Diterpenoids and triterpenoids in hairy roots of Salvia sclarea

Hairy root culture of Salvia sclarea L. was established following infection with Agrobacterium rhizogenes LBA 9402. The culture was grown in growth regulator-free half-strength B5 Gamborg medium with 30 g l⁻¹ sucrose and was investigated with respect to its capability of producing diterpenoids and triterpenoids. Four diterpenoids (ferruginol, salvipisone, aethiopinone and 1-oxoaethiopinone) and two ursene-type triterpenoids (2α,3α-dihydroxy-urs-12-en-28-oic acid and 2α,3α,24-trihydroxy-urs-12-en-28-oic acid) were isolated from the hairy roots. The presence of three sterols (β-sitosterol, stigmasterol and campesterol), as well as oleanolic and ursolic acids was also shown by GC–MS analysis. The quantitative and qualitative differences in diterpenoid and triterpenoid production patterns between hairy roots grown in the light and in the dark were described.     

A rearranged abietane diterpenoid from the root of Salvia aethiopis

From the root of Salvia aethiopis a new diterpenoid, salvipisone, has been isolated. Its structure, 12-hydroxy-4,5-seco-5,10-friedo-4(18),5(10),6,8,12-abietapentaen-11,14-dione, was established by spectroscopic means and by partial synthesis from aethiopinone. The previously known diterpenoids aethiopinone and royleanone were also found in the same source.