Diurno M V, Mazzoni O, Piscopo E, Bolognese A
Dipartimento di Chimica Farmaceutica e Tossicologica, Università di Napoli Federico II, Italy.
Farmaco. 1992 Feb;47(2):239-47.
A set of substituted 1,3,4-triaryl-2-azetidinones were synthesized and characterized. Their antimicrobial activity, against Gram+ and Gram- bacteria and Fungi, was tested. The compounds 23 and 30 showed remarkable activity against Pseudomonas aeruginosa.
合成并表征了一组取代的1,3,4-三芳基-2-氮杂环丁烷酮。测试了它们对革兰氏阳性菌、革兰氏阴性菌和真菌的抗菌活性。化合物23和30对铜绿假单胞菌表现出显著活性。
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