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Xiaowen Xue
Researcher at China Pharmaceutical University
Publications - 32
Citations - 444
Xiaowen Xue is an academic researcher from China Pharmaceutical University. The author has contributed to research in topics: Andrographolide & Biology. The author has an hindex of 10, co-authored 26 publications receiving 385 citations. Previous affiliations of Xiaowen Xue include University of Wisconsin-Madison & Fuzhou University.
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Journal ArticleDOI
The Strength of Parallel-Displaced Arene-Arene Interactions in Chloroform
TL;DR: Triptycene-derived compounds have been prepared to serve as conformational equilibrium reporters for direct measurements of arene-arene interactions in the parallel-displaced orientation and free energies derived from the syn/anti ratios in chloroform range from slightly positive to considerably negative values.
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Synthesis of CDDO-amino acid-nitric oxide donor trihybrids as potential antitumor agents against both drug-sensitive and drug-resistant colon cancer.
Yong Ai,Fenghua Kang,Zhangjian Huang,Xiaowen Xue,Yisheng Lai,Sixun Peng,Jide Tian,Yihua Zhang +7 more
TL;DR: Together, 4c is a novel trihybrid with potent antitumor activity and may be a promising candidate for the treatment of drug-resistant colon cancer.
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Off-Center Oxygen−Arene Interactions in Solution: A Quantitative Study
TL;DR: Triptycenes with C1-MeO/RCOO and C9-XC6H4CH2 have been prepared to determine lone pair-arene interactions in the off-center configuration, and compound 7 in the ester series with X = H and R = CF3 is the only compound that shows a slightly repulsive interaction.
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Synthesis and anticancer activity of some novel indolo[3,2-b]andrographolide derivatives as apoptosis-inducing agents
TL;DR: Preliminary anti-cancer mechanistic investigation was performed in terms of the cell cycle arrest and cell apoptosis assays of compound 6l against HCT116 using flow cytometry, and the results suggested that compounds 6l inhibited tumor proliferation through inducing early and late cellular apoptosis in a concentration-dependent manner and causing cell cycle Arrest in the S-phase.
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Synthesis and in vitro cytotoxicity of andrographolide-19-oic acid analogues as anti-cancer agents
TL;DR: The preliminary results indicated that the oxidation of C-19-hydroxyl group of andrographolide to corresponding carboxyl group and the subsequent esterification of the formed carboxylic acid led to considerable improvement in cytotoxicity against the cancer cells.