Ferrarini P L, Manera C, Mori C, Badawneh M, Saccomanni G
Dipartimento di Scienze Farmaceutiche, Università degli Studi di Pisa, Italy.
Farmaco. 1998 Dec 30;53(12):741-6. doi: 10.1016/s0014-827x(98)00094-9.
Some 4-phenyl-1,8-naphthyridine derivatives with a piperazino group in the 2- and/or 7-position have been synthesized and evaluated for their tuberculostatic activity. The compounds 1, 6, 10, 17b,c and 19i showed a marked activity against Mycobacterium tuberculosis H37Rv. For this series of compounds, submitted to biological screening, no structure-activity relationship can be deduced.
已经合成了一些在2-位和/或7-位带有哌嗪基的4-苯基-1,8-萘啶衍生物,并对其抑菌活性进行了评估。化合物1、6、10、17b、c和19i对结核分枝杆菌H37Rv显示出显著活性。对于这一系列经过生物筛选的化合物,无法推断出构效关系。