Abstract:
본 발명은 팜유의 제조 과정에서 부산물로 발생하는 과육 또는 이의 가수분해물을 이용하거나, 부원료를 추가로 혼합하여 탄수화물, 단백질 및 지방의 비율이 잘 조정된 농후사료로 전환할 수 있으므로, 팜유의 생산과정에서 지속적으로 생산되는 부산물을 고부가가치화할 수 있고, 폐기물을 획기적으로 줄이는 데 효과적이다.
Abstract:
The present invention uses pulp generated as by-products in a palm oil production process or hydrolysate thereof, or additionally mixes a supplementary material to convert to concentrate feed, which rates of carbohydrate, protein and fat are well adjusted. Therefore, high value can be added to the by-products continuously produced in the palm oil production process, and waste can be significantly reduced.
Abstract:
본 발명은 주원료로서 리그노셀룰로오스계 바이오매스, 및 접착제로서 탈지된 단백질계 천연물질 또는 바이오매스의 당화 후 잔사로 남는 리그닌계 접착성 물질로 구성된 연료용 또는 사료용 펠릿 및 이의 제조방법에 관한 것으로, 본 발명에 따른 펠릿은 부식성 물질이나 유독성 연소 기체가 발생하지 않고, 제조가 용이하며, 열량이 높고, 접착제를 사용하여 종래 목질 펠렛에 비해 높은 강도를 가지므로, 연료용, 사료용 또는 애완동물의 놀이용 또는 침대 재료로 유용하게 사용될 수 있다.
Abstract:
PURPOSE: A pharmaceutical composition containing Paeonia lactiflora seed extract, fraction thereof, or compound isolated from the same is provided to suppress BACE-1 activity and to treat and prevent neurodegenerative diseases. CONSTITUTION: A pharmaceutical composition for preventing or treating neurodegenerative diseases contains Paeonia lactiflora seed extract as an active ingredient. The neurodegenerative diseases include Alzheimer's dieses, Parkinsons's disease, progressive supranuclear palsy. The extract is prepared using water, alcohol of C1-C4, or mixture solvent thereof. The pharmaceutical composition contains Paeonia lactiflora seed fraction as an active ingredient. The pharmaceutical composition also contains compounds as an active ingredient. The method for preparing the compounds comprises: a step of adding water, C1-C3 alcohol, or mixture thereof to the Paeonia lactiflora seeds to prepare Paeonia lactiflora seed extract; a step of fractioning the extract with water, dichloromethane, and ethyl acetate to prepare a fraction; a step of performing silicagel column chromatography of the fraction.
Abstract:
본 발명은 유백피( Ulmus macrocarpa ) 추출물을 유효성분으로 함유하는 혈관 이완용 조성물에 관한 것으로서, 본 발명에 따른 조성물은 항산화 작용 및 혈관 평활근 이완 작용을 통해 우수한 혈압강하 효과를 나타내므로, 고혈압 및 고혈압의 합병증으로 인한 각종 심혈관계 질환의 예방 및 치료를 위한 약학 조성물 또는 건강기능 식품으로 유용하게 사용될 수 있다.
Abstract:
A composition comprising an extract of stembark of Vitis vinifera is provided to inhibit BACE-1(beta-site APP-cleaving enzyme 1) mediating formation of beta-amyloid, known to be a causing material of various dementia such as Alzheimer's disease, thereby being usefully used for preventing and treating neurodegenerative diseases such as senile dementia. A pharmaceutical composition for preventing or treating neurodegenerative diseases comprises a compound selected from the group consisting of vitisin A, epsilon-viniferin, ampelopsin A and a mixture thereof as an effective ingredient, wherein the compound is obtained by extracting stembark of Vitis vinifera with an organic solvent selected from the group consisting of C1-4 alcohol and an aqueous solution thereof, dichloromethane, ethyl acetate and a mixture thereof.
Abstract:
본 발명은 화학식 1로 표시되는 제초성 3-아릴-테트라히드로-1,2-벤즈이속사졸린-4-온 유도체에 관한 것이다.
상기식에서 Xn은 수소, C 1 -C 4 알킬기, C 2 -C 5 알케닐기, C 2 -C 5 알키닐기, C 1 -C 4 알콕시기, C 1 -C 4 할로알킬기, C 1 -C 4 알콕시카보닐기, 아미노카보닐기, 카복시기, 메탄설포닐기, 니트로기, 히드록시기, 니트릴기, 또는 이들의 둘이상의 복합치환기를 나타낸다.
Abstract:
Quinolinyl oxadiazole derivatives having strong herbicidal activities and excellent selectivity, especially on rice and barnyard grass, is disclosed in the present invention. Hydroxylamine chlorinate and nitrile compound are reacted in mixture solvent of water and alcohols in the presence of base to yield amidoxime. Thereafter, in the presence of base, said amidoxide is reacted with carboxylic acid chloride produced by the reaction of 3,7-dichloro-8-quinoline carboxylate and thionyl chloride to yield compound of general formula(I). In general formula(I), A and B represent hydrogen atom, sodium carbonate, etc., R represents low molecular weight alkyl, cyclo alkyl, etc.
Abstract:
The 5-substd phenyl-pyrazolo[3,4-d pyrimidine and 5-substd. phenyl-4-oxo-pyrazolo [3,4-d pyrimidine derivative of formula(I) is prepared. In (I), R1 is C1-4 alkyl or haloalkyl; R2 is H or C1-4 alkyl; R3 is H, C1-6 alkyl, haloalkyl, alkenyl or acyl, R4 and R5 are each halogen; A is H, alkyl, alkoxy, nitro, amino, alkyl amine, dialkyl amine or CO2R; R is H, C1-6 alkyl, substd. alkyl, haloalkyl or alkenyl [A = carboxylic acid or its ester . The cpd. (I) has a good selective herbicidal characteristic against esp. cotton plants.