Abstract:
본 발명은 하기 화학식 1로 표시되는 화합물을 유효성분으로 포함하는 약제학적 항암 조성물에 관한 것이다. 본 발명의 조성물은 종양세포의 증식에 대하여 IC 50 값이 0.16 μM 이하까지 나타내어 매우 효율적으로 종양세포의 증식을 억제함으로써, 암에 대하여 치료 또는 예방 효능을 나타낸다. 화학식 1
Abstract:
PURPOSE: Provided is a triazole derivative which has selective antibacterial effect on plant pathogenic bacteria, excellent invasion upon them and preventing and treating effect on them. Also, provided are a method for preparing the triazole derivative and antibacterial composition for agriculture comprising it. CONSTITUTION: The triazole derivative is represented by the formula(1), as defined in the specification. The triazole derivative is manufactured by reacting 1 equivalent weight of 1-phenacyl 5-bromotriazole of the formula(2) and 1-1.2 equivalent weight of a compound of the formula(3) of R2(NH)nNH2 in an organic solvent at 50-180 deg.C. The antibacterial composition for agriculture contains 0.01-90 wt.% of the triazole derivative of the formula(1).
Abstract:
PURPOSE: Provided is a fungicidal composition for agriculture and horticulture having as an active ingredient a 3-alkoxyindole-2-carboxylate derivative, and pharmaceutically acceptable carrier. It has selectively high fungicidal activity to resistant bacteria and plant pathogenic bacteria. CONSTITUTION: A fungicidal composition for agriculture and horticulture is characterized by containing a 3-alkoxyindole-2-carboxylate derivative, and pharmaceutically acceptable carrier, wherein the 3-alkoxyindole-2-carboxylate derivative is represented by the formula(1) as defined in the specification.
Abstract:
PURPOSE: A new methoxy acrylate compound introduced by an unsaturated carbonylthioenol group is provided which exhibits excellent germicidal activity against various plant pathogenic bacteria and is useful as an agricultural or horticultural fungicide. CONSTITUTION: The agricultural or horticultural fungicide contains a methoxy acrylate derivative represented by the formula(1). In formula, R1 represents a phenyl, substituted phenyl, naphthyl, substituted naphthyl, pyridyl, substituted pyridyl, furanyl, substituted furanyl, pyrrolyl, substituted pyrrolyl, thiopheneyl, substituted thiophenyl, indolinyl or substituted indolinyl group, in which the substituted group is selected from halogen, cyclo, C1-3 alkyl, C1-3 haloalkyl and C1-3 alkoxy group and can be substituted in the range of 1 to 4, two adjacent substituted groups can combine to form -OCH2CH2O-; R2 represents H or C1-3 alkyl; R3 represents C1-3 alkyl; X represents S or NH; Y represents CH or N.
Abstract:
PURPOSE: Provided is a fungicidal composition for agriculture and horticulture having as an active ingredient a 3-alkoxyindole-2-carboxylate derivative, and pharmaceutically acceptable carrier. It has selectively high fungicidal activity to resistant bacteria and plant pathogenic bacteria. CONSTITUTION: A fungicidal composition for agriculture and horticulture is characterized by containing a 3-alkoxyindole-2-carboxylate derivative, and pharmaceutically acceptable carrier, wherein the 3-alkoxyindole-2-carboxylate derivative is represented by the formula(1) as defined in the specification.
Abstract:
PURPOSE: An agricultural or horticultural fungicide composition containing a 4-azoyl-2-quinolinone derivative is provided which exhibits a preventive effect and treating effect against various fungi, in particular, excellent selective bactericidal activity against any plant pathogenic bacteria. CONSTITUTION: The titled composition contains a 4-azoyl-2-quinolinone derivative of formula(1) as an active component. In formula, X is O or S, Y is CH or N, R1 is C1-5 alkyl, R2, R3, R4 and R5 are the same or different, each differently H, H, C1-3 alkyl, C1-3 alkoxy, phenyl or NO2.
Abstract:
PURPOSE: A new oxazole derivative obtained by using amide as a starting material is provided which has a strong antibacterial effect on plant pathogenic bacteria with a small amount, for example Pyricularia oryzae Cavera, Rhizoctonia SolaniAG-1, Botrytis cinerea KCI, Phytophthora infestans or the like. CONSTITUTION: An amid compound(formula II) is refluxed in a solvent of dichloroacetone and ethanol to give chloromethyl oxazole(formula III). A chlorine atom of the chloromethyl oxazole is substituted to an iodine atom by use of sodium iodide and then reacted with 2-(2-hydroxyphenyl)-3-methoxy acrylic acid methylester(formula IV)(in case of A=C) or 2-methoxyimino-(2-hydroxyphenyl)-acetic acid methylester(formula IV)(in case of A=N) to produce an oxazole derivative(formula I).
Abstract:
하기 일반식 (I)의 항진균제 화합물 또는 그의 약제학적으로 허용 가능한 염:
상기 식에서, X는 CH 또는 N이고; Y는 O, 또는 이고; R 1 및 R 2 는 각각 F 또는 Cl이고; R 3 는 티오페닐, 나프틸, 또는 페닐(phenyl)기이고, 상기 페닐기는 C 1-4 알킬, C 1-4 할로알킬, C 1-4 알콕시, 메틸렌디옥시 및 할로겐으로 이루어진 군으로부터 선택된 하나 이상의 치환체로 선택적으로 치환되며, R 4 는 H 또는 트리플루오로메틸기이다.