JPH05271013A - Insect pest controlling agent comprising cyclic depsipeptide substance as active ingredient - Google Patents
Insect pest controlling agent comprising cyclic depsipeptide substance as active ingredientInfo
- Publication number
- JPH05271013A JPH05271013A JP7146392A JP7146392A JPH05271013A JP H05271013 A JPH05271013 A JP H05271013A JP 7146392 A JP7146392 A JP 7146392A JP 7146392 A JP7146392 A JP 7146392A JP H05271013 A JPH05271013 A JP H05271013A
- Authority
- JP
- Japan
- Prior art keywords
- substance
- controlling agent
- active ingredient
- insect pest
- cyclic depsipeptide
- 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
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は環状デプシペプチド物質
であるPF1022物質を有効成分として含有すること
を特徴とする害虫防除剤に関する。FIELD OF THE INVENTION The present invention relates to a pest control agent containing a PF1022 substance, which is a cyclic depsipeptide substance, as an active ingredient.
【0002】[0002]
【従来の技術】本発明に係る環状デプシペプチド物質で
あるPF1022物質は下記の化学構造式(I)を有す
る物質で駆虫作用を有する(特開平3−35796)。2. Description of the Related Art The PF1022 substance, which is a cyclic depsipeptide substance according to the present invention, is a substance having the following chemical structural formula (I) and has an anthelmintic action (JP-A-3-35796).
【0003】[0003]
【化1】 [Chemical 1]
【0004】上記の公報での駆虫剤は動物の寄生虫例え
ば、牛、羊の捻転胃虫、オステルターグ胃虫、毛円虫、
クーパー線虫、腸結節虫、双口吸虫、ベネディン条虫、
肺虫、肝蛭等、豚の回虫、鞭虫、腸結節虫等、犬の回
虫、鉤虫、鞭虫、糸状虫等、猫の回虫、マンソン裂頭条
虫等、鶏の回虫、毛様虫、盲腸虫等、ヒトの回虫、蟯
虫、鉤虫、東洋毛様線虫、糞線虫、鞭虫等の内部寄生虫
への効果が期待される旨記載されている。しかし、農園
芸分野や環境衛生分野の主要な害虫である昆虫類または
植物寄生性の線虫類に対する用途は記載されていない。The anthelmintic agents in the above publications are animal parasites such as bovine and sheep torsion gastropods, ostertag gastric caterpillars, caterpillars,
Cooper nematode, intestinal tuberculosis, double mouth fluke, Benedin tapeworm,
Lungworms, liver flukes, swine roundworms, whipworms, intestinal tuberculosis, dog roundworms, hookworms, whipworms, filamentous insects, cat roundworms, Manson's cephalopodis, etc. It is stated that an effect is expected on endoparasites such as caecum, human roundworm, pinworm, hookworm, oriental hairy nematode, dung nematode, whipworm and the like. However, there is no description of use for insects or plant parasitic nematodes, which are major pests in the fields of agriculture and horticulture and environmental hygiene.
【0005】上記公報記載の駆虫効果は明細書記載の麻
痺作用に基づく排虫効果によるものまであり、同様な寄
生虫の運動性麻痺作用を特徴とするピペラジンやモラン
テルが優れた駆虫剤であるにもかかわらず昆虫類に対す
る防除効果を有しないこと、あるいは豚等の回虫に優れ
た駆虫効果を有するデストマイシンがマツノザイセンチ
ュウに防除効果を示さない。このことから、PF102
2物質がこれらの害虫類に対して優れた防除効果を有す
るという本発明の発見は、容易に類推することの出来な
い驚くべき知見である。The anthelmintic effect described in the above publications is due to the worming effect based on the paralytic effect described in the specification, and piperazine and morantel, which are characterized by the similar motor paralytic effect of parasites, are excellent anthelmintic agents. Nonetheless, destomycin, which has no controlling effect on insects, or has an excellent anthelmintic effect on roundworms such as pigs, does not show a controlling effect on P. chinensis. From this, PF102
The discovery of the present invention that the two substances have excellent control effects against these pests is a surprising finding that cannot be easily analogized.
【0006】[0006]
【発明が解決しようとする課題】近年、有機リン酸エス
テル系、カーバメート系、ピレスロイド系等の、代表的
な殺虫剤の長年の使用により抵抗性の発達した害虫が出
現した結果、それらに対して優れた防除効果を示し、し
かも低毒性かつ低残留性の新たな害虫防除剤の開発が要
望されている。In recent years, pests with developed resistance have emerged as a result of the emergence of pests that have developed resistance due to the long-term use of typical insecticides such as organophosphates, carbamates, and pyrethroids. There is a demand for the development of a new pest control agent that exhibits an excellent control effect and has low toxicity and low residue.
【0007】[0007]
【課題を解決するための手段】本発明者らは上記問題点
を解決するため鋭意研究を重ねた結果、PF1022物
質が優れた害虫防除効果を示すことを発見し、本発明を
完成するに到った。即ち本発明の要旨は、環状デプシペ
プチド物質であるPF1022物質を有効成分として含
有することを特徴とする害虫防除剤に関する。As a result of intensive studies to solve the above problems, the present inventors have found that the PF1022 substance has an excellent pest control effect, and have completed the present invention. It was. That is, the gist of the present invention relates to a pest control agent containing a PF1022 substance which is a cyclic depsipeptide substance as an active ingredient.
【0008】以下本発明を詳細に説明する。本発明の有
効成分であるPF1022物質は前記の特開平3−35
796に記載された環状デプシペプチドであり、主とし
て無胞子不完全菌PF1022株(FERM BP−2
671)を好気的条件で培養し、その培養物から抽出、
精製することによって製造することができる。The present invention will be described in detail below. The PF1022 substance which is the active ingredient of the present invention is described in the above-mentioned JP-A-3-35.
796, which is a cyclic depsipeptide, and is mainly a non-sporeless bacterium PF1022 strain (FERM BP-2.
671) is cultivated under aerobic conditions and extracted from the culture,
It can be produced by purification.
【0009】本発明の害虫防除剤を実施するにあたって
はPF1022物質をそのまま用いることもできるが、
各種の液体担体又は固体担体と混合し、界面活性剤など
の補助剤の適当量を加えて水和剤、乳剤、水性液剤、油
性液剤、粉剤、粒剤、ベイト剤あるいは毒餌等に製剤化
して用いる。その場合の活性成分としては、PF102
2物質のみでもよいが、他の殺虫剤、殺菌剤、除草剤、
誘引剤、協力剤などと混合して使用すればより効果的、
かつ省力的に害虫防除の目的を達成することができる。In carrying out the pest control agent of the present invention, the PF1022 substance can be used as it is,
Mix with various liquid carriers or solid carriers, add appropriate amount of auxiliary agent such as surfactant, and formulate into wettable powder, emulsion, aqueous liquid, oily liquid, powder, granule, bait or poison bait etc. To use. In that case, the active ingredient is PF102.
Only two substances may be used, but other insecticides, fungicides, herbicides,
It is more effective if mixed with an attractant, synergist, etc.
In addition, the purpose of pest control can be achieved labor-savingly.
【0010】本発明の害虫防除剤は害虫防除が望まれる
作物に直接散布または植物体に注入して用いることがで
きる。また、必要に応じて水面や土壌表面などの作物の
生育環境に適用することができ、土壌中に混和して使用
することもできる。あるいは毒餌として害虫に直接摂取
させることもできる。The pest control agent of the present invention can be used by spraying it directly to a crop for which pest control is desired or by injecting it into a plant. In addition, it can be applied to the growing environment of crops such as the surface of water or the surface of soil, if necessary, and can also be mixed with soil for use. Alternatively, the pest can be directly ingested as poison bait.
【0011】本発明の害虫防除剤を散布剤として使用す
る場合には、通常、散布液中にPF1022物質が0.
1ないし1000ppmの濃度で含まれるようにするの
が望ましく、注入剤や餌中に混入して使用する場合に
は、0.01ないし500ppmの濃度で含まれるよう
にすることが望ましい。また濃厚少量散布などの場合に
は、本発明に係わるPF1022物質の温血動物に対す
る毒性が少ないので、より高濃度で効果的かつ安全に使
用することができる。When the pest control agent of the present invention is used as a spraying agent, the PF1022 substance is usually added to the spraying solution in an amount of 0.
It is desirable to be contained at a concentration of 1 to 1000 ppm, and when used by being mixed in an injectable or feed, it is desirable to be contained at a concentration of 0.01 to 500 ppm. Further, in the case of spraying in a concentrated small amount, since the PF1022 substance according to the present invention has little toxicity to warm-blooded animals, it can be used effectively and safely at a higher concentration.
【0012】[0012]
【発明の効果】本発明により、低毒性の優れた害虫防除
剤を提供できる。INDUSTRIAL APPLICABILITY According to the present invention, an excellent pest control agent having low toxicity can be provided.
【0013】[0013]
【実施例】次に本発明の害虫防除剤の効果を、以下の試
験例によって明らかにし、さらに製剤例も示す。 試験例1カイコ幼虫に対する効力試験 カイコ3令幼虫を1区10頭宛供試し、PF1022物
質が所定濃度になるように混入した人工飼料を入れた直
径9cmのプラスチックカップに放虫し、25℃の恒温
室で飼育した。6日後の生死虫数を調査し、下記の式に
より死虫率を求めた。結果を表1に示す。 死虫率(%)=(死虫数/放虫数)×100EXAMPLES Next, the effects of the pest control agent of the present invention will be clarified by the following test examples, and formulation examples will also be shown. Test Example 1 Efficacy test against silkworm larvae A third-instar larvae of silkworm was tested for 1 group and 10 larvae, and the insects were released in a plastic cup with a diameter of 9 cm containing an artificial feed mixed so that the PF1022 substance had a predetermined concentration at 25 ° C. It was kept in a constant temperature room. The number of live and dead insects after 6 days was investigated, and the mortality rate was calculated by the following formula. The results are shown in Table 1. Mortality rate (%) = (number of dead insects / number of released insects) x 100
【0014】[0014]
【表1】 表 1 供試薬剤 添加濃度 死虫率 (PPM) (%) PF1022物質 100 30 PF1022物質 500 100 無 添 加 0 0 [Table 1] Table 1 Reagents Concentration of added mortality rate (PPM) (%) PF1022 substance 100 30 PF1022 substance 500 100 No additive 0 0
【0015】試験例2ハスモンヨトウ幼虫に対する効力試験 PF1022物質20mgをアセトン5mlに溶解し、
水10mlを加えて希釈した。この希釈液を直径9cm
のプラスチックカップに入れた乾燥人工飼料(ビタシル
ク、共同飼料(株)製)4分の1片に注加し、十分に吸
収させた。室温でアセトンを蒸発させた後、ハスモンヨ
トウ3令幼虫5頭を放虫し、25℃の恒温室で飼育し
た。5日後の生死虫数を調査し、下記の式により死虫率
を求めた。死虫率は、80%であった。なお、試験は2
反復で行った。 死虫率(%)=(死虫数/放虫数)×100Test Example 2 Efficacy test against Larvae of Spodoptera litura, 20 mg of PF1022 substance was dissolved in 5 ml of acetone,
Diluted by adding 10 ml of water. This diluent is 9 cm in diameter
1/4 pieces of the dried artificial feed (Vitasilk, manufactured by Kyodo Feed Co., Ltd.) placed in the plastic cup of No. 1 was added to be sufficiently absorbed. After evaporating acetone at room temperature, 5 third-instar larvae of Spodoptera litura were released and were bred in a thermostatic chamber at 25 ° C. The number of live and dead insects after 5 days was investigated, and the mortality rate was calculated by the following formula. The mortality was 80%. The test is 2
Repeated. Mortality rate (%) = (number of dead insects / number of released insects) x 100
【0016】試験例3マツノザイセンチュウに対する効力試験 あらかじめ灰色かび病菌を接種したCzapek寒天培
地で培養したマツノザイセンチュウを供試した。薬剤は
乾熱滅菌した直径5mmの綿球に所定濃度に溶解、希釈
して調整した薬液を0.1ml宛処理した。Czape
k寒天に灰色かび病菌を接種して4日間培養した直径9
cmのプラスチックシャーレの中央に薬剤処理した綿球
を置き、マツノザイセンチュウの懸濁液0.1ml(1
500頭)を接種して、26℃暗黒下で培養した。5日
後に生存するマツノザイセンチュウをベールマン法で分
離し、顕微鏡下で生存虫数を計数調査し、下式によって
増殖阻止率を求めた。結果を表2に示す。 増殖阻止率(%)=(1−処理区の生存虫数/無処理区
の生存虫数)×100Test Example 3 Efficacy test against pine wood nematode A pine wood nematode cultivated on a Czapek agar medium previously inoculated with Botrytis cinerea was used as a test. The chemicals were prepared by dissolving and diluting a dry-heat sterilized cotton ball having a diameter of 5 mm to a predetermined concentration and treating it with 0.1 ml. Czape
k agar inoculated with Botrytis cinerea and cultured for 4 days Diameter 9
Place a chemically treated cotton ball in the center of a cm plastic dish, and add 0.1 ml (1 ml) of a pinewood nematode suspension.
(500 heads) were inoculated and cultured in the dark at 26 ° C. The pine wood nematodes that survived 5 days were separated by the Bertmann method, the number of surviving worms was counted and examined under a microscope, and the growth inhibition rate was determined by the following formula. The results are shown in Table 2. Growth inhibition rate (%) = (1-number of surviving insects in treated group / number of surviving insects in untreated group) × 100
【0017】[0017]
【表2】 表 2 供 試 薬 剤 薬剤処理量 増殖阻止率 (μg/綿球) (%) PF1022物質 5 45 無 添 加 0 0 [Table 2] Table 2 Test drug Agent Drug treatment amount Growth inhibition rate (μg / cotton ball) (%) PF1022 substance 5 45 No additive 0 0
【0018】製剤例1 PF1022物質、1.25重量部をN−メチルピロリ
ドン50重量部に溶解し、次いでポリオキシエチレンア
ルキルエーテル12.5重量部、およびプロピレングリ
コール脂肪酸エステル12.5重量部を添加溶解した。
さらに、水23.75重量部を加えて攪拌混合し、水性
液剤を調製した。Formulation Example 1 1.25 parts by weight of PF1022 substance was dissolved in 50 parts by weight of N-methylpyrrolidone, and then 12.5 parts by weight of polyoxyethylene alkyl ether and 12.5 parts by weight of propylene glycol fatty acid ester were added. Dissolved.
Further, 23.75 parts by weight of water was added and mixed with stirring to prepare an aqueous liquid preparation.
【0019】製剤例2 PF1022物質10重量部、ポリオキシエチレンアル
キルアリールエーテル10重量部、アルキルベンゼンス
ルホネート5重量部、クレー75重量部を粉砕混合し
て、水和剤を調製した。Formulation Example 2 10 parts by weight of PF1022 substance, 10 parts by weight of polyoxyethylene alkylaryl ether, 5 parts by weight of alkylbenzene sulfonate and 75 parts by weight of clay were pulverized and mixed to prepare a wettable powder.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 岡田 忠昭 神奈川県横浜市港北区師岡町760番地 明 治製菓株式会社薬品総合研究所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Tadaaki Okada 760 Shimooka-cho, Kohoku-ku, Yokohama-shi, Kanagawa Meiji Confectionery Co., Ltd.
Claims (1)
22物質を有効成分として含有することを特徴とする害
虫防除剤。1. A cyclic depsipeptide substance, PF10.
A pest control agent, which comprises 22 substances as active ingredients.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7146392A JPH05271013A (en) | 1992-03-27 | 1992-03-27 | Insect pest controlling agent comprising cyclic depsipeptide substance as active ingredient |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7146392A JPH05271013A (en) | 1992-03-27 | 1992-03-27 | Insect pest controlling agent comprising cyclic depsipeptide substance as active ingredient |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH05271013A true JPH05271013A (en) | 1993-10-19 |
Family
ID=13461315
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7146392A Pending JPH05271013A (en) | 1992-03-27 | 1992-03-27 | Insect pest controlling agent comprising cyclic depsipeptide substance as active ingredient |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH05271013A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999066794A1 (en) * | 1998-06-24 | 1999-12-29 | Bayer Aktiengesellschaft | Ectoparasiticide agents |
WO2001045512A1 (en) * | 1999-12-22 | 2001-06-28 | Bayer Aktiengesellschaft | Pest control agents / depsipeptides |
US6828300B2 (en) | 1999-12-22 | 2004-12-07 | Bayer Aktiengesellschaft | Pest control agent/PF 1022-221 |
WO2013187480A1 (en) | 2012-06-13 | 2013-12-19 | Meiji Seikaファルマ株式会社 | Novel cyclic depsipeptide derivative and pest control agent comprising same |
-
1992
- 1992-03-27 JP JP7146392A patent/JPH05271013A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999066794A1 (en) * | 1998-06-24 | 1999-12-29 | Bayer Aktiengesellschaft | Ectoparasiticide agents |
US6630569B1 (en) | 1998-06-24 | 2003-10-07 | Bayer Aktiengesellschaft | Ectoparasiticide agents |
WO2001045512A1 (en) * | 1999-12-22 | 2001-06-28 | Bayer Aktiengesellschaft | Pest control agents / depsipeptides |
US6828300B2 (en) | 1999-12-22 | 2004-12-07 | Bayer Aktiengesellschaft | Pest control agent/PF 1022-221 |
US6900176B2 (en) | 1999-12-22 | 2005-05-31 | Bayer Aktiengesellschaft | Pest control agents/depsipeptides |
WO2013187480A1 (en) | 2012-06-13 | 2013-12-19 | Meiji Seikaファルマ株式会社 | Novel cyclic depsipeptide derivative and pest control agent comprising same |
EP3441399A1 (en) | 2012-06-13 | 2019-02-13 | Meiji Seika Pharma Co., Ltd. | Novel cyclic depsipeptide derivatives and harmful organism control agents comprising the same |
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