Life Science

A synthetic intermediate for pharmaceutical synthesis.

A selective, positive allosteric modulator of mGluR2, stimulating the human and rat receptors with EC50 values of 33.2 and 96 nM, respectively can be used on cells, tissues, or animals.

A selective, positive allosteric modulator of mGluR2, stimulating the human and rat receptors with EC50 values of 33.2 and 96 nM, respectively can be used on cells, tissues, or animals.

A selective, positive allosteric modulator of mGluR2, stimulating the human and rat receptors with EC50 values of 33.2 and 96 nM, respectively can be used on cells, tissues, or animals.

An antagonist of cIAP1, cIAP2, and XIAP.

An antagonist of cIAP1, cIAP2, and XIAP.

An antagonist of cIAP1, cIAP2, and XIAP.

An antagonist of cIAP1, cIAP2, and XIAP.

A tacrine dimer, linked via a 7-carbon alkyl spacer inhibits AChE (IC50 = 0.40 nM), making it more than 1,000 times more potent than tacrine protects against hydrogen peroxide induced apoptosis in rat pheochromocytoma cells.

A tacrine dimer, linked via a 7-carbon alkyl spacer inhibits AChE (IC50 = 0.40 nM), making it more than 1,000 times more potent than tacrine protects against hydrogen peroxide induced apoptosis in rat pheochromocytoma cells.

A tacrine dimer, linked via a 7-carbon alkyl spacer inhibits AChE (IC50 = 0.40 nM), making it more than 1,000 times more potent than tacrine protects against hydrogen peroxide induced apoptosis in rat pheochromocytoma cells.

A tacrine dimer, linked via a 7-carbon alkyl spacer inhibits AChE (IC50 = 0.40 nM), making it more than 1,000 times more potent than tacrine protects against hydrogen peroxide induced apoptosis in rat pheochromocytoma cells.