1,2,4-옥사디아졸 유도체 및 그의 제조방법
    31.
    发明授权
    1,2,4-옥사디아졸 유도체 및 그의 제조방법 失效
    1,2,4-恶二唑衍生物及其制备方法

    公开(公告)号:KR1019900006555B1

    公开(公告)日:1990-09-13

    申请号:KR1019880008435

    申请日:1988-07-07

    Inventor: 조광연 정인화

    Abstract: 1,2,4-Oxadiazole derivs. of formula (I), useful as herbicides, are prepd.. In (I), R1 is dichlorophenoxymethyl, benzyl, ethyl, alkylamino-carbonyl, amido, methoxycarobnyl, amino, alkylureido, ethoxy carbonylalkoxy, diethylthiocarbamoylmethyl, allylaminocarbonyl opt. substd. by 1 or 2 haloen, or phenyl; R2 is dichlorophenoxymethyl, hydroxy, chloro, diethylthiocarbamoylmethyl, ethoxycarbonyl alkoxylphenoxy, dichlorophenoxy, nitrophenoxy, ethoxycarbonyl, amido or diethylphosphonyl.

    Abstract translation: 1,2,4-恶二唑衍生物。 在式(I)中,R 1是二氯苯氧基甲基,苄基,乙基,烷基氨基 - 羰基,酰胺基,甲氧基八烷基,氨基,烷基脲基,乙氧基羰基烷氧基,二乙基硫代氨基甲酰基甲基,烯丙基氨基羰基选择。 substd。 1或2个卤素,或苯基; R2是二氯苯氧基甲基,羟基,氯,二乙基硫代氨基甲酰基甲基,乙氧基羰基烷氧基苯氧基,二氯苯氧基,硝基苯氧基,乙氧基羰基,酰氨基或二乙基膦酰基。

    1,2,4-옥사디아졸 유도체
    33.
    发明授权
    1,2,4-옥사디아졸 유도체 失效
    1,2,4-OXADIAZINE DERIVATIVES

    公开(公告)号:KR1019900003273B1

    公开(公告)日:1990-05-12

    申请号:KR1019880001998

    申请日:1988-02-26

    Abstract: 1,2,4-Oxadiazole derivs. of formula (I) are provided. In (I), R1=lower alkyl, substd. phenyl by H or halogen, mehylphenyl, pyridine-2-yl, or pyridine-2-yloxymethyl; R2=substd. phenyl (or phenoxyalkyl or thiophenoxyalkyl) by H, halogen or phenyl, or 1-6C alkylhaloalkyl, cyclohexyl or hydroxy (I) are useful as a herbicide.

    Abstract translation: 1,2,4-恶二唑衍生物。 的式(I)。 在(I)中,R 1 =低级烷基,被取代。 苯基,H或卤素,甲苯基,吡啶-2-基或吡啶-2-基氧基甲基; R2 = substd。 H,卤素或苯基或1-6C烷基卤代烷基,环己基或羟基(I)的苯基(或苯氧基烷基或噻吩氧基烷基)可用作除草剂。

    생리활성을 가진 피리미딘 유도체 및 그 제조방법
    34.
    发明授权
    생리활성을 가진 피리미딘 유도체 및 그 제조방법 失效
    具有生理活性的吡啶并及其制备方法

    公开(公告)号:KR1019900002060B1

    公开(公告)日:1990-03-31

    申请号:KR1019870011154

    申请日:1987-10-06

    Abstract: 1=aryl sulfone, arylthio, alkylsulfone, alkylthio, alkyl carbonyl, dialkylphosphono; R2= amino, dialkylamino, lower alkyl, phenyl; R3=lower alkyl; R4= alkoxy, halogen-, nitro- substd. phenoxy, thiophenoxy, lower alkylthio; X=O,S) to prevent rice insect and acarid are prepd. Thus 10g (0.037 mol) 1-methoxycarbonyl-1-phenylsulfonyl-2-(N,Ndimethyl amino) ethene, 6.06g (0.022 mol) N,N-dimethyl guanidine sulfate and 3.52g (0.088 mol) NaOH in the mixed solvent of 60ml EtOH and 15ml H2O are stirred for 8 hr followed by removing solvent and recrystallizing with EtOH to give 7.8g I (R1=II; R2=N (CH3)2).

    Abstract translation: 1 =芳基砜,芳硫基,烷基砜,烷硫基,烷基羰基,二烷基膦酰基; R2 =氨基,二烷基氨基,低级烷基,苯基; R3 =低级烷基; R4 =烷氧基,卤素,硝基。 苯氧基,硫代苯氧基,低级烷硫基; X = O,S),以防止水稻昆虫和螨虫食用。 将10g(0.037mol)1-甲氧基羰基-1-苯基磺酰基-2-(N,N-二甲基氨基)乙烯,6.06g(0.022mol)N,N-二甲基硫酸胍和3.52g(0.088mol)NaOH在 将60ml EtOH和15ml H 2 O搅拌8小时,然后除去溶剂并用EtOH重结晶,得到7.8g I(R 1 = II; R 2 = N(CH 3)2)。

    토양 메타게놈 유래 인디루빈 및 인디고 생합성 유전자 및이로부터 코딩되는 단백질
    37.
    发明授权
    토양 메타게놈 유래 인디루빈 및 인디고 생합성 유전자 및이로부터 코딩되는 단백질 失效
    来源于土壤宏基因组的靛玉红和靛蓝生物合成基因以及由其编码的蛋白质

    公开(公告)号:KR100590053B1

    公开(公告)日:2006-06-19

    申请号:KR1020050000346

    申请日:2005-01-04

    Abstract: 본 발명은 토양 미생물의 메타게놈에서 분리한 인디루빈(indirubin) 및 인디고(indigo) 생합성 유전자 및 이로부터 코딩되는 단백질에 관한 것이다. 본 발명에 따른 인디루빈 및 인디고 생합성 유전자 및 이로부터 코딩되는 단백질은 미생물로부터 천연색소인 인디루빈 및 인디고를 대량으로 생산하는데 유용하게 사용될 수 있다.

    Abstract translation: 本发明涉及从土壤微生物的宏基因组中分离的吲哚布林和靛蓝生物合成基因和由其编码的蛋白质。 根据本发明的靛玉红和靛蓝生物合成基因和由其编码的蛋白质可以有效地用于从微生物大量生产作为天然着色剂的吲哚青和靛蓝。

    살균제의 약효증진제 조성물 및 이를 함유하는 살균제조성물
    38.
    发明公开
    살균제의 약효증진제 조성물 및 이를 함유하는 살균제조성물 有权
    用于增加防腐活性的组合物和含有该物质的防腐制剂有效地控制杀虫剂的制备和减少使用的杀真菌剂的数量

    公开(公告)号:KR1020050004343A

    公开(公告)日:2005-01-12

    申请号:KR1020030044486

    申请日:2003-07-02

    CPC classification number: A01N37/36 A01N37/50 A01N25/30 A01N25/04 A01N2300/00

    Abstract: PURPOSE: Provided are a composition for increasing fungicidal activity and a fungicidal preparation containing the same, thereby controlling phytopathogens effectively and decreasing the quantity of the fungicidal preparation used. CONSTITUTION: The fungicidal preparation is characterized by containing a fungicidal preparation selected from methyl (2E)-3-methoxy-2-(2'-(((3''-(1'''-fluor-2'''-phenyl-1'''-ethenyloxy)phenyl)methylimino)oxy)methylphenyl)propionate represented by the formula(1) and N-methyl (2E)-2-methoxyimino-2-(2'-(((3''-(1'''-fluor-2'''-phenyl-1'''-ethenyloxy)phenyl)methylimino)oxy)methylphenyl)acetamide represented by the formula(2); and the composition for increasing fungicidal activity in a weight ratio of 1:0.5 to 1:20.

    Abstract translation: 目的:提供一种提高杀真菌活性的组合物和含有该杀菌活性的杀真菌剂,从而有效控制植物病原体并减少所用杀真菌剂的用量。 构成:杀真菌制剂的特征在于含有选自(2E)-3-甲氧基-2-(2' - (((3“ - (1” - 氟-2“ - ” (1E)-2-甲氧基亚氨基-2-(2' - (((3“ - (( 苯基)甲基亚氨基)氧基)甲基苯基)乙酰胺;由式(2)表示的“1” - 氟-2“ - - 苯基-1” - - 以及以1:0.5至1:20的重量比提高杀真菌活性的组合物。

    식물 병원균인 피시움 미리오틸륨 균주 및 이를 이용한 잡초의 생물학적 방제 방법
    39.
    发明授权
    식물 병원균인 피시움 미리오틸륨 균주 및 이를 이용한 잡초의 생물학적 방제 방법 失效
    식물병원균인피시움미리오틸륨균주및이를이용한잡초의생물학적방제방

    公开(公告)号:KR100457069B1

    公开(公告)日:2004-11-10

    申请号:KR1020010054440

    申请日:2001-09-05

    Abstract: PURPOSE: Provided are a novel Pythium myriotylum strain, a pathogen of plants, and a method for the biological control of weeds using same, thereby effectively and selectively removing weeds from a rice field. CONSTITUTION: The novel strain, Pythium myriotylum MD2(KCTC 10034BP) is used for selectively controlling weeds selected from American black cherry, Monochoria vaginalis, yellow birtch, Chondostereum purpureum, Northern joint vetch, Colletotrichum gloeosporioides f. sp. aeschynomene, Morrenia odorata, Phyrophthora palmivora, Poa annua, Pseudomonas gladioli, etc.

    Abstract translation: 用途:提供了一种新型的Pythium myriotylum菌株,植物病原体,以及使用它的生物防治杂草的方法,由此有效地选择性地从稻田中除去杂草。 组成:新菌株Pythium myriotylum MD2(KCTC 10034BP)用于选择性控制选自美国黑樱桃,Monochoria vaginalis,黄色birtch,Chondostereum purpureum,Northern joint vetch,Colletotrichum gloeosporioides f。 SP。 aeschynomene,Morrenia odorata,Phyrophthora palmivora,Poa annua,唐菖蒲假单胞菌等

    케토미움 글로보숨 F0142 및 이에 의해 생산된 케토비리딘 A 및 B를 이용한 식물병의 생물학적 방제 방법
    40.
    发明公开
    케토미움 글로보숨 F0142 및 이에 의해 생산된 케토비리딘 A 및 B를 이용한 식물병의 생물학적 방제 방법 失效
    使用全氟辛酸F0142和其生产的乙酰胆碱酯酶A和B的植物病害生物控制方法

    公开(公告)号:KR1020030050072A

    公开(公告)日:2003-06-25

    申请号:KR1020010080458

    申请日:2001-12-18

    Abstract: PURPOSE: A method for biological control of plant diseases using Chaetomium globosum F0142 and chaetoviridins A and B produced by the same is provided, thereby effectively controlling plant diseases. CONSTITUTION: A method for biological control of plant diseases using Chaetomium globosum F0142(KCTC 0957BP) and chaetoviridins A and B produced by the same comprises spraying the cultured medium, mycelia or spores of Chaetomium globosum F0142, or chaetoviridins A and B isolated from the Chaetomium globosum cultured medium to plants, wherein the plant disease is rice blast disease, late blight, leaf rust or phytophthora blight. The chaetoviridins A and B are represented by the formula(1) and (2) respectively, and purified by extraction of Chaetomium globosum F0142(KCTC 0957BP) with ethyl acetate, first silica gel column chromatography, thin layer chromatography and second silica gel column chromatography, sequentially.

    Abstract translation: 目的:提供使用球毛壳菌F0142和由其生产的凝血酶原A和B的植物病害生物防治方法,从而有效控制植物病害。 构成:使用球毛壳菌F0142(KCTC 0957BP)和由其产生的切杆菌素A和B的植物病害的生物防治方法包括喷洒球形梭菌F0142的培养培养基,菌丝体或孢子,或从毛壳菌分离的凝血因子A和B 球藻培养基至植物,其中植物病是稻瘟病,晚疫病,叶锈病或疫病疫苗。 川to嗪A和B分别由式(1)和(2)表示,并用乙酸乙酯萃取球毛壳菌F0142(KCTC 0957BP),首先用硅胶柱层析,薄层色谱和第二次硅胶柱色谱法提纯 ,顺序。

Patent Agency Ranking