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

2 ityrosinase, anticancer, antihyperlipidemia, antiulcer, anti-inflammatory, and hepatoprotective activ

3 ioxidant, antimicrobial, prebiotic, healing, antiulcer, anti-inflammatory, anti-hyperlipidemic and sl

4    Interestingly, the short synthesis of the antiulcer drug irsogladine and the large-scale synthesis

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

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

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

8 : 10% received traditional NSAIDs along with antiulcer drugs at the recommended doses and 6% received

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

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

11                          We investigated the antiulcer efficacy of 3-indolyl furanoids (3g and 3c, i.

12 hich hinders the development of prophylactic antiulcer interventions.

13  mug/mL, respectively, indicating the higher antiulcer potency of 3g.

14 with mild dyspepsia continued NSAIDs but not antiulcer treatment.