JPH01102007A - Insect pest controlling agent - Google Patents
Insect pest controlling agentInfo
- Publication number
- JPH01102007A JPH01102007A JP25924187A JP25924187A JPH01102007A JP H01102007 A JPH01102007 A JP H01102007A JP 25924187 A JP25924187 A JP 25924187A JP 25924187 A JP25924187 A JP 25924187A JP H01102007 A JPH01102007 A JP H01102007A
- Authority
- JP
- Japan
- Prior art keywords
- phellodendron
- controlling agent
- palmatine
- berberine
- insect pest
- 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
Links
- 241000607479 Yersinia pestis Species 0.000 title claims abstract description 44
- 241000238631 Hexapoda Species 0.000 title abstract description 10
- YBHILYKTIRIUTE-UHFFFAOYSA-N berberine Chemical compound C1=C2CC[N+]3=CC4=C(OC)C(OC)=CC=C4C=C3C2=CC2=C1OCO2 YBHILYKTIRIUTE-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229940093265 berberine Drugs 0.000 claims abstract description 19
- QISXPYZVZJBNDM-UHFFFAOYSA-N berberine Natural products COc1ccc2C=C3N(Cc2c1OC)C=Cc4cc5OCOc5cc34 QISXPYZVZJBNDM-UHFFFAOYSA-N 0.000 claims abstract description 19
- PTPHDVKWAYIFRX-UHFFFAOYSA-N Palmatine Natural products C1C2=C(OC)C(OC)=CC=C2C=C2N1CCC1=C2C=C(OC)C(OC)=C1 PTPHDVKWAYIFRX-UHFFFAOYSA-N 0.000 claims abstract description 17
- QUCQEUCGKKTEBI-UHFFFAOYSA-N palmatine Chemical compound COC1=CC=C2C=C(C3=C(C=C(C(=C3)OC)OC)CC3)[N+]3=CC2=C1OC QUCQEUCGKKTEBI-UHFFFAOYSA-N 0.000 claims abstract description 17
- PTOJXIKSKSASRB-UHFFFAOYSA-O candicine Chemical compound C[N+](C)(C)CCC1=CC=C(O)C=C1 PTOJXIKSKSASRB-UHFFFAOYSA-O 0.000 claims abstract description 14
- 239000004480 active ingredient Substances 0.000 claims abstract description 8
- POIRVLZGTSWEMG-UHFFFAOYSA-N Magnoflorin Natural products N1CCC2=CC(OC)=C(O)C3=C2C1CC1=CC=C(OC)C(O)=C13 POIRVLZGTSWEMG-UHFFFAOYSA-N 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 abstract description 32
- XQINTCORIZHGFD-AWEZNQCLSA-O (6as)-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinoline-6-ium-11-ol Chemical compound C1=C(OC)C(OC)=C2C3=C(O)C(OC)=CC=C3C[C@@H]3[N+](C)(C)CCC1=C23 XQINTCORIZHGFD-AWEZNQCLSA-O 0.000 abstract description 26
- 238000000605 extraction Methods 0.000 abstract description 10
- -1 organic acid salt Chemical class 0.000 abstract description 10
- 239000003960 organic solvent Substances 0.000 abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 7
- 241000238876 Acari Species 0.000 abstract description 6
- 241000255925 Diptera Species 0.000 abstract description 6
- 241000972673 Phellodendron amurense Species 0.000 abstract description 6
- 230000000694 effects Effects 0.000 abstract description 6
- 239000000126 substance Substances 0.000 abstract description 5
- 231100000419 toxicity Toxicity 0.000 abstract description 5
- 230000001988 toxicity Effects 0.000 abstract description 5
- 241000256602 Isoptera Species 0.000 abstract description 4
- 241000196324 Embryophyta Species 0.000 abstract description 3
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- 241001674044 Blattodea Species 0.000 abstract description 2
- 241001466042 Fulgoromorpha Species 0.000 abstract description 2
- 238000010438 heat treatment Methods 0.000 abstract description 2
- 150000007522 mineralic acids Chemical class 0.000 abstract description 2
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- YLRXAIKMLINXQY-ZDUSSCGKSA-O (S)-magnoflorine Chemical compound C1=C(OC)C(O)=C2C3=C(O)C(OC)=CC=C3C[C@@H]3[N+](C)(C)CCC1=C23 YLRXAIKMLINXQY-ZDUSSCGKSA-O 0.000 abstract 2
- KYEAXNAYHSCLMT-CVVGWEDFSA-N Magnoflorine Natural products C[C@H]1OC=C2[C@@H]3[C@@H]1CN4CCc5c([nH]c6ccccc56)[C@@H]4[C@@H]3OC2=O KYEAXNAYHSCLMT-CVVGWEDFSA-N 0.000 abstract 2
- RBBVPNQTBKHOEQ-KKSFZXQISA-O Phellodendrine Chemical compound C1CC2=CC(OC)=C(O)C=C2[C@H]2[N@+]1(C)CC(C=C(C(=C1)O)OC)=C1C2 RBBVPNQTBKHOEQ-KKSFZXQISA-O 0.000 abstract 2
- 230000001747 exhibiting effect Effects 0.000 abstract 1
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- 239000000843 powder Substances 0.000 description 16
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- 238000007796 conventional method Methods 0.000 description 4
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- 239000000401 methanolic extract Substances 0.000 description 4
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
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- 235000021307 Triticum Nutrition 0.000 description 2
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000002574 poison Substances 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002728 pyrethroid Substances 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 238000010898 silica gel chromatography Methods 0.000 description 2
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- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000254032 Acrididae Species 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 206010004194 Bed bug infestation Diseases 0.000 description 1
- 241000238657 Blattella germanica Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
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- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 241000510032 Ellipsaria lineolata Species 0.000 description 1
- 235000019733 Fish meal Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920000715 Mucilage Polymers 0.000 description 1
- 241001477931 Mythimna unipuncta Species 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 241000256259 Noctuidae Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 241000500441 Plutellidae Species 0.000 description 1
- 241000283080 Proboscidea <mammal> Species 0.000 description 1
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- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 241000545593 Scolytinae Species 0.000 description 1
- 241000276699 Seriola Species 0.000 description 1
- 241000258242 Siphonaptera Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 241001454295 Tetranychidae Species 0.000 description 1
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- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
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- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
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- 150000002430 hydrocarbons Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
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Abstract
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は、ベルベリンもしくは、パルマチン。[Detailed description of the invention] (Industrial application field) The present invention relates to berberine or palmatine.
カンディシン、マグノフロリン、メニスペリン。Kandisin, Magnoflorin, Menisperine.
フェロデンドリンの一種およびまたは二種以上を有効成
分として含有せしめることを特徴とする害虫防除剤に関
する。The present invention relates to a pest control agent containing one or more types of ferrodendrin as an active ingredient.
(従来の技術)
近年における農作物生産の急速な増大に伴い農業害虫防
除のための薬剤の使用量が著しく増大している。また生
活環境の変化に伴い家屋やピル。(Prior Art) With the rapid increase in agricultural production in recent years, the amount of chemicals used for controlling agricultural pests has increased significantly. Also, due to changes in living environment, houses and pills.
倉庫、工場等における木材害虫、貯穀害虫、不快害虫、
衛生害虫防除等の被害も多様化し、その防除のための害
虫防除剤の使用も多くなっている。Wood pests, grain storage pests, unpleasant pests in warehouses, factories, etc.
The damage caused by sanitary pest control is also diversifying, and the use of pest control agents to control them is also increasing.
しかし、今日一般に害虫防除剤として使用きれている薬
剤はピレスロイド系、有機リン系、有機塩素系、カーバ
メイト系等合成薬剤があげられる(発明が解決しようと
する問題点)
現在使用されている害虫防除剤のほとんどは、化学合成
品であり、安全性および残留毒性が問題となっている。However, the chemicals that are generally used as insect pest control agents today include synthetic agents such as pyrethroid, organophosphorus, organochlorine, and carbamate (problems to be solved by the invention) Currently used pest control agents Most of the agents are chemically synthesized products, and safety and residual toxicity are issues.
害虫防除剤の使用量が著しく増大した結果、散布作業者
に対する直接被害だけでなく、収穫物への残留性や地下
水汚染等、環境への残留毒性、蓄積性が重大な社会問題
となっておりそのため安全性が高く残留毒性のより少な
い害虫防除剤が強く望まれている。As a result of the significant increase in the amount of pest control agents used, not only direct damage to sprayers, but also residual toxicity and accumulation in the environment, such as persistence in crops and groundwater contamination, have become serious social problems. Therefore, there is a strong demand for pest control agents that are highly safe and have less residual toxicity.
(問題点を解決するための手段)
本発明者らは、合成品でなく天然物南米の著効で、かつ
安全性が高く、残留毒性の少ない害虫防除剤を開発する
ために鋭意研究した結果、植物起源の物質が優れた害虫
防除効果を示すことを見い出し本発明を完成するに至っ
た。(Means for Solving the Problems) The present inventors have conducted intensive research to develop a pest control agent made from South America that is not a synthetic product but a natural product that is highly effective, highly safe, and has low residual toxicity. The inventors have discovered that plant-derived substances exhibit excellent pest control effects, and have completed the present invention.
即ち、ベルベリンもしくは、パルマチン、カンディシン
、マグノフロリン、メニスペリン、フェロデンドリンの
一種およびまたは二種以上を有効成分として含有せしめ
ることを特徴とする天然害虫肪除剤を提供するものであ
る。That is, the present invention provides a natural pest control agent containing as an active ingredient one or more of berberine, palmatine, candicin, magnoflorin, menisperine, and ferrodendrin.
本発明に用いるベルベリン、パルマチン、カンディシン
、マグノフロリン、メニスペリン、フェロデンドリンは
、キハダもしくは、ケキハダ、ヒロハノキハダ、ミヤマ
キハダ、シナキハダ、タイワンキハダから抽出精製する
ことにより得られるキハダ(Phellodendro
n amutense RUPRECHT)、ケキ
ハダ(Phellodendron amurens
eRUPRECHT var、japonicum(
MAXIM、)OHWI )、ヒロハノキハダ(Phe
llodendron amurense RUP
RECHT var、5achalinenae
FR,SCHM、)、ミヤマキハダ(Phellode
ndron amurense RUPREC
HT var、1avallei(DODE)SP
RAGUE)、シナキハダ(Phellodendro
n chinenseSCHNEID、)、タイワ
ンキハダ(Phellodendron wils
onii HAYATA et KANEHI
RA)は、ミカン科(Rutaceae)の植物である
・これらの樹皮からコルク層を除いた樹皮乾燥部は、古
来よりオウバクとして用いられており、安全性が高いこ
とがすでに確認されている。Berberine, palmatine, candicin, magnoflorin, menisperine, and ferrodendrin used in the present invention are obtained from yellowfin tuna, or yellowfin tuna (Phellodendro
n amutense RUPRECHT), Phellodendron amurens
eRUPRECHT var, japonicum (
MAXIM,)OHWI), Phe
llodendron amurense RUP
RECHT var, 5achalinenae
FR, SCHM, ), Yellowfin tuna (Phellode)
ndron amurense RUPREC
HT var, 1avallei (DODE) SP
RAGUE), Shinakihada (Phellodendro)
n chinenseSCHNEID, ), Formosan Yellowfin (Phellodendron wils)
onii HAYATA et KANEHI
RA) is a plant belonging to the Rutaceae family.The dried bark of these trees, after removing the cork layer, has been used as amberjack since ancient times, and has already been confirmed to be highly safe.
ベルベリン、パルマチン、カンディシン、マグノブロリ
ン、メニスペリン、フェロデンドリンの抽出操作はキハ
ダもしくは、ケキハダ、ヒロハノキハダ、ミヤマキハダ
、シナキハダ、タイワンキハダ、に有機溶媒または含水
有機溶媒または水を加え、常法により室温あるいは加熱
下に十分なる抽出処理を行いその後抽出残渣を濾別し、
濾液から°溶剤を留去または濃縮することにより実施さ
れる、抽出操作に用いられる有機溶媒または含水有機溶
媒としては、メタノール、エタノール、プロパツール、
イソプロパツール、フタノール、オクタツール等のアル
コール類;プロピレングリコール、グリセリン等のポリ
オール類;メチルエーテル、エチルエーテル、プロピル
エーテル、イソプロピルエーテル、テトラヒドロフラン
、ジオキサン等のエーテル類: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;クロ
ロホルム、ジクロロメタン等のハロゲン化炭化水素類;
ベンゼン、トルエン、キシレン等の炭化水素類およびこ
れらの含水物などが使われる。これらの溶媒の中では、
メタノール、エタノール、イソプロパツール等のアルコ
ール類が最適でアル。Berberine, palmatine, candicin, magnobroline, menisperine, and ferrodendrin are extracted by adding an organic solvent or a water-containing organic solvent or water to yellowfin tuna, yellowfin tuna, Japanese yellowfin tuna, Japanese yellowfin tuna, Chinese yellowfin tuna, Formosan yellowfin tuna, and adding an organic solvent or a water-containing organic solvent or water to the yellowfin tuna, and then extracting it at room temperature or under heating using a conventional method. Perform a sufficient extraction process, then filter the extraction residue,
Examples of organic solvents or water-containing organic solvents used in the extraction operation, which is carried out by distilling off or concentrating the solvent from the filtrate, include methanol, ethanol, propatool,
Alcohols such as isopropanol, phthanol, and octatool; Polyols such as propylene glycol and glycerin; Ethers such as methyl ether, ethyl ether, propyl ether, isopropyl ether, tetrahydrofuran, and dioxane; Ketones such as methyl ethyl ketone and acetone; Esters such as ethyl acetate; halogenated hydrocarbons such as chloroform and dichloromethane;
Hydrocarbons such as benzene, toluene, and xylene, and their hydrated substances are used. Among these solvents,
Alcohols such as methanol, ethanol, and isopropanol are most suitable.
ベルベリン、パルマチン、カンディシン、マグノフロリ
ン、メニスペリン、フェロデンドリンの精製手段として
は、通常のカラムクロマトグラフィー、薄層クロマトグ
ラフィー、沈殿法、酸沈殿法、再結晶法、超臨界流体抽
出法等又はこれらの組合わせを採用できる。Purification methods for berberine, palmatine, candicin, magnoflorin, menisperine, and ferrodendrin include ordinary column chromatography, thin layer chromatography, precipitation method, acid precipitation method, recrystallization method, supercritical fluid extraction method, etc. A combination of can be adopted.
ベルベリン、パルマチン、カンディシン、マグノフロリ
ン、メニスペリン、フェロデンドリンは、各種の無機酸
および有機酸と塩を形成するが、本発明に用いるベルベ
リン、パルマチン、カンディシン、マグノフロリン、メ
ニスベリン、フェロデンドリンは、各種の無機酸塩およ
び有機酸塩であってもよく、害虫防除効果は変わらない
。Berberine, palmatine, candicin, magnoflorin, menisperine, and ferrodendrin form salts with various inorganic acids and organic acids, and the berberine, palmatine, candicin, magnoflorin, menisperine, and ferrodendrin used in the present invention are Various inorganic acid salts and organic acid salts may be used, and the pest control effect remains the same.
無機酸塩としては、塩酸塩、臭化水素酸塩、ヨウ化水素
酸塩、硝酸塩等である。有機酸塩としては酢酸塩、シュ
ウ酸塩、パラトルエンスルホン酸塩等である。Examples of inorganic acid salts include hydrochloride, hydrobromide, hydroiodide, and nitrate. Examples of organic acid salts include acetate, oxalate, paratoluenesulfonate, and the like.
本発明の害虫防除剤の対象害虫としては、具体的には、
シロアリ、キクイムシ等の木材害虫、ウンカ類、ヨコバ
イ類、ヨトウ類、ヤガ類、コナガ類、ハマキ類、メイガ
類、アブラムシ類、ハダニ類等の農業害虫、ハエ、力、
ゴキブリ、ノミ、南京虫、家ダニ、シラミ等の衛生害虫
、コナダニ。Specifically, the target pests of the pest control agent of the present invention include:
Timber pests such as termites and bark beetles, agricultural pests such as planthoppers, leafhoppers, armyworms, noctuid moths, diamondback moths, leafhoppers, borer moths, aphids, spider mites, flies, power, etc.
Hygiene pests such as cockroaches, fleas, bed bugs, house mites, lice, and mites.
フクガ、コクゾウ等の貯穀害虫、マダニ類、ヒウヒダニ
、ツメダニ、アリガタバチ、ユスリカ、チョウバエ、ム
カデ、ゲジゲジ等の不快害虫およびシバムシを挙げるこ
とができる。従って、本発明の害虫防除剤は、これらの
害虫から農作物、貯蔵穀物等の保護、生活環境等の安全
衛生面の改善等に非常に有効に利用できる。Examples include grain storage pests such as fukumoths and brown elephants, unpleasant pests such as ticks, mites, black mites, wasps, midges, butterfly flies, centipedes, and grasshoppers, and grass beetles. Therefore, the pest control agent of the present invention can be very effectively used to protect agricultural crops, stored grains, etc. from these pests, and to improve the safety and hygiene of the living environment.
本発明の害虫防除剤は、ベルベリンもしくは、パルマチ
ン、カンディシン、マグノフロリン、メニスペリン、フ
ェロデンドリンを単独でまたは、二種以上の混合物をそ
のまま使用できるが、通常の製剤処方に従い適当な担体
およびまたは希釈剤と共に製剤化され実用きれる。In the pest control agent of the present invention, berberine, palmatine, candicin, magnoflorin, menisperine, or ferrodendrin can be used alone or as a mixture of two or more of them, but they can be used in combination with an appropriate carrier and/or dilution according to the usual pharmaceutical formulation. It is formulated with a drug and put into practical use.
また、該害虫防除剤には、他の有効成分を含有させて使
用することにより既存合成害虫肪除剤の使用量を減少な
らしめることができる。併用される他の有効成分として
は例えば、ピレスロイド系殺虫剤、有機リン系殺虫剤、
有機塩素系殺虫剤。Furthermore, by incorporating other active ingredients into the pest control agent, the amount of existing synthetic pest control agents used can be reduced. Other active ingredients used in combination include, for example, pyrethroid insecticides, organophosphorus insecticides,
Organochlorine insecticide.
カーバメイト系殺虫剤、殺ダニ剤、殺蟻剤等を挙げるこ
とができる。Examples include carbamate insecticides, acaricides, and termiticides.
本発明の害虫防除剤を製剤化するに当り、用いられる担
体およびまたは、希釈剤は通常慣用されるそれらと異な
るものではない、得られる製剤形態もまた通常のものと
同様でよく、例えば毒餌。In formulating the pest control agent of the present invention, the carrier and/or diluent used are not different from those commonly used, and the resulting formulation may also be the same as conventional ones, such as poison bait.
粉剤1粒剤、水和剤、乳剤、油剤、エアゾール剤、燻煙
剤、蚊取線香形態等の剤型を使用目的に応じて適宜に選
択することができる。これら各剤型の調製は、通常の方
法によることができる0例えば粉剤9粒剤等の固剤はベ
ルベリンもしくは、パルマチン、カンディシン、マグノ
フロリン、メニスベリン、フェロデンドリンの一種およ
びまたは二種以上と適当な担体とを混合し、必要に応じ
粉砕または造粒して調製される。一般に使用される担体
としては、例えば大豆粉、タバコ粉、小麦粉、木粉、澱
粉、白糖、乳糖等の植物性粉末、カオリン、ベントナイ
ト、酸性白土等のクレー類、滑石粉、ロウ石粉等のタル
ク類、珪藻土、雲母粉等のシリカ類その他炭酸マグ・ネ
シウム、醸化マグネシウム、リン酸カルシウム等の鉱物
性粉末等を挙げることができる。毒餌は、例えば小麦粉
、砂糖、魚粉等の各種の原料およびまたは昆虫用飼料を
用いて上記固剤と同様にして調製される。水和剤、乳剤
、油剤等の液剤は、常法に従い水その他の適当な溶剤お
よび必要に応じて各種界面活性剤等の分散剤を利用して
調製される。エアゾール剤。Dosage forms such as single powder, wettable powder, emulsion, oil, aerosol, smoke, and mosquito coil form can be appropriately selected depending on the purpose of use. The preparation of each of these dosage forms can be carried out by a conventional method.For example, a solid agent such as a powder 9-grain tablet may be suitably mixed with berberine, or one and/or two or more of palmatine, candicin, magnoflorin, menisberine, and ferrodendrin. It is prepared by mixing with a suitable carrier and grinding or granulating as necessary. Commonly used carriers include, for example, soybean powder, tobacco powder, wheat flour, wood flour, starch, vegetable powders such as white sugar and lactose, clays such as kaolin, bentonite, and acid clay, and talc powders such as talc powder and waxite powder. Examples include silicas such as diatomaceous earth, mica powder, and mineral powders such as magnesium carbonate, fermented magnesium, and calcium phosphate. Poison baits are prepared in the same manner as the solid formulations described above, using various raw materials such as wheat flour, sugar, and fishmeal, and/or insect feed. Liquid preparations such as wettable powders, emulsions, and oil preparations are prepared according to conventional methods using water or other suitable solvents and, if necessary, dispersants such as various surfactants. Aerosol agent.
燻煙剤、蚊取線香形態等もまた常法にしたがい、それぞ
れ噴射剤1発煙性基剤、燃焼性基材等を用いて調製され
る。上記各製剤中には、また必要に応じて通常添加配合
される乳化剤2分散剤、懸濁剤、R着剤、浸透剤等の界
面活性剤の他にも例えば湿潤剤、粘漿剤、安定剤、協力
剤等を温石配合することもできる。上記界面活性剤とし
ては各種石鹸類、高級アルコール硫酸エステル、アルキ
ルスルホン酸、アルキルアリールスルホン酸、第4級ア
ンモニウム塩、オキシアルキルアミン、脂肪酸エステル
、ポリアルキレンオキサイド等を例示できる。Fumigants, mosquito coil forms, etc. are also prepared in accordance with conventional methods using propellants, smoke bases, combustible bases, etc., respectively. In each of the above preparations, in addition to surfactants such as emulsifiers, dispersants, suspending agents, R adhesives, and penetrating agents, which are usually added and blended as needed, wetting agents, mucilage agents, stabilizing agents, etc. It is also possible to add hot stones such as agents, synergists, etc. Examples of the surfactant include various soaps, higher alcohol sulfates, alkylsulfonic acids, alkylarylsulfonic acids, quaternary ammonium salts, oxyalkylamines, fatty acid esters, polyalkylene oxides, and the like.
各製剤中に含有されるベルベリンもしくは、パルマチン
、カンディシン、マグノフロリン、メニスペリン、フェ
ロデンドリンの一種およびまたは二種以上の配合量は上
記製剤に応じて適宜に決定され特に制限はないが、一般
には約0.1〜90重量%の範囲とされるのがよい、各
製剤の使用方法はその剤型に応じて異なり、該剤型毎に
通常の方法と異なるわけではない0例えば固剤は通常こ
れによる処理を必要とする箇所に適当量を散布すること
により、液剤は塗布、噴霧、含浸等によりそれぞれ施用
される。施用すべき害虫の種類、所望の防除効果等に応
じて適宜に決定され、所望の防除効果が奏される限り限
定はない。The amount of one or more of berberine, palmatine, candicin, magnoflorin, menisperine, and ferrodendrin contained in each preparation is appropriately determined depending on the above preparation and is not particularly limited, but in general The usage method for each preparation differs depending on its dosage form, and does not differ from the usual method for each dosage form.For example, solid dosage forms are usually used. The liquid agent can be applied by coating, spraying, impregnating, etc. by dispersing an appropriate amount onto the area requiring treatment. It is determined as appropriate depending on the type of pest to be applied, the desired control effect, etc., and there is no limitation as long as the desired control effect is achieved.
(作用) 次に本発明の実施例および試験例を示す。(effect) Next, Examples and Test Examples of the present invention will be shown.
実施例1
キハダの乾燥樹皮500gにメタノール32を加え、室
温にて抽出を行った。得られた抽出混合物を濾過してメ
タノール抽出液を得た。抽出残渣に再びメタノール3i
を加え室温にて抽出を行った。この操作を計3回行い、
メタノール抽出液3回分を集め、ロータリーエバポレー
ターにて濃縮乾固して65.3.の黄褐色粉末を得た。Example 1 32 methanol was added to 500 g of dried bark of yellowfin tuna, and extraction was performed at room temperature. The obtained extraction mixture was filtered to obtain a methanol extract. Add methanol 3i to the extraction residue again.
was added and extracted at room temperature. Do this operation 3 times in total,
Three methanol extracts were collected and concentrated to dryness using a rotary evaporator to obtain 65.3. A yellowish brown powder was obtained.
この黄褐色粉末5gをシリカゲルカラムクロマトグラフ
ィー(富士デビイソン化学株式会社製シリカゲルBW−
300,溶出液;クロロホルム:メタノール:水−80
:20:1)にて分画を行いベルベリンフ20mg、パ
ルマチン260mg、カンディシン6mg、マグノフロ
リン4mg 、メニスペリン2mg 、フェロデンドリ
ン1mgを得た。5 g of this yellowish brown powder was subjected to silica gel column chromatography (Silica gel BW- manufactured by Fuji Davison Chemical Co., Ltd.).
300, eluent; chloroform:methanol:water-80
:20:1) to obtain 20 mg of berberinf, 260 mg of palmatine, 6 mg of candicin, 4 mg of magnoflorin, 2 mg of menisperine, and 1 mg of ferrodendrin.
実施例2
ケキハダの乾燥樹皮500gにメタノール3Nを加え、
室温にて抽出を行った。得られた抽出混合物を濾過して
メタノール抽出液を得た。抽出残渣に再びメタノール3
j!を加え室温にて抽出を行った。この操作を計3回行
い、メタノール抽出液3回分を集め、ロータリーエバポ
レーターにて濃縮乾固して45.2gの黄褐色粉末を得
た。この黄褐色粉末5gをシリカゲルカラムクロマトグ
ラフィー(富士デビイソン化学株式会社製シリカゲルB
W−300,溶出液;クロロホルム:メタノール:水−
80:20:1)にて分画を行いベルベリン640mg
、パルマチン210mg 、カンディシン5mg、マグ
ノフロリン4mg、メニスペリン1mg、フェロデンド
リン1mgを得た。Example 2 Add 3N methanol to 500g of dry bark of Kekihada,
Extraction was performed at room temperature. The obtained extraction mixture was filtered to obtain a methanol extract. Add 3 methanol to the extraction residue again.
j! was added and extracted at room temperature. This operation was performed three times in total, and three portions of the methanol extract were collected and concentrated to dryness using a rotary evaporator to obtain 45.2 g of yellowish brown powder. 5 g of this yellowish brown powder was subjected to silica gel column chromatography (Silica gel B manufactured by Fuji Davison Chemical Co., Ltd.).
W-300, eluent; chloroform:methanol:water-
80:20:1) and 640 mg of berberine.
, 210 mg of palmatine, 5 mg of candicin, 4 mg of magnoflorin, 1 mg of menisperine, and 1 mg of ferrodendrin were obtained.
実施例3
昆虫用飼料(オリエンタル酵母工業株式会社)を粉砕粉
末化した後、このもの95重量部とベルベリン5重量部
とをそれぞれ混合した。さらに、昆虫用飼料に対して、
10重量部の水を加えて練合・乾燥して一定量の本発明
害虫防除剤を得た。Example 3 After pulverizing insect feed (Oriental Yeast Co., Ltd.) into powder, 95 parts by weight of this feed and 5 parts by weight of berberine were mixed together. Furthermore, for insect feed,
10 parts by weight of water was added, kneaded and dried to obtain a certain amount of the pest control agent of the present invention.
実施例4
ハルマチ70.5重量部をメタノール30重量部に溶解
し、カオリン99.5重量部加え、十分攪拌後、メタノ
ールを留去して0.5%粉剤形態の本発明害虫防除剤を
得た。Example 4 70.5 parts by weight of harmachia was dissolved in 30 parts by weight of methanol, 99.5 parts by weight of kaolin was added, and after thorough stirring, the methanol was distilled off to obtain a pest control agent of the present invention in the form of a 0.5% powder. Ta.
試験例1
直径8mmの濾紙(東洋濾紙株式会社、ペパ−ディスク
、重量17mg)に、ベルベリンの処定量をメタノール
に溶解して調製した液を塗布して風乾した。これを直径
35mmのプラスチックシャーレ−に入れ、ヤマトシロ
アリを10匹放飼し、死亡率を求めた。ベルベリンの供
試量と死亡°率(%)とを第1表に示す。Test Example 1 A solution prepared by dissolving a prescribed amount of berberine in methanol was applied to a filter paper with a diameter of 8 mm (Toyo Roshi Co., Ltd., Pepper Disk, weight 17 mg) and air-dried. This was placed in a plastic Petri dish with a diameter of 35 mm, 10 Yamato termites were released, and the mortality rate was determined. Table 1 shows the amount of berberine tested and the mortality rate (%).
第1表
試験例2
直径8mmの濾紙(東洋濾紙株式会社、ペパー−ディス
ク、重量17mg)に、パルマチンの処定量をメタノー
ルに溶解して調製した液を塗布して風乾した。これを直
径35mmのプラスチックシャーレ−に入れ、ヤマトシ
ロアリを10匹放飼し、死亡率を求めた。パルマチンの
供試量と死亡率(%)とを第2表に示す。Table 1 Test Example 2 A solution prepared by dissolving a prescribed amount of palmatine in methanol was applied to a filter paper with a diameter of 8 mm (Toyo Roshi Co., Ltd., Pepper Disc, weight 17 mg) and air-dried. This was placed in a plastic Petri dish with a diameter of 35 mm, 10 Yamato termites were released, and the mortality rate was determined. Table 2 shows the amount of palmatine tested and the mortality rate (%).
第2表
試験例3
実施例3で調製したベルベリンを含有する害虫防除剤5
gにチャバネゴキブリ40匹を放飼し4週間後の死亡率
(%)と害虫防除剤の重量減少率(%)を求めた0本発
明害虫防除剤の殺虫効果を第3表に示す、尚、ベルベリ
ンを含まない人口飼料(オリエンタル酵母工業株式会社
、コンチュウ用粒剤飼料)のみを与えた場合の結果を対
照として併記する。Table 2 Test Example 3 Pest control agent 5 containing berberine prepared in Example 3
The insecticidal effect of the pest control agent of the present invention is shown in Table 3, where the mortality rate (%) and weight loss rate (%) of the pest control agent after 4 weeks were determined by releasing 40 German cockroaches in g. The results obtained when only an artificial feed containing no berberine (Oriental Yeast Kogyo Co., Ltd., granular feed for conch) was fed are also shown as a control.
第3表
(効果)
前記の試験例から明かなように、本発明の天然産植物抽
出物質を含有する害虫防除剤は、幅広い害虫に対して優
れた幼虫効果を示し、かつ安全性が高く残留毒性が少な
い害虫防除剤である。Table 3 (Efficacy) As is clear from the above test examples, the pest control agent containing the naturally occurring plant extract of the present invention exhibits excellent larval effects against a wide range of pests, is highly safe, and has no residual It is a pest control agent with low toxicity.
Claims (1)
ノフロリン、メニスベリン、フェロデンドリンの一種お
よびまたは二種以上を有効成分として含有せしめること
を特徴とする害虫防除剤。A pest control agent characterized by containing berberine, one or more of palmatine, candicin, magnoflorin, menisberine, and ferrodendrin as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25924187A JPH01102007A (en) | 1987-10-14 | 1987-10-14 | Insect pest controlling agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25924187A JPH01102007A (en) | 1987-10-14 | 1987-10-14 | Insect pest controlling agent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01102007A true JPH01102007A (en) | 1989-04-19 |
Family
ID=17331369
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25924187A Pending JPH01102007A (en) | 1987-10-14 | 1987-10-14 | Insect pest controlling agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01102007A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6814987B2 (en) | 2000-12-15 | 2004-11-09 | Npi, Llc. | Compositions and methods of use for extracts of magnoliaceae plants |
CN103548852A (en) * | 2013-10-31 | 2014-02-05 | 浙江农林大学天目学院 | Pesticide composition containing alkaloids and application thereof |
CN107094780A (en) * | 2017-03-31 | 2017-08-29 | 大连理工大学 | Jamaicin and its derivative as hexosaminidase inhibitor application |
-
1987
- 1987-10-14 JP JP25924187A patent/JPH01102007A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6814987B2 (en) | 2000-12-15 | 2004-11-09 | Npi, Llc. | Compositions and methods of use for extracts of magnoliaceae plants |
CN103548852A (en) * | 2013-10-31 | 2014-02-05 | 浙江农林大学天目学院 | Pesticide composition containing alkaloids and application thereof |
CN107094780A (en) * | 2017-03-31 | 2017-08-29 | 大连理工大学 | Jamaicin and its derivative as hexosaminidase inhibitor application |
CN107094780B (en) * | 2017-03-31 | 2020-04-14 | 大连理工大学 | Application of berberine and derivatives thereof as hexosaminidase inhibitor |
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