Title of article
Synthesis and morphological reversion activity on srctsNRK cells of pyrimidinylpropanamide antibiotics, sparsomycin, sparoxomycin A1, A2, and their analogues
Author/Authors
Noriyuki Nakajima، نويسنده , , Takeshi Enomoto، نويسنده , , Nobuyasu Matsuura، نويسنده , , Makoto Ubukata، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1998
Pages
4
From page
3331
To page
3334
Abstract
Three pyrimidinylpropanamide antibiotics sparsomycin (1), sparoxomycins A1, A2 (2, 3), and also six analogues (4–9) have been synthesized by employing asymmetric sulfide oxidation conditions as a key step. Sparsomycin (1) and its alkyl analogues (5–7) showed higher morphological reversion activities on srctsNMR cells than 2 and 3.
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
1998
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
789813
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