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- W4200418695 abstract "• Notoginsenoids T1−T7, a new class of hexa-nortriterpenoids, were obtained. • Spectral, single-crystal X-ray, Mo 2 (AcO) 4 -induced CD and ECD analyzes were applied. • T1-T7 possess an unprecedented 9-en-5-ketone tricyclic hexa-nordammar skeleton. • A plausible biotransformed pathway for T1−T7 by degradation from PNS was proposed. • T1−T5 showed growth inhibitory effects on probiotic and pathogenic fungi of sanqi. Notoginsenoids T1−T7, a new class of hexa-nortriterpenoids including two dimers and five monomers, possessing an unprecedented 9-en-5-ketone tricyclic hexa-nordammar skeleton and a variable side chain at C-17, were obtained from biotransformation of PPD-type dammarane saponins by the soil harvested with Panax notoginseng (Araliaceae), a famous traditional Chinese medicinal herb. Their structures were unambiguously determined by spectroscopic, single-crystal X-ray diffraction, Mo 2 (AcO) 4 -induced CD and ECD analyzes. A plausible biotransformed pathway for T1−T7 was proposed. Notoginsenoids T1−T5 showed growth inhibitory effects on the probiotic and pathogenic fungi of P. notoginseng ." @default.
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- W4200418695 date "2022-03-01" @default.
- W4200418695 modified "2023-10-16" @default.
- W4200418695 title "Notoginsenoids, a new class of hexa-nortriterpenoids from biotransformation of Panax notoginseng saponins" @default.
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- W4200418695 doi "https://doi.org/10.1016/j.molstruc.2021.132096" @default.
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