Pentobarbital sodium

A structural analog of melatonin that binds the melatonin MT2 receptor (Ki = 41 nM) acts as a melatonin receptor antagonist in frog skin and chicken retina and as a partial agonist in rabbit retina.

A structural analog of melatonin that binds the melatonin MT2 receptor (Ki = 41 nM) acts as a melatonin receptor antagonist in frog skin and chicken retina and as a partial agonist in rabbit retina.

A water-soluble receptor antagonist which targets both AMPA- and kainate-sensitive glutamate receptors (IC₅₀ = 0.15 and 4.8 &microM, respectively) does not block the NMDA-sensitive glutamate receptor (IC₅₀ = &ge 90 &microM).

General description A stable-labeled internal standard suitable for pentobarbital testing by GC/MS or LC/MS for clinical toxicology, forensic analysis, or urine drug testing applications. Pentobarbital is a short-acting barbiturate and hypnotic

General description A stable-labeled internal standard suitable for pentobarbital testing by GC/MS or LC/MS for clinical toxicology, forensic analysis, or urine drug testing applications. Pentobarbital is a short-acting barbiturate and hypnotic

General description Pentobarbital is a short-acting barbiturate and hypnotic approved for treatment of seizures and preoperative sedation. Also known as pentobarbitone, the sodium salt of pentobarbital is used as an anesthetic in veterinary

A potent antagonist highly selective for GluK1 (Kb = 10 nM), GluK3 (IC50 = 23 nM), and GluK1/K5 (Kb = 8 nM) subtype kainate receptors. Does not interact with GluK2 and GluK2/K5 receptors. Low affinity to AMPA receptors (Kd = 83 µM). Does not

A potent antagonist highly selective for GluK1 (Kb = 10 nM), GluK3 (IC50 = 23 nM), and GluK1/K5 (Kb = 8 nM) subtype kainate receptors. Does not interact with GluK2 and GluK2/K5 receptors. Low affinity to AMPA receptors (Kd = 83 µM). Does not

A potent antagonist highly selective for GluK1 (Kb = 10 nM), GluK3 (IC50 = 23 nM), and GluK1/K5 (Kb = 8 nM) subtype kainate receptors. Does not interact with GluK2 and GluK2/K5 receptors. Low affinity to AMPA receptors (Kd = 83 µM). Does not

A potent antagonist highly selective for GluK1 (Kb = 10 nM), GluK3 (IC50 = 23 nM), and GluK1/K5 (Kb = 8 nM) subtype kainate receptors. Does not interact with GluK2 and GluK2/K5 receptors. Low affinity to AMPA receptors (Kd = 83 µM). Does not

A potent antagonist highly selective for GluK1 (Kb = 10 nM), GluK3 (IC50 = 23 nM), and GluK1/K5 (Kb = 8 nM) subtype kainate receptors. Does not interact with GluK2 and GluK2/K5 receptors. Low affinity to AMPA receptors (Kd = 83 µM). Does not

General description Nytran SPC membrane is cast uniformly on both sides of a support matrix, demonstrating excellent symmetry. This gives the membrane the ability to lie flat without curling.