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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9a177f0fa84b1b2134e13caa36974ce3
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K8-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P13-02
filingDate 2005-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df641a586ac97f157b86c13f664d65b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79e2920e0eee9abcc685a6016707b95a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f30a7e5e7672229f957dc256c9cf687b
publicationDate 2007-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2007104926-A
titleOfInvention Method for producing phytoceramide and α-hydroxyceramide using ceramide synthase LASS6
abstract The present invention provides a method for producing phytoceramide and α-hydroxyceramide which are ceramides subjected to hydroxylation. A method for producing phytoceramide comprising reacting phytosphingosine and acyl CoA in the presence of ceramide synthase Lass6 to obtain phytoceramide, wherein the acyl of the acyl CoA has 14 or 16 carbon atoms. Or 18, the production method. A method for producing α-hydroxyceramide, comprising reacting a sphingoid base with α-hydroxyacyl CoA in the presence of ceramide synthase Lass6 to obtain α-hydroxyceramide. The acyl of α-hydroxyacyl CoA can be 14, 16 or 18 carbon atoms and the phytosphingoid base can be dihydrosphingosine, sphingosine or phytosphingosine. [Selection figure] None
priorityDate 2005-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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