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Biochemistry, Biophysics, and Structural Biology Commons

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Chemistry Faculty Publications

Fordham University

1955

Articles 1 - 3 of 3

Full-Text Articles in Biochemistry, Biophysics, and Structural Biology

Ultraviolet Absorption Spectra Of Derivatives Of 2,3,5- And 2,4,5-Trihydroxyacetophenone / By D. D. Clarke And F. F. Nord, Donald Dudley Clarke Phd, Friedrich F. Nord Jan 1955

Ultraviolet Absorption Spectra Of Derivatives Of 2,3,5- And 2,4,5-Trihydroxyacetophenone / By D. D. Clarke And F. F. Nord, Donald Dudley Clarke Phd, Friedrich F. Nord

Chemistry Faculty Publications

No abstract provided.


Radicinin: A Metabolite From Stemphylium Radicinum. Ii. On The Mechanism Of Its Biosynthesis / D. D. Clarke And F. F. Nord From The Department Of Organic Chemistry And Enzymology, Fordham University, New York, New York, Donald Dudley Clarke Phd, Friedrich F. Nord Jan 1955

Radicinin: A Metabolite From Stemphylium Radicinum. Ii. On The Mechanism Of Its Biosynthesis / D. D. Clarke And F. F. Nord From The Department Of Organic Chemistry And Enzymology, Fordham University, New York, New York, Donald Dudley Clarke Phd, Friedrich F. Nord

Chemistry Faculty Publications

After studying the effect of various substrates and also of certain enzyme inhibitors on the rate of formation of radicinin by Sterad, it is suggested that the carbohydrate molecule is utilized intact in the biosynthesis of radicinin


Radicinin: A Metabolite From Stemphylium Radicinum. I. Chemistry And Action / D. D. Clarke And F. F. Nord From The Department Of Organic Chemistry And Enzymology, Fordham University, New York, New York, Donald Dudley Clarke Phd, Friedrich F. Nord Jan 1955

Radicinin: A Metabolite From Stemphylium Radicinum. I. Chemistry And Action / D. D. Clarke And F. F. Nord From The Department Of Organic Chemistry And Enzymology, Fordham University, New York, New York, Donald Dudley Clarke Phd, Friedrich F. Nord

Chemistry Faculty Publications

The conditions for the growth of Sterad and isolation of radicinin are described. The formula C12H1205 wasas established for this compound by preparation and analyses of several derivatives. Degradation and spectrophotometric studies were employed to establish the molecular formula. Studies on the mode of action of radicinin revealed that it caused an increase in the rate of dehydrogenation of isopropyl alcohol by FIB, but that it had no effect on the quantity or degree of desaturation of the fat synthesized by FIB