未登录Design, synthesis, and characterization of a potent, nonpeptide, cell-permeable, bivalent smac mimetic that concurrently targets both the BIR2 and BIR3 domains in XIAP
Sun, Haiying; Nikolovska-Coleska, Zaneta; Lu, Jianfeng; Meagher, Jennifer L.; Yang, Chao-Yie; Qiu, Su; Tomita, York; Ueda, Yumi; Jiang, Sheng; Krajewski, Krzysztof; Roller, Peter P.; Stuckey, Jeanne A.; Wang, Shaomeng
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收藏Design and synthesis of novel and potent inhibitors of the type II transmembrane serine protease, matriptase, based upon the sunflower trypsin inhibitor-1
Li, Peng; Jiang, Sheng; Lee, Sheau-Ling; Lin, Cheng Yong; Johnson, Michael D.; Dickson, Robert B.; Michejda, Christopher J.; Roller, Peter P.
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收藏Structure-based design of flavonoid compounds as a new class of small-molecule inhibitors of the anti-apoptotic bcl-2 proteins
Tang, Guozhi; Ding, Ke; Nikolovska-Coleska, Zaneta; Yang, Chao-Yie; Qiu, Su; Shangary, Sanjeev; Wang, Renxiao; Guo, Jie; Gao, Wei; Meagher, Jennifer; Stuckey, Jeanne; Krajewski, Krzysztof; Jiang, Sheng; Roller, Peter P.; Wang, Shaomeng
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收藏Pyrogallol-based molecules as potent inhibitors of the antiapoptotic Bcl-2 proteins
Tang, Guozhi; Yang, Chao-Yie; Nikolovska-Coleska, Zaneta; Guo, Jie; Qiu, Su; Wang, Renxiao; Gao, Wei; Wang, Guoping; Stuckey, Jeanne; Krajewski, Krzysztof; Jiang, Sheng; Roller, Peter P.; Wang, Shaomeng
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收藏Structure-based design of potent small-molecule inhibitors of anti-apoptotic Bcl-2 proteins
Wang, Guoping; Nikolovska-Coleska, Zaneta; Yang, Chao-Yie; Wang, Renxiao; Tang, Guozhi; Guo, Jie; Shangary, Sanjeev; Qiu, Su; Gao, Wei; Yang, Dajun; Meagher, Jennifer; Stuckey, Jeanne; Krajewski, Krzysztof; Jiang, Sheng; Roller, Peter P.; Abaan, Hatice Ozel; Tomita, York; Wang, Shaomeng
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收藏Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction
Ding, Ke; Lu, Yipin; Nikolovska-Coleska, Zaneta; Wang, Guoping; Qiu, Su; Shangary, Sanjeev; Gao, Wei; Qin, Dongguang; Stuckey, Jeanne; Krajewski, Krzysztof; Roller, Peter P.; Wang, Shaomeng
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收藏Structure-based design of potent non-peptide MDM2 inhibitors
Ding, K; Lu, Y; Nikolovska-Coleska, Z; Qiu, S; Ding, YS; Gao, W; Stuckey, J; Krajewski, K; Roller, PP; Tomita, Y; Parrish, DA; Deschamps, JR; Wang, SM
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收藏Structure-based design of potent, conformationally constrained Smac mimetics
Sun, HY; Nikolovska-Coleska, Z; Yang, CY; Xu, L; Liu, ML; Tomita, Y; Pan, HG; Yoshioka, Y; Krajewski, K; Roller, PP; Wang, SM
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收藏Structure-based discovery of nonpeptidic small organic compounds to block the T cell response to myelin basic protein
Koehler, NKU; Yang, CY; Varady, J; Lu, YP; Wu, XW; Liu, M; Yin, DX; Bartels, M; Xu, BY; Roller, PP; Long, YQ; Li, P; Kattah, M; Cohn, ML; Moran, K; Tilley, E; Richert, JR; Wang, SM
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收藏Structure-based design, synthesis, and evaluation of conformationally constrained mimetics of the second mitochondria-derived activator of caspase that target the X-linked inhibitor of apoptosis protein/caspase-9 interaction site
Sun, HY; Nikolovska-Coleska, Z; Yang, CY; Xu, L; Tomita, Y; Krajewski, K; Roller, PP; Wang, SM
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收藏Discovery of embelin as a cell-permeable, small-molecular weight inhibitor of XLAP through structure-based computational screening of a traditional herbal medicine three-dimensional structure database
Nikolovska-Coleska, Z; Xu, L; Hu, ZJ; Tomita, Y; Li, P; Roller, PP; Wang, RX; Fang, XL; Guo, RB; Zhang, MC; Lippman, ME; Yang, DJ; Wang, SM
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