http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113930415-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d890ad239375a780e6827d3407f15ef3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Y405-01
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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-19
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P17-02
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filingDate 2021-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_180921320a8c95623db52f1e54d793eb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8bf23c2bbddc74a8e7cf7323a7acb37e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da35a7e35fc5021145c9b47e86d64368
publicationDate 2022-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-113930415-A
titleOfInvention Halogen alcohol dehalogenase mutant and application thereof
abstract The invention discloses a halohydrin dehalogenase mutant and application thereof in synthesizing a key chiral epoxy intermediate of an antifungal drug. The invention relates to the field of genetic engineering and enzyme engineering, in particular to a stereoselectively overturned halohydrin dehalogenase mutant N176G, the corresponding amino acid sequence of which is shown as SEQ ID No. 4. The halohydrin dehalogenase mutant can be applied to asymmetric dehalogenation of a catalytic compound I to synthesize a chiral epoxide II, the separation yield is 80%, and the optical purity is as high as 98% ee.
priorityDate 2021-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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