Eptazocine hydrobromide

5-Bromo-4-methyl-thiazol-2-ylamine hydrobromide.

5，6-Dihydro-4H-pyrrolo[3，4-d]thiazole Hydrobromide.

ABH (p-Azidobenzoyl Hydrazide)

A non-nucleoside pyridopyrimidine compound that selectively blocks the action of adenosine kinase in an adenosine-competitive manner (IC₅₀ = 1.7 nM in cell-free assays) suppresses nociception in various rodent pain models.

General description This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the

alpha-Amino-gamma-butyrolactone hydrobromide

Specificity Vanilloid receptor like protein 1 (VRL-1). Immunohistochemical analysis of rat dorsal root ganglia and spinal cord indicates that this antibody is of high specificity.

Specificity Vanilloid receptor like protein 1 (VRL-1). Immunohistochemical analysis of rat dorsal root ganglia and spinal cord indicates specific staining in a subpopulation of sensory neurons.

Produced endogenously via oxidation of AEA, or by transacylation of arachidonoyl CoA has analgesic activities in whole animal experiments, yet is a very poor ligand for the CB1 receptor.

An analog of AEA in which the alcohol of the ethanolamide group has been replaced with a fluorine atom, which increases the binding affinity and selectivity for the CB1 receptor in vivo activity is enhanced much less than the binding affinity,

An analog of AEA in which the alcohol of the ethanolamide group has been replaced with a fluorine atom, which increases the binding affinity and selectivity for the CB1 receptor in vivo activity is enhanced much less than the binding affinity,

A potent group IVA cPLA2 inhibitor (XI(50) = 0.022) reduces thermal hyperalgesia evoked by carrageenan injection of rat hind paw (ED₅₀ = 1.2 mg/kg) does not inhibit COX activity or interfere with CB1 receptor signaling.