14 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Highly potent tyrosinase inhibitor, neorauflavane from Campylotropis hirtella and inhibitory mechanism with molecular docking.
Gyeongsang National University
Sulfonamide chalcone as a new class of alpha-glucosidase inhibitors.
Gyeongsang National University
Potent inhibition of bacterial neuraminidase activity by pterocarpans isolated from the roots of Lespedeza bicolor.
Gyeongsang National University
Inhibition and structural reliability of prenylated flavones from the stem bark of Morus lhou on β-secretase (BACE-1).
Gyeongsang National University
Identification of potent virtual leads to design novel indoleamine 2,3-dioxygenase inhibitors: pharmacophore modeling and molecular docking studies.
Gyeongsang National University
Tyrosinase inhibitory study of flavonolignans from the seeds of Silybum marianum (Milk thistle).
Gyeongsang National University
Inhibition of tyrosinase activity by polyphenol compounds from Flemingia philippinensis roots.
Gyeongsang National University
Chemoselective regulation of TREK2 channel: activation by sulfonate chalcones and inhibition by sulfonamide chalcones.
Gyeongsang National University
Inhibition of protein tyrosine phosphatase 1B (PTP1B) and α-glucosidase by xanthones from Cratoxylum cochinchinense, and their kinetic characterization.
Gyeongsang National University
Competitive protein tyrosine phosphatase 1B (PTP1B) inhibitors, prenylated caged xanthones from Garcinia hanburyi and their inhibitory mechanism.
Gyeongsang National University
Inhibitors of pyruvate kinase and methods of treating disease
Beth Israel Deaconess Medical Center
The natural product dihydrotanshinone I provides a prototype for uncharged inhibitors that bind specifically to the acetylcholinesterase peripheral site with nanomolar affinity.
Mayo Clinic