| Bioactivity | Valpromide is an amide derivative of valproic acid and inhibits human epoxide hydrolase. | ||||||||||||
| Target | epoxide hydrolase | ||||||||||||
| Name | Valpromide | ||||||||||||
| CAS | 2430-27-5 | ||||||||||||
| Formula | C8H17NO | ||||||||||||
| Molar Mass | 143.23 | ||||||||||||
| Appearance | Solid | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
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| Reference | [1]. Pacifici GM, et al. Valpromide inhibits human epoxide hydrolase. Br J Clin Pharmacol. 1986 Sep;22(3):269-74. [2]. Gorres KL, et al. Valpromide Inhibits Lytic Cycle Reactivation of Epstein-Barr Virus. MBio. 2016 Mar 1;7(2):e00113. |