Diiodotyrosine

A natural quinoid diterpene that, at 10-20 &microM, stimulates AMPK in C2C12 myotubes and activates p38 MAPK in DU145 cells inhibits SHP2 in vitro (IC₅₀ = 22.5 &microM) and, at 4-8 &microM, blocks phosphorylation of STAT3 in MC-3

A natural quinoid diterpene that, at 10-20 &microM, stimulates AMPK in C2C12 myotubes and activates p38 MAPK in DU145 cells inhibits SHP2 in vitro (IC₅₀ = 22.5 &microM) and, at 4-8 &microM, blocks phosphorylation of STAT3 in MC-3

A natural quinoid diterpene that, at 10-20 &microM, stimulates AMPK in C2C12 myotubes and activates p38 MAPK in DU145 cells inhibits SHP2 in vitro (IC₅₀ = 22.5 &microM) and, at 4-8 &microM, blocks phosphorylation of STAT3 in MC-3

Deoxyneocryptotanshinone

DESTHIOPHENERIVAROXABAN PHTHALIMODO ANALOG

InformationDidanosine Didanosine is a reverse transcriptase inhibitor with an IC50 of 0.49 μM.In vitroDidanosine induces cytoplasmic lipid droplet accumulations, increases lactate production and decreases activities of COX (complex IV) and SDH (part

Dihydrotanshinone I.

DIPYRIDYL DITHIOCARBONATE

Droperidol is a potent antagonist of dopamine subtype 2 receptors in the limbic system.A D1DR and D2DR inhibitor.

A butyrophenone that acts as an antagonist at dopamine receptors (Kis = 0.25 and 0.84 nM at human D2 and D4) less potently inhibits the human voltage-gated potassium channel (IC₅₀ = 32 nM).

A butyrophenone that acts as an antagonist at dopamine receptors (Kis = 0.25 and 0.84 nM at human D2 and D4) less potently inhibits the human voltage-gated potassium channel (IC₅₀ = 32 nM).

A butyrophenone that acts as an antagonist at dopamine receptors (Kis = 0.25 and 0.84 nM at human D2 and D4) less potently inhibits the human voltage-gated potassium channel (IC₅₀ = 32 nM).