Ibodutant
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| Systematic (IUPAC) name | |
|---|---|
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Nα-[(1-{[(6-methyl-1-benzothien-2-yl)carbonyl]amino}cyclopentyl)carbonyl]-N-{[1-(tetrahydro-2H-pyran-4-ylmethyl)piperidin-4-yl]methyl}-D-phenylalaninamide | |
| Clinical data | |
| Routes of administration | Oral |
| Identifiers | |
| ATC code | none |
| PubChem | CID 11527495 |
| IUPHAR/BPS | 2117 |
| ChemSpider |
9702281  |
| UNII |
1H7RSQ28BJ  |
| Synonyms | 6-methyl-N-[1-[[(2R)-1-[[1-(oxan-4-ylmethyl)piperidin-4- yl]methylamino]-1-oxo-3-phenylpropan-2-yl]carbamoyl]cyclopentyl]-1-benzothiophene-2-carboxamide |
| Chemical data | |
| Formula | C37H48N4O4S |
| Molar mass | 644.866 g/mol |
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| (what is this?) (verify) | |
Ibodutant is a candidate drug for irritable bowel syndrome diarrhea, developed by The Menarini Group. As of March 2015, it is undergoing a multicentre double blind efficacy clinical study. Ibodutant selectively blocks the tachykinin receptor NK2, with blockade practically complete in nanomolar concentrations. A phase 2 trial in Europe(the IRIS-2 trial) completed in May 2012 with positive results. A 52-week phase 3 study in women is ongoing.[1]
See also
References
- ↑ "CLINICAL TRIALS DATABASE". Menarini Group. Retrieved 11 March 2015.
- H. Spreitzer (May 26, 2008). "Neue Wirkstoffe - Ibodutant". Österreichische Apothekerzeitung (in German) (11/2008): 541.
- S. Giuliani, M. Altamura, C. A. Maggi. "Ibodutant. Tachykinin NK2 receptor antagonist, Treatment of irritable bowel syndrome.". Drugs of the Future 33 (2): 111–115.
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