http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S60116628-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1374dd16777534b65ad4422333245af8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-557
filingDate 1983-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_843c54d61b0b19db5d4c2fd08571e979
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_167507e0b34f449f56f743239851c31c
publicationDate 1985-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S60116628-A
titleOfInvention Composition of pharmaceutical preparation of 7- thiaprostaglandin e1
abstract PURPOSE: The titled composition useful as an inhibitor of blood platelet aggregation, hyptotensor, etc. having higher action than existing PG, suitable as a pharmaceutical preparation for oral medication, having extremely improved stability, obtained by dissolving a 7-thiaprostaglandin E 1 in a vegetable oil. n CONSTITUTION: At least one 7-thiaprostaglandin E 1 shown by the formula (R 1 is H, or lower alkyl; R 2 is H, or CH 3 ; R 3 is 5W8C alkyl, or cycloalkyl; broken line shows single bond or double bond) is dissolved in a vegetable oil, to give the titled composition having improved stability. Especially a coconut oil or fractionated coconut oil is preferable as the vegetable oil, and an amount of it used is 100W200,000 times as heavy as the compound shown by the formula. By dissolving the compound in the vegetable oil, stability to acid, alkali, light rays, heat, oxygen, etc. is extremely improved. n COPYRIGHT: (C)1985,JPO&Japio
priorityDate 1983-11-29-04:00^^<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/SID419523291
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID977

Total number of triples: 13.