Fomicheva G K, Komarov E V
Antibiotiki. 1984 May;29(5):353-7.
The acid-base transformations of the gramicidin S molecule in water were studied. The protonization constants of the antibiotic amino group were calculated by the data of the potentiometric titration and the antibiotic distribution in the system of chloroform-water: K1 1.55 X 10(10), K2 1.38 X 10(6), the logarithm of the distribution coefficient of gramicidin S in the system of chloroform-water (1:1) lg alpha G 4.10. By the same data the constants of water solubility of gramicidin S base (1.02 X 10(7) mol/l), gramicidin S monohydrate (1.06 X 10(-4) mol/l) and gramicidin S dihydrochloride (2.08 X 10(-4) mol/l) were calculated.
研究了短杆菌肽S分子在水中的酸碱转化。通过电位滴定数据和短杆菌肽S在氯仿 - 水体系中的分配情况计算出抗生素氨基的质子化常数:K1为1.55×10(10),K2为1.38×10(6),短杆菌肽S在氯仿 - 水体系(1:1)中的分配系数对数lgαG为4.10。根据相同数据计算出短杆菌肽S碱(1.02×10(7) mol/l)、短杆菌肽S一水合物(1.06×10(-4) mol/l)和短杆菌肽S二盐酸盐(2.08×10(-4) mol/l)的水溶性常数。