Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Studies on Viomycin. IX. Amino Acid Derivatives of Viomycin
北川 常廣三浦 孝子高石 千恵子谷山 兵三
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1976 年 24 巻 6 号 p. 1324-1330

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The limited acylations of I on the two amino functions of β-lysine residue with protected amino acid active esters followed by de-protection by catalytic hydrogenolyses resulted N1-amino acid acylated viomycins. While, the limited carbobenzoxylation followed by the reaction with dicarbobenzoxylysine active ester and the decarbobenzoxylation gave N6-acylated product VI. Antimicrobial assay of the above obtained derivatives result that neutral amino acid derivatives of I have reduced potencies while, basic amino acid derivatives possess almost the similar potencies with I in vitro and in vivo tests. Thus, one of the provable reason for the importance of the two free amino functions of β-lysine residue for the exhibition of the potency of I is concluded to be due to their basicity.
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© The Pharmaceutical Society of Japan
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