Corymbulosins I-W, Cytotoxic Clerodane Diterpenes from the Bark of Laetia corymbulosa.
Simayijiang AimaitiAiri SuzukiYohei SaitoShuichi FukuyoshiMasuo GotoKatsunori MiyakeDavid J NewmanBarry R O'KeefeKuo-Hsiung LeeKyoko Nakagawa GotoPublished in: The Journal of organic chemistry (2018)
The isolation studies of a crude MeOH/CH2Cl2 (1:1) extract (N005829) of the bark of Laetia corymbulosa yielded 15 new clerodane diterpenes, designated corymbulosins I-W (1-15), as well as four known diterpenes, 16-19. The structures of 1-15 were characterized on the basis of extensive 1D and 2D NMR and HRMS analyses. The absolute configurations of newly isolated compounds 1-15, as well as known 16-19, which were reported previously with only relative configurations, were determined through ECD experiments, X-ray analysis, chemical methods, including Mosher esterification, and comparison of their spectroscopic data. The isolated compounds were evaluated for cytotoxicity against human cancer cell lines. Flow cytometric and immunocytochemical observations of cells treated with cytotoxic clerodanes demonstrated that the chromatin was fragmented and dispersed with formation of apoptotic microtubules.
Keyphrases
- high resolution
- induced apoptosis
- endothelial cells
- cell death
- cell cycle arrest
- papillary thyroid
- oxidative stress
- anti inflammatory
- gene expression
- magnetic resonance
- dna damage
- electronic health record
- molecular docking
- induced pluripotent stem cells
- squamous cell
- transcription factor
- genome wide
- endoplasmic reticulum stress
- pluripotent stem cells
- magnetic resonance imaging
- computed tomography
- case control
- signaling pathway
- data analysis
- room temperature
- mass spectrometry
- dna methylation
- newly diagnosed
- pi k akt
- molecular dynamics simulations