Magnesium salicylate/phenyltoloxamine

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.

BIS(CYCLOPENTADIENYL)MAGNESIUM.

Bis(cyclopentadienyl)magnesium(II).

An activator of the P2X receptors that exhibits 5-30-fold greater potency at the P2X7 receptor than ATP activates the human, rat, and mouse receptors with EC₅₀ values of 0.7, 3.6, and 285 &muM, respectively.

A potent, selective inhibitor of mTOR.

A potent, selective inhibitor of mTOR.

A potent, selective inhibitor of mTOR.

A potent, selective inhibitor of mTOR.

CCI-006 is a selective inhibitor and chemosensitizer of MLL-rearranged leukemia cells, by inhibits mitochondrial respiration resulting in insurmountable mitochondrial depolarization and a pro-apoptotic unfolded protein response (UPR) in a subset of

CCI-006 is a selective inhibitor and chemosensitizer of MLL-rearranged leukemia cells, by inhibits mitochondrial respiration resulting in insurmountable mitochondrial depolarization and a pro-apoptotic unfolded protein response (UPR) in a subset of

CCI-006 is a selective inhibitor and chemosensitizer of MLL-rearranged leukemia cells, by inhibits mitochondrial respiration resulting in insurmountable mitochondrial depolarization and a pro-apoptotic unfolded protein response (UPR) in a subset of