Dithioerythritol

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Oxidized form of dithioerythritol (DTE)
Oxidized form of dithioerythritol (DTE)

In chemistry, dithioerythritol (DTE) is an epimer of dithiothreitol (DTT). Its name derives from the corresponding 4-carbon sugar erythrose. DTE's formula is C4H10O2S2 (molecular weight 154.3 Da). Synonyms for DTE include

  • 2,3-dihydroxybutane-1,4-dithiol,
  • erythro-2,3-dihydroxy-1,4-butanedithiol,
  • erythro-1,4-dimercapto-2,3-butanediol, and
  • Cleland's reagent (also used for DTT)

Like dithiothreitol, DTE makes an excellent reducing agent, although its standard reduction potential is not quite as negative, i.e., DTE is slightly less effective at reducing than DTT, presumably because steric repulsion of its OH groups makes the cyclic disulfide-bonded form of DTE less favorable. In DTT, these hydroxyl groups are on opposite sides of the ring, whereas they are on the same side of the ring (and, hence, closer) in DTE.

[edit] References

  • Cleland WW. (1964) "Dithiothreitol, A New Protective Reagent for SH Groups", Biochemistry, 3, 480-482.


[edit] External links