Miyuki Kagawa scite author profile

Synthesis and Cytotoxicity of 5-Deazaflavins Containing o-and p-Quinone Moieties.-The substituent R1 has great influence on the activity of the title compounds, e.g. (III), whereas the chain length of the R2 substituent seems to be not interesting for activity. -(KIMACHI, T.; SUGITA, K.; TAMURA, Y.; KAGAWA, M.; YAMASAKI, K.; YONEDA, F.; SASAKI, T.; Bioorg. Med. Chem. Lett. 7 (1997) 6, 753-756; Fac. Pharm. Sci., Kyoto Univ., Sakyo, Kyoto 606, Japan; EN)

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Miyuki Kagawa

Nuclear magnetic resonance studies for the chiral recognition of (+)-(R)-18-crown-6-tetracarboxylic acid to amino compounds

Enantiomeric purity determination of acetyl-l-carnitine by reversed-phase high-performance liquid chromatography using chiral derivatization

Direct Enantiomeric Purity Determination of Acetyl-L-carnitine by LC with a Ligand-Exchange Chiral Stationary Phase

Enantiomeric purity determination of acetyl-l-carnitine by NMR with chiral lanthanide shift reagents

Synthesis and cytotoxicity of 5-deazaflavins containing o- and p-quinone moieties

ChemInform Abstract: Synthesis and Cytotoxicity of 5‐Deazaflavins Containing o‐ and p‐ Quinone Moieties.

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