Alvimopan
| Clinical data | |
|---|---|
| Trade names | Entereg |
| Other names | Alvimopan, Entereg |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a608051 |
| License data | |
| Routes of administration | Oral |
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| Pharmacokinetic data | |
| Bioavailability | 6% |
| Protein binding | 80% (parent drug), 94% (metabolite) |
| Metabolism | Gut microflora-mediated hydrolysis to active metabolite |
| Elimination half-life | 10-17 hours |
| Excretion | Faeces, urine (35%) |
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| Chemical and physical data | |
| Formula | C25H32N2O4 |
| Molar mass | 424.541 g·mol−1 |
| 3D model (JSmol) | |
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| (what is this?) (verify) | |
Alvimopan (trade name Entereg) is a drug which behaves as a peripherally acting μ-opioid receptor antagonist. With the limited ability to cross the blood–brain barrier and reach the μ-opioid receptors of the central nervous system, the clinically undesirable effects of centrally acting opioid antagonists (like reversal of opioid-mediated analgesia) are avoided without affecting the intended blockade of μ-opioid receptors in the gastrointestinal tract. It is currently only Food and Drug Administration approved for the treatment of postoperative ileus which it received in May 2008.