Chemistry:Isovaleramide

From HandWiki
Revision as of 23:35, 5 February 2024 by Jslovo (talk | contribs) (url)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Isovaleramide
Skeletal formula of isovaleramide
Ball-and-stick model of isovaleramide
Names
Preferred IUPAC name
3-Methylbutanamide
Other names
Isopentanamide
Isovaleric acid amide
Isovaleric amide
beta-Methylbutyramide
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 208-781-1
KEGG
UNII
Properties
C5H11NO
Molar mass 101.149 g·mol−1
Appearance colourless solid
Melting point 137 °C (279 °F; 410 K)
Boiling point 226 °C (439 °F; 499 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is ☑Y☒N ?)
Infobox references
Tracking categories (test):

Isovaleramide is an organic compound with the formula (CH3)2CHCH2C(O)NH2. The amide derived from isovaleric acid, it is a colourless solid.

Occurrence and biological activity

Isovaleramide is a constituent of valerian root.

In humans, it acts as a mild anxiolytic at lower doses and as a mild sedative at higher dosages.[1] Isovaleramide has been shown to be non-cytotoxic and does not act as a CNS stimulant. It inhibits the liver alcohol dehydrogenases and has a reported -1">50 of greater than 400 mg/kg when administered intraperitoneally in mice.[2]

It is a positive allosteric modulator of the GABAA receptor, similarly to isovaleric acid. [3]

References

  1. Balandrin, Manuel F. & Bradford C. Van Wagenen, "Use of isovaleramide as a mild anxiolytic and sedative agent", US patent 5506268, published 1996-04-09, assigned to NPS Pharmaceuticals Inc.
  2. Taillandier, Georges; Benoit-Guyod, Jean L.; Boucherle, Andre; Broll, Madeleine; Eymard, Pierre (1975). "Dipropylacetic series. XII. Anticonvulsant branched aliphatic acids and alcohols". European Journal of Medicinal Chemistry 10 (5): 453–462. 
  3. "[Isovaleramide, an anticonvulsant molecule isolated from Valeriana pavonii]" (in es). Biomedica 30 (2): 245–50. 2010. doi:10.7705/biomedica.v30i2.187. PMID 20890571.