Conivaptan
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| N-(4-(4,5-dihydro-2-methylimidazo[4,5-d][1]benzazepin- 6(1H)-yl)carbonyl)phenyl)- (1,1'-biphenyl)-2-carboxamide | |
| CAS number 210101–16–9 | ATC code not yet available |
| Chemical formula | C32H26N4O2 |
| Molecular weight | 498.583 |
| Bioavailability | N/A |
| Metabolism | ? |
| Elimination half-life | ? |
| Excretion | ? |
| Pregnancy category | ? |
| Legal status | ? |
| Routes of administration | Intravenous |
Conivaptan (YM 087) is a non-peptide inhibitor of antidiuretic hormone (vasopressin). It was approved in 2004 for hyponatremia (low blood sodium levels) caused by syndrome of inappropriate antidiuretic hormone (SIADH). It is marketed by Yamanouchi Pharmaceutical.
Conivaptan inhibits both isotypes of the vasopressin receptor (V1a and V2). Effectively, it causes iatrogenic nephrogenic diabetes insipidus.
See also
- Tolvaptan
Categories: Medical treatment stubs | Pharmacologic agents