http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002177720-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0f25cafda3ea58ec9999a6d5873e8ce1
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01D15-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01D15-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-18
filingDate 2001-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_32b2673d22a789eec7c82d235f56fbab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4688efe49394513260ac17d0cb8a7db4
publicationDate 2002-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002177720-A1
titleOfInvention Isolation of natural L-beta-3-indolylalanine and enrichment of natural aliphatic amino acid mixtures with natural L-beta-3-indolylalanine
abstract Processes for isolating substantially pure natural L-β-3-indolylalanine (L-β-3) from a mixture of amino acids, such as a protein hydrolysate. A protein hydrolysate, for example of casein or soy protein, is passed over a polymeric resin attractive to aromatic amino acids but not attractive to aliphatic amino acids. The aromatic amino acids are retained on the resin while the aliphatic amino acids pass over the resin and are collected. The resin is then washed to displace any residual aliphatic acids which may be physically associated with but not bound to the resin. Thereafter, the resin is eluted with a dilute acid to displace L-phenylalanine and L-tyrosine and provide a solution thereof while allowing L-β-3 to be retained on the resin. The resin is then further eluted with a dilute base to displace L-β-3 from the resin and provide a solution of L-β-3. Substantially pure natural L-β-3 is recoverable from this solution.
priorityDate 1998-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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