Clinical data | |
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Routes of administration | Oral |
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Pharmacokinetic data | |
Metabolism | Hepatic (CYP2C19-mediated) |
Elimination half-life | 4.8 to 7.7 hours |
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IUPAC name
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CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.120.697 |
Chemical and physical data | |
Formula | C16H18N4O3S |
Molar mass | 346.41 gยทmol |
3D model (JSmol) | |
Chirality | Racemic mixture |
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Tenatoprazole is a proton pump inhibitor drug candidate that was undergoing clinical testing as a potential treatment for reflux oesophagitis and peptic ulcer as far back as 2003. The compound was invented by Mitsubishi Tanabe Pharma and was licensed to Negma Laboratories (part of Wockhardt as of 2007).
Mitsubishi reported that tenatoprazole was still in Phase I clinical trials in 2007 and again in 2012.
Tenatoprazole has an imidazopyridine ring in place of the benzimidazole moiety found in other proton pump inhibitors, and has a half-life about seven times longer than other PPIs.
See also
References
- "Gastrointestinal Disease Update". Digestive Disease Week. DataMonitor. March 2003.
- "Investors unwilling to forgive Wockhardt, promoter for failings". Economic Times. 3 March 2011. Archived from the original on November 16, 2014.
- ^ "State of New Product Development" (PDF). Mitsubishi Tanabe Pharma. 8 May 2012.
- "FY2007 Interim Financial Results". Mitsubishi Tanabe Pharma.
- Li H, Meng L, Liu F, Wei JF, Wang YQ (January 2013). "H+/K+-ATPase inhibitors: a patent review". Expert Opinion on Therapeutic Patents. 23 (1): 99โ111. doi:10.1517/13543776.2013.741121. PMID 23205582. S2CID 44647770.
Drugs for peptic ulcer and GERD/GORD (A02B) | |
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H2 antagonists ("-tidine") | |
Prostaglandins (E)/ analogues ("-prost-") | |
Proton-pump inhibitors ("-prazole") | |
Potassium-competitive acid blockers ("-prazan") | |
Others | |
Combinations | |
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