Valiloxybate
Pharmaceutical compound
From Wikipedia, the free encyclopedia
Valiloxybate (INN, USAN;[2] developmental code name XW-10172) is an extended-release prodrug of γ-hydroxybutyrate (GHB; oxybate) which is under development for the treatment of narcolepsy.[1][3][4][5][6] It is also being investigated for treatment of excessive daytime sleepiness (EDS) in people with Parkinson's disease.[7] The drug is taken orally once per night.[1][4][5][8][6]
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| Other names | Valiloxibic acid; Valiloxybic acid; 4-((L-Valyl)oxy)butanoic acid; XW-10172; XW10172; XWL-008; XWL008 |
| Routes of administration | Oral[1] |
| Drug class | GABAB receptor agonist; GHB receptor agonist; Hypnotic |
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| Formula | C9H17NO4 |
| Molar mass | 203.238 g·mol−1 |
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Pharmacology
It is an amino acid (L-valine) ester prodrug of GHB,[6][2] which itself acts as a GABAB and GHB receptor agonist.[9][10] Relative to administration of GHB itself, valiloxybate showed a delayed time to peak levels and an extended duration of GHB exposure in humans.[6] It is said to maintain desired GHB levels for 6 to 7 hours.[11] This profile is compatible with once-nightly dosing,[6] in contrast to GHB itself which is typically administered twice per night due to its very short elimination half-life.[12][13][14] In addition, unlike sodium oxybate, valiloxybate contains no sodium or cation, and hence avoids excessive sodium intake.[6][15]
History
See also
- List of investigational narcolepsy and hypersomnia drugs
- JZP-386 (deuterated sodium oxybate)
- Aceburic acid
- Ethyl acetoxy butanoate
- 1,6-Dioxecane-2,7-dione