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filingDate 1998-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba211fe43109fbc8fb031e0ed8a9a670
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63ffe4a082dd72f9b684b8100eb9670c
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publicationDate 2001-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6235912-B1
titleOfInvention Sphingosine analogues
abstract The present invention aims to provide a novel sphingosine analogue, which is useful as an intermediate for syntheses of novel lipid derivatives such as sphingolipid derivatives and the like that can regulate the effects of sphingolipid.The present invention relates to a sphingosine analogue represented by the general formula (I) described below.In the formula, as for Q1, Q2 and Q3, Q1 and Q2, which are the same or different each other, are hydrogen, alkyl groups having 1-4 of carbon atoms, acyl groups having 2-5 of carbon atoms, or protecting groups of the amino group, and Q3 is a hydrogen or a protecting group of the hydroxyl group; or Q2 and Q3 make up an isopropylidene group and Q1 is a hydrogen or a protecting group of the amino group. Q4 and Q5, which are the same or different each other, are hydroxyl groups, acyl groups having 2-5 of carbon atoms, -O-Q6, or hydrogen; or Q4 and Q5 make up a covalent bond. Q6 is a protecting group of the hydroxyl group. X1 is -COOH, -CONH2, -CO-Q7, -CH2OH, or -CH2O-Q8. Q7 is a protecting group of the carboxyl group, and Q8 is a protecting group of the hydroxyl group.
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