作者:Thomas Philip Robinson、Richard B. Hubbard、Tedman J. Ehlers、Jack L. Arbiser、David J. Goldsmith、J. Phillip Bowen
DOI:10.1016/j.bmc.2005.03.054
日期:2005.6
It has been specifically shown to be an effective inhibitor of angiogenesis both in vitro and in vivo. Using curcumin as a lead compound for anti-angiogenic analog design, a series of structurally related compounds utilizing a substituted chalcone backbone have been synthesized and tested via an established SVR cell proliferation assay. The results have yielded a wide range of compounds that equal or
姜黄素是从香料姜黄中分离得到的天然产物,已显示出广泛的药理活性,包括某些抗癌特性。它已被明确地证明是在体外和体内血管生成的有效抑制剂。使用姜黄素作为抗血管生成类似物设计的先导化合物,已经合成了一系列利用取代的查尔酮骨架的结构相关化合物,并通过已建立的SVR细胞增殖测定法进行了测试。结果产生了范围广泛的化合物,这些化合物等于或超过姜黄素体外抑制内皮细胞生长的能力。由于它们的商业可获得性和相当简单的合成制备方法,这些低分子量化合物是开发未来血管生成抑制剂的诱人线索。