JPH02115107A - Antibiotic agent - Google Patents

Antibiotic agent

Info

Publication number
JPH02115107A
JPH02115107A JP26661888A JP26661888A JPH02115107A JP H02115107 A JPH02115107 A JP H02115107A JP 26661888 A JP26661888 A JP 26661888A JP 26661888 A JP26661888 A JP 26661888A JP H02115107 A JPH02115107 A JP H02115107A
Authority
JP
Japan
Prior art keywords
extract
clove
extraction
antibiotic agent
active ingredient
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
JP26661888A
Other languages
Japanese (ja)
Inventor
Yasuhiro Saihara
康弘 才原
Nobuji Nakatani
中谷 延二
Haruyuki Date
伊達 晴行
Atsuko Kishimoto
岸本 篤子
Koji Osada
光司 長田
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.)
Panasonic Electric Works Co Ltd
Original Assignee
Matsushita Electric Works 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 Matsushita Electric Works Ltd filed Critical Matsushita Electric Works Ltd
Priority to JP26661888A priority Critical patent/JPH02115107A/en
Publication of JPH02115107A publication Critical patent/JPH02115107A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain antibiotic agent expectable of very wide range of use having excellent safety, sufficient antibiosis and wide antimicrobial spectrum against, e.g., microorganism by containing extract from clove as active ingredient. CONSTITUTION:Any extracting solvent, preferably organic solvent such as methanol, acetone, ethyl acetate or n-hexane is added to crushed or finely cut material of preferably flower bud of, e.g., clove and extraction is performed by conventional method preferably under heating at room temperature - 100 deg.C, then resultant extract is purified by preferably extracting again with non-polar organic solvent and fractionating to afford the extract of clove. Said extract is contained as active ingredient in the aimed antibiotic agent especially used for food or industrial material, etc., having excellent safety because natural and edible plant is used as raw material and having the above-mentioned effect, e.g., having strong antibiosis such as sterilization, insecticide, bacterium control, mold control or insect control.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、殺菌、殺虫、防菌、防カビ、防虫等の抗生
物作用を有し、植物質を含んでなる抗生物剤に関するも
のであって、特に、食品や工業材料等に用いられ、カビ
や細菌等の微生物の生育。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to an antibiotic agent containing plant matter and having antibiotic effects such as bactericidal, insecticidal, antibacterial, antifungal, and insect repellent. In particular, it is used in foods and industrial materials, etc., and the growth of microorganisms such as mold and bacteria.

増殖の抑制および殺菌等の作用を及ぼす抗生物剤に関す
る。
This invention relates to antibiotics that inhibit proliferation and have sterilizing effects.

〔従来の技術〕[Conventional technology]

従来、カビや細菌等の微生物によって引き起こされる病
気、食物の腐敗、化粧品や各種工業材料の微生物劣化等
を防止するために、様々な防菌防カビ剤の研究が行われ
ている。他方、農業目的や人体の健康目的のための殺虫
剤や防虫剤の研究開発も進められている。
BACKGROUND ART Research has been carried out on various antibacterial and antifungal agents in order to prevent diseases caused by microorganisms such as mold and bacteria, food spoilage, and microbial deterioration of cosmetics and various industrial materials. On the other hand, research and development of insecticides and repellents for agricultural purposes and human health purposes is also progressing.

上記食品や化粧品の保存性向上の観点からは、従来、合
成保存料として、ソルビン酸およびその塩(K塩等)、
安息香酸およびその塩(Na塩等)、デヒドロ酢酸およ
びその塩(Na塩等)、バラオキシ安息香酸エステル(
イソブチル、イソプロピル、エチル、ブチル各エステル
等)、プロピオン酸塩(Ca、Na塩等)、エタノール
、グリシン、重合リン酸等が使用されてきた。また、殺
菌剤としては、重金属化合物、有機金属化合物、硫黄化
合物、ハロゲン化物、フェノール類、アルコール類、界
面活性剤、酸化剤、抗生物質等が広く用いられている。
From the perspective of improving the shelf life of the above foods and cosmetics, conventional synthetic preservatives such as sorbic acid and its salts (K salt, etc.),
Benzoic acid and its salts (Na salt, etc.), dehydroacetic acid and its salts (Na salt, etc.), roseoxybenzoic acid ester (
Isobutyl, isopropyl, ethyl, butyl esters, etc.), propionate salts (Ca, Na salts, etc.), ethanol, glycine, polymerized phosphoric acid, etc. have been used. Furthermore, as disinfectants, heavy metal compounds, organometallic compounds, sulfur compounds, halides, phenols, alcohols, surfactants, oxidizing agents, antibiotics, etc. are widely used.

ところが、上記の合成保存料は、一般に、安全性に問題
があり、添加量や対象食品等が制限されざるを得ないの
が現状である。また、殺菌剤についても、毒性が強い、
人体に副作用がある等の欠点を持つものが多く、抗菌ス
ペクトルの狭いものも少なくない。
However, the above-mentioned synthetic preservatives generally have safety problems, and the current situation is that the amount added and the foods to which they can be used must be restricted. In addition, disinfectants are highly toxic,
Many have drawbacks such as side effects on the human body, and many have a narrow antibacterial spectrum.

こうしたことから、近年、天然物からの抽出物を有効成
分とする、毒性の低い抗生物剤、特に抗微生物剤の開発
が進んでおり、特開昭60−41473号公報には、ツ
バキ科植物からの分離物を有効成分とする抗微生物剤が
報告されている。
For this reason, in recent years, the development of low-toxicity antibiotics, especially antimicrobials, which contain extracts from natural products as active ingredients has progressed. An antimicrobial agent containing isolates from .

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかしながら、上記公報記載の抗微生物剤について発明
者らが詳しく検討した結果、このものの抗微生物作用(
抗菌抗カビ作用等)は強いものではなく、また、抗菌ス
ペクトルも狭いことが判明した。
However, as a result of the inventors' detailed study of the antimicrobial agent described in the above publication, the antimicrobial action (
It was found that the antibacterial and antifungal effects were not strong, and the antibacterial spectrum was also narrow.

以上の事情に鑑み、この発明は、安全性が高いとともに
、充分な抗生物作用を有し、たとえば、微生物に対する
抗菌スペクトルの広い抗生物剤を提供することを課題と
する。
In view of the above circumstances, it is an object of the present invention to provide an antibiotic agent that is highly safe, has sufficient antibiotic activity, and has a broad antibacterial spectrum against microorganisms, for example.

〔課題を解決するための手段〕[Means to solve the problem]

上記課題を解決するため、発明者らは香辛料の抽出物に
ついて研究を行った結果、クローブからの抽出物に優れ
た作用があることを見出し、この発明を完成させるに至
った。
In order to solve the above problems, the inventors conducted research on spice extracts and found that extracts from cloves have excellent effects, leading to the completion of this invention.

したがって、この発明にかかる抗生物剤は、クローブか
らの抽出物を有効成分としている。
Therefore, the antibiotic according to the present invention contains an extract from cloves as an active ingredient.

〔作   用〕[For production]

この発明の抗生物剤は、その有効成分が合成品ではなく
、天然物、しかも食用に供される植物であるクローブか
らの抽出物であるため安全性が高いとともに、殺菌、殺
虫、防菌、防カビ、防虫等の抗生物作用の強いものであ
って、たとえば微生物に対して広い抗菌スペクトルを有
している。
The antibiotic of this invention is highly safe because its active ingredient is not a synthetic product but a natural product, moreover, an extract from cloves, which are edible plants. It has strong antimicrobial effects such as antifungal and insecticidal properties, and has a broad antibacterial spectrum against microorganisms.

〔実 施 例〕〔Example〕

以下に、この発明の詳細な説明する。 The present invention will be explained in detail below.

この発明にかかる抗生物剤は、出発原料クローブから抽
出された抽出物を有効成分とするものであって、その抽
出方法等は特に限定されることはない、たとえば、クロ
ーブの、好ましくは花蕾を粉砕あるいは細断したものに
任意の抽出溶媒を加え、常法に従って抽出処理を行った
後、抽出残渣を濾別し、濾液より溶剤を留去または濃縮
することにより、液体または固形物として目的とする抽
出物を得ることができる。なお、抽出処理は、室温ある
いは100℃以下の加熱下で、充分に行われることが好
ましい。
The antibiotic according to the present invention has as an active ingredient an extract extracted from cloves as a starting material, and the extraction method is not particularly limited. For example, cloves, preferably flower buds, are Add any extraction solvent to the pulverized or shredded material, perform extraction according to a conventional method, filter the extraction residue, and distill or concentrate the solvent from the filtrate to obtain the desired product as a liquid or solid. An extract can be obtained. Note that the extraction treatment is preferably carried out sufficiently at room temperature or under heating at 100° C. or lower.

上記抽出溶媒としては、水および/または有機溶媒、特
に有機溶媒を用いることが好ましい。固有Ia溶媒では
、たとえば、メタノール、エタノール、プロパツール、
イソプロパツール、ブタノール等のアルコール類、エチ
ルエーテル、プロピルエーテル、テトラヒドロフラン等
のエーテル類(酸素複素環化合物も含む)、メチルエチ
ルケトン、アセトン等のケトン類、酢酸エチル等のエス
テル類や、ヘキサン、イソオクタン、ベンゼン、トルエ
ン等の炭化水素などが挙げられ、−層好ましくは、メタ
ノール、アセトン、酢酸エチル、nヘキサン等が選択さ
れる。以上の有機溶媒は、単独で用いられる他、任意に
複数種を組み合わせて用いることもできる。
It is preferable to use water and/or an organic solvent, particularly an organic solvent, as the extraction solvent. Specific Ia solvents include, for example, methanol, ethanol, propatool,
Alcohols such as isopropanol and butanol, ethers (including oxygen heterocyclic compounds) such as ethyl ether, propyl ether, and tetrahydrofuran, ketones such as methyl ethyl ketone and acetone, esters such as ethyl acetate, hexane, isooctane, Examples include hydrocarbons such as benzene and toluene, and methanol, acetone, ethyl acetate, n-hexane and the like are preferably selected. The above organic solvents can be used alone or in any combination of two or more kinds.

さらに、上記抽出溶媒による抽出が行われたのち、得ら
れた抽出物を、再度、非極性有機溶媒で抽出1分画する
ことが好ましい。それにより、抽出物の精製が行われる
ためである。用いられる非極性有機溶媒としては、特に
限定はされないが、各種炭化水素類、たとえばヘキサン
等を好ましく用いることができる。
Furthermore, after the extraction with the above-mentioned extraction solvent is performed, it is preferable that the obtained extract is extracted and fractionated again with a non-polar organic solvent. This is because the extract is purified thereby. The nonpolar organic solvent used is not particularly limited, but various hydrocarbons, such as hexane, can be preferably used.

以上のようにして得られる抗生物剤は、たとえばその抗
微生物作用についてみると、JIS Z 2911のカ
ビ抵抗性試験方法に規定されているアスペルギルス・ニ
ゲル(Aspergillus niger)、アスペ
ルギルス・テレウス(Aspergillus ter
reus)、ペニシリウム・シトリナム(Penici
llium citrinum)、ペニシリウム・フニ
クロスム(Penicillium funiculo
sum) +リゾープス・オリゼー(Rhizopus
 oryzac)+タラトスポリウム・クラドスポリオ
イデス(Cladosporium cladospo
rioides)、ケトミウム・グロボスム(Chae
tomium globosum)+フザリウム・プロ
リフエラーツム(Fusarium prolifer
aLum)等のカビ、または、サツカロミセス・セレヴ
イシエー(Saccharo+nyces cerev
isiae)等の酵母、エシェリヒア・コリー(Esc
herichia coli)、バチルス・スプヂリス
(Bacil!us 5ubLilis)、シュードモ
ナス・エアルギノーサ(r’seudomonas a
eruginosa)+ スタフィロコッカス0オウレ
ンス(SLaphylococcus aureus)
等のバクテリア等の生育を抑えることができる。
The antibiotics obtained as described above, for example, have antimicrobial effects on Aspergillus niger and Aspergillus terreus as specified in the mold resistance test method of JIS Z 2911.
reus), Penicillium citrinum (Penici
llium citrinum), Penicillium funiculo
sum) + Rhizopus oryzae
oryzac) + Talatosporium cladosporioides (Cladosporium cladospo)
rioides), Chaetomium globosum (Chae
tomium globosum) + Fusarium proliferatum
aLum) or Saccharomyces cerevisiae (Saccharo+nyces cerev)
yeast such as Escherichia coli (Esc
herichia coli), Bacillus spudilis (Bacillus!us 5ubLilis), Pseudomonas aeruginosa (r'seudomonas a)
eruginosa) + SLaphylococcus aureus
It is possible to suppress the growth of bacteria such as.

このような抗菌抗カビ作用をはじめとする抗生物作用は
、抗生物剤中に含まれる種々の成分の協力作用によって
得られるものと考えられる。
Antibiotic effects including such antibacterial and antifungal effects are thought to be obtained through the cooperative effects of various components contained in antibiotics.

また、抗生物剤の有効成分である抽出物の適用量は、そ
の剤型や適用方法1通用場所に応じて適宜設定すればよ
く、特に限定はされない。剤型についても、任意の選択
が可能で、分散乳化剤、希釈剤や水和剤などを加えた液
体状のほか、ゼリー状であってもよ(、シート状基材や
家具部材等の表面に塗布されていてもよい。さらに、担
体に保持させた面材、粉材等であってもよい。ここで、
面材、粉材の担体としては、たとえば、珪酸、カオリン
、活性炭、ベントナイト珪藻±5タルク、クレー、炭酸
カルシウム、陶磁器粉等の鉱物質粉末、木粉、大豆粉、
小麦粉、デンプン等の植物質粉末、シクロデキストリン
等の包接化合物などを用いることができるが、これらに
限定されることはない。
Further, the amount of the extract, which is an active ingredient of the antibiotic, may be appropriately set depending on its dosage form, application method, and place of application, and is not particularly limited. The dosage form can also be selected arbitrarily; it may be in a liquid form containing a dispersing emulsifier, diluent, or hydrating agent, or in a jelly form (for example, it can be applied to the surface of sheet-like base materials or furniture parts, etc.). It may be applied.Furthermore, it may be a face material, powder material, etc. held on a carrier.Here,
Examples of carriers for face materials and powders include silicic acid, kaolin, activated carbon, bentonite diatom ±5 talc, clay, calcium carbonate, mineral powders such as ceramic powder, wood flour, soybean flour,
Vegetable powders such as wheat flour and starch, clathrate compounds such as cyclodextrin, etc. can be used, but are not limited to these.

以上のように、この発明にかかる抗生物剤は、殺生物剤
、有害生物忌避剤または誘引剤、あるいは植物生長調節
剤等として幅広く用いられ、その使用形態は、溶液状態
、ゲル状態、ペースト状、あるいは無機や有機の担体に
含浸させた系など、特に限定されない。
As described above, the antibiotic according to the present invention is widely used as a biocide, a pest repellent or attractant, a plant growth regulator, etc., and can be used in the form of a solution, gel, or paste. , or a system impregnated with an inorganic or organic carrier, but is not particularly limited.

続いて、この発明のさらに詳しい実施例について、比較
例と併せて説明するが、この発明にかかる抗生物剤が、
これらの実施例に限定されることはない。たとえば、以
下では特に抗微生物作用について詳細な検討を加えてい
るが、この発明の抗生物剤が防虫、殺虫等においても有
用であることは言うまでもない。
Next, more detailed examples of the present invention will be explained together with comparative examples.
The invention is not limited to these examples. For example, although the antimicrobial action will be discussed in detail below, it goes without saying that the antibiotic of the present invention is also useful for insect repellent, insecticide, and the like.

一実施例1 クローブの花蕾を粉砕して得られた微粉末205にメタ
ノール120−を加え、80℃還流下、7時間抽出を行
った。得られた抽出混合物を濾過して濾液を得、これを
濃縮して目的とする抽出物8.53を得た。
Example 1 Methanol 120- was added to fine powder 205 obtained by crushing clove buds, and extraction was performed under reflux at 80°C for 7 hours. The obtained extraction mixture was filtered to obtain a filtrate, which was concentrated to obtain the desired extract 8.53.

一実施例2− 抽出溶媒としてn−ヘキサンを用い、抽出温度70℃で
行うようにする他は、上記実施例1と同様に抽出を行い
、抽出物5,2)を得た。
Example 2 Extracts 5 and 2) were obtained by performing extraction in the same manner as in Example 1, except that n-hexane was used as the extraction solvent and the extraction temperature was 70°C.

一実施例3− 上記実施例1で得られた抽出物をメタノール:水=1:
lの混合溶媒に熔かして分液ロートに入れ、n−ヘキサ
ンを添加して振とうして、n−ヘキサン画分を得た。濃
縮後の抽出物収量は、4滲であった。
Example 3 - The extract obtained in Example 1 above was mixed with methanol:water = 1:
The mixture was dissolved in a mixed solvent of 1 ml and put into a separating funnel, and n-hexane was added and shaken to obtain an n-hexane fraction. The extract yield after concentration was 4 extracts.

実施例4 抽出溶媒としてアセトンを用い、抽出温度50°Cで行
うようにする他は、上記実施例1と同様に抽出を行い、
抽出物6.83を得た。
Example 4 Extraction was carried out in the same manner as in Example 1 above, except that acetone was used as the extraction solvent and the extraction temperature was 50°C.
6.83 extracts were obtained.

実施例5 抽出溶媒として酢酸エチルを用い、拙句温度75℃で行
うようにする他は、上記実施例1と同様に抽出を行い、
抽出物7.23を得た。
Example 5 Extraction was carried out in the same manner as in Example 1 above, except that ethyl acetate was used as the extraction solvent and the temperature was 75°C.
Extract 7.23 was obtained.

比較例1〜3− 出発原料としてオレガノ、タイム、シナモンをそれぞれ
用い、以下は実施例1と同様にして、それらの抽出物を
得た。
Comparative Examples 1 to 3 - Extracts of oregano, thyme, and cinnamon were obtained in the same manner as in Example 1 using oregano, thyme, and cinnamon as starting materials.

上記得られた実施例および比較例の抽出物につき、以下
に述べる寒天希釈塗抹試験法により、種々の微生物に対
する生育最低阻止濃度(重量%)を調べた。
The extracts of Examples and Comparative Examples obtained above were examined for minimum growth inhibitory concentration (% by weight) against various microorganisms by the agar dilution smear test method described below.

まず、各抽出物の所定量を、滅菌溶解させた寒天培地に
添加2分散させた。ここで、供試菌がカビおよび酵母で
ある場合はバレイショ・ブドウ糖培地を、バクテリアに
は標準寒天培地を用いた。
First, a predetermined amount of each extract was added to and dispersed in a sterilized and dissolved agar medium. Here, when the test bacteria were molds and yeasts, a potato-glucose medium was used, and for bacteria, a standard agar medium was used.

これらの寒天培地に、あらかじめ試験管斜面培地で培養
した下記の供試菌を白金耳で画線し、それぞれの培地を
温度28℃、湿度95%で1週間培養して、各画の生育
の有無を調べた。
The following test bacteria, which had been previously cultured on test tube slants, were streaked onto these agar media with a platinum loop, and each culture medium was cultured for one week at a temperature of 28°C and a humidity of 95%, and the growth of each streak was evaluated. I checked to see if it existed.

なお、供試菌としてはJIS Z 2911に規定され
ている次の8種のカビ、および1種の酵母、4種のバク
テリアを用いた。
The test bacteria used were the following eight types of molds specified in JIS Z 2911, one type of yeast, and four types of bacteria.

カビとしては; ■アスペルギルス・ニゲル IFO6341■アスペル
ギルス・テレウス IFO6346■ペニシリウム・シ
トリナム IFO6352■ペニシリウム・フニクロス
ム IFO6345 ■リゾーブス・オリゼー IFO31005■クラドス
ポリウム・クラドスポリオイデスIFO6348 ■ケトミウム・グロボスム IFO634,7■フザリ
ウム・プロリフエラーツム IFO6349 酵母としては: ■サン力ロミセス・セレヴイシェー IFO0203 バクテリアとしては; [相]エシェリヒア・コリー IFO33010バチル
ス・スブチリス IFO3009@シユードモナス・エ
アルギノーサ IF0 3080 0スタフイロコツカス・オウレンス IFO3060 結果を、第1表および第2表に示す。
As for molds; ■ Aspergillus niger IFO6341 ■ Aspergillus terreus IFO6346 ■ Penicillium citrinum IFO6352 ■ Penicillium funiculosum IFO6345 ■ Rhizorbus oryzae IFO31005 ■ Cladosporium cladosporioides IFO6348 ■ Chaetomium globosum IFO63 4,7 ■ Fusarium Pro Rifferatum IFO6349 As a yeast: ■Romyces cerevisiae IFO0203 As a bacterium; [Phase] Escherichia coli IFO33010 Bacillus subtilis IFO3009 @ Pseudomonas aeruginosa IF0 3080 0 Staphylococcus aurens IFO3060 Results , Table 1 and shown in Table 2.

第 表 第   2   表 第1表および第2表にみるように、クローブから得られ
た実施例の抽出物はいずれも、比較例のその他の香辛料
に比べ、カビ、酵母、バクテリア等の微生物に対し、抗
菌スペクトルの広い、強力な抗微生物作用を有している
ことが判明した。特に、実施例3の抽出物は、実施例1
の抽出物に対して非極性有機溶媒による分画が行われた
ものであるため、実施例1の抽出物に比べて抽出物中の
抗微生物成分濃度が高く、重量当たりの抗菌活性の高い
(生育最低阻止濃度の低い)ものとなっている。
Table 2 As shown in Tables 1 and 2, the extracts obtained from cloves in the Examples are more effective against microorganisms such as mold, yeast, and bacteria than other spices in the Comparative Examples. It was found that it has a strong antimicrobial effect with a broad antibacterial spectrum. In particular, the extract of Example 3 is similar to that of Example 1.
Since the extract was fractionated using a non-polar organic solvent, the concentration of antimicrobial components in the extract is higher than that of the extract of Example 1, and the antimicrobial activity per weight is high ( It has a low minimum inhibitory concentration for growth.

さらに、実施例2の抽出物のラットの経口急性致死量は
、LDs。値は1.Bit/kg以上であり、安全性の
高いものであると判明した。
Furthermore, the oral acute lethal dose of the extract of Example 2 in rats was LDs. The value is 1. Bit/kg or more, and it was found to be highly safe.

〔発明の効果〕〔Effect of the invention〕

以上みてきたように、この発明にかかる抗生物剤は、安
全性が高く、充分な抗生物件用を有するとともに、たと
えば微生物に対する抗菌スペクトルの広いものであって
、非常に広範囲の用途が期待される。
As described above, the antibiotic according to the present invention is highly safe and has sufficient antibiotic use, and has a broad antibacterial spectrum against microorganisms, so it is expected to have a very wide range of uses. .

代理人 弁理士  松 本 武 彦Agent: Patent Attorney Takehiko Matsumoto

Claims (1)

【特許請求の範囲】[Claims] 1 クローブからの抽出物を有効成分とする抗生物剤。1.An antibiotic agent whose active ingredient is an extract from cloves.
JP26661888A 1988-10-22 1988-10-22 Antibiotic agent Pending JPH02115107A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26661888A JPH02115107A (en) 1988-10-22 1988-10-22 Antibiotic agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26661888A JPH02115107A (en) 1988-10-22 1988-10-22 Antibiotic agent

Publications (1)

Publication Number Publication Date
JPH02115107A true JPH02115107A (en) 1990-04-27

Family

ID=17433317

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26661888A Pending JPH02115107A (en) 1988-10-22 1988-10-22 Antibiotic agent

Country Status (1)

Country Link
JP (1) JPH02115107A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04108708A (en) * 1990-08-29 1992-04-09 Miwako Kondo Production of pollution-free agricultural chemical
JPH06256129A (en) * 1993-02-18 1994-09-13 Eiho Ko Nontoxic disinfectant
KR100425926B1 (en) * 2001-03-19 2004-04-03 (주)제이엔헬스존 A Method for controlling plant disease is caused by Meloidogyne sp. using Eugenia caryophyllate
KR100513258B1 (en) * 2002-08-05 2005-10-06 케이지바텍 주식회사 Controller of plant disease and noxious insects using herb medicine extracts and producing method thereof
CN106234437A (en) * 2016-08-05 2016-12-21 郭迎庆 A kind of preparation method of efficiency natural Tableware disinfectant

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54119035A (en) * 1976-11-22 1979-09-14 Dechiyuudo De Rushierushiyu De Insecticidal composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54119035A (en) * 1976-11-22 1979-09-14 Dechiyuudo De Rushierushiyu De Insecticidal composition

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04108708A (en) * 1990-08-29 1992-04-09 Miwako Kondo Production of pollution-free agricultural chemical
JPH06256129A (en) * 1993-02-18 1994-09-13 Eiho Ko Nontoxic disinfectant
KR100425926B1 (en) * 2001-03-19 2004-04-03 (주)제이엔헬스존 A Method for controlling plant disease is caused by Meloidogyne sp. using Eugenia caryophyllate
KR100513258B1 (en) * 2002-08-05 2005-10-06 케이지바텍 주식회사 Controller of plant disease and noxious insects using herb medicine extracts and producing method thereof
CN106234437A (en) * 2016-08-05 2016-12-21 郭迎庆 A kind of preparation method of efficiency natural Tableware disinfectant

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