期刊
PLANTA MEDICA
卷 73, 期 1, 页码 77-83出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/s-2006-951766
关键词
Perovskia abrotanoides; Labiatae; tetracyclic diterpenes; NMR spectral assignment
The phytochemical investigation of the n-hexane, the EtOAc, and the n-BuOH soluble fractions of the methanolic extract of the arial parts of Perovskia abrotanoides Karelin furnished ten compounds including the two new tetracyclic diterpenes abrotandiol (7) and abrotanone (8) besides the known cirsimaritin (9), hespiriclin (10), rosmarinic acid (11), stigmast-5-en-3 beta-of (12), stigmast-5,22-dien-3 beta-ol (13), stigmast-5-en-3 beta,7 alpha-diol (14), ursolic acid (15) and betulinic acid (16). Compounds 7 and 8 both show a 6,5,6,6 ring skeleton with a trans-1,1 -dimethylcyclohexa- no[ e,b Itetrahydrofu ran element perpendicular to a benzodihydropyran system. The complete structure elucidation of these compounds has been achieved with NMR techniques.
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