http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1268230-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J17-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J9-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J17-005
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J19-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J19-00
filingDate 1969-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1972-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1268230-A
titleOfInvention Steroid glycosides and process for their manufacture
abstract 1,268,230. Steriod dehydroglycosides. FARBWERKE HOECHST A.G. 1 April, 1969 [6 April, 1968], No. 16961/69. Heading C2U. The invention comprises compounds of formula wherein R is a steroid-3-yl radical of the 20(22)- cardenolide or 20,22-bufadienolide series (other than that derived by removal of the 3-hydroxyl group from strophanthidin); R<SP>1</SP> is H or an aliphatic or aromatic acyl group; and R<SP>2</SP> is H, Me, Et, CH 2 OR<SP>1</SP> or CHOR<SP>1</SP>-CH 2 OR<SP>1</SP> (where R<SP>1</SP> is as above). Compounds I are prepared from steroid alcohols R-OH by reaction with acylated glycols of formula (wherein R<SP>1</SP> is aliphatic or aromatic acyl and R<SP>2</SP> is as above) followed when required by hydrolysis of acyl groups in the glycoside moiety. Compounds I are said to possess inotropic, cardiovascular, diuretic and antidiarrhoeal properties and may be made up with carriers into pharmaceutical compositions for oral administration.
priorityDate 1968-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419574558
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6185

Total number of triples: 15.