http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-286395-B6

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_edce709207c77ee12489dbd4bf113669
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D457-02
filingDate 1993-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8395b56bb8569a426eed3d7cc6bdfe1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f1c57bad0ac65a7e56fe8114eaad3ed
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ac2f4d89d65948283868d71a82068f40
publicationDate 2000-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-286395-B6
titleOfInvention 2-acetamido-2-deoxy-0-beta-D-glukopyranosides and 2 acetamido-2-deoyy-0-beta-D-galactopyranosides of ergot alkaloids and process of their preparation
abstract In the present invention there are disclosed 2-acetamido-2-deoxy-O-{beta}-D-glucopyranosides and 2-acetamido-2-deoxy-O-{beta}-D-galactopyranosides of ergot alkaloids - elymoclavine lysergol, 9,10 dihydrolysergol of the general formula I, chanoclavine of the general formula II and ergometrine of the general formula III, in which R = Ri1 or Ri2. Said compounds are prepared in such a manner that elymoclavine lysergol, l9,10-dihydrolysergol, chanoclavine or ergometrine is treated with N-acetylhexosaminidase in the presence of p-nitrophenyl-{beta}-N-acetylgalactosaminide or p-nitrophenyl-{beta}-N-acetylglucosaminide in buffer solution with pH value ranging from 4 to 7 at a temperature in the range of 4 to 35 degC, whereupon the obtained product is isolated for instance by silica gel chromatography of by high-efficient liquid chromatography.
priorityDate 1993-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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