JPH10279432A5 - - Google Patents

Info

Publication number
JPH10279432A5
JPH10279432A5 JP1997099813A JP9981397A JPH10279432A5 JP H10279432 A5 JPH10279432 A5 JP H10279432A5 JP 1997099813 A JP1997099813 A JP 1997099813A JP 9981397 A JP9981397 A JP 9981397A JP H10279432 A5 JPH10279432 A5 JP H10279432A5
Authority
JP
Japan
Prior art keywords
extract
lignan
glycosides
glycoside
products
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP1997099813A
Other languages
Japanese (ja)
Other versions
JPH10279432A (en
Filing date
Publication date
Application filed filed Critical
Priority to JP9099813A priority Critical patent/JPH10279432A/en
Priority claimed from JP9099813A external-priority patent/JPH10279432A/en
Publication of JPH10279432A publication Critical patent/JPH10279432A/en
Publication of JPH10279432A5 publication Critical patent/JPH10279432A5/ja
Pending legal-status Critical Current

Links

Description

【0005】
すなわち、本発明は、次の成分(A)及び(B)
(A)リグナン配糖体
(B)皮脂分泌調整剤及び/または殺菌剤から選ばれる薬効剤
を含有することを特徴とする組成物を提供するものである。本発明の好ましい実施態様としては、以下の特徴を有する。
(1)該リグナン配糖体が、下記の構造式(I)で示されるリグナン配糖体である。
【化5】
(2)該リグナン配糖体が、下記の構造式(II−a)、(II−b)もしくは(II−c)で示されるリグナン配糖体の1種または2種以上を主成分とするリグナン配糖体である。
【化6】
【化7】
【化8】
(3)該リグナン配糖体が、ゴマ種子やその加湿物もしくは発芽体、またはそれらの粉砕物、またはそれらの脱脂物の含水低級アルコール抽出物である。
(4)該皮脂分泌調整剤が、ピリドキシン及びその誘導体並びにそれらの塩、ビオチン、酸化亜鉛、塩化アルミニウム、塩化ナトリウム、アルミニウムヒドロキシクロライド、クエン酸及びその塩、海水乾燥物、アロエ抽出物、イブキトラノオ抽出物、オウバク抽出物、クレソン抽出物、メリッサ抽出物、ハマメリス抽出物、紅茶抽出物、緑茶抽出物、ウーロン茶抽出物、スギナ抽出物、ホップ抽出物、ローズマリー抽出物から選ばれる1種または2種以上である。
(5)該殺菌剤が安息香酸及びその誘導体並びにその塩、塩化ベンザルコニウム、イソプロピルメチルフェノール、レゾルシン、ビス(2−ピリジルチオ−1−オキシド)亜鉛、イオウ、ショウガ抽出物、クジン抽出物、ティーツリー抽出物、ユーカリ抽出物及びドクダミ抽出物から選ばれる1種または2種以上である。
[0005]
That is, the present invention provides a composition comprising the following components (A) and (B):
(A) Lignan glycosides
(B) a medicinal agent selected from a sebum secretion regulator and/or a bactericide
A preferred embodiment of the present invention has the following features.
(1) The lignan glycoside is a lignan glycoside represented by the following structural formula (I):
[C5]
(2) The lignan glycoside is a lignan glycoside having as its main component one or more of the lignan glycosides represented by the following structural formula (II-a), (II-b) or (II-c):
[C6]
[Chemical 7]
[Chemical formula 8]
(3) The lignan glycoside is a hydrous lower alcohol extract of sesame seeds, their moistened or germinated products, or their pulverized products, or their defatted products.
(4) The sebum secretion regulator is one or more selected from pyridoxine and its derivatives and salts thereof, biotin, zinc oxide, aluminum chloride, sodium chloride, aluminum hydroxychloride, citric acid and its salts, seawater dried products, aloe extract, Ibuki toranoo extract, Phellodendron bark extract, watercress extract, Melissa extract, Hamamelis extract, black tea extract, green tea extract, oolong tea extract, horsetail extract, hop extract, and rosemary extract.
(5) The disinfectant is one or more selected from benzoic acid and its derivatives and salts, benzalkonium chloride, isopropylmethylphenol, resorcinol, zinc bis(2-pyridylthio-1-oxide), sulfur, ginger extract, lily of the valley extract, tea tree extract, eucalyptus extract, and Houttuynia cordata extract.

【0028】
参考例3 高純度リグナン配糖体精製物の製造
参考例2に記載の方法で得られた粗リグナン配糖体を、ODSを担体とする分配クロマトグラフィーに供した。YMC−GEL ODS−A(山村化学(株)製)60gを直径3cm、長さ50cmのガラス製カラムに充填して水を流して平衡化した。これに前記粗リグナン配糖体1gをカラムの上部に負荷した。水から順次メタノール濃度を増加させる段階溶出法によって、分画成分を溶出させた。30〜60%(v/v)メタノールで溶出する画分を集め、減圧濃縮したところ、約100mgのカラム分画物が得られた。
[0028]
Reference Example 3: Preparation of Highly Purified Lignan Glycosides The crude lignan glycosides obtained by the method described in Reference Example 2 were subjected to partition chromatography using ODS as a carrier. 60 g of YMC-GEL ODS-A (Yamamura Chemical Co., Ltd.) was packed into a glass column 3 cm in diameter and 50 cm in length, and equilibrated with water. 1 g of the crude lignan glycosides was loaded onto the top of the column. The fractionated components were eluted by a stepwise elution method, starting with water and gradually increasing the methanol concentration. The fractions eluted with 30-60% (v/v) methanol were collected and concentrated under reduced pressure, yielding approximately 100 mg of column fractions.

【0036】
【表1】
[0036]
[Table 1]

【0037】
(製法)
A.成分(1)〜(7)を混合し、加熱して70℃に保つ。
B.成分(11)(13)を混合し、加熱して70℃に保つ。
C.AにBを加え、混合した後、冷却する。
D.Cに(8)〜(10)及び(12)を加えてクリームを得た。
[0037]
(Manufacturing method)
A. Mix ingredients (1) to (7) and heat to 70°C.
B. Mix ingredients (11) and (13) and heat to 70°C.
C. Add B to A, mix, and then cool.
D. C was added with (8) to (10) and (12) to obtain a cream.

【0042】
【表2】
[0042]
[Table 2]

JP9099813A 1997-04-01 1997-04-01 Composition Pending JPH10279432A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9099813A JPH10279432A (en) 1997-04-01 1997-04-01 Composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9099813A JPH10279432A (en) 1997-04-01 1997-04-01 Composition

Publications (2)

Publication Number Publication Date
JPH10279432A JPH10279432A (en) 1998-10-20
JPH10279432A5 true JPH10279432A5 (en) 2005-03-03

Family

ID=14257301

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9099813A Pending JPH10279432A (en) 1997-04-01 1997-04-01 Composition

Country Status (1)

Country Link
JP (1) JPH10279432A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI20021184L (en) 2002-06-19 2003-12-20 Hormos Nutraceutical Oy Ltd Lignan preparations
WO2004012655A2 (en) * 2002-08-06 2004-02-12 The Quigley Corporation Anti-microbial compositions and methods of using same
KR101252554B1 (en) * 2006-03-17 2013-04-08 (주)아모레퍼시픽 Composition capable of inhibiting sebum secretion
FR2906716B1 (en) * 2006-10-06 2013-05-17 Clarins Lab USE OF A COSMETIC COMPOSITION FOR THE CARE OF OIL SKIN.

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