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Isoxerophilusins A and B, Two Novel Polycyclic Asymmetric Diterpene Dimers from Isodon xerophilus : Structural Elucidation, Modification, and Inhibitory Activities against α-Glucosidase.

Jia-Meng DaiBing-Chao YanKun HuXing-Ren LiXiao-Nian LiHan-Dong SunPema-Tenzin Puno
Published in: Organic letters (2024)
Isoxerophilusins A ( 1 ) and B ( 2 ), two unprecedented diterpene heterodimers biogenetically from ent -atisanes and abietanes, were isolated from the rhizomes of Isodon xerophilus . Their structures were determined by extensive spectroscopic analysis and single-crystal X-ray diffraction. Selective esterification of 1 generated 11 new derivatives. All derivatives showed excellent α -glucosidase inhibitory activity in comparison to acarbose. Compounds 12 and 13 demonstrated significant inhibition against α -glucosidase with IC 50 values of 4.92 and 3.83 μ M, respectively.
Keyphrases
  • molecular docking
  • high resolution
  • molecular dynamics simulations
  • structure activity relationship
  • solid state
  • electron microscopy
  • dual energy
  • computed tomography