17 articles for thisTarget
              
              The following articles (labelled with PubMed ID or TBD) are for your review
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Functional 1,3a,6a-triazapentalene scaffold: Design of fluorescent probes for kinesin spindle protein (KSP).

University of Shizuoka
 
Structure-Guided Design of Novel l-Cysteine Derivatives as Potent KSP Inhibitors.

University of Shizuoka
 
Structure-Activity Relationship Study on Isothiocyanates: Comparison of TRPA1-Activating Ability between Allyl Isothiocyanate and Specific Flavor Components of Wasabi, Horseradish, and White Mustard.

University of Shizuoka
 
Identification of Indole Alkaloid Structural Units Important for Stimulus-Selective TRPM8 Inhibition: SAR Study of Naturally Occurring Iboga Derivatives.

University of Shizuoka
 
Activation and inhibition of thermosensitive TRP channels by voacangine, an alkaloid present in Voacanga africana, an African tree.

University of Shizuoka
 
S-benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase.

University of Shizuoka
 
Ellagitannins and hexahydroxydiphenoyl esters as inhibitors of vertebrate squalene epoxidase.

University of Shizuoka
 
Inhibition of vertebrate squalene epoxidase by isoprenyl gallates and phenylalkyl gallates.

University of Shizuoka
 
Syntheses of 2-deoxy-2,3-didehydro-N-acetylneuraminic acid analogues modified by N-sulfonylamidino groups at the C-4 position and biological evaluation as inhibitors of human parainfluenza virus type 1.

University of Shizuoka
 
Selective inhibition of methoxyflavonoids on human CYP1B1 activity.

University of Shizuoka
 
Phenolic constituents of the aerial parts of Cimicifuga simplex and Cimicifuga japonica.

University of Shizuoka
 
Bis(hetero)aryl derivatives as unique kinesin spindle protein inhibitors.

University of Shizuoka
 
Synthesis and biological evaluation of L-cysteine derivatives as mitotic kinesin Eg5 inhibitors.

University of Shizuoka
 
Ligand Screening System for the RXRα Heterodimer Using the Fluorescence RXR Agonist CU-6PMN.

University of Shizuoka
 
Design, synthesis, and evaluation of a novel prodrug, a S-trityl-

University of Shizuoka
 
Propolis Components from Stingless Bees Collected on South Sulawesi, Indonesia, and Their Xanthine Oxidase Inhibitory Activity.

University of Shizuoka
 
Ligand-Phospholipid Conjugation: A Versatile Strategy for Developing Long-Acting Ligands That Bind to Membrane Proteins by Restricting the Subcellular Localization of the Ligand.

University of Shizuoka