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    • 4. 发明专利
    • Terphenyl derivative and application
    • 泰勒衍生物和应用
    • JP2003306409A
    • 2003-10-28
    • JP2003148687
    • 2003-05-27
    • Kanebo Ltdカネボウ株式会社
    • SAKAI SHINGOSAYO TETSUYAINOUE SHINTAROKAWAGISHI HIROKAZUMURAKAMI HIROAKI
    • A61K8/49A61K8/00A61K8/02A61K8/06A61K31/343A61P17/16A61Q11/00A61K7/00A61K7/16
    • PROBLEM TO BE SOLVED: To obtain a hyaluronic acid decomposition inhibitor and a therapeutic agent, a rough skin or dry skin inhibitor having preventive and therapeutic effect to diseases more physiologically accelerated in decomposition of hyaluronic acid than that in normal state such as xeroderma, psoriasis, rough skin, dry skin and the like and provide a cosmetic effective for preventing wrinkles, improving flexibility and so forth.
      SOLUTION: The cosmetic, the hyaluronic acid decomposition inhibitor, the rough skin or dry skin inhibitor and a therapeutic agent for anomalous decomposition of hyaluronic acid contain an extract of Boletopsis leucomelas or a terphenyl derivative expressed by formula 1 (wherein R
      1 to R
      4 express each OH or acetyl).
      COPYRIGHT: (C)2004,JPO
    • 待解决的问题:为了获得透明质酸分解抑制剂和治疗剂,对透明质酸分解中比在正常状态如透皮质中分解更加生理上加速的疾病具有预防和治疗效果的粗糙皮肤或干性皮肤抑制剂 牛皮癣,皮肤粗糙,皮肤干燥等,并提供有效防止皱纹,提高柔韧性等的化妆品。 解决方案:化妆品,透明质酸分解抑制剂,粗糙皮肤或干性皮肤抑制剂和用于透明质酸异常分解的治疗剂含有Boletopsis leucomelas或由式1表示的三联苯衍生物的提取物(其中R 1 至R SB 表示每个OH或乙酰基)。 版权所有(C)2004,JPO
    • 6. 发明专利
    • ERGOSTEROL GLYCOSIDE DERIVATIVE AND USE
    • JPH11106396A
    • 1999-04-20
    • JP28440597
    • 1997-09-30
    • KANEBO LTD
    • SAKAI SHINGOSAYO TETSUYAINOUE SHINTAROKAMIO MICHIKOKAWAGISHI HIROKAZUHOSOKAWA SATOSHI
    • C12N9/99A61K8/00A61K31/575A61P17/00A61Q11/00C07J17/00
    • PROBLEM TO BE SOLVED: To obtain the subject new derivative useful for a preventive/ therapeutic agent for diseases observed to have hyaluronic acid abnormal decomposition and decomposition accentuation, an inhibitor against hyaluronic acid decomposition, a preventive for chapped skin and dried skin, a cosmetic, etc., comprising a specific ergosterol glycoside. SOLUTION: This new ergosterol glycoside derivative is shown by the formula, is expected to have preventing and treating effects on diseases followed by abnormal decomposition of hyaluronic acid and gingivitis, xeroderma, chapped skin, dried skin, etc., in which hyaluronic acid decomposition is more aggravated than a physiologically normal state and is useful as a medicine composition directly acting on fibroblast, an inhibitor against hyaluronic acid decomposition, a preventive for chapped skin and dried skin, a cosmetic, etc. The glycoside is obtained by extracting a lyophilized substance of a fruit body of Naemaroloma sublateritium a mushroom derived from the family Strophariaceae with an extraction solvent such as water, methanol, etc., filtering or centrifuging the extraction solution to remove impurities, concentrating the filtrate under reduced pressure, reextracting the concentrate with ethyl acetate and drying the extracted essence by lyophilization, etc.
    • 9. 发明专利
    • HYARULONIC ACID PRODUCTION PROMOTER
    • JPH08163983A
    • 1996-06-25
    • JP33399394
    • 1994-12-15
    • KANEBO LTD
    • SAYO TETSUYASAKAI SHINGOINOUE SHINTARO
    • C12N9/50A61K36/06C12P19/26
    • PURPOSE: To obtain a hyarulonic acid production promoter containing, as active ingredient, yeast extract, capable of promoting the hyarulonic acid productivity in human skin fibroblast, thus useful for preventing skin aging and treating such diseases as to involve the abnormal decomposition of hyarulonic acid, and safe to the human body. CONSTITUTION: A mixture comprising cetanol, lipophilic monostearic acid glycerin-polyoxyethylene cetyl ether, liquid paraffin, methylpolysiloxane, etc., is first prepared by homogeneously mixing these components at 80 deg.C, and butyl p-oxybenzoate is added to and dissolved in the mixture. Separately, a second mixture comprising sodium N-stearoyl-L-glutamate, dipropylene glycol and water is prepared by homogeneously mixing these components at 80 deg.C, and a yeast extract is added to and dissolved in this mixture. Subsequently, the resultant two solutions are mutually mixed and then cooled to 30 deg.C under through agitation, thus obtaining the objective promoter having the above- mentioned advantages.