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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Chemical Compound Review: 

CHEBI:16155     [(1R,3S,4S,6R)-2,5-dihydroxy- 3,4,6...

Synonyms: HMDB01187, DB04300, Ins-1,3,4,6-P4, AC1L3TR1, C04477, ...
 
 
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Disease relevance of 110298-84-5

 

High impact information on 110298-84-5

  • The structure of one of these new InsP4 isomers, which is a phosphorylation product of Ins-1,3,4-P3, was deduced by its resistance to periodate oxidation to be Ins-1,3,4,6-P4 [2].

References

  1. Synthesis of myo-inositol 1,3,4,5,6-pentakisphosphate from inositol phosphates generated by receptor activation. Stephens, L.R., Hawkins, P.T., Barker, C.J., Downes, C.P. Biochem. J. (1988) [Pubmed]
  2. Formation of inositol 1,3,4,6-tetrakisphosphate during angiotensin II action in bovine adrenal glomerulosa cells. Balla, T., Guillemette, G., Baukal, A.J., Catt, K.J. Biochem. Biophys. Res. Commun. (1987) [Pubmed]
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