Abstract:
A bathing preparation comprising an alkyl phthalide and/or an alkoxy phthalide and/or an alkylidene phthalide optionally together with carbon dioxide gas or a material capable of generating carbon dioxide gas and an extract of a plant belonging to the family Umbelliferae is disclosed. This bathing preparation has excellent effects of warming, retaining the warmth and accelerating blood circulation.
Abstract:
A bathing preparation comprising an alkyl phthalide and/or an alkoxy phthalide and/or an alkylidene phthalide optionally together with carbon dioxide gas or a material capable of generating carbon dioxide gas and an extract of a plant belonging to the family Umbelliferae is disclosed. This bathing preparation has excellent effects of warming, retaining the warmth and accelerating blood circulation.
Abstract:
PROBLEM TO BE SOLVED: To provide a skin care preparation for external use having efficacy for preventing or improving skin aging such as wrinkles and also having efficacy for inhibiting hair growth. SOLUTION: There are provided fructosyl dipeptide represented by general formula (1): Fru-A-B-R or its salt, as well as a skin care preparation for external use, a hair growth inhibitor and a wrinkle-preventing or improving agent, each containing the same. In the general formula (1), Fru represents a fructosyl residue; A represents a valine residue or an isoleucine residue; B represents a tyrosine residue, a phenylalanine residue, a valine residue or an isoleucine residue; R represents a hydroxy group or a methoxy group. COPYRIGHT: (C)2010,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a simple and efficient method for producing a useful branched fatty acid using industrially available raw materials. SOLUTION: The method for producing a branched fatty acid comprises (a) causing a cyclic ester represented by formula (1) (in the formula, n represents an integer of 9 to 17) to react with hydrogen bromide in an acetic acid solvent to obtain a bromocarboxylic acid represented by formula (2): Br-(CH 2 ) n -CO 2 H (in the formula, n is the same as defined above) and (b) subsequently causing the resulting bromocarboxylic acid to react with a Grignard reagent represented by formula (3): R 1 MgX (in the formula, R 1 represents a 3-8C branched alkyl group, and X represents a halogen atom) to obtain a 13-26C branched fatty acid represented by formula (4): R 1 -(CH 2 ) n -CO 2 H (in the formula, R 1 is the same as defined above, and n is the same as defined above). COPYRIGHT: (C)2009,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a new nuclear factor of activated T cells (NFAT) signal inhibitor which can inhibit NFAT signal. SOLUTION: This NFAT signal inhibitor comprises at least one selected from the group consisting of at least plant selected from Dolichandrone spthacea, Cocculus orbiculatus, and Siegesbeckia orientalis L., the extract of the plant, and an ingredient contained in the extract, as an active ingredient. The NFAT signal inhibitor of the present invention can be applied to various fields such as external preparations, pharmaceutical compositions, cosmetics and foods. COPYRIGHT: (C)2009,JPO&INPIT
Abstract translation:要解决的问题:提供可抑制NFAT信号的活化T细胞(NFAT)信号抑制剂的新核因子。 解决方案:该NFAT信号抑制剂包括至少一种选自至少一种选自杜立丹酮,,藜,Coc and L.,植物提取物,以及提取物中所含的成分的植物, 作为活性成分。 本发明的NFAT信号抑制剂可以应用于外用制剂,药物组合物,化妆品,食品等各种领域。 版权所有(C)2009,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a method for producing a cross-coupled compound. SOLUTION: The method for producing the cross-coupled compound comprises conducting a reaction between a Grignard compound and an organic electrophilic agent in the presence of a copper catalyst and a phosphine of formula R 3 3 P (wherein, R 3 is a 1-6C alkyl, cyclohexyl or a phenyl group optionally having a methyl or methoxy group) or a phosphite of the formula (R 4 O) 3 P (wherein, R 4 is a 1-4C alkyl). COPYRIGHT: (C)2009,JPO&INPIT