Eisai Research Institute of Boston, 4 Corporate Drive, Andover, MA 01810, USA.
Bioorg Med Chem Lett. 2009 Nov 1;19(21):6196-9. doi: 10.1016/j.bmcl.2009.08.096. Epub 2009 Sep 3.
With bioactivity-guided phenotype screenings, a potent anti-inflammatory compound f152A1 has been isolated, characterized and identified as the known natural product LL-Z1640-2. Metabolic instability precluded its use for the study on animal disease models. Via total synthesis, a potent, metabolically stabilized analog ER-803064 has been created; addition of the (S)-Me group at C4 onto f152A1 has resulted in a dramatic improvement on its metabolic stability, while preserving the anti-inflammatory activities.
通过生物活性导向的表型筛选,分离得到了一种有效的抗炎化合物 f152A1,并对其进行了鉴定,确定为已知天然产物 LL-Z1640-2。由于代谢不稳定性,该化合物不能用于动物疾病模型的研究。通过全合成,得到了一种有效的、代谢稳定的类似物 ER-803064;在 f152A1 的 C4 位上加上(S)-Me 基团,显著提高了其代谢稳定性,同时保持了抗炎活性。