Magnesium salicylate/phenyltoloxamine

DMEOB is a negative allosteric modulator at mGluR-5. DMEOB exhibits reversible noncompetitive inhibition of mGluR-5-mediated responses. In general, group I metabotropic glutamate receptors are coupled to G|q/11|and are activators of phospholipase C.

DMEOB is a negative allosteric modulator at mGluR-5. DMEOB exhibits reversible noncompetitive inhibition of mGluR-5-mediated responses. In general, group I metabotropic glutamate receptors are coupled to G|q/11|and are activators of phospholipase C.

DMEOB is a negative allosteric modulator at mGluR-5. DMEOB exhibits reversible noncompetitive inhibition of mGluR-5-mediated responses. In general, group I metabotropic glutamate receptors are coupled to G|q/11|and are activators of phospholipase C.

Eosin Y, a red xanthene dye, has been noted to reduce the affinity of Mg2+-ATPase for ATP and increase the enzyme affinity for Mg2+ at concentrations of 10-50 μM. At higher concentrations near 100 μM the affinity for Mg2+-ATPase for the

Potent and selective negative allosteric modulator of mGlu1receptors.

Potent and selective negative allosteric modulator of mGlu1receptors.

Potent and selective negative allosteric modulator of mGlu1receptors.

Potent and selective negative allosteric modulator of mGlu1receptors.

GMP Human FLT3 Ligand, 100 æg

GMP Human FLT3 Ligand, 50 æg

KU-0063794 is a potent and highly specific dual-mTOR inhibitor of mTORC1 and mTORC2 with IC50 of ~10 nM in cell-free assays: no effect on PI3Ks.A FRAP (mTOR) inhibitor for both mTORC1 and mTORC2.

KU-0063794 is a potent and highly specific dual-mTOR inhibitor of mTORC1 and mTORC2 with IC50 of ~10 nM in cell-free assays: no effect on PI3Ks.A FRAP (mTOR) inhibitor for both mTORC1 and mTORC2.