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羊毛甾烷型三萜类 N-糖苷的合成及其对人癌细胞系的细胞毒性

Synthesis of Lanostane-Type Triterpenoid N-Glycosides and Their Cytotoxicity against Human Cancer Cell Lines.

作者信息

Ukiya Motohiko, Hayakawa Teppei, Okazaki Kouta, Hikawa Maiko, Akazawa Hiroyuki, Li Wei, Koike Kazuo, Fukatsu Makoto

机构信息

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.

出版信息

Chem Biodivers. 2018 Jul;15(7):e1800113. doi: 10.1002/cbdv.201800113. Epub 2018 Jun 10.

Abstract

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.

摘要

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。

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