Donitriptan hydrochloride

Powerful silylating agent Reagent for N-acetyl-N, trimethylsilyl, N-trimethylsilyl-N-triflu?oroacetyl, and O-trimethylsilyl (TMS)Derivatisation of Non-Steroidal Anti-Inflammatory Drugs with Activated Silylating Reagents Suitable for the

Powerful silylating agent Reagent for N-acetyl-N, trimethylsilyl, N-trimethylsilyl-N-triflu?oroacetyl, and O-trimethylsilyl (TMS)Derivatisation of Non-Steroidal Anti-Inflammatory Drugs with Activated Silylating Reagents Suitable for the

Powerful silylating agent Reagent for N-acetyl-N, trimethylsilyl, N-trimethylsilyl-N-triflu?oroacetyl, and O-trimethylsilyl (TMS)Derivatisation of Non-Steroidal Anti-Inflammatory Drugs with Activated Silylating Reagents Suitable for the

A reversible, selective S-COMT inhibitor (IC₅₀s = 300 and 20 nM in rat liver and brain, respectively) reduces 3-OMD formation and elevates serum and brain L-DOPA, dopamine, and DOPAC levels at 3&ndash30 mg/kg in rats when combined with

Biochem/physiol Actions Noladin ether (2-Arachidonyl glycerol ether) is a stable analog of the endogenous cannabanoid 2-Arachidonylglycerol (2-AG) with selectivity for CB1 receptors. Noladin ether is a CB1 agonist.

Biochem/physiol Actions Noladin ether (2-Arachidonyl glycerol ether) is a stable analog of the endogenous cannabanoid 2-Arachidonylglycerol (2-AG) with selectivity for CB1 receptors. Noladin ether is a CB1 agonist.

Noladin ether (2-Arachidonyl glycerol ether) is a stable analog of the endogenous cannabanoid 2-Arachidonylglycerol (2-AG) with selectivity for CB1 receptors. Noladin ether is a CB1 agonist. The Ki values for CB1 vs CB2 receptors are 21.2 nM and 3

Biochem/physiol Actions Nonyloxytryptamine (5-nonyloxytryptamine) is a potent and selective 5-HT1B receptor agonist. Nonyloxytryptamine is a polysialic acid (PSA) mimick that triggers PSA-mediated functions.

Biochem/physiol Actions Nonyloxytryptamine (5-nonyloxytryptamine) is a potent and selective 5-HT1B receptor agonist. Nonyloxytryptamine is a polysialic acid (PSA) mimick that triggers PSA-mediated functions.

A selective D1 dopamine receptor agonist.

Less active enantiomer of (±)-SKF-38393: D1 dopamine receptor agonist.

Biochem/physiol Actions T-0080 is a blood-brain barrier (BBB)-permeable formyl peptide receptor 1 (FPR1) antagonist that effectively inhibits fMLF-dependent response in human and murine neutrophils cultures (10 nM fMLF-induced human neutrophil