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Isolation and purification of diterpenoids from the aerial parts of Isodon excisoides target-guided by UPLC-LTQ-Orbitrap-MS
Authors:Li-Ping Dai  Ling-Xia Zhang  Ya-Lin Liu  Hong Wu  Rui-Xin Liu  Meng Zhao
Institution:1. School of pharmacy, Henan University of Traditional Chinese Medicine, Zhengzhou, China;2. Collaborative Innovation Center for Respiratory Disease Diagnosis and Treatment &3. Chinese Medicine Development of Henan Province, Henan College of Traditional Chinese Medicine;4. Department of pharmacy, The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou, China
Abstract:Cytotoxic diterpenoids were enriched and orientation prepared from the aerial parts of Isodon excisoides target-guided by UPLC-LTQ-Orbitrap-MS. Four diterpenoids were obtained, including a novel compound: 1α-acetoxy-7α, 14β, 20α-trihydroxy-ent-kaur-16-en-15-one (1); together with three known compounds kamebakaurin (2), lasiokaurin (3), enmenol-1-β-glucoside (4). Their structures were elucidated on the basis of spectroscopic methods in conjunction with published data for their analogues. All compounds were tested for their cytotoxic effects against five human cancer cell lines HCT-116, HepG2, A2780, NCI-H1650 and BGC-823, respectively. Compounds 1 and 2 showed obviously cytotoxic activity against the five cancer cell lines with IC50 ranging from 1.06 to 3.60 μM. Compounds 3 and 4 showed selective cytotoxic activity.
Keywords:Isodon excisoides  diterpenoid  orientational preparation  cytotoxic activity
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