http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1043401-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P13-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P13-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00 |
filingDate | 2000-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c848d962a0b538bd8269cd74980c1d2e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5eaaf8eb00e001668544b86dfdc808e0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11aa39f7e315ee45df89715b5c14af61 |
publicationDate | 2000-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | EP-1043401-A1 |
titleOfInvention | Methods for producing optically active amino acids |
abstract | A method for producing from one of the optical isomers (optical isomernI) of an amino acid represented by Formula (1):R-CH(NH 2 )-COOH (1),nwherein R is defined in the specification, the other of the optical isomersn(optical isomer II), said method comprising reacting a biological materialnwhich has an ability of converting said one of the optical isomers (opticalnisomer I) to said the other of the optical isomers (optical isomer II), thenisomerism being on the basis of an assymetric carbon atom to which both of annamino group and a carboxyl group are bound and said ability being notninhibited seriously by an amino acid transferase inhibitor β-chloro-D-alanine,nβ-chloro-L-alanine or gabaculine, with said one of the optical isomers (opticalnisomer I). |
priorityDate | 1999-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 149.