Krapcho A P, Landi J J, Shaw K J, Phinney D G, Hacker M P, McCormack J J
J Med Chem. 1986 Aug;29(8):1370-3. doi: 10.1021/jm00158a008.
A number of unsymmetrically substituted 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones have been synthesized and evaluated for their antitumor activity against L1210 in vitro and in vivo. The high activity of several compounds observed in vitro was not paralleled by comparable activity in vivo. The activities of the substituted 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones as inhibitors of cell growth were generally much higher than those of the related 1-[(aminoalkyl)amino]-4-methoxyanthracene-9,10-diones, and this correlated with the relative abilities of compounds of the two types to interact with calf thymus DNA.
已合成了多种不对称取代的1,4 - 双[(氨基烷基)氨基]蒽 - 9,10 - 二酮,并对其在体外和体内对L1210的抗肿瘤活性进行了评估。在体外观察到的几种化合物的高活性在体内并未表现出相应的活性。取代的1,4 - 双[(氨基烷基)氨基]蒽 - 9,10 - 二酮作为细胞生长抑制剂的活性通常远高于相关的1 - [(氨基烷基)氨基] - 4 - 甲氧基蒽 - 9,10 - 二酮,这与这两种类型的化合物与小牛胸腺DNA相互作用的相对能力相关。