Gold(I)‐Catalyzed Selective Cyclization and 1,2‐Shift to Prepare Pseudorutaecarpine Derivatives von Wang, Wang, Chen, Nan‐Ying, Zou, Pei‐Sen, Pang, Li, Mo, Dong‐Liang, Pan, Cheng‐Xue, Su, Gui‐Fa

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Assessing IRAK4 Functions in ABC DLBCL by IRAK4 Kinase Inhibition and Protein Degradation von Zhang, Jing, Fu, Liqiang, Shen, Bin, Liu, Yingtao, Wang, Wenqian, Cai, Xin, Kong, Linglong, Yan, Yilin, Meng, Ryan, Zhang, Zhuming, Chen, Ying-Nan P., Liu, Qian, Wan, Zhao-Kui, Zhou, Tianyuan, Wang, Xiaotao, Gavine, Paul, Del Rosario, Amanda, Ahn, Kay, Philippar, Ulrike, Attar, Ricardo, Yang, Jennifer, Xu, Yanping, Edwards, James P., Dai, Xuedong

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Synthesis of spiroindolenine-3,3'-pyrrolo[2,1- b ]quinazolinones through gold(I)-catalyzed dearomative cyclization of N -alkynyl quinazolinone-tethered indoles von Wang, Wang, Zou, Pei-Sen, Pang, Li, Lei, Yao, Huang, Zi-Yi, Chen, Nan-Ying, Mo, Dong-Liang, Pan, Cheng-Xue, Su, Gui-Fa

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Allosteric Inhibition of SHP2: Identification of a Potent, Selective, and Orally Efficacious Phosphatase Inhibitor von Garcia Fortanet, Jorge, Chen, Christine Hiu-Tung, Chen, Ying-Nan P, Chen, Zhouliang, Deng, Zhan, Firestone, Brant, Fekkes, Peter, Fodor, Michelle, Fortin, Pascal D, Fridrich, Cary, Grunenfelder, Denise, Ho, Samuel, Kang, Zhao B, Karki, Rajesh, Kato, Mitsunori, Keen, Nick, LaBonte, Laura R, Larrow, Jay, Lenoir, Francois, Liu, Gang, Liu, Shumei, Lombardo, Franco, Majumdar, Dyuti, Meyer, Matthew J, Palermo, Mark, Perez, Lawrence, Pu, Minying, Ramsey, Timothy, Sellers, William R, Shultz, Michael D, Stams, Travis, Towler, Christopher, Wang, Ping, Williams, Sarah L, Zhang, Ji-Hu, LaMarche, Matthew J

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Cryptolepine and aromathecin based mimics as potent G-quadruplex-binding, DNA-cleavage and anticancer agents: Design, synthesis and DNA targeting-induced apoptosis von Yuan, Jing-Mei, Wei, Kai, Zhang, Guo-Hai, Chen, Nan-Ying, Wei, Xin-Wei, Pan, Cheng-Xue, Mo, Dong-Liang, Su, Gui-Fa

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Small-molecule antagonists of the oncogenic Tcf/β-catenin protein complex von Lepourcelet, Maina, Chen, Ying-Nan P., France, Dennis S., Wang, Huisheng, Crews, Phillip, Petersen, Frank, Bruseo, Charles, Wood, Alexander W., Shivdasani, Ramesh A.

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3-(Benzo[ d ]thiazol-2-yl)-4-aminoquinoline derivatives as novel scaffold topoisomerase I inhibitor via DNA intercalation: design, synthesis, and antitumor activities von Yuan, Jing-Mei, Chen, Nan-Ying, Liao, Hao-Ran, Zhang, Guo-Hai, Li, Xiao-Juan, Gu, Zi-Yu, Pan, Cheng-Xue, Mo, Dong-Liang, Su, Gui-Fa

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Validating cancer drug targets von Benson, John D, Chen, Ying-Nan P, Cornell-Kennon, Susan A, Dorsch, Marion, Kim, Sunkyu, Leszczyniecka, Magdalena, Sellers, William R, Lengauer, Christoph

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Allosteric inhibition of SHP2 phosphatase inhibits cancers driven by receptor tyrosine kinases von Chen, Ying-Nan P., LaMarche, Matthew J., Chan, Ho Man, Fekkes, Peter, Garcia-Fortanet, Jorge, Acker, Michael G., Antonakos, Brandon, Chen, Christine Hiu-Tung, Chen, Zhouliang, Cooke, Vesselina G., Dobson, Jason R., Deng, Zhan, Fei, Feng, Firestone, Brant, Fodor, Michelle, Fridrich, Cary, Gao, Hui, Grunenfelder, Denise, Hao, Huai-Xiang, Jacob, Jaison, Ho, Samuel, Hsiao, Kathy, Kang, Zhao B., Karki, Rajesh, Kato, Mitsunori, Larrow, Jay, La Bonte, Laura R., Lenoir, Francois, Liu, Gang, Liu, Shumei, Majumdar, Dyuti, Meyer, Matthew J., Palermo, Mark, Perez, Lawrence, Pu, Minying, Price, Edmund, Quinn, Christopher, Shakya, Subarna, Shultz, Michael D., Slisz, Joanna, Venkatesan, Kavitha, Wang, Ping, Warmuth, Markus, Williams, Sarah, Yang, Guizhi, Yuan, Jing, Zhang, Ji-Hu, Zhu, Ping, Ramsey, Timothy, Keen, Nicholas J., Sellers, William R., Stams, Travis, Fortin, Pascal D.

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Rutaecarpine analogues with potent anti-inflammation to alleviate acute ulcerative colitis via regulating TLR4/MAPK/NF-κB pathway von Qin, Li-Qing, Gu, Zi-Yu, Chen, Nan-Ying, Liu, Pei-Dong, Lan, Liu-Song, Li, Xin-Wei, Su, Jun-Cheng, Su, Gui-Fa, Mo, Dong-Liang, Pan, Cheng-Xue

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6‑Amino-3-methylpyrimidinones as Potent, Selective, and Orally Efficacious SHP2 Inhibitors von Sarver, Patrick, Acker, Michael, Bagdanoff, Jeffrey T, Chen, Zhouliang, Chen, Ying-Nan, Chan, Homan, Firestone, Brant, Fodor, Michelle, Fortanet, Jorge, Hao, Huaixiang, Hentemann, Murphy, Kato, Mitsunori, Koenig, Robert, LaBonte, Laura R, Liu, Gang, Liu, Shumei, Liu, Chen, McNeill, Eric, Mohseni, Morvarid, Sendzik, Martin, Stams, Travis, Spence, Stan, Tamez, Victoriano, Tichkule, Ritesh, Towler, Christopher, Wang, Hongyun, Wang, Ping, Williams, Sarah L, Yu, Bing, LaMarche, Matthew J

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DNA binding and antibacterial properties of ternary lanthanide complexes with salicylic acid and phenanthroline von Yue, Bin, Sun, Hui-Juan, Chen, Ying-Nan, Kong, Kai, Chu, Hai-Bin, Zhao, Yong-Liang

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Optimization of Fused Bicyclic Allosteric SHP2 Inhibitors von Bagdanoff, Jeffrey T, Chen, Zhouliang, Acker, Michael, Chen, Ying-Nan, Chan, Homan, Dore, Michael, Firestone, Brant, Fodor, Michelle, Fortanet, Jorge, Hentemann, Murphy, Kato, Mitsunori, Koenig, Robert, LaBonte, Laura R, Liu, Shumei, Mohseni, Movarid, Ntaganda, Rukundo, Sarver, Patrick, Smith, Troy, Sendzik, Martin, Stams, Travis, Spence, Stan, Towler, Christopher, Wang, Hongyun, Wang, Ping, Williams, Sarah L, LaMarche, Matthew J

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Synthesis of Rutaecarpine Analogues by Borrowing Hydrogen Strategy von Wang, Liangfeng, Zhang, Linfeng, Zhou, Chao, Gou, Tiantian, Chen, Nan‐Ying, Feng, Ke, Li, Shiqing, Su, Jun‐Cheng, Yu, Jingxian, Wang, Guixia, Kong, Xiangfei

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Enhancing the reproductive performance of tiger shrimp, Penaeus monodon, by incorporating sodium alginate in the broodstock and larval diets von Chung, Meng-Yuan, Liu, Chun-Hung, Chen, Ying-Nan, Cheng, Winton

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Selective Killing of Transformed Cells by Cyclin/Cyclin-Dependent Kinase 2 Antagonists von Chen, Ying-Nan P., Sharma, Sushil K., Ramsey, Timothy M., Jiang, Li, Martin, Mary S., Baker, Kayla, Adams, Peter D., Bair, Kenneth W., Kaelin, William G.

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Expression and functional divergence of a type-A response regulator paralog pair formed by dispersed duplication during Populus deltoides evolution von Lu, Jing, Chen, Ying-nan, Yin, Tong-ming

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A green synthesized medicine residue carbon-based iron composite for the removal of chromium (VI) and cadmium (II): Performance, kinetics and mechanism von Diao, Fa-Ming, Chen, Man-Li, Tong, Lin-Yin, Chen, Ying-Nan, Diao, Zeng-Hui

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Identification of 3-(benzazol-2-yl)quinoxaline derivatives as potent anticancer compounds: Privileged structure-based design, synthesis, and bioactive evaluation in vitro and in vi... von Liu, Qing-Qing, Lu, Ke, Zhu, Hai-Miao, Kong, Shi-Lin, Yuan, Jing-Mei, Zhang, Guo-Hai, Chen, Nan-Ying, Gu, Chen-Xi, Pan, Cheng-Xue, Mo, Dong-Liang, Su, Gui-Fa

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2-Styryl-4-aminoquinazoline derivatives as potent DNA-cleavage, p53-activation and in vivo effective anticancer agents von Wei, Xin-Wei, Yuan, Jing-Mei, Huang, Wan-Yun, Chen, Nan-Ying, Li, Xiao-Juan, Pan, Cheng-Xue, Mo, Dong-Liang, Su, Gui-Fa

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