Abstract:
PURPOSE: A method for preventing hardening pills by adding a water-soluble high polymer and liquid-keeping agent to Chinese herbal drug powder during the manufacture of the pills is provided which permits easy digestion and enhancement of absorption efficiency of the pills. CONSTITUTION: A water-soluble high polymer and a liquid-keeping agent are added to crude drug powder during manufacture of pills. The water-soluble high polymer is selected from the group consisting of a boiled agar solution, boiled starch, aloe, methyl cellulose and methyl acetate. And the liquid-keeping agent is natural oils containing vegetable oils and animal oils, glycerin or propanediol.
Abstract:
PURPOSE: Provided is a kit for examining water quality by measuring the concentration of nitrogen and phosphorus contained in a water soluble sample. CONSTITUTION: The kit for examining water quality contains reagents for measurement of each concentration of ammonia, nitrous acid, nitric acid and phosphoric acid, each comparative color band and a reaction vessel. Water quality is examined by measuring the concentration of ammonia, nitrous acid, nitric acid and phosphoric acid contained in a sample using reagents; analyzing the result to confirm if the sample is contaminated and to estimate what causes its contamination.
Abstract:
PURPOSE: Provided are kinase inhibitory compounds with dihydrobenzofuran scaffold, which has therapeutic effect on hepatocirrhosis, rheumatism, cancer, sclerosis of the arteries, and the like. CONSTITUTION: Kinase inhibitory compound is characterized by comprising dihydrobenzofuran scaffold, and a functional group attached to the dihydrobenzofuran scaffold and providing hydrogen bond. The kinase inhibitory compound is characteristically represented by the formula(1).
Abstract:
PURPOSE: A composition containing an extract of Opuntia ficus-indica var. Saboten Makino and a compound isolated therefrom which exhibit antioxidative action and nerve cell protecting activity is provided. The composition inhibits neurotoxicity caused by cell death and exhibits nerve cell protecting effect on animal models of brain ischemia and is thus expected to be useful for prevention and treatment of cerebral apoplexy, cerebral concussion, Alzheimer's disease, Parkinson's disease, myocardial infarction and brain infarction. CONSTITUTION: A composition for protecting nerve cells contains an ethyl acetate extract of Opuntia ficus-indica and a compound isolated from therefrom as an active ingredient. The ethyl acetate extract contains campherol, dihydroquercetin or quercetin-3-methyl ether as an active ingredient and is prepared by adding 0.1 to 10L of an alcohol solvent to stems, fruits or processed fruits of Opuntia ficus-indica, followed by leaving them at room temperature for 4 to 5 days, filtering, distilling under reduced pressure and then extracting with 0.5 to 2L of ethyl acetate.
Abstract:
PURPOSE: Provided is DNA sequence that codes variable region of an antibody having enzymatic activity degrading glycosidic bond. And its expression method is also provided. CONSTITUTION: A DNA sequence coding variable region of an antibody having enzymatic activity degrading glycosidic bond is as follows: DNA sequence represented by sequence ID. No. 1 coding VH chain of antibody for glycosidase, 4f4r; DNA sequence represented by sequence ID. No. 3 coding VH chain of antibody for glycosidase, 6h4h; DNA sequence represented by sequence ID. No. 5 coding VH chain of antibody for glycosidase, Ab2l; DNA sequence represented by sequence ID. No. 7 coding antibody for glycosidase, 4f4r; DNA sequence represented by sequence ID. No. 9 coding VL chain of antibody for glycosidase, 6h4h; or DNA sequence represented by sequence ID. No. 11 coding VL chain of antibody for glycosidase, Ab2l. Wherein, all sequences are described as in the description. The antibody is prepared by expressing a fusion protein of VH and VL in an eukaryote cell or bacteria.
Abstract:
황련 또는 황백으로부터 약리 활성 물질을 보다 신속하게 정제해내는 방법이 제공된다. 이 방법에 의하면, 황련 또는 황백의 유기 용매 추출액에 ClO 4 - 카운터 이온을 형성하는 화합물을 첨가함으로써 약리 활성 물질을 침전시키고, 침전물을 분배 계수가 높은 용매로 재추출함으로써 베르베린 및 기타 약리 활성을 나타내는 성분들을 간편하고 신속하게 추출·정제할 수 있다.
Abstract:
본 발명은 16-페녹시 프로스타트리에노산 유도체의 제조에 유용한 중간체(Ⅰ)을 제조하고, 이 화합물을 이용한 다음 일반식(Ⅱ)의 16-페녹시 프로스타트리에노 산 유도체를 제조하는 방법에 관한 것이
상기식에서 R은 테트라하이드로피라닐, 테트라하이드로푸라닐, 2-에톡시에틸 또는 3-t-부틸 디메틸실릴, 트리이소프로필실릴, 트리에틸실릴과 같은 에테르형성그룹으로, R 1 ,R 2 는 수소, 또는 아세틸과 같은 에스테르 형성그룹이고, P는 수소, 트리메틸실릴, 또는 트리부틸틴이고, Z는 산소 또는 α-히드록실기이며, 파상선은 에피입체 혼합물이다.
Abstract:
A process for prepg. pyrazolone dervis. of formula (I) comprises: (a) reacting halogen derivs. of formula (II) with primary amine of formula R4-NH2 in org. solvent(i.e. water, MeOH, EtOH) for 10 hr at 10-30 deg. C; (b) reacting with secondary haloketo cpd. in org. solvent i.e. benzene, toluene, dioxane in basic media i.e. NaHCO3, NaOH, triethylamine at 20-120 deg. C; and (c) reacting with hydrazine of formula R5NH-NH2 in org. solvent i.e. diethyleneglycole, THF in basic media i.e. KHCO3, NaOH. In the formulas, R1=isopropyl; R4=Me; R5=H or methanesulfonyl; X=Cl, Br or I. (I) are useful as an antipyretic analgesic.