Department of Chemistry , Emory University , Atlanta , Georgia 30322 , United States.
Cherry L. Emerson Centre for Scientific Computation , Emory University , Atlanta , Georgia 30322 , United States.
Org Lett. 2018 Sep 21;20(18):5922-5926. doi: 10.1021/acs.orglett.8b02599. Epub 2018 Sep 10.
Natural products from environmental microbiomes provide exquisite templates for elucidating biological activity in the search for new drugs. A recently discovered marine Brevibacillus sp. metabolite, ulbactin F, was found to inhibit tumor cell migration and invasion at IC < 3 μM. Herein, we disclose the first total synthesis of ulbactin F and epi-ulbactin F, which was modeled after the biosynthetic pathway. The scaffold bears structural similarity to siderophores of human pathogens but contains a novel tricyclic ring system derived from cysteine. We have found that ulbactin F forms low-affinity metal complexes, with a preference for Fe and Cu, which may hint both at its environmental role and its antimetastatic mechanism of action.
从环境微生物组中提取的天然产物为阐明生物活性提供了极好的模板,有助于寻找新药。最近发现的海洋 Brevibacillus sp. 代谢产物 ulbactin F 在 IC < 3 μM 时可抑制肿瘤细胞迁移和侵袭。本文首次全合成了 ulbactin F 和 epi-ulbactin F,这是基于生物合成途径进行的。该支架与人类病原体的铁载体具有结构相似性,但含有一个源自半胱氨酸的新型三环系统。我们发现 ulbactin F 形成低亲和力的金属配合物,对 Fe 和 Cu 具有偏好性,这可能暗示了它的环境作用及其抗转移作用机制。