Specific tritium labeling of cerebrosides at the 3-positions of erythro-sphingosine and threo-sphingosine.

Abstract:

:Cerebrosides containing either threo- or erythro-[3-3-H]sphingosine were synthesized by a new procedure. Glucopyranosyl or galactopyranosyl ceramides were converted to their 3-keto derivatives with 2,3-dichloro-5,6-dicyanobenzoquinone and reduced with 3-H-labeled sodium borohydride. The resulting tritiated cerebrosides, which contained erythro- and threo-sphingosines in the ratio of 84:16, were deacylated with butanol-KOH, and the erythro- and threo-psychosines were separated by silica gel column chromatography and reacylated with lignoceroyl chloride.

journal_name

J Lipid Res

authors

Iwamori M,Moser HW,Kishimoto Y

keywords:

subject

Has Abstract

pub_date

1975-07-01 00:00:00

pages

332-6

issue

4

eissn

0022-2275

issn

1539-7262

journal_volume

16

pub_type

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