Olvanil
Chemical Name: N-Vanillyloleoylamide
Purity: ≥98%
Biological Activity
Olvanil is a potent vanilloid receptor agonist (pEC50 values are 8.1 and 7.7 at rat and human VR1 receptors respectively). Also blocks anandamide uptake (IC50 = 9 μM) and may bind to CB1 cannabinoid receptors. Antinociceptive following systemic administration.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Interactions between synthetic vanilloids and the endogenous cannabinoid system.
Di Marzo et al.
FEBS Lett., 1998;436:449 -
NE-19550 and NE-21610, antinociceptive capsaicin analogues: studies on nociceptive fibres of the neonatal rat tail in vitro.
Dray et al.
Eur.J.Pharmacol., 1990;181:289 -
Vanilloids. 1. Analogs of capsaicin with antinociceptive and antiinflammatory activity.
Janusz et al.
J.Med.Chem., 1993;36:2595 -
Cannabinoid activation of recombinant and endogenous vanilloid receptors.
Ralevic et al.
Eur.J.Pharmacol., 2001;424:211
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Citation for Olvanil
The citations listed below are publications that use Tocris products. Selected citations for Olvanil include:
1 Citation: Showing 1 - 1
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Use of a fluorescent imaging plate reader--based calcium assay to assess pharmacological differences between the human and rat vanilloid receptor.
Authors: Witte Et al.
Am J Physiol Endocrinol Metab 2002;7:466
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