Click Glycosylation for the Synthesis of 1,2,3-Triazole-Linked Picropodophyllotoxin Glycoconjugates and Their Anticancer Activity
文献类型：期刊论文
| 作者 | Zi, Cheng-Ting1; Yang, Liu2; Gao, Wei2; Li, Yan2 ; Zhou, Jun2; Ding, Zhong-Tao3; Hu, Jiang-Miao2; Jiang, Zi-Hua4
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| 刊名 | CHEMISTRYSELECT
 |
| 出版日期 | 2017-07-21 |
| 卷号 | 2期号:18页码:5038-5044 |
| ISSN号 | 2365-6549 |
| 关键词 | Anticancer Activity Cu(i)-catalyzed Click Reaction Glycoconjugates Picropodophyllotoxin Podophyllotoxin |
| DOI | 10.1002/slct.201700347 |
| 英文摘要 | Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction was employed successfully to prepare a series 4 beta-triazole-linked picropodophyllotoxin glycoconjugates (25 - 34). Maltose residue, 1,6-beta-D-diglucose residue, and several triazole-linked disaccharide and trisaccharide residues were coupled to 4 beta-azido-podophyllotoxin derivatives through click glycosylation strategy. The initial click glycosylation products were treated with catalytic amount of NaOCH3 to facilitate global deacylation and epimerization at C-2 position to yield the cis-gamma-lactone moiety in the picropodophyllotoxin glycoconjugates. Most of these picropodophyllotoxin glycoconjugates show weak cytotoxicity (IC50 > 40 mu M) against a panel of five human cancer cell lines (HL-60, SMMC-7721, A-549, MCF-7, SW480) as indicated by in vitro MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay. However, compound 27 that contains a 1,6-beta-D-di-glucose residue displays strong anticancer activity against all cancer cell lines tested, with IC50 values ranging from 0.67 to 7.41 mu M, which is significantly more potent than the control drug etoposide against four of the five cancer cells tested. Structure activity relationship analysis suggests that the 4'-O-methyl group on the E ring of podophyllotoxin scaffold is perhaps important for the anticancer activity of glycosylated picropodophyllotoxin derivatives with a cis-g-lactone moiety. |
| 学科主题 | Chemistry, Multidisciplinary |
| 语种 | 英语 |
| WOS记录号 | WOS:000406674900009 |
| 源URL | [http://ir.kib.ac.cn/handle/151853/54940]  |
| 专题 | 昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室 |
| 作者单位 | 1.Yunnan Agr Univ, Key Lab Pu Er Tea Sci, Minist Educ, Kunming 650201, Yunnan, Peoples R China 2.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China 3.Yunnan Univ, Sch Chem Sci & Technol, Key Lab Med Chem Nat Resource, Minist Educ, Kunming 650091, Yunnan, Peoples R China 4.Lakehead Univ, Dept Chem, 955 Oliver Rd, Thunder Bay, ON P7B 5E1, Canada |
| 推荐引用方式 GB/T 7714 | Zi, Cheng-Ting,Yang, Liu,Gao, Wei,et al. Click Glycosylation for the Synthesis of 1,2,3-Triazole-Linked Picropodophyllotoxin Glycoconjugates and Their Anticancer Activity[J]. CHEMISTRYSELECT,2017,2(18):5038-5044. |
| APA | Zi, Cheng-Ting.,Yang, Liu.,Gao, Wei.,Li, Yan.,Zhou, Jun.,...&Jiang, Zi-Hua.(2017).Click Glycosylation for the Synthesis of 1,2,3-Triazole-Linked Picropodophyllotoxin Glycoconjugates and Their Anticancer Activity.CHEMISTRYSELECT,2(18),5038-5044. |
| MLA | Zi, Cheng-Ting,et al."Click Glycosylation for the Synthesis of 1,2,3-Triazole-Linked Picropodophyllotoxin Glycoconjugates and Their Anticancer Activity".CHEMISTRYSELECT 2.18(2017):5038-5044. |
入库方式： OAI收割
来源：昆明植物研究所
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