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Department of Applied Chemistry, Niigata University | 論文
- Costunolide and Dehydrocostus Lactone as Inhibitors of Killing Function of Cytotoxic T LymPhocytes
- A New Taxoid from a Callus Culture of Taxus cuspidata as an MDR Reversal Agent
- The Structure of a New Cardenolide Diglycoside and the Biological Activities of Eleven Cardenolide Diglycosides from Nerium oleander
- The biological activities of cardenolide triglycosides from stems, twigs, and leaves of Nerium oleander
- Synthesis and reactions of 2-arylhydrazinotropones. II. Synthesis of 5-aryltropolones and B-ring-open colchicine analogues via benzidine type rearrangement of 2-(2-arylhydrazino)tropones.
- Studies on the syntheses of sesquiterpene lactones. III. Improved synthesis of vulgarin.
- The total syntheses of chamaecynone, isochamaecynone, and dihydroisochamaecynone.
- The total syntheses of (-)-occidentalol and its C7-epimer. The stereochemical assignment of (+)-occidentalol.
- The total synthesis of hydroxyisochamaecynone and its stereochemical assignment.
- The Diazotization of 2-Aminoazulene Derivatives. The Formation of 2-Diazo-2,6-azulenoquinone Derivatives
- Santonin-Related Compound 2 Inhibits the Nuclear Translocation of NF-κB Subunit p65 by Targeting Cysteine 38 in TNF-α-Induced NF-κB Signaling Pathway
- Studies on the syntheses of sesquiterpene lactones. I. Chemical transformation of .ALPHA.-santonin into vulgarin, C4-epivulgarin, and arglanine.