Yang, Huibin published the artcileDesign and synthesis of thiazolylhydrazone derivatives as inhibitors of chitinolytic N-acetyl-β-D-hexosaminidase, Related Products of ethers-buliding-blocks, the main research area is thiazolylhydrazone derivative acetylhexosaminidase inhibitor mol docking.
N-acetyl-β-D-hexosaminidase (Hex) is potential target for pesticide design. Here, a series of thiazolylhydrazone derivatives were designed, synthesized and evaluated as competitive inhibitors of OfHex1, a Hex from the agricultural pest Ostrinia furnacalis. The derivative 3k, with a (benzyloxy)methyl group at the N3 atom, demonstrated greater potency with a Ki of 10.2 μM. Mol. docking anal. indicated that the (benzyloxy)methyl group of 3k was bound to a previously unexplored pocket formed by Loop 478-496. Then further optimization around naphthalene ring led to find the more potency substituent Ph. The derivative 7, with phenoxyethyl group at R1 and a Ph group at R2, demonstrated an augmented potency with a Ki of 2.1 μM. Mol. docking anal. indicated that 7 was bound to the active pocket of OfHex1 more favorably than 3k. This work suggests a novel scaffold for developing specific Hex inhibitors.
Bioorganic & Medicinal Chemistry published new progress about Drug design. 622-86-6 belongs to class ethers-buliding-blocks, name is (2-Chloroethoxy)benzene, and the molecular formula is C8H9ClO, Related Products of ethers-buliding-blocks.
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem