 80 ° C., mixed well, and then stirred and cooled to obtain Lotion 2.
- Comparative Example 3 in which the ursolic acid phosphate was replaced with ursolic acid was prepared in the same manner. Lotion 2 was transparent and stable after 3 months of storage at 5 ° C, 20 ° C and 40 ° C, but Comparative Example 3 had already become cloudy immediately after production.
- a mouth preparation for suppressing melanin production which is an external preparation for skin of the present invention, was prepared. That is, the prescription ingredients were heated to 80 ° C., mixed well, and then stirred and cooled to obtain Lotion 3.
- a comparative example 4 in which the ursolic acid phosphate was replaced with ursolic acid was also prepared in the same manner. Lotion 3 was clear and stable after storage at 5 ° C, 20 ° C and 40 ° C for 3 months, but Comparative Example 4 was already turbid immediately after production.
- a mouth preparation for suppressing melanin production which is an external preparation for skin of the present invention, was prepared. That is, the prescription ingredients were heated to 80 ° C., mixed well, and then stirred and cooled to obtain Lotion 4.
- Replace ursolic acid phosphate with ursolic acid Comparative Example 5 was prepared in the same manner. Lotion 4 was transparent and stable after storage at 5 ° C, 20 ° C and 40 ° C for 3 months, but Comparative Example 5 was already turbid immediately after production.
- the present invention a variety of physiological activities are known, and a technique for improving the solubility of triterpenic acid having a hydroxyl group such as ruursolic acid without impairing the physiological activity can be provided.
- the skin external preparation of the present invention can be suitably applied to cosmetics (quasi-drugs) for anti-inflammation or melanin production suppression.
Abstract
Description
Claims
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020087000637A KR101254938B1 (ko) | 2005-06-10 | 2006-04-13 | 신규 트리테르펜산 유도체 및 이를 포함하는 피부 외용제 |
AU2006256351A AU2006256351B2 (en) | 2005-06-10 | 2006-04-13 | Novel triterpenic acid derivative and preparation for external application for skin comprising the same |
US11/912,477 US7718635B2 (en) | 2005-06-10 | 2006-04-13 | Triterpenic acid derivative and preparation for external application for skin comprising the same |
EP06731754.5A EP1889850B1 (en) | 2005-06-10 | 2006-04-13 | Novel triterpenic acid derivative and preparation for external application for skin comprising the same |
CN2006800205185A CN101193907B (zh) | 2005-06-10 | 2006-04-13 | 三萜酸衍生物和包含其的皮肤外用剂 |
JP2007520036A JP5080249B2 (ja) | 2005-06-10 | 2006-04-13 | 新規トリテルペン酸誘導体及びそれを含有してなる皮膚外用剤 |
CA2611435A CA2611435C (en) | 2005-06-10 | 2006-04-13 | Novel triterpenic acid derivative and preparation for external application for skin comprising the same |
ES06731754.5T ES2469566T3 (es) | 2005-06-10 | 2006-04-13 | Nuevo derivado de ácido triterp�nico y preparación para aplicación externa para la piel que lo comprende |
HK08110563.8A HK1121766A1 (en) | 2005-06-10 | 2008-09-23 | Triterpenic acid derivative and preparation for external application for skin comprising the same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2005170220 | 2005-06-10 | ||
JP2005-170220 | 2005-06-10 |
Publications (1)
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WO2006132033A1 true WO2006132033A1 (ja) | 2006-12-14 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/JP2006/307818 WO2006132033A1 (ja) | 2005-06-10 | 2006-04-13 | 新規トリテルペン酸誘導体及びそれを含有してなる皮膚外用剤 |
Country Status (12)
Country | Link |
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US (1) | US7718635B2 (ja) |
EP (1) | EP1889850B1 (ja) |
JP (1) | JP5080249B2 (ja) |
KR (1) | KR101254938B1 (ja) |
CN (1) | CN101193907B (ja) |
AU (1) | AU2006256351B2 (ja) |
CA (1) | CA2611435C (ja) |
ES (1) | ES2469566T3 (ja) |
HK (1) | HK1121766A1 (ja) |
RU (1) | RU2407748C2 (ja) |
TW (1) | TWI376368B (ja) |
WO (1) | WO2006132033A1 (ja) |
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JP2009035512A (ja) * | 2007-08-02 | 2009-02-19 | Pola Chem Ind Inc | 乳化剤形の皮膚外用剤 |
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WO2019039170A1 (ja) * | 2017-08-23 | 2019-02-28 | 一丸ファルコス株式会社 | 美白剤、美白用皮膚外用剤および皮膚の美白方法 |
WO2020013415A1 (ko) * | 2018-07-11 | 2020-01-16 | 차의과학대학교 산학협력단 | 극난용성이 개선 된 신규한 우르솔릭산 공결정 또는 복합제 |
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JP2007332066A (ja) * | 2006-06-14 | 2007-12-27 | Nikko Chemical Co Ltd | チロシナーゼ産生抑制剤 |
JP2009035512A (ja) * | 2007-08-02 | 2009-02-19 | Pola Chem Ind Inc | 乳化剤形の皮膚外用剤 |
JP2014040382A (ja) * | 2012-08-21 | 2014-03-06 | Pola Chem Ind Inc | 皮膚外用組成物 |
JP2014040383A (ja) * | 2012-08-21 | 2014-03-06 | Pola Chem Ind Inc | 皮膚外用組成物 |
JP2014097943A (ja) * | 2012-11-14 | 2014-05-29 | Pola Chem Ind Inc | 高い紫外線吸収効果を有する皮膚外用組成物 |
JP2014037448A (ja) * | 2013-11-29 | 2014-02-27 | Pola Chem Ind Inc | エージング対応用の皮膚外用剤の製造方法 |
RU2667652C2 (ru) * | 2014-04-03 | 2018-09-21 | Пола Кемикал Индастриз, Инк. | Ингибитор меланогенеза, содержащий d-пантотениловый спирт, и косметическое средство для отбеливания кожи, содержащее такой ингибитор меланогенеза |
JPWO2015152384A1 (ja) * | 2014-04-03 | 2017-04-13 | ポーラ化成工業株式会社 | D−パントテニルアルコールからなるメラニン産生抑制剤、及び該メラニン産生抑制剤を含む美白化粧料 |
WO2015152384A1 (ja) * | 2014-04-03 | 2015-10-08 | ポーラ化成工業株式会社 | D-パントテニルアルコールからなるメラニン産生抑制剤、及び該メラニン産生抑制剤を含む美白化粧料 |
EP3536306A2 (en) | 2014-04-03 | 2019-09-11 | Pola Chemical Industries Inc. | Melanogenesis inhibitor comprising d-pantothenyl alcohol, and skin-whitening cosmetic containing same melanogenesis inhibitor |
US10568822B2 (en) | 2014-04-03 | 2020-02-25 | Pola Chemical Industries, Inc. | Melanogenesis inhibitor comprising d-pantothenyl alcohol, and skin-whitening cosmetic containing same melanogenesis inhibitor |
EP3708148A1 (en) | 2014-04-03 | 2020-09-16 | Pola Chemical Industries Inc. | Melanogenesis inhibitor comprising d-pantothenyl alcohol, and skin-whitening cosmetic containing same melanogenesis inhibitor |
IL248114B (en) * | 2014-04-03 | 2022-07-01 | Pola Chem Ind Inc | A melanogenesis suppressant containing pentotanyl-d alcohol, skin whitening preparations containing it and its uses |
EP4234042A1 (en) | 2014-04-03 | 2023-08-30 | Pola Chemical Industries, Inc. | Melanogenesis inhibitor comprising d-pantothenyl alcohol, and skin-whitening cosmetic containing same melanogenesis inhibitor |
WO2019039170A1 (ja) * | 2017-08-23 | 2019-02-28 | 一丸ファルコス株式会社 | 美白剤、美白用皮膚外用剤および皮膚の美白方法 |
WO2020013415A1 (ko) * | 2018-07-11 | 2020-01-16 | 차의과학대학교 산학협력단 | 극난용성이 개선 된 신규한 우르솔릭산 공결정 또는 복합제 |
Also Published As
Publication number | Publication date |
---|---|
RU2008100042A (ru) | 2009-07-20 |
TW200716661A (en) | 2007-05-01 |
HK1121766A1 (en) | 2009-04-30 |
EP1889850A4 (en) | 2011-08-03 |
RU2407748C2 (ru) | 2010-12-27 |
JPWO2006132033A1 (ja) | 2009-01-08 |
ES2469566T3 (es) | 2014-06-18 |
JP5080249B2 (ja) | 2012-11-21 |
AU2006256351A2 (en) | 2006-12-14 |
AU2006256351B2 (en) | 2011-08-04 |
CA2611435A1 (en) | 2006-12-14 |
EP1889850B1 (en) | 2014-03-05 |
CN101193907B (zh) | 2012-07-11 |
US20090075946A1 (en) | 2009-03-19 |
US7718635B2 (en) | 2010-05-18 |
CN101193907A (zh) | 2008-06-04 |
KR101254938B1 (ko) | 2013-04-16 |
CA2611435C (en) | 2013-01-08 |
EP1889850A1 (en) | 2008-02-20 |
TWI376368B (en) | 2012-11-11 |
AU2006256351A1 (en) | 2006-12-14 |
KR20080016948A (ko) | 2008-02-22 |
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