COMPOSITION FOR EXTERNAL USE
    1.
    发明授权
    COMPOSITION FOR EXTERNAL USE 有权
    ZUSAMMENSETZUNG ZURÄUßERLICHENANWENDUNG

    公开(公告)号:EP1640025B1

    公开(公告)日:2010-12-15

    申请号:EP04746481.3

    申请日:2004-06-25

    IPC分类号: A61L31/00

    摘要: It is intended to provide a skin composition for external use that contains an ascorbic acid derivative having a high stability, being continuously usable in vivo, having a strong antioxidant effect and showing little skin irritation and has an excellent skin permeability. A composition for external use characterized by containing 2-O-(β-D-glucopyranosyl)ascorbic acid represented by the formula (I) or its salt or ester being safe to the human body together with optionally treated koji mold cells.

    摘要翻译: 一种外用组合物,其包含由式(I)表示的2-O-(2-D-吡喃葡萄糖基)抗坏血酸:或其对人体安全的盐或酯,以及曲霉或加工曲 。 外用组合物的皮肤透过性优异,含有稳定性优异,抗生素活性强,抗氧化活性强的抗坏血酸衍生物。

    Method for producing oligosaccharides
    4.
    发明公开
    Method for producing oligosaccharides 失效
    生产寡糖的方法

    公开(公告)号:EP0266177A3

    公开(公告)日:1989-01-25

    申请号:EP87309496.5

    申请日:1987-10-27

    IPC分类号: C12P19/00 C12N9/38

    摘要: The present invention provides a method of producing oligosaccharides by the reaction between lactose and β-galactosidase from Aspergillus oryzae in which an concentration of lactose in an enzyme reaction mixture is between 50 and 90% (w/v) and a reaction temperature is within the range of 55°C to the temperature at which the β-galactosidase in the reaction mixture is inactivated. This invention therefore makes it possible to obtain the sugar mixture containing high-purity oligosaccharides, small amounts of unreacted lactose and by produced monosaccharides.

    摘要翻译: 本发明提供了一种通过来自米曲霉的乳糖和β-半乳糖苷酶之间的反应生产寡糖的方法,其中酶反应混合物中乳糖的浓度为50-90%(w / v),反应温度在 从55℃到反应混合物中β-半乳糖苷酶失活的温度。 因此,本发明可以获得含有高纯度寡糖,少量未反应的乳糖和产生的单糖的糖混合物。

    Method for producing oligosaccharides
    5.
    发明公开
    Method for producing oligosaccharides 失效
    Verfahren zur Herstellung von Oligosacchariden。

    公开(公告)号:EP0266177A2

    公开(公告)日:1988-05-04

    申请号:EP87309496.5

    申请日:1987-10-27

    IPC分类号: C12P19/00 C12N9/38

    摘要: The present invention provides a method of producing oligosaccharides by the reaction between lactose and β-galactosidase from Aspergillus oryzae in which an concentration of lactose in an enzyme reaction mixture is between 50 and 90% (w/v) and a reaction temperature is within the range of 55°C to the temperature at which the β-galactosidase in the reaction mixture is inactivated. This invention therefore makes it possible to obtain the sugar mixture containing high-purity oligosaccharides, small amounts of unreacted lactose and by produced monosaccharides.

    摘要翻译: 本发明提供了通过乳糖和β-半乳糖苷酶与米曲霉之间的反应制备寡糖的方法,其中酶反应混合物中的乳糖浓度为50-90%(w / v),反应温度在 范围为55℃至反应混合物中β-半乳糖苷酶失活的温度。 因此,本发明使得可以获得含有高纯度寡糖,少量未反应的乳糖和产生的单糖的糖混合物。

    PROCESS FOR PRODUCING OPTICALLY ACTIVE 3-QUINUCLIDINOL DERIVATIVES
    7.
    发明公开
    PROCESS FOR PRODUCING OPTICALLY ACTIVE 3-QUINUCLIDINOL DERIVATIVES 失效
    VERFAHREN ZUR HERSTELLUNG OPTISCH AKTIVER 3-QUINUCLIDINOL DERIVATE

    公开(公告)号:EP0945518A4

    公开(公告)日:1999-11-17

    申请号:EP97909738

    申请日:1997-11-04

    摘要: A process for producing optically active quinuclidinol derivatives characterized by treating racemic 3-quinuclidinol esters represented by general formula (I) (wherein R represents linear or branched alkyl; and (H ) means an optional formation of a salt with a mineral or organic acid) with cells of microorganisms belonging to the genus Aspergillus, Rhizopus, Candida or Pseudomonas and capable of asymmetrically hydrolyzing the ester bond, liquid cultures of the microbial cells, treated microbial cells, enzymes produced by these microorganisms, or enzymes of swine or bovine origin. This process makes it possible to easily produce optically active 3-quinuclidinol derivatives which are valuable intermediates in synthesizing drugs, etc.

    摘要翻译: 一种制备光学活性的奎宁醇衍生物的方法,其特征在于处理由通式(I)表示的外消旋3-奎核醇醇酯(其中R代表直链或支链烷基;和(H +)意指任意形成与矿物或 有机酸)与属于曲霉属,根霉属,假丝酵母​​属或假单胞菌属的微生物的细胞并且能够不对称地水解酯键,微生物细胞的液体培养物,经处理的微生物细胞,由这些微生物产生的酶或猪或牛的酶 起源。 该过程使得可以容易地制备光学活性的3-奎宁环醇衍生物,其是合成药物等中有价值的中间体。

    Procédé microbiologique d'obtention de méthylcétones
    10.
    发明公开
    Procédé microbiologique d'obtention de méthylcétones 失效
    为甲基酮的制备微生物处理。

    公开(公告)号:EP0390624A1

    公开(公告)日:1990-10-03

    申请号:EP90400518.8

    申请日:1990-02-26

    申请人: ELF SANOFI

    IPC分类号: C12P7/26

    摘要: L'invention a pour objet un procédé d'obtention de méthylcétones en C₅ à C₁₀ par bioconversion d'acides gras en C₆ à C₁₁ par des spores de champignons filamenteux du genre Amastigomycota . Ce procédé est mis en oeuvre dans un solvant organique inerte dont le logarithme du coefficient de partage entre l'eau et l'octane est supérieur à 4, avantageusement dans un hydrocarbure aliphatique en C₈ à C₂₀ ou un mélange de tels hydrocarbures, contenant au plus 20% d'eau. Application : obtention de méthylcétones arômatiques comme aromes.