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氨苄西林三唑和异恶唑衍生物的合成及其抗菌活性

Synthesis and antibacterial activity of triazole and isoxazole derivatives of ampicillin.

作者信息

Yasuda N, Iwagami H, Sasaki Y

出版信息

J Antibiot (Tokyo). 1983 Nov;36(11):1516-24. doi: 10.7164/antibiotics.36.1516.

Abstract

In order to improve the antibacterial activity of ampicillin, new penicillin derivatives having a 1-aryltriazole-4-carboxamide group or a 5-arylisoxazole-3-carboxamide group at the alpha-position of benzylpenicillin or p-hydroxybenzylpenicillin were synthesized. Some compounds in these series were found to possess high activity against Pseudomonas and other Gram-negative bacteria. In addition, structure-activity relationships, especially the effect of the hydrophobic character of the compounds on activity, were investigated.

摘要

为了提高氨苄西林的抗菌活性,合成了在苄青霉素或对羟基苄青霉素的α位具有1-芳基三唑-4-甲酰胺基或5-芳基异恶唑-3-甲酰胺基的新型青霉素衍生物。发现这些系列中的一些化合物对假单胞菌和其他革兰氏阴性菌具有高活性。此外,还研究了构效关系,特别是化合物的疏水特性对活性的影响。

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