L-838,417
Chemical Name: 3-(2,5-Difluorophenyl)-7-(1,1-dimethylethyl)-6-[(1-methyl-1H-1,2,4-triazol-5-yl)methoxy]-1,2,4-triazolo[4,3-b]pyridazine
Purity: ≥98%
Biological Activity
L-838,417 is a subtype-selective GABAA receptor partial agonist. Selectively binds to α1, α2, α3 and α5 subunits (Ki values are 0.79, 0.67, 0.67 and 2.25 nM respectively) but displays no efficacy at α1 (α1-sparing). Exhibits non-sedative anxiolytic, antinociceptive and anti-inflammatory activity in vivo.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.
Additional Information
Background References
-
Probing the molecular basis for affinity/potency- and efficacy-based subtype-selectivity exhibited by benzodiazepine-site modulators at GABAA receptors.
Soderhielm et al.
Biochem.Pharmacol., 2018;158:339 -
Subtype-selective GABAergic drugs facilitate extinction of mouse operant behaviour.
McCabe et al.
Neuropharmacology, 2004;46:171 -
Differential behavioural effects of low efficacy positive GABAA modulators in combination with benzodiazepines and a neuroactive steroid in rhesus monkeys.
McMahon and France
Br.J.Pharmacol., 2006;147:260 -
Reversal of pathological pain through specific spinal GABAA receptor subtypes.
Knabl et al.
Nature, 2008;451:330
Product Datasheets
Reconstitution Calculator
Molarity Calculator
Citations for L-838,417
The citations listed below are publications that use Tocris products. Selected citations for L-838,417 include:
3 Citations: Showing 1 - 3
-
Blockade of spinal α5-GABAA receptors differentially reduces reserpine-induced fibromyalgia-type pain in female rats.
Authors: De la Luz-Cuellar Et al.
Eur J Pharmacol 2019;858:172443
-
Probing the molecular basis for affinity/potency- and efficacy-based subtype-selectivity exhibited by benzodiazepine-site modulators at GABAA receptors.
Authors: Soderhielm Et al.
Biochem Pharmacol 2018;158:339
-
Limiting activity at beta1-subunit-containing GABAA receptor subtypes reduces ataxia.
Authors: Gee Et al.
J Pharmacol Exp Ther 2010;332:1040
FAQs
No product specific FAQs exist for this product, however you may
View all Small Molecule FAQsReviews for L-838,417
There are currently no reviews for this product. Be the first to review L-838,417 and earn rewards!
Have you used L-838,417?
Submit a review and receive an Amazon gift card.
$25/€18/£15/$25CAN/¥75 Yuan/¥2500 Yen for a review with an image
$10/€7/£6/$10 CAD/¥70 Yuan/¥1110 Yen for a review without an image