JPS62142193A - Novel tannin - Google Patents

Novel tannin

Info

Publication number
JPS62142193A
JPS62142193A JP29189386A JP29189386A JPS62142193A JP S62142193 A JPS62142193 A JP S62142193A JP 29189386 A JP29189386 A JP 29189386A JP 29189386 A JP29189386 A JP 29189386A JP S62142193 A JPS62142193 A JP S62142193A
Authority
JP
Japan
Prior art keywords
acetone
substance
formula
present
soluble substance
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.)
Granted
Application number
JP29189386A
Other languages
Japanese (ja)
Other versions
JPH0246598B2 (en
Inventor
Itsuo Nishioka
西岡 五夫
Genichiro Nonaka
源一郎 野中
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Shinyaku Co Ltd
Original Assignee
Nippon Shinyaku Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nippon Shinyaku Co Ltd filed Critical Nippon Shinyaku Co Ltd
Priority to JP29189386A priority Critical patent/JPH0246598B2/en
Publication of JPS62142193A publication Critical patent/JPS62142193A/en
Publication of JPH0246598B2 publication Critical patent/JPH0246598B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)

Abstract

NEW MATERIAL:A compound shown by formula I (G is galloyl shown by formula II). USE:An antiallergic agent and an antiviral agent. PREPARATION:For example, sanguisorba Radix is extracted with aqueous acetone and acetone is distilled away. Then, the residue is partitioned with ethyl acetate and a water-soluble substance is collected, incorporated with sellaite and air-dried. The prepared substance is packed into a column and eluted with acetone to give an acetone-soluble substance. This substance is separated and purified by liquid chromatography.

Description

【発明の詳細な説明】 本発明は医薬品として有用な新規タンニンに関する。[Detailed description of the invention] The present invention relates to novel tannins useful as pharmaceuticals.

タンニンは広く植物界に分布し、収斂作用のあることか
ら古くから知られ、収斂薬として、また皮を革に変化さ
せるなめし剤として多く用いられてきた。
Tannins are widely distributed in the plant kingdom and have long been known for their astringent properties, and have been widely used as an astringent and as a tanning agent to transform hides into leather.

タンニンは分子量600〜2000はどの植物の@量成
分で複雑な構造を有しており、単離精製の困難さとあい
まって研究が遅れていた。
Tannin has a molecular weight of 600 to 2,000 and is a component of all plants, and has a complex structure, which, combined with the difficulty of isolation and purification, has delayed research.

一方、従来より、地検等の植物が、酵素阻害作用等に基
づく有用な医薬的効果を有することが知られていた。
On the other hand, it has been known for a long time that plants such as Chiken have useful medicinal effects based on enzyme inhibitory effects and the like.

本発明者らは、これらの植物の薬効成分を検索する目的
でこれらに含まれる成分を単離取得して薬理効果を調べ
た結果、幸運にも新規なるタンニンに酵素阻害作用のあ
ることを見出し本発明を完成した。
In order to search for medicinal components in these plants, the present inventors isolated and obtained the components contained in these plants and investigated their pharmacological effects. Fortunately, the inventors discovered that a new tannin has an enzyme-inhibiting effect. The invention has been completed.

本発明に係る化合物は、体中酵素蛋白と結合することに
よってその活性を低下させる作用を有している。
The compound according to the present invention has the effect of reducing the activity of enzyme proteins in the body by binding to them.

本発明に係る化合物が抗ヒアルロニダーゼ活性を有して
いることが明らかになっており、本発明化合物は抗アレ
ルギー剤として有用である。
It has been revealed that the compound according to the present invention has anti-hyaluronidase activity, and the compound of the present invention is useful as an anti-allergic agent.

また、本発明に係る化合物には、ヘルペスウィルスの発
育を阻害する作用が認められ、抗ウィルス剤としてその
活用が期待される。
Furthermore, the compound according to the present invention has been found to have an effect of inhibiting the growth of herpesvirus, and is expected to be used as an antiviral agent.

本発明に係る化合物は、地楡、ウラジロガシ皮、茶菓、
ザクロ葉、メヒルギ皮、櫟樹皮等の植物から、アセトン
による抽出、酢酸エチル:水の分配、あるいはカラムク
ロマト等の公知の方法により容易に得ることができる。
The compounds according to the present invention include elm, Japanese oak bark, tea confectionery,
It can be easily obtained from plants such as pomegranate leaves, cane bark, and oak bark by known methods such as extraction with acetone, ethyl acetate:water partitioning, or column chromatography.

以下に本発明に係る化合物の製造に関する実施例を掲げ
る。
Examples related to the production of compounds according to the present invention are listed below.

実施例 地楡16kgを、80%の水性アセトン60βで3回抽
出し、アセトンを留去する。留去後、酢酸エチルの5β
で8回分液し、水可溶物質を集める。セライトを加えて
風乾する。これをカラムにつめてアセトンで溶出し、ア
セトン可溶物質を得る。これをさらにセファデックスL
H−20クロマトで分離精製したところ、19gの褐色
の無晶形粉末■を得た。
EXAMPLE 16 kg of elms are extracted three times with 80% aqueous acetone 60β and the acetone is distilled off. After distillation, 5β of ethyl acetate
Separate the solution 8 times and collect water-soluble substances. Add Celite and air dry. This is packed into a column and eluted with acetone to obtain an acetone-soluble substance. Add this to Sephadex L
Separation and purification using H-20 chromatography yielded 19 g of brown amorphous powder (2).

■Sanguiin H−11 rr Lan amorpl+ous powder〔
αlo  +33.9° (C=0.94 aceto
ne)PMR(acetone−d6)δ: 3.09
7,3.928.3.954゜4.039  (eac
hlH,br、d、J = 13.2)1z、12.7
,12.3.13.211zrespectively
、 H−6,6’、6” and 6”’ ) 、4.
146.4.36Q。
■Sanguiin H-11 rr Lan amorpl+ous powder
αlo +33.9° (C=0.94 aceto
ne) PMR (acetone-d6) δ: 3.09
7,3.928.3.954゜4.039 (eac
hlH, br, d, J = 13.2) 1z, 12.7
,12.3.13.211zrespectively
, H-6,6', 6" and 6"'), 4.
146.4.36Q.

4.485〜4.550 (4Hin total、m
、ll−5+5’、5” and 5”’)4.111
81,4.947,5.022,5.081,5.11
2,5.157  (8111nLoLal、each
 t、J=9.52,9.77.10.01.10.2
5,8.55,9.76Hz respectivel
y H−2+3+3’+3” +4+4’+4” an
d 4”’) +5.2111  (III、 t、 
J−a、 7911z山2’り)  、5.291 (
2+1.dd、J=3.41,9.10Hz、)l−2
and 2”) 、5.366 (1+l、dd、J 
=6.80゜13.6Hz、  H−6”’)  、5
.426  (IH,t、   J= 9.28+1z
、  11−3″)5.523.5.682 (eac
h ill、dd、J= 6.5,1311z、If−
6or 6’)、5.920 (111,d、J=8.
311z、It−1’)  、  5.940  (I
II、  m、  Iトロ′)  、  6.1?5.
 6.212  (each  Ill、  s、  
八r−It)  、  6.311   (LH。
4.485~4.550 (4Hin total, m
, ll-5+5', 5" and 5"') 4.111
81, 4.947, 5.022, 5.081, 5.11
2,5.157 (8111nLoLal, each
t, J=9.52,9.77.10.01.10.2
5, 8.55, 9.76Hz spectivel
y H-2+3+3'+3"+4+4'+4" an
d 4”') +5.2111 (III, t,
J-a, 7911z mountain 2'ri), 5.291 (
2+1. dd, J=3.41, 9.10Hz, )l-2
and 2”), 5.366 (1+l, dd, J
=6.80°13.6Hz, H-6''), 5
.. 426 (IH, t, J= 9.28+1z
, 11-3″) 5.523.5.682 (eac
h ill, dd, J= 6.5, 1311z, If-
6or 6'), 5.920 (111, d, J=8.
311z, It-1'), 5.940 (I
II, m, Itro'), 6.1?5.
6.212 (each Ill, s,
8r-It), 6.311 (LH.

d、 J=8.8)1z、 If−1”’) 、 6.
330.6.335.6.363.6.3B3゜6.3
86.6.513 (each IH,s、 Ar−I
f) 、 6.525 (III、 d。
d, J=8.8)1z, If-1"'), 6.
330.6.335.6.363.6.3B3゜6.3
86.6.513 (each IH,s, Ar-I
f), 6.525 (III, d.

J=3.9)1z、  H−1or  1”  )  
、  6.540   (LH,s、  八r−11)
6.549  (l)I、  d、  J−3,4Hz
、  H−1or  1”  )  6.774゜6.
795. 6.8[37,6,907(esch  I
H,s、  Ar−H)  7.018゜?、116 
(each d、 J = 2.011z、 Ar−1
1)  、 ’7.24 (311,br、s。
J=3.9)1z, H-1or 1”)
, 6.540 (LH,s, 8r-11)
6.549 (l) I, d, J-3,4Hz
, H-1or 1”) 6.774°6.
795. 6.8[37,6,907(esch I
H, s, Ar-H) 7.018°? , 116
(each d, J = 2.011z, Ar-1
1), '7.24 (311, br, s.

galloyl−H,Ar−II)、7.188,7.
20?、7.386  (eachlll。
galloyl-H, Ar-II), 7.188, 7.
20? , 7.386 (eachllll.

d、  J  =2.0IIz、  Ar−If )以
d, J = 2.0IIz, Ar-If) or more

Claims (1)

【特許請求の範囲】 次の式〔 I 〕 ▲数式、化学式、表等があります▼〔 I 〕 (Gはガロイル基▲数式、化学式、表等があります▼ を表わす。)で表わされる新規なるタンニン。[Claims] The following formula [I] ▲There are mathematical formulas, chemical formulas, tables, etc.▼〔I〕 (G is galloyl group ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ represents. ) is a new tannin.
JP29189386A 1986-12-08 1986-12-08 SHINKINARUTANNIN Expired - Lifetime JPH0246598B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29189386A JPH0246598B2 (en) 1986-12-08 1986-12-08 SHINKINARUTANNIN

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29189386A JPH0246598B2 (en) 1986-12-08 1986-12-08 SHINKINARUTANNIN

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP58070774A Division JPS59196884A (en) 1983-04-20 1983-04-20 Novel tannin

Publications (2)

Publication Number Publication Date
JPS62142193A true JPS62142193A (en) 1987-06-25
JPH0246598B2 JPH0246598B2 (en) 1990-10-16

Family

ID=17774815

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29189386A Expired - Lifetime JPH0246598B2 (en) 1986-12-08 1986-12-08 SHINKINARUTANNIN

Country Status (1)

Country Link
JP (1) JPH0246598B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0374888A2 (en) * 1988-12-20 1990-06-27 Yamanouchi Pharmaceutical Co. Ltd. Sulfated tannins and theirs salts
EP0727218A3 (en) * 1995-02-10 1997-01-15 Suntory Ltd Anti-allergic composition containing god-type ellagitannin as active ingredient
EP0727217A3 (en) * 1995-02-10 1997-01-15 Suntory Ltd Pharmaceutical composition containing god-type ellagitannin as active ingredient
JP2005179285A (en) * 2003-12-22 2005-07-07 Lotte Co Ltd Histamine liberation inhibitor and food and drink containing the same

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0374888A2 (en) * 1988-12-20 1990-06-27 Yamanouchi Pharmaceutical Co. Ltd. Sulfated tannins and theirs salts
US5159069A (en) * 1988-12-20 1992-10-27 Yamanouchi Pharmaceutical Co., Ltd. Sulfated tannins and their salts
EP0727218A3 (en) * 1995-02-10 1997-01-15 Suntory Ltd Anti-allergic composition containing god-type ellagitannin as active ingredient
EP0727217A3 (en) * 1995-02-10 1997-01-15 Suntory Ltd Pharmaceutical composition containing god-type ellagitannin as active ingredient
JP2005179285A (en) * 2003-12-22 2005-07-07 Lotte Co Ltd Histamine liberation inhibitor and food and drink containing the same
JP4491065B2 (en) * 2003-12-22 2010-06-30 株式会社ロッテ Histamine release inhibitor

Also Published As

Publication number Publication date
JPH0246598B2 (en) 1990-10-16

Similar Documents

Publication Publication Date Title
KR100315495B1 (en) Taxanes with antitumor activity
JPS6222990B2 (en)
EP0006060A1 (en) Inula extract, process for preparing it and its use as a medicament
NO863329L (en) PHARMACOLOGICAL EFFECT.
JPS62142181A (en) Novel tannin
JPS62142193A (en) Novel tannin
CN103494806B (en) Application of benzene a pair of horses going side by side alpha-pyrone compound and preparation method thereof
JPH0229078B2 (en)
JPS6248677A (en) Novel tannin
CN116606269B (en) Renilla diterpenoid compound and extract L01 and application thereof in pharmacy
KR100205045B1 (en) Novel triterpene glycosidic compound process thereof
JP5462996B2 (en) A hepatoprotective agent obtained from the bonsai, a pharmaceutical or food containing the hepatoprotectant, and a novel Megastigman compound obtained from the bonsai.
CN109331052B (en) Parthenocissus tricuspidata extract and extraction method and application thereof
JPS6353993B2 (en)
JP2003221333A (en) Agent for inhibiting hyaluronidase
Kupchan et al. Zygadenus Alkaloids. VI. 1 Active Principles of Zygadenus paniculatus2
JP2001316398A (en) Antiallergic agent
Anderson et al. Nonpolar pentacyclic triterpenes of the medicinal fern Polypodium subpetiolatum
JPS61112080A (en) Novel tannin
JPS61112089A (en) Novel tannin
JPS61112090A (en) Novel tannin
CN110218208B (en) Diels-Alder type compound and preparation method and application thereof
JPS6249277B2 (en)
Larit et al. A new phloroglucinol derivative isolated from Hypericum afrum, a plant endemic to Algeria
JPS61118395A (en) Novel tannin