http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2458061-C2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f83ac68f68cfabd0fd5daf622d775ad4
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-00
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filingDate 2008-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb66eaf241a2ada0b034e7a1fa5f28a6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d69d8af343b6576633800f5ea1ae5d08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebf0486dcf9d45df24f5f14ec2360acb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d2b52320efc97da71408e425033295f
publicationDate 2012-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2458061-C2
titleOfInvention Crystalline forms of 8-azabicyclo[3,2,1]octane compound
abstract FIELD: medicine, pharmaceutics. n SUBSTANCE: present invention refers to a crystalline salt form representing a sulphate salt of 3-endo-(8-{2-[cyclohexylmethyl-((S)-2,3-dihydroxypropionyl)amino]ethyl}-8-azabicyclo[3.2.1]oct-3-yl)benzamide or its hydrate which are used as mu-opioid receptor antagonists, to a based pharmaceutical composition, to applying them for preparing a drug, as well as to a method of treating, improving gastrointestinal motility and mu-opioid receptor antagonisation. n EFFECT: invention refers to versions of the method for preparing the crystalline sulphate salt of 3-endo-(8-{2-[cyclohexylmethyl-((S)-2,3-dihydroxypropionyl)amino]ethyl}-8-azabicyclo[3,2,1]oct-3-yl)benzamide and to a bisulphite adduct of benzene ester of N-cyclohexylmethyl-(2-oxoethyl)carbamic acid. n 26 cl, 26 ex, 6 dwg
priorityDate 2007-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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