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2000
Volume 13, Issue 1
  • ISSN: 1570-1794
  • E-ISSN: 1875-6271

Abstract

Novel α-amino acids bearing 1,2,4-triazinone and steroidal moieties (N,C-disubstituted glycine) (5a and 5b) and the related systems (6 and 7) have been produced from condensation of 6-(8-aminophenyl)-4-phenyl-3-thioxo-1,2,4-triazin(2H)-5-one (1) with the selective steroids, 5-α-Androstan-17β-ol-3-one (2a) and Transandrosterone (2b) followed by addition of hydrocyanic acid and acidic hydrolysis. A nucleophilic substitution of mercapto group by 4-fluoro aniline and sulfanilamide of 5 afforded the corresponding α-amino acids 6 and 7. These newly synthesis compounds are further evaluated for enzymatic effects against some fungi (Cellobiase activity).

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/content/journals/cos/10.2174/1570179412666150703162953
2016-02-01
2025-06-26
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/content/journals/cos/10.2174/1570179412666150703162953
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  • Article Type:
    Research Article
Keyword(s): cellobiase activities; steroid; Synthesis α-amino acids; transandrosterone; triazine
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