“…The 1 H and 13 C-NMR spectra of 2 exhibited a pregnane aglycone, one tigloyl unit, and three sugar units (Table 1). In addition, the NMR data of 2 were similar to those of gymsyloside A ( 1 The aglycone of 1 was supposed to have the same configurations as those of gymnepregoside F and 12-O-(E)-cinnamoylgymnepregoside F from G. sylvestre [12], biogenetic derivatives of 1 at C-3, C-8, C-12, C-14, C-17, and C-20. In addition, the alkaline hydrolysis of 1 gave sarcostin, ((20S)-3β,8β,12β,14β,17β,20-hexahydroxypregn-5-ene) [13].…”