4.6 Article

Notoginsenoids, a new class of hexa-nortriterpenoids from biotransformation of Panax notoginseng saponins

Journal

JOURNAL OF MOLECULAR STRUCTURE
Volume 1252, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molstruc.2021.132096

Keywords

Panax notoginseng saponins; Hexa-nortriterpenoids; Biotransformation; Antifungal activity; X-ray analysis

Funding

  1. Science and Technology Planning Project of Yunnan Province [2013FC008]
  2. Major Science and Technique Programs in Yunnan Province [2016ZF001-001]

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Notoginsenoids T1-T7, a new class of hexa-nortriterpenoids obtained from the biotransformation of PPD-type dammarane saponins by soil harvested with Panax notoginseng, possess unique structures and show inhibitory effects on probiotic and pathogenic fungi of P. notoginseng.
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. (C) 2021 Elsevier B.V. All rights reserved.

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