Biologically Active Small Molecules

A potent dopamine receptor agonist that binds the D2 receptor with highest affinity (Ki = 2.5 nM) avidly binds the serotonin receptors 5-HT1A and 5-HT1D (Ki = 12.9 and 10.7 nM, respectively), as well as &alpha and &beta adrenoreceptors.

A potent dopamine receptor agonist that binds the D2 receptor with highest affinity (Ki = 2.5 nM) avidly binds the serotonin receptors 5-HT1A and 5-HT1D (Ki = 12.9 and 10.7 nM, respectively), as well as &alpha and &beta adrenoreceptors.

A potent dopamine receptor agonist that binds the D2 receptor with highest affinity (Ki = 2.5 nM) avidly binds the serotonin receptors 5-HT1A and 5-HT1D (Ki = 12.9 and 10.7 nM, respectively), as well as &alpha and &beta adrenoreceptors.

A potent dopamine receptor agonist that binds the D2 receptor with highest affinity (Ki = 2.5 nM) avidly binds the serotonin receptors 5-HT1A and 5-HT1D (Ki = 12.9 and 10.7 nM, respectively), as well as &alpha and &beta adrenoreceptors.

BEL is a selective, irreversible, mechanism-based inhibitor of iPLA2 with a Ki value of 180 nM. It inhibits macrophage iPLA2 in a concentration-dependent manner with an IC₅₀ value of 60 nM.

BEL is a selective, irreversible, mechanism-based inhibitor of iPLA2 with a Ki value of 180 nM. It inhibits macrophage iPLA2 in a concentration-dependent manner with an IC₅₀ value of 60 nM.

BEL is a selective, irreversible, mechanism-based inhibitor of iPLA2 with a Ki value of 180 nM. It inhibits macrophage iPLA2 in a concentration-dependent manner with an IC₅₀ value of 60 nM.

BEL is a selective, irreversible, mechanism-based inhibitor of iPLA2 with a Ki value of 180 nM. It inhibits macrophage iPLA2 in a concentration-dependent manner with an IC₅₀ value of 60 nM.

An internal standard for the quantification of BEL by GC- or LC-MS.

An internal standard for the quantification of BEL by GC- or LC-MS.

An internal standard for the quantification of BEL by GC- or LC-MS.

Commonly used as a pH indicator, a color marker in agarose or polyacrylamide gel electrophoresis, and a dye to detect proteins and nucleic acids (absorbance at 610 nm), particularly when staining living tissues.