Abstract:
콩나물류의 부패가 일어나지 않아 위생적이고 생산성이 높음과 아울러 폐수에 의한 환경오염문제가 없는 콩나물류 재배방법 및 그 장치에 관한 것으로, 콩나물 재배부로부터 배출된 오염물질 내지 불순물이 포함된 재배수에 응집제를 투입하여 오염물질 내지 불순물을 응집시켜 슬러지가 되게 하는 단계와, 응집된 슬러지를 포함한 재배수를 DAF처리하여 슬러지를 제거하는 단계와, 슬러지가 제거된 깨끗한 재배수를 상기 콩나물 재배부로 재공급하는 단계를 구비하는 것을 특징으로 하는 콩나물류 재배방법과 그를 실현하기 위한 장치가 제공된다.
Abstract:
PURPOSE: A method for cultivation of Paecilomyces Japonica using a silkworm without a pupa as a host and a freeze drying method is provided. Therefore, a product having an excellent therapeutic effect on diabetic is produced with high productivity without causing the depletion of nutrients. CONSTITUTION: In the process for artificial cultivation of Paecilomyces Japonica, a 5 day old silkworm as a host is subjected to sterilization using chlorine dioxide water with a concentration of 1 to 5ppm without using heat treatment, a compound selected from the group consisting of silk amino acid, sugar and a mixture thereof is added to a medium for cultivation thereof, and then the silkworm is freeze dried and killed through an electric shock method.
Abstract:
PURPOSE: A method for preparing chlorine dioxide in high yield is accomplished by proper adjustment of the supply ratio of sodium chlorite and chlorine, by which hydrogen-ion concentration condition is optimized. The chlorine dioxide, when applied to cooling water, showed excellent bactericidal effect against Legionella pneumophila when applied to cooling water. In addition, chlorine dioxide has proven to be effective in eliminating alien algae in cultivating lava. CONSTITUTION: In the generation of chlorine dioxide using sodium chlorite and chlorine, by using a flowmeter and a chemical pump, Cl2 supply rate and NaClO2 supply rate are controlled to adjust pH in the range 1.9 to 2.0. For the smooth dissolving of chlorine gas into sodium chlorite solution, chlorine gas is supplied through glass wool(7), and a baffle(8) is installed to be perpendicular to a sodium chlorite/chlorine inlet. The baffle plays role in converting laminar flow to turbulent flow within short time.
Abstract:
PURPOSE: A purine compound having a substitutent group at the C-8 position is provided which is expected to be useful as an inhibitor of cyclin-dependent kinase. CONSTITUTION: A purine compound represented by the formula 1 having a substitutent group at the C-8 position is prepared, Thus, urea and ethylisocyanoacetate are subjected to heating reflux in the presence of a base to give a compound of formula 2, which is subjected to heating reflux after nitration and treated with sodium hydrosulfide to give a compound of formula 3, which is subjected to reaction continuously to give the title compound. In formula, R1 is methyl or phenyl; R2 is ethanolamine, or 2-amino-3-methyl-1-butanol.
Abstract:
PURPOSE: A thiol derivative having a novel bicyclic and 1-beta-methyl-carbaphenem having them as a substituent group at its 2-position are provided which are useful for resolving the reduction of activity of conventional carbaphenem by DHP-1. CONSTITUTION: A bicyclic thiol derivative of formula (1) and 1-beta-methyl-2-thio based carbaphenem of formula (2) having two methyl groups at its 2-position are described. In formula, R denotes H, C1-6 lower alkyl, C1-6 lower cycloalkyl, aryl, benzyl, or amino group-substituted C1-6 lower alkyl. Preferably the lower alkyl is methyl, ethyl, propyl, cyclopropylmethyl and the amino group-substituted C1-6 lower alkyl is amino ethyl.
Abstract:
PURPOSE: Title derivatives useful as radioactive pharmaceuticals are prepared which can extend a residual time in heart, and minimize a radioactive disturbance. CONSTITUTION: 1,12-Dodecane diol is alcohol-substituted by bromic acid to give 12-bromo-dodecane-1-ol, and protected by tetrahydropyrane. Obtained dodecane, 2-ethyl-4,4-dimethyl-2-oxazoline and n-butyl lithium are reacted to give 2(R/S)-(4,4-dimethyl-2-oxazoline-2-yl)-12-tetrahydropyranyl oxy-tetradecane, and esterified with sulfuric acid to give ethyl-2(R/S)-methyl-12-hydroxytetradecaneate. Obtained tetradecaneate is protected to give ethyl-2(R/S)-methyl-14-tetra butyl dimethyl silyloxy-tetradecaneate, followed by reduction with lithium aluminum hydride to give 2(R/S)-methyl-14-t-butyl dimethyl silyloxy-tetradecane-1-ol, tosylated by tosyl chloride, and to give 3(R/S)-methyl-15-t-butyl dimethyl silyloxy-pentadecane-nitrile by substituting with sodium cyanide. Obtained nitride is treated with 1N-hydrochloric acid, hydrolyzed and mesylated to give 16-methane sulfonyl-3-methyl-pentadecanic acid. The pentadecanic acid is brominated, followed by reaction of thiourea and NaOH to give 15-mercapto-3-methyl-pentadecanic acid(formula 1).
Abstract:
본 발명은 신규한 에틸 3-이소시아노 부티레이트 및 의학진단용 영상화제로서 유용한 그의 테크네슘 착화합물에 관한 것이다. 본 발명의 에틸 3-이소시아노 부티레이트는 테크네슘과의 표지 효율이 우수하고 특히 심장/허파 업테이크 비율이 우수하여 배경 장기에 대한 좋은 영상을 얻을 수 있다.
Abstract:
PURPOSE: A method for preparing a cephalosporin antibiotics intermediate using a novel enzyme is provided to industrially synthesize an acrystalline hydrate. CONSTITUTION: A method for preparing cephalosporin antibiotic intermediate of chemical formula 1 comprises: a step of adding cresol or phenol to a compound of chemical formula 2 and stirring to deprotecting a protection group of carboxyl groups; a step of adjusting pH concentration with a base, adding Sinta CLEC-PA enzyme, and deprotecting; and a step of adjusting pH concentration with inorganic acid. The base is a carbonate alkali metal, alkali metal hydroxide, ammonia solution, or trialkyl amine.