Agricultural and Biological Chemistry
Online ISSN : 1881-1280
Print ISSN : 0002-1369
ISSN-L : 0002-1369
Modification at the 5-Position of 4-Deoxypyridoxol and α4-Norpyridoxol
Yasuhiro MORISAWAMitsuru KATAOKATaiichiro WATANABENoritoshi KITANOToshiaki MATSUZAWA
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1975 Volume 39 Issue 6 Pages 1275-1281

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Abstract
In an attempt to relate structure to anticoccidial activity, a number of 5-modified analogs of 4-deoxypyridoxol (4-DOP) and α4-norpyridoxol have been synthesized and their biological activities examined. The compounds prepared include the 5-(3-hydroxypropyl), 5-(2-hydroxyethyl), 5-(1-hydroxyethyl), formyl and acetyl analogs of 4-DOP, and 5-(3-hydroxypropyl), formyl, ethoxycarbonyl, carbamoyl and hydroxyl analogs of α4-norpyridoxol. Among these compounds, 4-deoxyisopyridoxal and α4-norisopyridoxal were found to exhibit anticoccidal activity.
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© Japan Society for Bioscience, Biotechnology, and Agrochemistry
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