Lee K H, Okano M, Hall I H, Brent D A, Soltmann B
J Pharm Sci. 1982 Mar;71(3):338-45. doi: 10.1002/jps.2600710320.
A series of new bisbrusatolyl and brusatolyl esters and related compounds were synthesized and tested for in vivo antileukemia activity against a quassinoid sensitive strain of P-388 lymphocytic leukemia in BDF1 mice. The bisbrusatolyl malonate, succinate, glutarate, adipate, and sebacate were as active or more active than brusatol. The C-3 esters of brusatol and bruceantin were also found to be as active or more active than brusatol or bruceantin in general. The free hydroxyl groups at C-11 and C-12 as well as the enone double bond in ring A of both bisbrusatolyl and brusatolyl esters are required for antileukemic activity. The presence of a double bond in the ester side chain contributes to the enhanced activity of these esters.
合成了一系列新的双布鲁萨特醇酯和布鲁萨特醇酯以及相关化合物,并针对BDF1小鼠中对苦木素敏感的P-388淋巴细胞白血病菌株进行了体内抗白血病活性测试。丙二酸双布鲁萨特醇酯、琥珀酸双布鲁萨特醇酯、戊二酸双布鲁萨特醇酯、己二酸双布鲁萨特醇酯和癸二酸双布鲁萨特醇酯与布鲁萨特醇活性相当或更具活性。一般而言,布鲁萨特醇和鸦胆子丁的C-3酯也与布鲁萨特醇或鸦胆子丁活性相当或更具活性。双布鲁萨特醇酯和布鲁萨特醇酯的C-11和C-12位的游离羟基以及A环中的烯酮双键是抗白血病活性所必需的。酯侧链中双键的存在有助于增强这些酯的活性。