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Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Cespitulones A and B, cytotoxic diterpenoids of a new structure class from the soft coral Cespitularia taeniata
Yu-Chi Lin1, Shih-Sheng Wang2, Chung-Hsiung Chen3
1School of Pharmacy, College of Medicine, National Taiwan University, Taipei 100, Taiwan. z10108042@email.ncku.edu.tw.
Abstract:
Two novel diterpenoids, cespitulones A (1) and B (2), were isolated from extracts of the soft coral Cespitularia taeniata. Both compounds possess an unprecedented bicyclo [10.3.1] ring system with C-C bond connections between C-10 and C-20, and between C-20 and C-11. Their structures were elucidated on the basis of extensive spectroscopic analyses. Compound 1 exhibited significant cytotoxicity against human medulloblastoma and colon adenocarcinoma cancer cells.
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