Publications

44. eIF3d and eIF3e mediate selective translational control of hypoxia that can be inhibited byÌýsmall molecules, Purdy, S. C.; Matlin, K.; Alderman, C.; Baldwin, A.; Shrivastava, N.; Dutta, S.; Webb, K. J.; Wolin, A.; Boulton, D.; Kapali, J.; Landua, J.; Lewis, M.; Caino, C.; Old, W.; Wang, X.; Zhao, R.;Mukherjee, N.; Ford, H. L. Cell Report 2025 44, 116643. doi: 10.1016/j.celrep.2025.116643. PMID: 41364558


43. Potent synthetic lethality between PLK1 and EYA family inhibitors in tumors of the central and peripheral nervous systems, Nelson CB, Wells JK, Kesarwani E, Sobinoff AP, Fernando M, Gao J, MacKenzie KL, Poulos RC, Nawaz U, Wang X, Ford HL, Pickett HA. Genes Dev. 2026, 40, 267. doi: 10.1101/gad.353271.125. PMID: 41266088.


42. Extended structure-activity relationship studies of the [1,2,5]oxadiazolo[3,4-b]pyrazine-containing colistin adjuvants, Harris, S. L.; Dutta, S.; Liu, N.; Wollenberg, T.; Wang, X.ÌýBioorg. Med. Chem. Lett.Ìý2025,Ìý115, 130008. https://doi.org/10.1016/j.bmcl.2024.130008. [].


41.ÌýRational design of novel allosteric EYA2 inhibitors as potential therapeutics for multiple brain cancers, Gardner, L.; ÌýRossi, J.;ÌýArmstrong, B.;ÌýMuse, M.;ÌýLaVeck, A.; ÌýBlevins, M.;ÌýZhang, L.;ÌýFord, H.; ÌýZhao, R.;ÌýWang, X. °ä³ó±ð³¾µþ¾±´Ç°ä³ó±ð³¾.Ìý2024,Ìýe202400179. doi: 10.1002/cmdc.202400179 [].


40.ÌýPractical synthesis of isoindolines yields potent colistin potentiators for multidrug-resistantÌý´¡³¦¾±²Ô±ð³Ù´Ç²ú²¹³¦³Ù±ð°ùÌý²ú²¹³Ü³¾²¹²Ô²Ô¾±¾±, Dutta, S.; Eyolfson, S.; Zhu, Y.; Gao, Y.; Wang, X. Org. & Biomol. Chem.Ìý2024,Ìý22, 4057–4061 [].


39.ÌýA Small-Molecule Membrane Fluidizer Re-sensitizes Methicillin-ResistantÌýStaphylococcus aureusÌý(MRSA) toÌýβ-Lactam Antibiotics, Podoll, J. D.; Rosen, E.; Wang, W.; Gao, Y.; Zhang, J.; Wang, X. Antimicrob. Agents Chemother. 2023,Ìý18;67(10):e0005123. doi: 10.1128/aac.00051-23Ìý[].


38. ÌýRecent Developments of Isoindole Chemistry, Weintraub, R. A.; Wang, X.Ìý³§²â²Ô³Ù³ó±ð²õ¾±²õ, 2023, 519Ìý[].

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37. ÌýStructure-Activity Relationship Studies of [1,2,5]Oxadiazolo[3,4-b]pyrazine-ContainingÌýPolymyxin-Selective Resistance-Modifying Agents,ÌýSomnath, D.; Liu, N.;ÌýGao, Y.; Beck, L.;ÌýWang, X.ÌýBioorg. Med. Chem. Lett. 2022, 72, 128878.Ìý[].

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36. ÌýSerendipitous Discovery of a Highly Active and Selective Resistance-Modifying Agent for Colistin-Resistant Gram-Negative Bacteria,ÌýGao, Y.;ÌýSomnath, D.;ÌýWang, X.ÌýACS Omega 2022, 7, 12442. []ÌýÌý

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35. ÌýA Cell-Free Screen for Bacterial Membrane Disruptors Identifies Mefloquine as a Novel Antibiotic Adjuvant, Podoll, J.; Olson, J.; Wang, W.; ÌýWang, X.ÌýAntibioticsÌý2021, 10(3), 315. []

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34. ÌýOne-Pot Synthesis of Polycyclic Isoindolines Using Isoindole Umpolung,ÌýWeintraub, R. A.; He, W.;ÌýWang, X. Tetrahedron Lett. 2020, 61, 152128. []

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33. ÌýTryptoline-BasedÌýBenzothiazolesÌýRe-sensitize MRSA to β-LactamÌýAntibiotics,ÌýWang, X.; Chen, J.; Wang, W.; Jaunaraj, A.;ÌýWang, X.ÌýBioorg. & Med. Chem.Ìý2019,Ìý27, 115095–115106. []Ìý

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32. ÌýIdentification and Characterization of a Novel Anti-inflammatory Lipid Isolated fromÌýMycobacterium vaccae, a Soil-Derived Bacterium with Immunoregulatory and Stress Resilience Properties,ÌýSmith, D. G.; Martinelli, R.; Besra, G. S.; Illarionov, P. A.; Szatmari, I.; Brazda, P.; Allen, M. A.; Xu, W.;ÌýWang, X.; Nagy, L.; Dowell, R. D.; Rook G. A. W.; Brunet, L. R.; Lowry, C. A.ÌýPhycopharmacology,Ìý2019,Ìý236(5),Ìý1653–1670. []

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31. Enantioselective Tandem Cyclization of Alkyne-Tethered Indoles Using Cooperative Silver(I) and Chiral Phosphoric Acid Catalysis. Zhu Y,ÌýHe W, Wang W, Pitsch CE, Wang X,ÌýWang X, AngewÌýChem,ÌýInt. Ed.Ìý2017,Ìý40, 12206–12209.

DOI: 10.1002/anie.201706694 and 10.1002/ange.201706694 []

cooperative catalysis

30. ÌýDiastereoselective Synthesis and Biological Evaluation of Enantiomerically Pure Tricyclic Indolines. He W, Griffiths BM,ÌýWang W, Wang X, Org. Biomol. Chem., 2017;15:4241-4245.

DOI: 10.1039/C7OB00897J []

Diastereoselective synthesis of tricyclic indolines

29. Tetracyclic Indolines as aÌýNovel Class of β-Lactam-Selective Resistance Modifying Agent for MRSA.ÌýZhu Y, Cleaver L, Wang W, Podoll JD, Walls S, Jolly A, Wang X.ÌýEurÌýJÌýMedÌýChem.Ìý2017;125:130-142.

DOI: 10.1016/j.ejmech.2016.09.034 []

tetracyclic indoline

28. Bioinspired Discovery of Chemical Reactions and Biological Probes. Griffiths B, Burl J, Wang X.ÌýSynlett. 2016;27:2039-2042.

DOI: 10.1055/s-0035-1561638Ìý[]

bioinspired discovery

27.ÌýProperty-Guided Synthesis of Aza-Tricyclic Indolines: Development of Gold Catalysis En Route. Barbour PM, Wang W, Chang L, Pickard KL, Rais R, Slusher BS, Wang X. AdvÌýSynthÌýCatal. 2016;358:1482-1490.Ìý[Theme: Gold Catalysis: Quo Vadis?]

DOI: 10.1002/adsc.201501101 []

aza-tricyclic indoline

26. A Fluorescence Polarization Biophysical Assay for theÌýNaegleriaÌýDNA Hydroxylase Tet1. Marholz LJ, Wang W, Zheng Y, Wang X.ÌýACS Med Chem Lett. 2016;7:167-171. [Theme: Epigenetics]Ìý

DOI: 10.1021/acsmedchemlett.5b00366 []

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25.ÌýGold-Catalyzed Cyclization Leads to A Bridged Tetracyclic Indolenine That Represses β-Lactam Resistance. Xu W, Wang W, Wang X. Angew Chem Int Ed. 2015;54:9546-9549; Angew Chem. 2015;127:9682-9685.

DOI: 10.1002/anie.201503736 (International)Ìýand 10.1002/ange.201503736 (German)Ìý[]

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24. Novel Scaffolds of Cell-Active Histone Demethylase Inhibitors Identified from High-Throughput Screening. Wang W, Marholz LJ, Wang X. J Biomol Screen.Ìý2015;20:821-827.Ìý

DOI: 10.1177/1087057115579637Ìý[]; Featured on GMD []

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23.ÌýDiscovery and Initial Structure-Activity Relationships ofÌýN-Benzyl Tricyclic Indolines as Antibacterials for Methicillin-ResistantÌýStaphylococcus Aureus. Barbour PM, Podoll JD, Marholz LJ, Wang X. Bioorg Med Chem Lett. 2014;24:5602-5605. Ìý

DOI:Ìý10.1016/j.bmcl.2014.10.094. []Ìý

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22. Development of Substrate-Selective Probes for Affinity Pulldown of Histone Demethylases. Marholz LJ, Chang L, Old WM, Wang X. ACS Chem Biol. 2015;10:129-137.

DOI: 10.1021/cb5006867 []

Ìý


21.ÌýA Histone Demethylase Inhibitor, Methylstat, Inhibits Angiogenesis in vitro and in vivo. Cho Y, Kim KH, Xu W, Wang X, Kwon HJ.ÌýRSC Adv. 2014;4:38230-38233.

DOI: 10.1039/c4ra07154a []

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20.ÌýStructure-Activity Relationship Studies of the Tricyclic Indoline Resistance-Modifying Agent. Chang L, Podoll JD, Wang W, Walls S,ÌýO'Rourke CP, Wang X. J Med Chem. 2014;57:3803-3817.Ìý

DOI: 10.1021/jm500146gÌý

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19. Gold Approaches to Polycyclic Indole Alkaloids. Barbour PM, Marholz LJ, Chang L, Xu W, Wang X. Chem Lett. 2014;43:572-578.Ìý

DOI: 10.1246/cl.131230Ìý[]

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18. Bio-Inspired Synthesis Yields A Tricyclic Indoline That Selectively Resensitizes MRSA to β-Lactam Antibiotics. Podoll JD, Liu Y, Chang L, Walls S, Wang W, Wang X. Proc Natl Acad Sci USA. 2013;110:15573-15578.Ìý

DOI: 10.1073/pnas.1310459110Ìý;ÌýHighlighted by PNASÌý;ÌýRecommended by Faculty of 1000Ìý

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17. Quantitative Analysis of Histone Demethylase Probes Using Fluorescence Polarization. Xu W, Podoll JD, Dong X, Tumber A, Oppermann U, Wang X. J Med Chem. Ìý2013;56:5198-5202.Ìý

DOI: 10.1021/jm3018628Ìý;ÌýHighlighted by Nature SciBXÌý

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16. A One-Pot Three-Component Reaction for the Preparation of Highly Functionalized Tryptamines. Yeo SJ, Liu Y, Wang X. Tetrahedron.Ìý2012;68:813-818.Ìý

DOI:Ìý10.1016/j.tet.2011.11.032Ìý

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15. A Selective Inhibitor and Probe of the Cellular Functions of Jumonji C Domain-Containing Histone Demethylases. Luo X,ÌýLiu Y,ÌýKubicek S,ÌýMyllyharju J,ÌýTumber A,ÌýNg S,ÌýChe KH,ÌýPodoll J,ÌýHeightman TD,ÌýOppermann U,ÌýSchreiber SL,ÌýWang X. J Am Chem Soc. 2011;133:9451-9456.Ìý

DOI: 10.1021/ja201597bÌý;ÌýHighlighted by Nature SciBXÌý

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14. Selective Gold(I)-Catalyzed Formation of Tetracyclic Indolines: A Single Transition State and Bifurcations Lead to Multiple Products. Noey EL, Wang X, Houk KN. J Org Chem. 2011;76:3477-83.Ìý

DOI:Ìý10.1021/jo200556fÌý

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13. Gold(I)-Catalyzed Tandem Cyclization Approach to Tetracyclic Indolines. Liu Y, Xu W, Wang X. Org Lett. 2010;12:1448-51.Ìý

DOI: 10.1021/ol100153hÌý

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12. AAK1 Identified as an Inhibitor of Neuregulin-1/ErbB4-Dependent Neurotrophic Factor Signaling Using Integrative Chemical Genomics and Proteomics. Kuai L, Ong SE, Madison JM, Wang X, Duvall JR, Lewis TA, Luce CJ, Conner SD, Pearlman DA, Wood JL, Schreiber SL, Carr SA, Scolnick EM, Haggarty SJ. Chem & Biol. 2011;18;891-906.Ìý

11. Chemical genetics identifies small-molecule modulators of neuritogenesis involving neuregulin-1/ErbB4 signaling. Kuai L, Wang X, Madison JM, Schreiber SL, Scolnick EM, Haggarty SJ. ACS Chem Neurosci. 2010;1;325-42.Ìý

10. Syntheses of aminoalcohol-derived macrocycles leading to a small-molecule binder to and inhibitor of sonic hedgehog. Peng LF, Stanton BZ, Maloof N, Wang X, Schreiber SL. Bioorg Med Chem Lett. 2009;19: 6319-25.Ìý

9. Identifying the proteins to which small-molecule probes and drugs bind in cells. Ong SE, Schenone M, Margolin AA, Li X, Do K, Doud MK, Mani DR, Kuai L, Wang X, Wood JL, Tolliday NJ, Koehler AN, Marcaurelle LA, Golub TR, Gould RJ, Schreiber SL, Carr SA. Proc Natl Acad Sci U S A. 2009;106;4617-22.Ìý

8. A small molecule that binds Hedgehog and blocks its signaling in human cells. Stanton B, Peng LF, Maloof N, Nakai K, Wang X, Duffner JL, Taveras KM, Hyman JM,ÌýLee SW, Koehler AN, Chen JK, Fox JL, Mandinova A, Schreiber SL. Nat Chem Biol. 2009;5:154-6.ÌýÌý

7. Diversity synthesis of complex pyridines yields a probe of a neurotrophic signalling pathway. Gray BL, Wang X, Brown WC, Kuai L, Schreiber SL. Org Lett. 2008;10:2621-4.Ìý

6. Small-molecule reagents for cellular pull-down experiments. Wang X, Imber BS, Schreiber SL. Bioconjug Chem. 2008;19:585-7.Ìý

5. Synthesis of the tetracyclic core of the tetrapetalones via transannular oxidative [4+3] cyclization. Wang X, Porco JA Jr. Angew Chem Int Ed Eng. 2005;44:3067-71;ÌýCorrigendum: 2006;45:6607.Ìý

4. Total synthesis of the salicylate enamide macrolide oximidine III: application of relay ring-closing metathesis. Wang X, Bowman EJ, Bowman BJ, Porco JA Jr. Angew Chem Int Ed Eng. 2004;43:3601-5.Ìý

3. Total synthesis of the salicylate enamide macrolide oximidine II. Wang X, Porco JA Jr. J Am Chem Soc. 2003;125:6040-1.Ìý

2. Modification of C-terminal peptides to form peptide enamides: synthesis of chondriamides A and C. Wang X, Porco JA Jr. J Org Chem. 2001;66:8215-21.Ìý

1. Parallel synthesis and purification using anthracene-tagged substrates. Wang X, Parlow JJ, Porco JA Jr. Org Lett. 2000;2:3509-12.Ìý

1.Histone demethylase inhibitors and methods for using the same. Wang, Xiang; Xu, Wenqing. U.S. 8,735,622.

2.Ìý“Indoline Alkaloid Compounds,â€� Podoll JD; Chang L; Wang, Xiang PCT/US14/32585.

3. "Polycycilc Indoline and Indolenine Compounds," Barbour PM, Wang, Xiang PCT/US62/154,792.

4.Ìý“1,3,4,9-Tetrahydro-2H-Pyrido[3,4-B]Indole Derivative Compounds and Uses Thereof,â€� Zhang, Jing; Podoll, Jessica D.;ÌýWang, Xiang.ÌýÌýUSÌý62/719,048.

5. “Tryptoline-Based Benzothiazoles and their use as Antibiotics and Antibiotic Resistance-Modifying Agents,â€� Wang, Xinfeng.;ÌýWang, Xiang. US 62/895,380.

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