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Chemical Compound Review

Prosapogenin     bis[3,4,5-trihydroxy-6- (hydroxymethyl)oxan...

Synonyms: NSC-124670, AC1L9JTZ, NSC124670, ro-pyran-2-yl) ester
 
 
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Disease relevance of AIDS126730

 

High impact information on AIDS126730

  • The biological activity of compounds 1-10, 12, and 13 and prosapogenin 1b were examined against pancreatic lipase [2].
  • A novel prosapogenin (3) was obtained on the alkaline hydrolysis of 1 and its structure defined as 3-O-[beta-D-glucopyranosyl(1-->4)-beta-D-glucopyranosyl(1-->3)-alpha-L- rhamnopyranosyl(1-->2)-beta-D-xylopyranosyl] hederagenin [3].
  • The partialy hydrolysis products of formosanin C, dioscin (II) and prosapogenin A of dioscin (III), also increased 3H-thymidine incorporation of Con A-stimulated lymphocytes maximally at 0.01 micrograms/ml, whereas formosanin C did so at 0.0001 micrograms/ml [4].

References

  1. In vitro anticomplementary activity of hederagenin saponins isolated from roots of Dipsacus asper. Oh, S.R., Jung, K.Y., Son, K.H., Park, S.H., Lee, I.S., Ahn, K.S., Lee, H.K. Arch. Pharm. Res. (1999) [Pubmed]
  2. New biologically active triterpenoid saponins from Scabiosa tschiliensis. Zheng, Q., Koike, K., Han, L.K., Okuda, H., Nikaido, T. J. Nat. Prod. (2004) [Pubmed]
  3. Triterpenoid saponins from Cephalaria transsylvanica. Kirmizigül, S., Anil, H., Rose, M.E. J. Nat. Prod. (1996) [Pubmed]
  4. Immunomodulating effects of the hydrolysis products of formosanin C and beta-ecdysone from Paris formosana Hayata. Chiang, H.C., Wang, J.J., Wu, R.T. Anticancer Res. (1992) [Pubmed]
 
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