Department of Pharmaceutical Chemistry, University of Dhaka , Dhaka-1000, Bangladesh.
School of Cancer and Pharmaceutical Science, King's College London , 150 Stamford Street, London SE1 9NH, U.K.
J Nat Prod. 2018 Feb 23;81(2):236-242. doi: 10.1021/acs.jnatprod.7b00377. Epub 2018 Feb 3.
Two new cis-clerodane-type furanoditerpenes, crispenes F and G (1 and 2), together with seven known compounds, were isolated from the stems of Tinospora crispa. Crispenes F and G (1 and 2) inhibited STAT3 dimerization in a cell-free fluorescent polarization assay and were found to have significant cytotoxicity against a STAT3-dependent MDA-MB 231 breast cancer cell line, while being inactive in a STAT3-null A4 cell line. These two compounds share structural similarities with a previously reported STAT3 inhibitor, crispene E, isolated from the same plant. Molecular docking studies suggested that the molecules inhibit STAT3 by interacting with its SH2 domain.
从三叶崖爬藤茎中分离得到了两个新的顺式-克氏烷型呋喃二萜类化合物,crispenes F 和 G(1 和 2),以及七个已知化合物。Crispenes F 和 G(1 和 2)在无细胞荧光偏振测定中抑制 STAT3 二聚化,并且对 STAT3 依赖性 MDA-MB 231 乳腺癌细胞系表现出显著的细胞毒性,而在 STAT3 缺失的 A4 细胞系中则无活性。这两个化合物与从同一植物中分离得到的先前报道的 STAT3 抑制剂 crispene E 具有结构相似性。分子对接研究表明,这些分子通过与 STAT3 的 SH2 结构域相互作用来抑制 STAT3。