Classifications

• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
  • A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
  • A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
  • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
  • A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
  • A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
  • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
  • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
  • A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring

Definitions

• the present inventors have intensively studied to find out a composition having an excellent control effect on a plant disease. As a result, they have found that a composition comprising a compound represented by the formula (1) and one or more antibiotic fungicidal compound selected from the following group (A) shows a synergistic activity, and thus has an excellent control effect on a plant disease, and therefore the present invention has been completed.
• antibiotic fungicidal compound selected from the following group (A):
• antibiotic fungicidal compound selected from the following group (A) to a plant or a soil for cultivating the plant,
• composition of the present invention may be a mixture as itself of the present amide compound and the present antibiotic compound
• the composition of the present invention is usually prepared by mixing the present amide compound, the present antibiotic compound and an inert carrier, and if necessary, adding a surfactant or other pharmaceutical additives, and then formulating into the form of oil solution, emulsificale concentrate, flowable formulation, wettable powder, granulated wettable powder, dust formulation, granules and so on.
• Such formulations can be used by itself or with an addition of other inert components as an agent for controlling a plant disease.
• the composition of the present invention can contain 0.1 to 99% by weight, preferably 0.2 to 90% by weight, and more preferably 1 to 80% by weight of the present amide compound and the present antibiotic compound in total.
• liquid carrier examples include aromatic hydrocarbons (e.g., xylene, alkyl benzene, or methylnaphtalene), alcohols (e.g., 2-propanol, ethylene glycol, propylene glycol, or ethylene glycol monoethyl ether), ketones (e.g., acetone, cyclohexanone, or isophorone), vegetable oils (e.g., soybean oil, or cotton oils), petroleum-derived aliphatic hydrocarbons, esters, dimethylsulfoxide, acetonitrile and water.
• aromatic hydrocarbons e.g., xylene, alkyl benzene, or methylnaphtalene
• alcohols e.g., 2-propanol, ethylene glycol, propylene glycol, or ethylene glycol monoethyl ether
• ketones e.g., acetone, cyclohexanone, or isophorone
• vegetable oils e
• surfactant examples include anionic surfactant (e.g., alkyl sulfate salts, alkylaryl sulfate salts, dialkyl sulfosuccinate salts, polyoxyethylene alkylaryl ether phosphates, lignin sulfonate, or naphthalenesulfonate formaldehyde polycondensation), nonionic surfactant (e.g., polyoxyethylene alkylaryl ether, polyoxyethylene alkyl polyoxypropylene block copolymer, or sorbitan fatty acid ester) and cationic surfactant (e.g., alkyltrimethyl ammonium salts).
• anionic surfactant e.g., alkyl sulfate salts, alkylaryl sulfate salts, dialkyl sulfosuccinate salts, polyoxyethylene alkylaryl ether phosphates, lignin sulfonate, or na
• the plant disease which can be controlled by the present invention is exemplified below:
• Rapeseed diseases Sclerotinia rot ( Sclerotinia sclerotiorum ), black spot ( Alternaria brassicae ), powdery mildew ( Erysiphe cichoracearum ), blackleg ( Leptosphaeria maculans );
• Adzuki-bean diseases Gray mold ( Botrytis cinerea ), Sclerotinia rot ( Sclerotinia sclerotiorum );
• the present amide compound and the present antibiotic compound may be applied separately around the same time to the plant or the soil for cultivating the plant, but is usually applied as the composition of the present invention in terms of a convenience on applying.
• test examples are given below.
• Test Example 1 The same operations as described in Test Example 1 are carried out with kasugamycin or streptomycin instead of validamycin or polyoxins, so as to calculate respective preventive values.

Landscapes

• Life Sciences & Earth Sciences (AREA)
• Agronomy & Crop Science (AREA)
• Pest Control & Pesticides (AREA)
• Plant Pathology (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Dentistry (AREA)
• General Health & Medical Sciences (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)

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• 2011
  • 2011-02-10 JP JP2011026897A patent/JP5691595B2/ja active Active
  • 2011-03-02 KR KR1020127022635A patent/KR101793305B1/ko not_active Expired - Fee Related
  • 2011-03-02 EP EP11710039A patent/EP2542068A2/fr not_active Withdrawn
  • 2011-03-02 AU AU2011221767A patent/AU2011221767B2/en not_active Ceased
  • 2011-03-02 WO PCT/JP2011/055432 patent/WO2011108753A2/fr not_active Ceased
  • 2011-03-02 US US13/579,620 patent/US20120329745A1/en not_active Abandoned
  • 2011-03-02 MX MX2012009658A patent/MX2012009658A/es active IP Right Grant
  • 2011-03-02 CA CA2790281A patent/CA2790281C/fr not_active Expired - Fee Related
  • 2011-03-02 CN CN201180012285.5A patent/CN102834004B/zh not_active Expired - Fee Related
  • 2011-03-02 BR BR112012021680A patent/BR112012021680B1/pt not_active IP Right Cessation
  • 2011-03-02 AR ARP110100654A patent/AR081732A1/es active IP Right Grant
• 2012
  • 2012-08-08 ZA ZA2012/05988A patent/ZA201205988B/en unknown
  • 2012-08-31 CL CL2012002409A patent/CL2012002409A1/es unknown
• 2015
  • 2015-07-31 US US14/815,449 patent/US10051860B2/en active Active

Non-Patent Citations (4)

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