16 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Structural and computational study on inhibitory compounds for endonuclease activity of influenza virus polymerase.
Chiba University
9-Hydroxycanthin-6-one, aß-Carboline Alkaloid from Eurycoma longifolia, Is the First Wnt Signal Inhibitor through Activation of Glycogen Synthase Kinase 3ß without Depending on Casein Kinase 1a.
Chiba University
Hedgehog/GLI-mediated transcriptional inhibitors from Zizyphus cambodiana.
Chiba University
Sesquiterpenoids and plasmin-inhibitory flavonoids from Blumea balsamifera.
Chiba University
Discovery of indole alkaloids with cannabinoid CB1 receptor antagonistic activity.
Chiba University
Derivatives of 5-nitro-furan-2-carboxylic acid carbamoylmethyl ester inhibit RNase H activity associated with HIV-1 reverse transcriptase.
Chiba University
Sticklac-Derived Natural Compounds Inhibiting RNase H Activity of HIV-1 Reverse Transcriptase.
Chiba University
Design, synthesis, and pharmacological evaluation of 2-(4-sulfonylphenyl)-2-[(E)-pyrrolidin-1-ylimino]-N-thiazoleacetamides as glucokinase activators.
Chiba University
In vitro and in vivo evaluation of polymethylene tetraamine derivatives as NMDA receptor channel blockers.
Chiba University
Structural and biochemical study on the inhibitory activity of derivatives of 5-nitro-furan-2-carboxylic acid for RNase H function of HIV-1 reverse transcriptase.
Chiba University
Design, synthesis, and biological evaluation of tricyclic heterocycle-tetraamine conjugates as potent NMDA channel blockers.
Chiba University
Studies on the synthesis and opioid agonistic activities of mitragynine-related indole alkaloids: discovery of opioid agonists structurally different from other opioid ligands.
Chiba University