Thioester enantiomeric compounds and their therapeutic uses
AssigneeSociete Civile Bioprojet
InventorsPierre Duhamel, Lucette Duhamel, Denis Danvy, Jean-Christophe Plaquevent, Bruno Giros, Claude Gros, Jean-Charles Schwartz, Jeanne-Marie Lecomte
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Abstract
The (R) or (S) isomer of acetorphan or N-/(acetylthiomethyl)-2-oxo-1-phenyl-3-propyl/(S) alanine methyl ester is prepared by splitting of racemic acetylthio-3-benzyl-2-propanoic acid by reaction with ephedrin, separation of the enantiomeric salt obtained, then freeing of the acid and coupling with the corresponding amino acid ester. The obtained preparations possess remarkable therapeutic activities and can notably be used as drugs.
Claims9
An enantiomer (R) compound having the formula:
- ##STR4## in which R.sub.1 =CH.sub.3 or CH2-C.sub.6 H.sub.5.
A drug composition having both central and peripheral activities, being useful as an antalgic, psychotropic, anti gastric acid and antidiarrhea agent and being useful for treatment of irritable bowel syndrome, gastro-oesophageal regurgitation or acute cholecystitis, characterized in that it contains, as an active ingredient, a compound selected from the group consisting of ##STR7##
A method for treatment of irritable bowel syndrome, gastro-oesophageal regurgitation or acute cholecystitis by the administration to a patient having same of a therapeutically effective dose of a compound selected from the group consisting of:
- ##STR8##
A method for treatment of diarrhea by the administration to a patient of a therapeutically effective dose of a compound selected from the group consisting of ##STR9##
Dependencies are inferred from the claim text.