The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review

AC1O3DO0     (2R)-4- (hydroxymethyl)oxolane-2,3,4- triol

Synonyms:
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

High impact information on Apiose

  • Methylation analysis of the lithium degradation products from each PG-2 also indicated that these oligosaccharide alditols mainly consisted of terminal Rha, Araf, Fuc, Xyl, and Gal, 4-linked Rha, 3-linked Fuc, and 3'-linked Api [1].
  • Two apiose-containing kaempferol triosides, together with nine known flavonoids were isolated from the leaves of Silphium perfoliatum L [2].
  • Methylation analysis of these degradation products indicated that they contained terminal Rha, Araf, Fuc, Xyl, and Gal, 4-linked Rha, 3-linked Fuc, 3-linked Ara, and 3'-linked Api [3].
  • The neutral sugar content of the successive fractions increased with increasing molecular weight, but each fraction also contained, in addition to Rha, Ara, and Gal, 2-Me-Fuc, 2-Me-Xyl, and Api [3].
  • Two compounds have this structure physiologically: ribose in ribonucleotides and RNA, and apiose in the plant cell wall [4].
 

Biological context of Apiose

  • The acetylation of apiitol in the determination of apiose [5].
  • Fragment LMPH deprived of some terminal apiose residues as a result of partial acidic hydrolysis failed to have an effect on the inflammatory response.Thus, the data obtained reveal an enhancement by lemnan of the inflammatory response [6].

References

  1. Existence of a rhamnogalacturonan II-like region in bioactive pectins from medicinal herbs. Hirano, M., Kiyohara, H., Yamada, H. Planta Med. (1994) [Pubmed]
  2. Kaempferol triosides from Silphium perfoliatum. el-Sayed, N.H., Wojcińska, M., Drost-Karbowska, K., Matławska, I., Williams, J., Mabry, T.J. Phytochemistry (2002) [Pubmed]
  3. Structural studies of endopolygalacturonase-resistant fragments of an antiulcer pectin from the roots of Bupleurum falcatum L. Hirano, M., Kiyohara, H., Matsumoto, T., Yamada, H. Carbohydr. Res. (1994) [Pubmed]
  4. Chemistry and biology of boron. Loomis, W.D., Durst, R.W. Biofactors (1992) [Pubmed]
  5. The acetylation of apiitol in the determination of apiose. Kindel, P.K., Cheng, L.A. Carbohydr. Res. (1990) [Pubmed]
  6. Effect of lemnan, pectin from Lemna minor L., and its fragments on inflammatory reaction. Popov, S.V., Ovodova, R.G., Ovodov, Y.S. Phytotherapy research : PTR. (2006) [Pubmed]
 
WikiGenes - Universities