4.7 Article

Synthesis and evaluation of sphinganine analogues of KRN7000 and OCH

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 70, Issue 25, Pages 10260-10270

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo051147h

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Funding

  1. NIAID NIH HHS [AI054346, AI45889, AI45053, AI057519] Funding Source: Medline

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The phytosphingosine-containing alpha-galactosylceramides (alpha-GalCers), KRN7000 and OCH, have been shown to activate NKT cells via interaction with CD1d, a member of the CD1 family of antigen presenting proteins. Evidence from KRN7000 stimulation of NKT cells suggests that alpha-GalCers may have applications in the treatment or prevention of a range of viral, bacterial, and autoimmune conditions. Moreover, OCH, a truncated analogue of KRN7000, appears to induce a T(H)2 bias, which could have implications for the treatment of autoimmune and inflammatory conditions. We have prepared the direct sphinganine-containing analogues of KRN7000 and OCH, 1 and 2, and found them to be comparable in activity to the parent compounds in inducing the release of IL-2, IL-4, and IFN gamma. In addition, compound 2 leads to a cytokine bias similar to that seen with OCH. This is significant because sphinganines are more easily accessed than phytosphingosines, which should facilitate SAR studies.

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