a Harbin University of Commerce , Harbin 150076 , P.R. China.
Nat Prod Res. 2014;28(18):1446-53. doi: 10.1080/14786419.2014.910663. Epub 2014 Apr 22.
Timosaponin B-III (TB-III) is a steroidal saponin isolated from the rhizome of Anemarrhenae asphodeloides (Liliaceae). The biotransformation of TB-III by β-glucosidase was investigated. Three biotransformation products were isolated and their structures were identified as timosaponin B-III-a (M1), (20R,25S)-5β-spirostane-3β-ol-3-O-β-D-glucopyranosyl-(1 → 2)-β-D-galacopyanoside (M2) and timosaponin AIII (M3). Then the four compounds were evaluated for their anti-depressive activity in mice by the open field test, tail suspension test and forced swimming test. As a result, TB-III, M1 and M3 exhibited modest anti-depressive activity. Structure-activity relationships were investigated and the preliminary conclusions are summarised as follows: the glycosyl at C-3 and C-26 can increase the activity, the double bond between C-20 and C-22 might be important for the anti-depressive activity, the R-configuration at C-22 and S-configuration at C-20 are necessary for its anti-depressive activity.
知母皂苷 B-III(TB-III)是从百合科知母的根茎中分离得到的一种甾体皂苷。研究了β-葡萄糖苷酶对 TB-III 的生物转化。分离得到三种转化产物,并鉴定其结构为知母皂苷 B-III-a(M1)、(20R,25S)-5β-螺甾烷-3β-醇-3-O-β-D-吡喃葡萄糖基-(1 → 2)-β-D-吡喃半乳糖苷(M2)和知母皂苷 AIII(M3)。然后通过旷场试验、悬尾试验和强迫游泳试验评价了这四种化合物对小鼠的抗抑郁活性。结果表明,TB-III、M1 和 M3 表现出中等的抗抑郁活性。对构效关系进行了研究,得出以下初步结论:C-3 和 C-26 的糖苷化可以提高活性,C-20 和 C-22 之间的双键可能对其抗抑郁活性很重要,C-22 的 R-构型和 C-20 的 S-构型是其抗抑郁活性所必需的。