ABSTRACT
This phytochemistry investigation on the trunk of Morus alba L. resulted in the isolation of three triterpenoids, including a new gammacerane triterpenoid - morusacerane (1); along with two known compounds of betulinic acid (2) and ursolic acid (3). The structure elucidation was thoroughly conducted based on 1D, 2D-NMR and HRESIMS spectra, followed by a comparison with existing literatures. The evaluation on α-glucosidase inhibitory exhibited the great potential of the application of these isolated compounds in diabetes treatments. The results show that morusacerane (1), betulinic acid (2), and ursolic acid (3) demonstrate the strong inhibitory with the IC50 values of 106.1, 11.12, and 7.20 µM, respectively. All of these compounds interacted well with the allosteric site enzyme α-glucosidase MAL32 through H-bonds and hydrophobic interaction.
ABSTRACT
Chemical investigation of the lichen Parmotrema tinctorum (Nyl.) Hale led to the isolation of two new phenolic compounds, 2-ethylhexyl orsellinate (1) and tinctorinone (2). The structures were determined by analysis of their MS and NMR data as well as by comparison with literature data. The 2-ethylhexyl ester group of 2-ethylhexyl orsellinate is uncommon among lichen metabolites. Tinctorinone revealed strong inhibition towards α-glucosidase.
Subject(s)
Lichens , Parmeliaceae , Asian People , Humans , Lichens/chemistry , Parmeliaceae/chemistry , Phenols/chemistryABSTRACT
In an age of mass extinctions, confirming the survival of lost species provides rare second chances for biodiversity conservation. The silver-backed chevrotain Tragulus versicolor, a diminutive species of ungulate known only from Vietnam, has been lost to science for almost three decades. Here, we provide evidence that the silver-backed chevrotain still exists and the first photographs of the species in the wild, and urge immediate conservation actions to ensure its survival.
