Valerenic acid

Valerenic acid

Chembox new
ImageFile1=ValerenicAcid2d.pngImageSize1=120px
ImageFile2=ValerenicAcid3d.pngImageSize2=120px
IUPACName=(E)-3- [(4S,7R,7aR)-3,7-dimethyl- 2,4,5,6,7,7a-hexahydro- 1H-inden-4-yl] - 2-methylprop-2-enoic acid
OtherNames=
Section1= Chembox Identifiers
CASNo=3569-10-6
PubChem= 6440940
SMILES=CC1CCC(C2=C(CCC12)C)C=C(C)C(=O)O

Section2= Chembox Properties
Formula=C15H22O2
MolarMass=234.334
Appearance=
Density=
MeltingPt=
BoilingPt=
Solubility=

Section3= Chembox Hazards
MainHazards=
FlashPt=
Autoignition=

Valerenic acid is a constituent of the essential oil of the Valerian plant.

Valerian is used as a herbal sedative which may be helpful in the treatment of insomnia. While the precise mechanism of this action has not been established and it is likely that several different components of the plant contribute to the effect, valerenic acid is thought to be at least partly responsible for the sedative effects.

Valerenic acid has been demonstrated to be both a subtype-selective GABAA agonist [Yuan CS, Mehendale S, Xiao Y, Aung HH, Xie JT, Ang-Lee MK. The gamma-aminobutyric acidergic effects of valerian and valerenic acid on rat brainstem neuronal activity. "Anesthesia and Analgesia". 2004 Feb;98(2):353-8.] acting mainly at α1β2 and α1β3 subtypes, [Khom S, Baburin I, Timin E, Hohaus A, Trauner G, Kopp B, Hering S. Valerenic acid potentiates and inhibits GABA(A) receptors: molecular mechanism and subunit specificity. "Neuropharmacology". 2007 Jul;53(1):178-87.] and also a 5HT5A partial agonist. [Dietz BM, Mahady GB, Pauli GF, Farnsworth NR. Valerian extract and valerenic acid are partial agonists of the 5-HT5a receptor in vitro. "Brain Research. Molecular Brain Research". 2005 Aug 18;138(2):191-7.] Both of these actions are likely to play a role in the sedative effects of this compound, as other GABAA agonists such as benzodiazepines are commonly used as sedative drugs, and while no selective 5HT5A agonists are currently used medically, the 5HT5A receptor is known to be highly expressed in the suprachiasmatic nucleus of the brain, which is believed to be involved in the sleep-wake cycle.

Valerenic acid has also been reported to be an NF-κB inhibitor, and may be partly responsible for the reported anti-inflammatory action of the valerian plant. [Jacobo-Herrera NJ, Vartiainen N, Bremner P, Gibbons S, Koistinaho J, Heinrich M. NF-kappaB modulators from Valeriana officinalis. "Phytotherapy Research". 2006 Oct;20(10):917-9.]

References


Wikimedia Foundation. 2010.

Игры ⚽ Поможем написать курсовую

Look at other dictionaries:

  • Gamma-Hydroxybutyric acid — γ Hydroxybutyric acid Systematic (IUPAC) name 4 Hydroxybutanoic acid …   Wikipedia

  • Lysergic acid diethylamide — LSD redirects here. For other uses, see LSD (disambiguation). LSD 25 redirects here. For the dock landing ship, see USS San Marcos (LSD 25). For the Fringe episode, see Lysergic Acid Diethylamide (Fringe). Lysergic acid diethylamide …   Wikipedia

  • Valproic acid — Systematic (IUPAC) name 2 propylpentanoic …   Wikipedia

  • Tolfenamic acid — Systematic (IUPAC) name 2 [(3 chloro 2 methylphenyl)amino]benzoic acid)[1] …   Wikipedia

  • Lysergic acid hydroxyethylamide — Systematic (IUPAC) name 9,10 didehydro N (1 hydroxyethyl) 6 methylergoline 8 carboxamide Clinical data …   Wikipedia

  • Nipecotic acid — Systematic (IUPAC) name piperidine 3 carboxylic acid Clinical data Pregnancy cat.  ? …   Wikipedia

  • (+)-cis-2-Aminomethylcyclopropane carboxylic acid — Systematic name (1S,2R) 2 (Aminomethyl)cyclopropane 1 carboxylic acid …   Wikipedia

  • (1,2,5,6-Tetrahydropyridin-4-yl)methylphosphinic acid — IUPAC name methyl (1,2,3,6 tetrahydropyridin 4 yl)phosphinic acid …   Wikipedia

  • Valerian (herb) — For other uses, see Valerian. Valerian (plant) Scientific classification Kingdom: Plantae (unranked) …   Wikipedia

  • Propofol — Systematic (IUPAC) name 2,6 diisopropylphenol …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”