1 oprostol, a PGE1 analog, was developed as an antiulcer agent because it prevents gastrointestinal ulc

2 umber of clinically used drugs including the antiulcer drug omeprazole, the anxiolytic drug diazepam,

3 ntagonist, the authors hypothesize that this antiulcer drug reduces IL-6, MMP-1, and MMP-9 immunoexpr

4  Enantiopure stereomers of rosaprostol 1, an antiulcer drug, were synthesized from diastereomeric bui

5 : 10% received traditional NSAIDs along with antiulcer drugs at the recommended doses and 6% received

6 eroidal saponins from S. paniculatum and the antiulcer effect of this species at this lower dose.

7    The lower dose of extract able to promote antiulcer effect was 125 mg/kg.

8 with mild dyspepsia continued NSAIDs but not antiulcer treatment.