WT161 Low Form

WT161 Low FormWT161 is a potent, selective, and bioavailable HDAC6 inhibitor with IC50 values of 0. 4 nM, 8. 35 nM and 15. 4 nM for HDAC6, HDAC1 and HDAC2, respectively; shown to have >100 fold selectivity over other HDACs.

27 Standard Taper PYREX(r) stoppered neck and a side delivery tube

Atipamezole is a synthetic

Corning These 9

Terbinafine HCl inhibits ergosterol synthesis by inhibiting squalene epoxidase

CA-074 Me is a membrane-permeable derivative of CA-074 and acts as an irreversible cathepsin B inhibitor

norepinephrine (noradrenaline)

bipolar I depression and shows affinity for various neurotransmitter receptors including serotonin

thereby inhibiting c-Myc/Max heterodimer formation and inhibiting its transcriptional activity (IC50 = 146 µM)

50-fold selectivity against MK2 and CDK5

5 nM and 303

INO-1001 is a potent inhibitor of PARP with IC50 of <50 nM in CHO cells and a mediator of oxidant-induced myocyte dysfunction during reperfusion

Flubendazole is an autophagy inducer by targeting Atg4B