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Neolignans from the Arils of Myristica fragrans as Potent Antagonists of CC Chemokine Receptor 3.

Kindai University

Hydrophobic substituents increase the potency of salacinol, a potenta-glucosidase inhibitor from Ayurvedic traditional medicine 'Salacia'.

Kindai University

Enhanced inhibitory activity of compounds containing purine scaffolds compared to protein kinase CK2α considering crystalline water.

Kindai University

Discovery of pimozide derivatives as novel T-type calcium channel inhibitors with little binding affinity to dopamine D

Kindai University

Elongation of the side chain by linear alkyl groups increases the potency of salacinol, a potent α-glucosidase inhibitor from the Ayurvedic traditional medicine "Salacia," against human intestinal maltase.

Kindai University

STAT3 inhibitory activity of naphthoquinones isolated from Tabebuia avellanedae.

Kindai University

Synthesis and biological evaluation of histone deacetylase and DNA topoisomerase II-Targeted inhibitors.

Kindai University