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:
A novel agricultural chemical, especially an insecticide or acaricide; and a substituted benzanilide compound represented by the general formula (1): (1) G-7 G-13 G-71 [wherein G represents a ring represented by G-7, G-13, G-71, etc.; W1 and W2 each independently represents oxygen or sulfur; X represents halogeno, etc.; Y represents C1-6 alkyl, etc.; R1, R2, and R3 each independently represents hydrogen, C1-12 alkyl, C1-6 alkylthio(C1-6 alkyl), etc.; R4, R5, R6a, and R6b each independently represents hydrogen, C1-6 alkyl, C1-6 haloalkyl, phenyl optionally substituted by (Z2)p1, etc.; R6i, R6j, and R6k each independently represents hydrogen, halogeno, etc.; Z2 represents halogeno, C1-6 haloalkoxy, C1-6 alkylsulfonyl, etc.; m and n each independently is an integer of 0 to 4; and p1 is an integer of 1 to 5] or a salt of the compound. The pest control agent contains either of the compound and salt.
摘要:
Verbindungen der Formel worin die Substituenten die in Anspruch 1 angegebenen Bedeutungen besitzen, sowie agronomisch verträgliche Salze, Isomere und Enantiomere dieser Verbindungen eignen sich zur Verwendung als Herbizide.
摘要翻译:芳基取代的(杂)环酮 - 烯醇(I)是新的。 还有新的含有这些酮 - 烯醇和安全剂的选择性除草剂。 烯醇醚由部分新的卤代取代的甲苯中间体制备。 芳基取代的(杂)环酮 - 烯醇是式(I)化合物及其异构体,对映异构体和盐:[图像] R 1,R 3Et,OMe或OEt(各自任选被卤素,乙炔基,COMe,COEt CH 2 OH,C 2H 5 OH,COOMe或COOEt; Q:包括基团Q 1和Q 6的10个基团之一; [图像] R 4,任选被28个基团取代的R 5烷基,烯基,炔基,环烷基,芳基或杂芳基; 或R 4 + R 5 +相关的N原子:任选地含有杂原子的环,任选地带有稠合或螺键键合的亚烷基或亚链烯基,并任选被苯基或苄基取代(各自任选被9个基团取代); R 13,任选被8个基团取代的R 14烷基,烯基,炔基,环烷基,芳基或杂芳基;或R 13 + R 14 +相关原子:环; G 1,G 6H,-C(X 1)-R 20, C(X 2)-X 3 -R 21,-C(X 4)-N(R 22)-R 23,-SO 2 -R 24,碱金属,碱土金属,锍或铵阳离子,-P(X 5)(R 25)-R 26或-CH 2 -X 6 -R 27; X 1-X 6O或S; R 20 -R 23 H,烷基 由25个基团取代,烯基,炔基,卤代烯基,环烷基,苯基,杂芳基,杂芳基氨基,二杂芳基氨基,苯基氨基或二苯基氨基(各自任选被7个基团取代),环烷基氨基,二环烷基氨基或环烷氧基; R 24-R 26H,任选被25个基团取代的烷基,烯基,炔基,卤代烯基,环烷基,苯基,杂芳基,杂芳基氨基,二杂芳基氨基,苯基氨基或二苯基氨基(各自任选被7个基团取代),环烷基氨基,二环烷基氨基,环烷氧基,烷氧基,卤代烷氧基 ,烷基氨基,二烷基氨基,苯氧基或苄氧基(各自任选被7个基团取代); R 27烷基羰基或除H之外的任何R 20 -R 23值。完整定义在定义(完全定义)领域中给出。 还包括独立权利要求:(1)化合物(I)的制备; (2)含有化合物(I)的选择性除草剂(除了Q = Q 1组之外)和选自20个给定式的安全剂(解毒剂)(公式和相关的全部定义在定义(完全定义)领域中给出; 化合物(I其中R 1 = R 3 = C 2H 5; Q = Q 1; R 4)的功效;(3)式(ⅩⅩⅪa)的卤代甲苯衍生物 + R 5 = - (CH 2)4-; G =新戊酰氧基)当以0.5kg / ha的出苗前测量时,所用结果范围为1 =总杀灭数为9 =无效果; 表现出良好的非常好的活动,得分分别为:1对Alopecurus,Avena,Lolium,Setaria,Panicum,Sorghum,Echinochloaand Brachiaria和4对Digitaria的作用机制:没有给出。
摘要:
Nucleoside and nucleotide compounds and their analogs/prodrugs are provided. Particularly contemplated compounds include 1-β-L-ribofuranosyl-1,2,4-triazole-3-carboxamide, which may be modified and/or phosphorylated. Contemplated compounds may further be combined with other pharmacological compounds, especially including Ribavirin, antibodies, and cytokines. Preferred uses of contemplated compounds include use as an antiviral compound, anti-inflammatory compound, antineoplastic compound, and as a compound to stimulate cellular growth.
摘要:
Compounds of the formula I in which Z is -CO-NHNH 2 , COOH, COCl, CONHNHCOR 4 or CON=C(R 4 )NMe 2 are intermediates for the preparation of compounds of the formula I in which Z is a group
a)
or b)
or c)
or d)
The end compounds can be used for pest control, in particular as microbicides, insecticides and acaricides in agriculture, in horticulture and in the hygiene sector.
摘要:
A system for inhibiting the germination or growth of a fungus comprises (a) fungal cell wall degrading chitinolytic or glucanolytic enzyme and (b) antifungal cell membrane affecting compound. Exemplified antifungal fungal cell membrane affecting compounds include flusilazole, miconazole, osmotin, gramicidin, valinomycin, phospholipase B, and trichorzianines. The system components (a) and (b) may be supplemented with polyene macrolide antibiotic, antifungal epithiodiketopiperazine antibiotic (e.g., gliotoxin), fungal cell wall biosynthesis inhibitor (e.g., L-sorbose) and/or detergent. Embodiments include method of contacting a plan which expresses cell wall degrading enzyme with antifungal fungal cell membrane affecting compound.