スポンサーリンク
School Of Pharmacy National Defense Medical Center | 論文
- Antioxidative and Anti-Inflammatory Activities of Polyhydroxyflavonoids of Scutellaria baicalensis GEORGI
- Novel Synthesis of Flavonoids of Scutellaria baicalensis GEORGI
- HIV-1 Integrase Inhibition of Biscoumarin Analogues
- Synthesis and Antitumor Activity of 1,8-Diaminoanthraquinone Derivatives
- Synthesis and Antitumor Evaluation of Symmetrical 1,5-Diamidoanthraquinone Derivatives as Compared to Their Disubstituted Homologues
- Synthesis of Symmetrical 1,5-bis-thio-Substituted Anthraquinones for Cytotoxicity in Cultured Tumor Cells and Lipid Peroxidation
- Studies on Anthracenes.2.Synthesis and Cytotoxic Evaluation of 9-Acyloxy 1, 8-Dichloroanthracene Derivatives
- New Constituent from Podocarpus macrophyllus var. macrophyllus Shows Anti-tyrosinase Effect and Regulates Tyrosinase-Related Proteins and mRNA in Human Epidermal Melanocytes
- Small-Molecule Anthracene-Induced Cytotoxicity and Induction of Apoptosis through Generation of Reactive Oxygen Species(Medicinal Chemistry)
- Glycosides from Paeonia suffruticosa
- Synthesis and HIV-1 Integrase Inhibition of Novel Bis- or Tetra-Coumarin Analogues
- Synthesis and Human Telomerase Inhibition of a Series of Regioisomeric Disubstituted Amidoanthraquinones
- Determination of anticancer drug vitamin K_3 in plasma by high-performance liquid chromatography
- Stduies on Anthracenes.3.Synthesis, Lipid Peroxidation and Cytotoxic Evaluation of 10-Substituted 1, 5-Dichloro-9(10H)-anthracenone Derivatives
- Studies on Anthracenes. 1. Human Telomerase Inhibition and Lipid Peroxidation of 9-Acyloxy 1, 5-Dichloroanthracene Derivatives
- Chemical Constituents of Taraxacum formosanum
- Synthesis of Selenium-Containing Polyphenolic Acid Esters and Evaluation of Their Effects on Antioxidation and 5-Lipoxygenase Inhibition
- Evaluation of Polyphenolic Acid Esters as Potential Antioxidants(Medicinal Chemistry)
- Synthesis and Biological Evaluation of Ebselen and Its Acyclic Derivatives
- Synthesis and Biological Activity of Sulfur-Containing Aryl-aldehyde Schiff Bases