Fötsch G, Pfeifer S, Bartoszek M, Franke P, Hiller K
Sektion Chemie, Wissenschaftsbereich Pharmazie, Humboldt-Universität zu Berlin.
Pharmazie. 1989 Aug;44(8):555-8.
Leiocarposide (1; 3-beta-D-glucopyranosyloxy-2-methoxy-6-hydroxy-benzoic acid -2'-beta-D-glucopyranosyloxybenzyl ester) is a phenolic glycoside from Solidago virgaurea L. After oral administration to rats it will be only poorly absorbed and mostly unchanged fecaly excreted. In the urine were found less than 10% as metabolites: leiocarpic acid (3; 3,6-dihydroxy-2-methoxy-benzoic acid, 2% of the administered dose), 3-conjugates (2%), salicylic acid (5; 0.5%), 5-conjugates (0.1%) and salicyluric acid (6; 0.5%). On the other hand salicin (2), structural part of 1, is good absorbed. In the urine were excreted 15% of the unchanged drug and the following metabolites: 0.1% saligenin (4), 30% 5, 5% 5-conjugates, 0.1% 6, 2% gentisic acid (7) and 0.1% 2,3-dihydroxy-benzoic acid (8). The different metabolic rates are explicable by the high stability of the ester bond of 1. It is hydrolyzed in artificial intestinal fluid only very slowly (t1/2 = 41.7 h).
地锦草苷(1;3-β-D-吡喃葡萄糖氧基-2-甲氧基-6-羟基苯甲酸-2'-β-D-吡喃葡萄糖氧基苄酯)是来自兴安一枝黄花的一种酚苷。给大鼠口服后,它的吸收很差,大部分以原形经粪便排出。在尿液中发现作为代谢产物的量不到10%:地锦草酸(3;3,6-二羟基-2-甲氧基苯甲酸,占给药剂量的2%)、3-缀合物(2%)、水杨酸(5;0.5%)、5-缀合物(0.1%)和水杨尿酸(6;0.5%)。另一方面,1的结构部分水杨苷(2)吸收良好。在尿液中排出了15%的原形药物以及以下代谢产物:0.1%的水杨醇(4)、30%的5、5%的5-缀合物、0.1%的6、2%的龙胆酸(7)和0.1%的2,3-二羟基苯甲酸(8)。不同的代谢率可以通过1的酯键的高稳定性来解释。它在人工肠液中水解非常缓慢(t1/2 = 41.7小时)。