FUNGICIDAL PYRANONES AND OXAZINONES
    51.
    发明申请
    FUNGICIDAL PYRANONES AND OXAZINONES 审中-公开
    杀真菌剂和氧化亚氮

    公开(公告)号:US20120329787A1

    公开(公告)日:2012-12-27

    申请号:US13166248

    申请日:2011-06-22

    摘要: Disclosed are compounds of Formula 1, including all geometric and stereoisomers, tautomers, N-oxides, and salts thereof, wherein Q, Z, R2, R3 and R4 are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling plant disease caused by a fungal pathogen comprising applying an effective amount of a compound or a composition of the invention.

    摘要翻译: 公开了式1的化合物,包括所有几何和立体异构体,互变异构体,N-氧化物及其盐,其中Q,Z,R 2,R 3和R 4如本公开所定义。 还公开了含有式1化合物的组合物和用于控制由真菌病原体引起的植物病害的方法,包括施用有效量的本发明化合物或组合物。

    Amino substituted benzo(hetero)cyclic derivatives

    公开(公告)号:US20060166984A1

    公开(公告)日:2006-07-27

    申请号:US10547914

    申请日:2004-02-20

    IPC分类号: A01N43/84

    CPC分类号: A01N43/72 A01N43/60

    摘要: Use of compounds Formula (I), A=a 5- to 7-membered ring which may contain 1-3 heteroatoms and which may be saturated or partially or completely unsaturated; R1═OH, SH, NH2, CN, NO2, halogen, C1-C6-alkyl, C1-C6-haloalkyl; C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-haloalkylthio, C2-C6-alkenyl, C2-C6alkenyloxy, C2-C6-alkenylthio, C2-C6-alkynyl, C2-C6-alkynyloxy, C2-C6-alkynylthio, C1-C6-alkylsulfonyl, C1-C6-alkylsulfoxyl, C2-C6-alkenylsulfonyl, C2-C6-alkylsulfoxyl, C1-C6-alkylcarbonyl, C1-C6-alkoxycarbonyl, C1-C6-aklylcarbonyloxy; R2═C1-C6-alkyl or a mono- or bicyclic 5- to 10-membered aromatic ringsystem which may contain 1 to 4 heteroatoms and which is either bonded directly or through an O, S, C1-C6-alkylene or C1-C6-alkyleneoxy linkage to A or fused to A and which may be substituted; R3, R4═H, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkyl-amino, C1-C6-alkoxy, C3-C6-cycloalkyl, or R3 and R4 together with the nitrogen atom to which they are attached form a saturated or partially saturated mono- or bicyclic 5- to 10-membered ring system containing 1 to 3 heteroatoms or a 5-membered hetaryl containing 1 to 4 nitrogen atoms, wherein the carbon and/or nitrogen atoms in the ring systems may be substituted or phenyl or benzyl which may be substituted; or R3 and R4 together form the chains —(CH2)2N+(O—)(CH2)2— or —(CH2)3N+(O−)(CH2)2—; m=0 to 4; n is 0 to 4; and the enantiomers, diastereomers, cis/trans isomers or salts thereof for combatting insects, arachnids or nematodes, methods for the control of these pests and of protecting growing plants attack or infestation by these pests by applying a pesticidally effective amount of a compound of formula (I), processes for preparing them, and compositions comprising them.

    Novel substance fki-1033 and process for producing the same
    57.
    发明申请
    Novel substance fki-1033 and process for producing the same 有权
    新物质fki-1033及其制备方法

    公开(公告)号:US20060111280A1

    公开(公告)日:2006-05-25

    申请号:US10532662

    申请日:2002-11-12

    摘要: The present invention is comprised of culturing microorganism having ability to produce FKI-1033 substance represented by the formula: in a medium, accumulating FKI-1033 substance in the cultured medium, and isolating FKI-1033 substance from the cultured mass. The thus obtained FKI-1033 substance has ryanodine binding inhibition activity, insecticidal activity and anthelmintic activity, and is expected as useful drugs as agrochemicals, veterinary drugs and medicaments in effectiveness and toxicity.

    摘要翻译: 本发明包括培养具有下式表示的FKI-1033物质的能力的微生物:在培养基中积聚FKI-1033物质的培养基中,并从培养物质中分离FKI-1033物质。 由此获得的FKI-1033物质具有兰诺定结合抑制活性,杀虫活性和驱虫活性,并且作为农药,兽药和药物的有效性和毒性被期待为有用的药物。