Abstract
The structures of two triterpene oligosides from the holothurianStichopus cloronotus (Brandt) have been established; they are: 23ξ-acetoxy-3β-[O-β-D-quinovopyranosyl-(1→2)-β-D-xylopyranosyloxy]holost-7(8)-ene and 23ξ-acetoxy-3β-[O-β-D-glucopyranosyl-(1→2)-β-D-xylopyranosyloxy]holost-7(8)-ene.
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Additional information
Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Scientific Center, Academy of Sciences of the USSR, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 181–184, March–April, 1981.
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Sharypov, V.F., Chumak, A.D., Stonik, V.A. et al. Glycosides of marine invertebrates. X. The structure of stichoposides A and B from the holothurianStichopus cloronotus . Chem Nat Compd 17, 139–142 (1981). https://doi.org/10.1007/BF00634731
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DOI: https://doi.org/10.1007/BF00634731