Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H14O6 |
Molecular Weight | 266.2467 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(=CC(OC)=C1OC)C(=O)\C=C\C(O)=O
InChI
InChIKey=PVCWLTQMJSUKGZ-SNAWJCMRSA-N
InChI=1S/C13H14O6/c1-17-10-6-8(9(14)4-5-12(15)16)7-11(18-2)13(10)19-3/h4-7H,1-3H3,(H,15,16)/b5-4+
Baxitozine is a Histamine H2 receptor antagonist. It has a cytoprotective, antisecretory and antiulcer properties. In situ, baxitozine inhibited acid secretion stimulated by histamine or pentagastrin but was inactive against carbachol. It also had antiulcer activity against stress ulcers (restraint plus cold). It had marked gastric cytoprotective activity in rats against the necrotizing effects of ethanol. This cytoprotective activity was not significantly affected by indomethacin pre-treatment. Baxitozine has been in phase II clinical trials for the treatment of gastric ulcer. However, this research has been discontinued.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4084342
Curator's Comment: Rat data
Single doses 2.5, 5 or 10 mg/kg
Route of Administration:
Oral
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C29698
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C73191
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ACTIVE MOIETY