 | This article needs additional citations for
verification. (February 2022) |
| |
| Names | |
|---|---|
|
Preferred IUPAC name
3-Methyl-5,6,7,8-tetrahydroquinoline-8-carbothioamide | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C11H14N2S | |
| Molar mass | 206.31 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Tiquinamide is a gastric acid synthesis inhibitor. [1]
- ^ Pierce, DM; Franklin, RA; Southgate, RJ (1976). "Pharmacokinetic studies on tiquinamide, a novel inhibitor of gastric acid secretion". British Journal of Clinical Pharmacology. 3 (5): 943–945. doi: 10.1111/j.1365-2125.1976.tb00655.x. PMC 1428943. PMID 973994.
 | This organic chemistry article is a stub. You can help Wikipedia by expanding it. |
| This article needs additional citations for
verification. (February 2022) |
|
| |
| Names | |
|---|---|
|
Preferred IUPAC name
3-Methyl-5,6,7,8-tetrahydroquinoline-8-carbothioamide | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C11H14N2S | |
| Molar mass | 206.31 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Tiquinamide is a gastric acid synthesis inhibitor. [1]
- ^ Pierce, DM; Franklin, RA; Southgate, RJ (1976). "Pharmacokinetic studies on tiquinamide, a novel inhibitor of gastric acid secretion". British Journal of Clinical Pharmacology. 3 (5): 943–945. doi: 10.1111/j.1365-2125.1976.tb00655.x. PMC 1428943. PMID 973994.
|
| This organic chemistry article is a stub. You can help Wikipedia by expanding it. |