Zolimidine

Zolimidine
Names
	Preferred IUPAC name 2-[4-(Methanesulfonyl)phenyl]imidazo[1,2-a]pyridine
Identifiers
CAS Number	1222-57-7 ;
3D model (JSmol)	Interactive image;
ChemSpider	13985 ;
ECHA InfoCard	100.013.589
KEGG	D07075 ;
PubChem CID	14652;
UNII	YCF001N8QB ;
CompTox Dashboard (EPA)	DTXSID9057630 ;
	InChI InChI=1S/C14H12N2O2S/c1-19(17,18)12-7-5-11(6-8-12)13-10-16-9-3-2-4-14(16)15-13/h2-10H,1H3 Key: VSLIUWLPFRVCDL-UHFFFAOYSA-N ; InChI=1/C14H12N2O2S/c1-19(17,18)12-7-5-11(6-8-12)13-10-16-9-3-2-4-14(16)15-13/h2-10H,1H3 Key: VSLIUWLPFRVCDL-UHFFFAOYAK;
	SMILES CS(=O)(=O)C1=CC=C(C=C1)C2=CN3C=CC=CC3=N2;
Properties
Chemical formula	C14H12N2O2S
Molar mass	272.32 g/mol
Density	1.31 g/cm3
Pharmacology
ATC code	A02BX10 (WHO)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Zolimidine (zoliridine, brand name Solimidin) is a gastroprotective^[1] drug previously used for peptic ulcer^[2] and gastroesophageal reflux disease.^[3]

References[edit]

^ Parisio, C; Clementi, F (November 1976). "Surface Alterations Induced by Stress in Gastric Mucosa: Protective Effect of Zolimidine. A Transmission and Scanning Electron Microscope Investigation". Laboratory Investigation. 35 (5): 484–95. PMID 136548.
^ Belohlavek, D; Malfertheiner, P (1979). "The Effect of Zolimidine, Imidazopyridine-derivate, on the Duodenal Ulcer Healing". Scandinavian Journal of Gastroenterology. Supplement. 54: 44. PMID 161649.
^ Materia, A; Basso, N; Bagarani, M; Basoli, A; Speranza, V (30 April 1981). "Treatment of Alkaline Reflux Gastritis with Zolimidine. Controlled Study". La Clinica Terapeutica. 97 (2): 183–91. PMID 6453678.

This drug article relating to the gastrointestinal system is a stub. You can help Wikipedia by expanding it.

v t e Drugs for peptic ulcer and GERD/GORD (A02B)
H₂ antagonists ("-tidine")	Cimetidine Famotidine Lafutidine Lavoltidine (loxtidine) Nizatidine Ranitidine^#‡ Roxatidine
Prostaglandins (E)/ analogues ("-prost-")	Misoprostol Enprostil
Proton-pump inhibitors ("-prazole")	Azeloprazole Dexlansoprazole Esomeprazole Ilaprazole Lansoprazole Omeprazole^# Pantoprazole Picoprazole Rabeprazole Tenatoprazole Timoprazole
Potassium-competitive acid blockers ("-prazan")	Linaprazan Revaprazan Soraprazan Vonoprazan
Others	Aceglutamide aluminum Acetoxolone Alginic acid Arbaclofen placarbil Bismuth subcitrate Carbenoxolone Cetraxate Gefarnate Irsogladine Lesogaberan Pirenzepine Proglumide Rebamipide Sucralfate Sulglicotide Telenzepine Teprenone Troxipide Zinc L-carnosine Zolimidine
Combinations	Bismuth subcitrate/metronidazole/tetracycline Omeprazole/amoxicillin/rifabutin Vonoprazan/amoxicillin Vonoprazan/amoxicillin/clarithromycin
See also: Helicobacter pylori* eradication protocols*
^#WHO-EM ^‡Withdrawn from market Clinical trials: ^†Phase III ^§Never to phase III

Names


Preferred IUPAC name 2-[4-(Methanesulfonyl)phenyl]imidazo[1,2-a]pyridine
Identifiers
CAS Number	1222-57-7^Y
3D model (JSmol)	Interactive image
ChemSpider	13985^N
ECHA InfoCard	100.013.589
KEGG	D07075^Y
PubChem CID	14652
UNII	YCF001N8QB^Y
CompTox Dashboard (EPA)	DTXSID9057630
InChI InChI=1S/C14H12N2O2S/c1-19(17,18)12-7-5-11(6-8-12)13-10-16-9-3-2-4-14(16)15-13/h2-10H,1H3^N Key: VSLIUWLPFRVCDL-UHFFFAOYSA-N^N InChI=1/C14H12N2O2S/c1-19(17,18)12-7-5-11(6-8-12)13-10-16-9-3-2-4-14(16)15-13/h2-10H,1H3 Key: VSLIUWLPFRVCDL-UHFFFAOYAK
SMILES CS(=O)(=O)C1=CC=C(C=C1)C2=CN3C=CC=CC3=N2
Properties
Chemical formula	C₁₄H₁₂N₂O₂S
Molar mass	272.32 g/mol
Density	1.31 g/cm³
Pharmacology
ATC code	A02BX10 (WHO)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references