The important role of 4-[2-(Boc-amino)ethyl]piperidine

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 165528-81-4, help many people in the next few years.category: piperidines

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, category: piperidines, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 165528-81-4, Name is 4-[2-(Boc-amino)ethyl]piperidine, molecular formula is C12H24N2O2. In a Article, authors is Thomson, Christopher G.,once mentioned of 165528-81-4

A series of inhibitors of Autotaxin (ATX) has been developed using the binding mode of known inhibitor, PF-8380, as a template. Replacement of the benzoxazolone with a triazole zinc-binding motif reduced crystallinity and improved solubility relative to PF-8380. Modification of the linker region removed hERG activity and led to compound 12 ? a selective, high affinity, orally-bioavailable inhibitor of ATX. Compound 12 concentration-dependently inhibits autotaxin and formation of LPA in vivo, as shown in pharmacokinetic-pharmacodynamic experiments.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 165528-81-4, help many people in the next few years.category: piperidines

Reference:
Piperidine – Wikipedia,
Piperidine | C5H18442N – PubChem