Figure 1. Rat pharmacokinetic study of GJG and structure of ignavine.
(A) A dose of 1 g/kg GJG was orally administered and blood samples were collected 1 h after administration. Quantitative analysis of the ingredients in PAT was performed using LC/MS/MS. Data are expressed as mean +/− SD (n = 5). (B) Ignavine is a diterpene alkaloid and has a different core structure from the aconitine alkaloids.