Hopp D C, Alali F Q, Gu Z M, McLaughlin J L
Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN 47907-1333, USA.
Bioorg Med Chem. 1998 May;6(5):569-75. doi: 10.1016/s0968-0896(98)00018-2.
Continuing work on the bioactivity-directed fractionation of the bark of Annona squamosa has resulted in the discovery of three new Annonaceous acetogenins, (2,4-cis and trans)-squamolinone (1), (2,4-cis and trans)-9-oxoasimicinone (2), and bullacin B (3). Compounds 1-3 are all adjacent bis-THF ring acetogenins with 2 representing the first bis-ring acetogenin to contain a carbonyl along its aliphatic chain. Compound 3 was selectively cytotoxic in a panel of six human tumor cell lines with a potency of nearly a million times that of adriamycin against the MCF-7 (human breast adenocarcinoma) cell line.
对番荔枝树皮进行生物活性导向分级分离的持续研究,已发现三种新的番荔枝乙酰精宁,即(2,4-顺式和反式)-鳞叶酮(1)、(2,4-顺式和反式)-9-氧代阿西米酮(2)和布拉西辛B(3)。化合物1-3均为相邻的双四氢呋喃环乙酰精宁,化合物2是首个在其脂肪链上含有羰基的双环乙酰精宁。化合物3在一组六种人类肿瘤细胞系中具有选择性细胞毒性,其效力比阿霉素对MCF-7(人乳腺腺癌)细胞系的效力高近一百万倍。