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      • Sulfa劑-Ni 錯化合物 形成에 關한 硏究

        고우영 朝鮮大學校 大學院 1974 국내석사

        RANK : 248655

        This is to study the molar Ratio, the precipitation Condition and the Color of Nickel Sulfa-drugs Complexes. I Can observe the Colors of the Complexes Whenever precipitation Condition is obtained With PH 8~9 The molar ratio of Complexes is determined by gravimetric method and Solvent extraction method. By Both methods as above we found the molar ratio of Sulfadrugs and Nikel of indentified Complexes 2:1

      • 수검제가 小腸內에서의 Sulfa劑 吸收에 미치는 影響

        이진환 朝鮮大學校 大學院 1970 국내박사

        RANK : 248607

        Auther examined the absorption of sulfonamides influencing to the such antidiarrhoics as the bismuth-subnitrats of heavy metal salt, and as the tannic acid of organic astringency by the Wiseman's apparatus, through the small intestine of rat. The experiments carried out, two kinds of the concentration, the wateric buffor solution contained 0.5 mile - mole or 0.05 mili-mole of the each antidiarrhoics of the fixed administration of sulfonamides. The views of the determined are as followings; ① Generally, the absorptions of sulfonamides are augmentation by their antidiarrhoics which the bismuth subnitrate effected than the tannic acid, and N'-(2-thiazolyl) sulfanilamido have been influenced than the N'-(6-methoxy 3-pyridazinyl) sulfonamide. ② The velocity constants of absorbability are 6.43×10^(-4) per a minute of N'-(2-thiazolyl) sulfonilamide and 5.80×10^(-4) per a minute of N'-(6-methoxy 3-pyridazinyl ) sulfonamide versus the bismuth subnitrate combined with the 0.05 mili-mole concentration, the higher concentration of the antidiarrhoics have practically tended than that of lower concentrations on the absorption rates. ③ According to the estimated value, N'-(2-thiazolyl) sulfanilamide are inhibited than the N'-(6-methoxy 3-pyridazinyl) sulfonamide by the combined drugr are fact that N'-(2-thiazolyl) sulfanilamide bismuth salt on the chemical structure.

      • Nitrofuran誘導體로써 抗菌劑合成에 關한 硏究 : 5-(2-nitro)pyromucic aldehyde와 sulfa劑의 縮合反應

        김영수 朝鮮大學校 大學院 1974 국내석사

        RANK : 248606

        For the purpose of synthesizing new antibacterial agents, the author designated the 5-nitropyromucic aldehyde possessig antimicrobial activity as an antibacterial body, and also designated that sulfanilamide derivatives possessing antibacterial activity are in the Auxo-antibacterial group. in order to synthesize New antibacterial agents, new five 5-nitropyromucic sulfanilamide derivatives are synthesized which are obtained by the action of the 5-nitropyromucic aldehyde as an antibacterial body on sulfonamide derivatives as an Auxo-antibacterial group, such as N'-acetylsulfanilamide, P-aminobenzen sulfonamide, N'-guanylsulfanilamide, N'-(4-methyl-2-thiazol) sulfanilamide, N'-(4-methyl-2- pyrimidinyl) sulfanilamide.

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