Ukiya Motohiko, Hayakawa Teppei, Okazaki Kouta, Hikawa Maiko, Akazawa Hiroyuki, Li Wei, Koike Kazuo, Fukatsu Makoto
College of Science and Technology, Nihon University, 1-8-14 Kanda Surugadai, Chiyoda-ku, Tokyo, 101-8308, Japan.
Faculty of Pharmaceutical Science, Toho University, 2-2-1 Miyama, Funabashi-shi, Chiba, 274-8510, Japan.
Chem Biodivers. 2018 Jul;15(7):e1800113. doi: 10.1002/cbdv.201800113. Epub 2018 Jun 10.
Seventeen lanostane-type triterpenoid derivatives (2 - 18), including 11N-glycosides (8 - 18), were synthesized from the natural triterpenoid, lanosterol (1), and were evaluated for their cytotoxicity against the human cancer cell lines, HL-60, A549, and MKN45, as well as the normal human lung cells, WI-38. Among them, N-β-d-2-acetamido-2-deoxyglucoside (10) showed cytotoxicity against HL-60, A549, MKN45, and WI-38 cells (IC 0.0078 - 2.8 μm). However, N-β-d-galactoside (12) showed cytotoxicity against HL-60 and MKN45 cells (IC 0.0021 - 4.0 μm), but not the normal WI-38 cells. Furthermore, Western blot analysis suggested that 12 induces apoptosis by activation of caspases-3, 8, and 9. These results will be useful for the synthesis of other tetracyclic triterpenoids or steroid N-glycosides to increase their cytotoxicity and apoptosis-inducing activities.
从天然三萜类化合物羊毛甾醇(1)合成了17种羊毛甾烷型三萜衍生物(2 - 18),包括11种N-糖苷(8 - 18),并评估了它们对人癌细胞系HL-60、A549和MKN45以及正常人肺细胞WI-38的细胞毒性。其中,N-β-d-2-乙酰氨基-2-脱氧葡萄糖苷(10)对HL-60、A549、MKN45和WI-38细胞显示出细胞毒性(IC 0.0078 - 2.8μm)。然而,N-β-d-半乳糖苷(12)对HL-60和MKN45细胞显示出细胞毒性(IC 0.0021 - 4.0μm),但对正常WI-38细胞没有细胞毒性。此外,蛋白质印迹分析表明,12通过激活半胱天冬酶-3、8和9诱导细胞凋亡。这些结果将有助于合成其他四环三萜或甾体N-糖苷,以提高它们的细胞毒性和诱导细胞凋亡的活性。