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ECB-ART-40078
Chem Biodivers 2006 Nov 01;311:1249-54. doi: 10.1002/cbdv.200690126.
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Structure and cytotoxicity of a new lanostane-type triterpene glycoside from the sea cucumber Holothuria hilla.

Wu J , Yi YH , Tang HF , Zou ZR , Wu HM .


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A new triterpene glycoside, hillaside C (1), was isolated from the sea cucumber Holothuria hilla Lesson, which is found in the South China Sea, and its structure has been elucidated by spectral analysis (ESI-MS and NMR) and chemical transformations. Four known compounds, holothuria A, thymine, uracil, and cholesterol, were also obtained. Compound 1 exhibited significant cytotoxicity against eight human tumor cell lines (A-549, MCF-7, IA9, CAKI-1, PC-3, KB, KB-VIN, and HCT-8) with IC50 values in the range of 0.15-3.20 microg/ml.

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Genes referenced: LOC100887844 LOC100893907 LOC115919910