Rahman S, Fukamiya N, Okano M, Tagahara K, Lee K H
Department of Interdisciplinary Studies on Natural Environment, Faculty of Integrated Arts and Sciences, Hiroshima University, Japan.
Chem Pharm Bull (Tokyo). 1997 Sep;45(9):1527-9. doi: 10.1248/cpb.45.1527.
In vitro evaluation of anti-tuberculosis activity was conducted for fifty-six quassinoids isolated in our laboratory from Simaroubaceous plants, Ailanthus altissima (= Aa, 10 compounds), Brucea antidysenterica (= Ba, 16 compounds), Picrasma ailanthoides (= Pa, 14 compounds), and Brucea javanica (= Bj, 16 compounds). Of the compounds tested, shinjulactone K (1), ailanthone (2), shinjudilactone (3), and dehydrobruceantin (4) were the most potent. Although the activities were very low (0-19%), the resulting data provided a picture of structure-activity relationships.
对我们实验室从苦木科植物臭椿(=Aa,10种化合物)、鸦胆子(=Ba,16种化合物)、苦木(=Pa,14种化合物)和鸦胆子(=Bj,16种化合物)中分离得到的56种苦木素类化合物进行了抗结核活性的体外评估。在所测试的化合物中,新朱内酯K(1)、臭椿酮(2)、新朱地内酯(3)和脱氢鸦胆子苦素(4)活性最强。尽管活性非常低(0 - 19%),但所得数据提供了构效关系的情况。