Thiabendazole uoroacetate salt It displays >200 fold selectivity

It displays >200 fold selectivity over other HDAC isoforms 1

Smiles: CC(C)(C)OC1=CC=CC2=NC(N)=NC(N)=C21

orientated in such a way to enable potential nucleophilic attack on the carbonyl of the amide bond by the hydroxyl of MoCo

InChiKey: FPPNZSSZRUTDAP-UWFZAAFLSA-N

It can enhance survival of human embryonic stem cells (hESCs) or iPSCs after single cell dissociation by trypsin

Thiabendazole uoroacetate salt It displays >200 fold selectivityThiabendazole is a fungicide and parasiticide. Tiabendazole works by inhibition of the mitochondrial, helminth specific enzyme, fumarate reductase, with possible interaction with endogenous quinone. Tiabendazole serves to block angiogenesis in both frog embryos and human cells. It has also been shown to serve as a vascular disrupting agent to reduce newly established blood vessels. Tiabendazole has been shown to effectively do this in certain cancer