http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2320737-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_602bf5a30fd79d91d8b45d22d6299f0c
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F3-003
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-412
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F3-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-41
filingDate 1975-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1977-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2320737-A1
titleOfInvention PROCESS FOR PREPARING MAGNESIUM SALTS OF ARYLOXY-ALKANOIC ACIDS AND SALTS OBTAINED BY ITS IMPLEMENTATION
abstract Mg salts of aryloxyalkanoc acids of formula (in which R1 is H, CL, Br or F; R2 is 1-3C alkyl; R3 is 1-3C alkyl) are prepd. by reacting metallic Mg with the corresp. acid in a solvent, pref. at 50-100 deg C. The resulting salts can be dehydrated at 90-150 deg C. These salts are used in medicine to diminish the formation of triglycinde-rich, very-low-density lipoproteins, tissue lipides and steroids (Mg salts are superior in this respect to esters of these acids which are susceptible to esterase). Mg activates enzymes in the main synthesis of aftty acids; diminishes the excitability of myocardium and reduces the toxicity of digitalis, and suppresses the formation of cholestin and accumulation of Ca in blood vessels walls. The use of metallic Mg instead of Mg salts employed in conventional processes simplifies the procedures as impurities are not introduced and pure Mg aryloxyalkanoates are obtd.
priorityDate 1974-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 16.