Fengtian Xue, Ph.D.
Affiliations: | 2007 | Brown University, Providence, RI |
Area:
molecular recognition in biological systemsGoogle:
"Fengtian Xue"Mean distance: 7.76 | S | N | B | C | P |
Parents
Sign in to add mentor| Christopher T. Seto | grad student | 2007 | Brown | |
| (Small synthetic molecules for biomolecular functions: Design, synthesis and biological studies.) | ||||
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Publications
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| Liang D, Li L, Lynch C, et al. (2019) Human constitutive androstane receptor agonist DL5016: A novel sensitizer for cyclophosphamide-based chemotherapies. European Journal of Medicinal Chemistry. 179: 84-99 |
| Zhao J, Liang D, Robinson E, et al. (2019) The effects of novel heme oxygenase inhibitors on the growth of Pseudomonas aeruginosa. Microbial Pathogenesis |
| Liang D, Robinson E, Hom K, et al. (2018) Structure-based design and biological evaluation of inhibitors of the pseudomonas aeruginosa heme oxygenase (pa-HemO). Bioorganic & Medicinal Chemistry Letters |
| Liang D, Yu W, Nguyen N, et al. (2017) Iodobenzene-Catalyzed Synthesis of Phenanthridinones via Oxidative C-H Amidation. The Journal of Organic Chemistry |
| Cardenas MG, Oswald E, Yu W, et al. (2016) The expanding role of the BCL6 oncoprotein as a cancer therapeutic target. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research |
| Cardenas MG, Yu W, Beguelin W, et al. (2016) Rationally designed BCL6 inhibitors target activated B cell diffuse large B cell lymphoma. The Journal of Clinical Investigation |
| Heinzl GA, Huang W, Yu W, et al. (2016) Iminoguanidines as Allosteric Inhibitors of the Iron-Regulated Heme Oxygenase (HemO) of Pseudomonas aeruginosa. Journal of Medicinal Chemistry |
| Holden JK, Dejam D, Lewis MC, et al. (2015) Inhibitor Bound Crystal Structures of Bacterial Nitric Oxide Synthase. Biochemistry. 54: 4075-82 |
| Lakkaraju SK, Mbatia H, Hanscom M, et al. (2015) Cyclopropyl-containing positive allosteric modulators of metabotropic glutamate receptor subtype 5. Bioorganic & Medicinal Chemistry Letters. 25: 2275-9 |
| Li T, He X, Thomas JM, et al. (2015) A novel GTP-binding inhibitor, FX2149, attenuates LRRK2 toxicity in Parkinson's disease models. Plos One. 10: e0122461 |