Bukin Iu V, Plikhtiak I L, Draudin-Krylenko V A, Iartseva I V, Orlova L M
Bioorg Khim. 1987 Apr;13(4):539-45.
New derivatives of 2-C-/(indolyl-3)methyl/-beta-L-threo-L-glycero-3-hexulofuranosono- 1,4-lactone, vis. 1'-ethylascorbigen, 1'-benzylascorbigen and 1',2'-dimethyl-5'-methoxyascorbigen were obtained. In aquous solutions at physiological temperature and pH values ascorbigens disintegrate rather rapidly to yield L-ascorbic acid, the rate of the latter's formation depending on the substituent in the indole nucleus and increasing with growth of pH and temperature. Intraperitoneal injection of 1'-methylascorbigen to mice leads to steady rise of L-ascorbic acid level in blood plasma.
2-C-/(吲哚-3)甲基/-β-L-苏式-L-甘油-3-己酮呋喃糖-1,4-内酯的新衍生物,即1'-乙基抗坏血酸原、1'-苄基抗坏血酸原和1',2'-二甲基-5'-甲氧基抗坏血酸原已被制得。在生理温度和pH值的水溶液中,抗坏血酸原相当迅速地分解,生成L-抗坏血酸,后者的生成速率取决于吲哚核中的取代基,并随pH值和温度的升高而增加。给小鼠腹腔注射1'-甲基抗坏血酸原会导致血浆中L-抗坏血酸水平稳步上升。