product summary
Loading...
company name :
Tocris Bioscience
product type :
chemical
product name :
JZL 184
catalog :
3836
quantity :
10 mg (also 50 mg)
price :
149 USD
more info or order :
citations: 7
Reference
Argueta D, Perez P, Makriyannis A, DiPatrizio N. Cannabinoid CB1 Receptors Inhibit Gut-Brain Satiation Signaling in Diet-Induced Obesity. Front Physiol. 2019;10:704 pubmed publisher
Hu H, Kruijssen D, Frias C, Rozsa B, Hoogenraad C, Wierenga C. Endocannabinoid Signaling Mediates Local Dendritic Coordination between Excitatory and Inhibitory Synapses. Cell Rep. 2019;27:666-675.e5 pubmed publisher
Martin H, Bernabeu A, Lassalle O, Bouille C, Beurrier C, Pelissier Alicot A, et al. Endocannabinoids Mediate Muscarinic Acetylcholine Receptor-Dependent Long-Term Depression in the Adult Medial Prefrontal Cortex. Front Cell Neurosci. 2015;9:457 pubmed publisher
Bashashati M, Nasser Y, Keenan C, Ho W, Piscitelli F, Nalli M, et al. Inhibiting endocannabinoid biosynthesis: a novel approach to the treatment of constipation. Br J Pharmacol. 2015;172:3099-111 pubmed publisher
Sardinha J, Kelly M, Zhou J, Lehmann C. Experimental cannabinoid 2 receptor-mediated immune modulation in sepsis. Mediators Inflamm. 2014;2014:978678 pubmed publisher
Valdeolivas S, Pazos M, Bisogno T, Piscitelli F, Iannotti F, Allarà M, et al. The inhibition of 2-arachidonoyl-glycerol (2-AG) biosynthesis, rather than enhancing striatal damage, protects striatal neurons from malonate-induced death: a potential role of cyclooxygenase-2-dependent metabolism of 2-AG. Cell Death Dis. 2013;4:e862 pubmed publisher
Maleńczyk K, Jazurek M, Keimpema E, Silvestri C, Janikiewicz J, Mackie K, et al. CB1 cannabinoid receptors couple to focal adhesion kinase to control insulin release. J Biol Chem. 2013;288:32685-99 pubmed publisher
product information
brand :
Tocris
master code :
3836
SKU :
3836/10
product name :
JZL 184
description :
Potent MAGL inhibitor
target :
Monoacylglycerol Lipase Inhibitors
category :
Small Molecules
unit size :
10 mg (also 50 mg)
purity :
98%
observed molecular weight :
520.49
url print :
?utm_source=distributor&utm_medium=referral&utm_campaign=product&utm_term=smallmolecules
details of functionality :
Potent and selective MAGL inhibitor. Blocks hydrolysis of the endocannabinoid 2-arachidonyl glycerol (2-AG) in vivo in the mouse brain (IC50 = 8 nM). Potentiates depolarization-induced suppression of excitability in cerebellar Purkinje neurons. Exhibits 300-fold selectivity for MAGL over FAAH in vitro . Attenuates nociception in neuropathic and inflammatory pain models. Also reduces free fatty acid levels in primary tumors.
catalog number base :
3836
product keywords :
JZL184 MAGL inhibitor MAG lipase monoacylglycerol lipase inhibitors inhibits MGL MAGL 3836, MAGL
extended description :
Potent MAGL inhibitor
chemical name text :
4-[Bis(1,3-benzodioxol-5-yl)hydroxymethyl]-1-piperidinecarboxylic acid 4-nitrophenyl ester
formula :
C 27 H 24 N 2 O 9
formula text :
C27H24N2O9
cas num :
1101854-58-3
2020 USD :
146
2021 USD :
149 USD
storage :
Store at -20°C
more info or order :
company information
Tocris Bioscience
The Watkins Building
Atlantic Road
Avonmouth, Bristol
BS11 9QD
info@bio-techne.com
https://www.tocris.com
800-343-7475
headquarters: UK