沼沢光輝 | Tohoku College Of Pharmacy

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著作論文

Conformational Analysis of 19-Oxygenated Steroids with a 4-Ene or 2,4-Diene Structure, Potential Intermediates of Aromatase Reaction, with Semiempirical Molecular Orbital PM3 Calculations
Biochemical Studies of Estr-4-ene-3,6,17-trione and 5α-Androstan-17-ones with or without a Carbonyl Function at C-3 and/or C-6 as Aromatase Inhibitors
Synthesis of Deuterium-Labeled 16α, 19-Dihydroxy C_ Steroids as Internal Standards for Gas Chromatography-Mass Spectrometry
A Radiometric Assay Method for Aromatase Activity Using [1β-^3H]16α-Hydroxyandrostenedione
Competitive Inhibition and Suicide Inactivation of Human Placental Aromatase by Androst-4-ene-3,6-dione Derivatives and 3α-Methoxyandrost-4-ene-6,17-dione
Synthesis of 16α-Hydroxyandrost-4-ene-3,17,19-trione and 3β, 16α-Dihydroxyandrost-5-ene-17,19-dione : Potential Intermediates of Estriol Biosynthesis
Oxygenation of 2,4-Dibromoestrogens with Nitric Acid : A New Synthesis of 19-Nor Steroids
Radioimmunoassay of 2-Hydroxyestrone Using Antisera Raised against Antigenic Complexs Obtained by Convenient Methods
Time-Dependent Inactivation of Human Placental Aromatase by Bromoacetoxy 4-Androsten-3-ones in the Presence of Reduced Nicotinamide Adenine Dinucleotide Phosphate (NADPH)
Reactions of Enolizable Steroidal 4-En-3-ones and 17-Ones with Hypervalent Iodine
Stereospecific 1,2-Hydride Shift in the Rearrangement of 16β-Hydroxy-17-oxo Steroids to 17β-Hydroxy-16-ones with Acid and Base(Organic,Chemical)
Preparation of [1,2-^3H,4-^C]16α-Hydroxyandrostenedione and Its Use for Radiometric Determination of Human Placental Aromatase Activity(Analytical,Chemical)
Regiospecific Deoxygenation of the Dihydroxyacetone Moiety at C-17 of Corticoid Steroids with Iodotrimethylsilane
Reaction of 21-Bromo-17α-methoxy-20-ketopregnenes with Sodium Methoxide or Potassium Acetate
Synthesis of Deuterium-Labelled 16α-Hydroxy-4-androstene-3,17-dione and 16α-Hydroxydehydroepiandrosterone
Synthesis of Deuterium-labelled Estriol, 16α-Hydroxyestrone and Estriol 16-Glucuronide via 2,4,16α-Tribromoestrone as Internal Standards for Mass Fragmentography

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