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Volumn 11, Issue 6, 2019, Pages 521-532

Diverse compounds from pleuromutilin lead to a thioredoxin inhibitor and inducer of ferroptosis

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; AZULENE DERIVATIVE; CYSTEINE; DITERPENE; IMMUNOLOGIC FACTOR; PLEUROMUTILIN; PYRIDAZINE DERIVATIVE; THIOREDOXIN;

EID: 85065757498     PISSN: 17554330     EISSN: 17554349     Source Type: Journal    
DOI: 10.1038/s41557-019-0261-6     Document Type: Article
Times cited : (180)

References (64)
  • 1
    • 71049126548 scopus 로고    scopus 로고
    • Escape from flatland: increasing saturation as an approach to improving clinical success
    • COI: 1:CAS:528:DC%2BD1MXht1KjtLvN
    • Lovering, F., Bikker, J. & Humblet, C. Escape from flatland: increasing saturation as an approach to improving clinical success. J. Med. Chem. 52, 6752–6756 (2009).
    • (2009) J. Med. Chem. , vol.52 , pp. 6752-6756
    • Lovering, F.1    Bikker, J.2    Humblet, C.3
  • 2
    • 79959929769 scopus 로고    scopus 로고
    • How were new medicines discovered?
    • COI: 1:CAS:528:DC%2BC3MXotlCmsbs%3D
    • Swinney, D. C. & Anthony, J. How were new medicines discovered? Nat. Rev. Drug Discov. 10, 507–519 (2011).
    • (2011) Nat. Rev. Drug Discov. , vol.10 , pp. 507-519
    • Swinney, D.C.1    Anthony, J.2
  • 3
    • 84880296641 scopus 로고    scopus 로고
    • Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules
    • Galloway, W. R. J. D., Isidro-Llobet, A. & Spring, D. R. Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules. Nat. Commun. 1, 80–93 (2010).
    • (2010) Nat. Commun. , vol.1 , pp. 80-93
    • Galloway, W.R.J.D.1    Isidro-Llobet, A.2    Spring, D.R.3
  • 4
    • 85045978359 scopus 로고    scopus 로고
    • Chemical probes and drug leads from advances in synthetic planning and methodology
    • COI: 1:CAS:528:DC%2BC1cXnsFCnsbs%3D
    • Gerry, C. J. & Schreiber, S. L. Chemical probes and drug leads from advances in synthetic planning and methodology. Nat. Rev. Drug Discov. 17, 333–352 (2018).
    • (2018) Nat. Rev. Drug Discov. , vol.17 , pp. 333-352
    • Gerry, C.J.1    Schreiber, S.L.2
  • 5
    • 84890069342 scopus 로고    scopus 로고
    • Natural products as starting points for the synthesis of complex and diverse compounds
    • COI: 1:CAS:528:DC%2BC3sXhvVyqsr%2FN
    • Morrison, K. C. & Hergenrother, P. J. Natural products as starting points for the synthesis of complex and diverse compounds. Nat. Prod. Rep. 31, 6–14 (2014).
    • (2014) Nat. Prod. Rep. , vol.31 , pp. 6-14
    • Morrison, K.C.1    Hergenrother, P.J.2
  • 6
    • 84875466221 scopus 로고    scopus 로고
    • A ring-distortion strategy to construct stereochemically complex and structurally diverse compounds from natural products
    • COI: 1:CAS:528:DC%2BC3sXhtFSgurg%3D
    • Huigens, R. W. III et al. A ring-distortion strategy to construct stereochemically complex and structurally diverse compounds from natural products. Nat. Chem. 5, 195–202 (2013).
    • (2013) Nat. Chem. , vol.5 , pp. 195-202
    • Huigens, R.W.1
  • 7
    • 85014699798 scopus 로고    scopus 로고
    • A novel complexity-to-diversity strategy for the diversity-oriented synthesis of structurally diverse and complex macrocycles from quinine
    • COI: 1:CAS:528:DC%2BC2sXjvF2nurw%3D
    • Ciardiello, J. J. et al. A novel complexity-to-diversity strategy for the diversity-oriented synthesis of structurally diverse and complex macrocycles from quinine. Bioorg. Med. Chem. 25, 2825–2843 (2017).
    • (2017) Bioorg. Med. Chem. , vol.25 , pp. 2825-2843
    • Ciardiello, J.J.1
  • 8
    • 84890955037 scopus 로고    scopus 로고
    • Synthesis of complex and diverse compounds through ring distortion of abietic acid
    • COI: 1:CAS:528:DC%2BC3sXhvValtbfN
    • Rafferty, R. J., Hicklin, R. W., Maloof, K. A. & Hergenrother, P. J. Synthesis of complex and diverse compounds through ring distortion of abietic acid. Angew. Chem. Int. Ed. 53, 220–224 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 220-224
    • Rafferty, R.J.1    Hicklin, R.W.2    Maloof, K.A.3    Hergenrother, P.J.4
  • 9
    • 84990911231 scopus 로고    scopus 로고
    • Access to a structurally complex compound collection via ring distortion of the alkaloid sinomenine
    • COI: 1:CAS:528:DC%2BC28XhsFait7bN
    • Garcia, A., Drown, B. S. & Hergenrother, P. J. Access to a structurally complex compound collection via ring distortion of the alkaloid sinomenine. Org. Lett. 18, 4852–4855 (2016).
    • (2016) Org. Lett. , vol.18 , pp. 4852-4855
    • Garcia, A.1    Drown, B.S.2    Hergenrother, P.J.3
  • 10
    • 85053502091 scopus 로고    scopus 로고
    • Preparation of structurally diverse compounds from the natural product lycorine
    • COI: 1:CAS:528:DC%2BC1cXhs1Orur7I
    • Tasker, S. Z., Cowfer, A. E. & Hergenrother, P. J. Preparation of structurally diverse compounds from the natural product lycorine. Org. Lett. 20, 5894–5898 (2018).
    • (2018) Org. Lett. , vol.20 , pp. 5894-5898
    • Tasker, S.Z.1    Cowfer, A.E.2    Hergenrother, P.J.3
  • 11
    • 85012928687 scopus 로고    scopus 로고
    • A tryptoline ring‐distortion strategy leads to complex and diverse biologically active molecules from the indole alkaloid yohimbine
    • COI: 1:CAS:528:DC%2BC2sXitVKmsr4%3D
    • Paciaroni, N. G. et al. A tryptoline ring‐distortion strategy leads to complex and diverse biologically active molecules from the indole alkaloid yohimbine. Chem. Eur. J. 23, 4327–4335 (2017).
    • (2017) Chem. Eur. J. , vol.23 , pp. 4327-4335
    • Paciaroni, N.G.1
  • 12
    • 85041225146 scopus 로고    scopus 로고
    • Novel topologically complex scaffold derived from alkaloid haemanthamine
    • Govindaraju, K. et al. Novel topologically complex scaffold derived from alkaloid haemanthamine. Molecules 23, 255–263 (2018).
    • (2018) Molecules , vol.23 , pp. 255-263
    • Govindaraju, K.1
  • 13
    • 85042912605 scopus 로고    scopus 로고
    • Reagent-controlled regiodivergent ring expansions of steroids
    • Charaschanya, M. & Aubé, J. Reagent-controlled regiodivergent ring expansions of steroids. Nat. Commun. 9, 934–942 (2018).
    • (2018) Nat. Commun. , vol.9 , pp. 934-942
    • Charaschanya, M.1    Aubé, J.2
  • 14
    • 85045380919 scopus 로고    scopus 로고
    • A ring‐distortion strategy from marine natural product ilimaquinone leads to quorum sensing modulators
    • Laurent, E. et al. A ring‐distortion strategy from marine natural product ilimaquinone leads to quorum sensing modulators. Eur. J. Org. Chem. 2018, 2486–2497 (2018).
    • (2018) Eur. J. Org. Chem. , vol.2018 , pp. 2486-2497
    • Laurent, E.1
  • 15
    • 85008177116 scopus 로고    scopus 로고
    • Identification of a diverse synthetic abietane diterpenoid library for anticancer activity
    • COI: 1:CAS:528:DC%2BC28XitFCmt7zF
    • Xu, H. et al. Identification of a diverse synthetic abietane diterpenoid library for anticancer activity. Bioorg. Med. Chem. Lett. 27, 505–510 (2017).
    • (2017) Bioorg. Med. Chem. Lett. , vol.27 , pp. 505-510
    • Xu, H.1
  • 16
    • 85009740903 scopus 로고    scopus 로고
    • Discovery of novel cinchona‐alkaloid‐inspired oxazatwistane autophagy inhibitors
    • Luca, L. et al. Discovery of novel cinchona‐alkaloid‐inspired oxazatwistane autophagy inhibitors. Angew. Chem. Int. Ed. 56, 2145–2150 (2017).
    • (2017) Angew. Chem. Int. Ed. , vol.56 , pp. 2145-2150
    • Luca, L.1
  • 17
    • 85019581867 scopus 로고    scopus 로고
    • Predictive compound accumulation rules yield a broad-spectrum antibiotic
    • COI: 1:CAS:528:DC%2BC2sXnsVeis7Y%3D
    • Richter, M. F. et al. Predictive compound accumulation rules yield a broad-spectrum antibiotic. Nature 545, 299–304 (2017).
    • (2017) Nature , vol.545 , pp. 299-304
    • Richter, M.F.1
  • 18
    • 0035788806 scopus 로고    scopus 로고
    • The pleuromutilin drugs tiamulin and valnemulin bind to the RNA at the peptidyl transferase centre on the ribosome
    • COI: 1:CAS:528:DC%2BD3MXntlGhsLw%3D
    • Poulsen, S. M., Karlsson, M., Johansson, L. B. & Vester, B. The pleuromutilin drugs tiamulin and valnemulin bind to the RNA at the peptidyl transferase centre on the ribosome. Mol. Microbiol. 41, 1091–1099 (2001).
    • (2001) Mol. Microbiol. , vol.41 , pp. 1091-1099
    • Poulsen, S.M.1    Karlsson, M.2    Johansson, L.B.3    Vester, B.4
  • 19
    • 85046135913 scopus 로고    scopus 로고
    • Directed C–H bond oxidation of (+)-pleuromutilin
    • COI: 1:CAS:528:DC%2BC1cXnslKmtbs%3D
    • Ma, X. et al. Directed C–H bond oxidation of (+)-pleuromutilin. J. Org. Chem. 83, 6843–6892 (2018).
    • (2018) J. Org. Chem. , vol.83 , pp. 6843-6892
    • Ma, X.1
  • 20
    • 85041458889 scopus 로고    scopus 로고
    • Total synthesis of (+)-pleuromutilin
    • COI: 1:CAS:528:DC%2BC1cXotVyluw%3D%3D
    • Farney, E. P., Feng, S. S., Schäfers, F. & Reisman, S. E. Total synthesis of (+)-pleuromutilin. J. Am. Chem. Soc. 140, 1267–1270 (2018).
    • (2018) J. Am. Chem. Soc. , vol.140 , pp. 1267-1270
    • Farney, E.P.1    Feng, S.S.2    Schäfers, F.3    Reisman, S.E.4
  • 21
    • 85020294119 scopus 로고    scopus 로고
    • A modular and enantioselective synthesis of the pleuromutilin antibiotics
    • COI: 1:CAS:528:DC%2BC2sXosV2rtL8%3D
    • Murphy, S. K., Zeng, M. & Herzon, S. B. A modular and enantioselective synthesis of the pleuromutilin antibiotics. Science 356, 956–959 (2017).
    • (2017) Science , vol.356 , pp. 956-959
    • Murphy, S.K.1    Zeng, M.2    Herzon, S.B.3
  • 23
    • 0019982412 scopus 로고
    • Total synthesis of (±)-pleuromutilin
    • COI: 1:CAS:528:DyaL38Xhs1aqtbk%3D
    • Gibbons, E. G. Total synthesis of (±)-pleuromutilin. J. Am. Chem. Soc. 104, 1767–1769 (1982).
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 1767-1769
    • Gibbons, E.G.1
  • 24
    • 0023876532 scopus 로고
    • (+)-Pleuromutilin synthetic studies. Degradative and de novo acquisition of a levorotatory tricyclic lactone subunit
    • COI: 1:CAS:528:DyaL1cXhs1OksLY%3D
    • Paquette, L. A., Wiedeman, P. E. & Bulman-Page, P. C. (+)-Pleuromutilin synthetic studies. Degradative and de novo acquisition of a levorotatory tricyclic lactone subunit. J. Org. Chem. 53, 1441–1450 (1988).
    • (1988) J. Org. Chem. , vol.53 , pp. 1441-1450
    • Paquette, L.A.1    Wiedeman, P.E.2    Bulman-Page, P.C.3
  • 25
    • 78751544589 scopus 로고    scopus 로고
    • A concise synthesis of the molecular framework of pleuromutilin
    • COI: 1:CAS:528:DC%2BC3MXot1Cgsg%3D%3D
    • Liu, J., Lotesta, S. D. & Sorensen, E. J. A concise synthesis of the molecular framework of pleuromutilin. Chem. Commun. 47, 1500–1502 (2011).
    • (2011) Chem. Commun. , vol.47 , pp. 1500-1502
    • Liu, J.1    Lotesta, S.D.2    Sorensen, E.J.3
  • 26
    • 49949137644 scopus 로고
    • The structure and some aspects of the biosynthesis of pleuromutilin
    • Birch, A. J., Holzapfel, C. W. & Rickards, R. W. The structure and some aspects of the biosynthesis of pleuromutilin. Tetrahedron 22, 359–387 (1966).
    • (1966) Tetrahedron , vol.22 , pp. 359-387
    • Birch, A.J.1    Holzapfel, C.W.2    Rickards, R.W.3
  • 27
    • 0014399306 scopus 로고
    • Some studies in the biosynthesis of terpenes and related compounds
    • COI: 1:CAS:528:DyaE3cXktFGjsrg%3D
    • Arigoni, D. Some studies in the biosynthesis of terpenes and related compounds. Pure Appl. Chem. 17, 331–348 (1968).
    • (1968) Pure Appl. Chem. , vol.17 , pp. 331-348
    • Arigoni, D.1
  • 28
    • 0016785248 scopus 로고
    • Antimicrobial activities of 81.723 hfu, a new pleuromutilin derivative
    • COI: 1:CAS:528:DyaE2MXltVygsLk%3D
    • Drews, J. et al. Antimicrobial activities of 81.723 hfu, a new pleuromutilin derivative. Antimicrob. Agents Chemother. 7, 507–516 (1975).
    • (1975) Antimicrob. Agents Chemother. , vol.7 , pp. 507-516
    • Drews, J.1
  • 29
    • 42249101746 scopus 로고    scopus 로고
    • Retapamulin: a review of its use in the management of impetigo and other uncomplicated superficial skin infections
    • COI: 1:CAS:528:DC%2BD1cXmvVeltLk%3D
    • Yang, L. P. & Keam, S. J. Retapamulin: a review of its use in the management of impetigo and other uncomplicated superficial skin infections. Drugs 68, 855–873 (2008).
    • (2008) Drugs , vol.68 , pp. 855-873
    • Yang, L.P.1    Keam, S.J.2
  • 30
    • 0009501175 scopus 로고
    • Synthese ab-trans-anellierter derivate des tricyclischen diterpens pleuromutilin durch intramolekulare 1,5-hydrid-verschiebung
    • COI: 1:CAS:528:DyaL3MXmsFyrtw%3D%3D
    • Berner, H., Schulz, G. & Schneider, H. Synthese ab-trans-anellierter derivate des tricyclischen diterpens pleuromutilin durch intramolekulare 1,5-hydrid-verschiebung. Tetrahedron 36, 1807–1811 (1980).
    • (1980) Tetrahedron , vol.36 , pp. 1807-1811
    • Berner, H.1    Schulz, G.2    Schneider, H.3
  • 31
    • 68349160587 scopus 로고    scopus 로고
    • Process development for a novel pleuromutilin-derived antibiotic
    • COI: 1:CAS:528:DC%2BD1MXotV2ltL8%3D
    • Andemichael, Y. et al. Process development for a novel pleuromutilin-derived antibiotic. Org. Process Res. Dev. 13, 729–738 (2009).
    • (2009) Org. Process Res. Dev. , vol.13 , pp. 729-738
    • Andemichael, Y.1
  • 32
    • 79960245266 scopus 로고    scopus 로고
    • The synthesis of C-13 functionalized pleuromutilins via C–H amidation and subsequent novel rearrangement product
    • COI: 1:CAS:528:DC%2BC3MXptVWkt70%3D
    • Uccello, D. P. et al. The synthesis of C-13 functionalized pleuromutilins via C–H amidation and subsequent novel rearrangement product. Tetrahedron Lett. 52, 4247–4251 (2011).
    • (2011) Tetrahedron Lett. , vol.52 , pp. 4247-4251
    • Uccello, D.P.1
  • 33
    • 84906946560 scopus 로고    scopus 로고
    • Synthesis of bridged oxafenestranes from pleuromutilin
    • COI: 1:CAS:528:DC%2BC2cXhtFyqsb%2FO
    • Hicklin, R. W., López Silva, T. L. & Hergenrother, P. J. Synthesis of bridged oxafenestranes from pleuromutilin. Angew. Chem. Int. Ed. 53, 9880–9883 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 9880-9883
    • Hicklin, R.W.1    López Silva, T.L.2    Hergenrother, P.J.3
  • 34
    • 84893487711 scopus 로고    scopus 로고
    • Dual small-molecule targeting of procaspase-3 dramatically enhances zymogen activation and anticancer activity
    • COI: 1:CAS:528:DC%2BC2cXitFKnsQ%3D%3D
    • Botham, R. C. et al. Dual small-molecule targeting of procaspase-3 dramatically enhances zymogen activation and anticancer activity. J. Am. Chem. Soc. 136, 1312–1319 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 1312-1319
    • Botham, R.C.1
  • 35
    • 84886519739 scopus 로고    scopus 로고
    • Efficient NQO1 substrates are potent and selective anticancer agents
    • COI: 1:CAS:528:DC%2BC3sXht1Cqtb7M
    • Parkinson, E. I., Bair, J. S., Cismesia, M. & Hergenrother, P. J. Efficient NQO1 substrates are potent and selective anticancer agents. ACS Chem. Biol. 8, 2173–2183 (2013).
    • (2013) ACS Chem. Biol. , vol.8 , pp. 2173-2183
    • Parkinson, E.I.1    Bair, J.S.2    Cismesia, M.3    Hergenrother, P.J.4
  • 36
    • 84947583848 scopus 로고    scopus 로고
    • A small molecule that induces intrinsic pathway apoptosis with unparalleled speed
    • COI: 1:CAS:528:DC%2BC2MXhvVOqsbnO
    • Palchaudhuri, R. et al. A small molecule that induces intrinsic pathway apoptosis with unparalleled speed. Cell Rep. 13, 2027–2036 (2015).
    • (2015) Cell Rep. , vol.13 , pp. 2027-2036
    • Palchaudhuri, R.1
  • 37
    • 84922394053 scopus 로고    scopus 로고
    • Regulated cell death and inflammation: an auto-amplification loop causes organ failure
    • COI: 1:CAS:528:DC%2BC2cXhslKmu73J
    • Linkermann, A., Stockwell, B. R., Krautwald, S. & Anders, H.-J. Regulated cell death and inflammation: an auto-amplification loop causes organ failure. Nat. Rev. Immunol. 14, 759–767 (2014).
    • (2014) Nat. Rev. Immunol. , vol.14 , pp. 759-767
    • Linkermann, A.1    Stockwell, B.R.2    Krautwald, S.3    Anders, H.J.4
  • 38
    • 84857789296 scopus 로고    scopus 로고
    • The secret ally: immunostimulation by anticancer drugs
    • COI: 1:CAS:528:DC%2BC38Xhs1Gitb4%3D
    • Galluzzi, L., Senovilla, L., Zitvogel, L. & Kroemer, G. The secret ally: immunostimulation by anticancer drugs. Nat. Rev. Drug Discov. 11, 215–233 (2012).
    • (2012) Nat. Rev. Drug Discov. , vol.11 , pp. 215-233
    • Galluzzi, L.1    Senovilla, L.2    Zitvogel, L.3    Kroemer, G.4
  • 39
    • 85019592597 scopus 로고    scopus 로고
    • Reactive oxygen species synergize to potently and selectively induce cancer cell death
    • COI: 1:CAS:528:DC%2BC2sXkvFWjs74%3D
    • Lee, H. Y. et al. Reactive oxygen species synergize to potently and selectively induce cancer cell death. ACS Chem. Biol. 12, 1416–1424 (2017).
    • (2017) ACS Chem. Biol. , vol.12 , pp. 1416-1424
    • Lee, H.Y.1
  • 40
    • 85030552365 scopus 로고    scopus 로고
    • Ferroptosis: a regulated cell death nexus linking metabolism, redox biology and disease
    • COI: 1:CAS:528:DC%2BC2sXhs1Wqs7%2FL
    • Stockwell, B. R. et al. Ferroptosis: a regulated cell death nexus linking metabolism, redox biology and disease. Cell 171, 273–285 (2017).
    • (2017) Cell , vol.171 , pp. 273-285
    • Stockwell, B.R.1
  • 41
    • 84861541814 scopus 로고    scopus 로고
    • Ferroptosis: an iron-dependent form of nonapoptotic cell death
    • COI: 1:CAS:528:DC%2BC38XnslSntrw%3D
    • Dixon, S. J. et al. Ferroptosis: an iron-dependent form of nonapoptotic cell death. Cell 149, 1060–1072 (2012).
    • (2012) Cell , vol.149 , pp. 1060-1072
    • Dixon, S.J.1
  • 42
    • 84892685001 scopus 로고    scopus 로고
    • Regulation of ferroptotic cancer cell death by GPX4
    • COI: 1:CAS:528:DC%2BC2cXhtF2is70%3D
    • Yang, W. S. et al. Regulation of ferroptotic cancer cell death by GPX4. Cell 156, 317–331 (2014).
    • (2014) Cell , vol.156 , pp. 317-331
    • Yang, W.S.1
  • 43
    • 84965000436 scopus 로고    scopus 로고
    • Global survey of cell death mechanisms reveals metabolic regulation of ferroptosis
    • COI: 1:CAS:528:DC%2BC28XnsFaitrs%3D
    • Shimada, K. et al. Global survey of cell death mechanisms reveals metabolic regulation of ferroptosis. Nat. Chem. Biol. 12, 497–503 (2016).
    • (2016) Nat. Chem. Biol. , vol.12 , pp. 497-503
    • Shimada, K.1
  • 44
    • 85044753310 scopus 로고    scopus 로고
    • 2 initiates ferroptosis through GPX4 inactivation and iron oxidation
    • COI: 1:CAS:528:DC%2BC1cXosFGmsbY%3D
    • 2 initiates ferroptosis through GPX4 inactivation and iron oxidation. Nat. Chem. Biol. 14, 507–515 (2018).
    • (2018) Nat. Chem. Biol. , vol.14 , pp. 507-515
    • Gaschler, M.M.1
  • 45
    • 85046081206 scopus 로고    scopus 로고
    • Oxytosis/ferroptosis—(re-)emerging roles for oxidative stress-dependent non-apoptotic cell death in diseases of the central nervous system
    • Lewerenz, J. et al. Oxytosis/ferroptosis—(re-)emerging roles for oxidative stress-dependent non-apoptotic cell death in diseases of the central nervous system. Front. Neurosci. 12, 214 (2018).
    • (2018) Front. Neurosci. , vol.12 , pp. 214
    • Lewerenz, J.1
  • 46
    • 0023833551 scopus 로고
    • Calcium-dependent glutamate cytotoxicity in a neuronal cell line
    • COI: 1:CAS:528:DyaL1cXhs1aqsLg%3D
    • Murphy, T. H. et al. Calcium-dependent glutamate cytotoxicity in a neuronal cell line. Brain Res. 444, 325–332 (1988).
    • (1988) Brain Res. , vol.444 , pp. 325-332
    • Murphy, T.H.1
  • 47
    • 0024446419 scopus 로고
    • Antioxidants protect against glutamate-induced cytotoxicity in a neuronal cell line
    • COI: 1:CAS:528:DyaL1MXlvVOntLs%3D, PID: 2778712
    • Miyamoto, M., Murphy, T. H., Schnaar, R. L. & Coyle, J. T. Antioxidants protect against glutamate-induced cytotoxicity in a neuronal cell line. J. Pharmacol. Exp. Ther. 250, 1132–1140 (1989).
    • (1989) J. Pharmacol. Exp. Ther. , vol.250 , pp. 1132-1140
    • Miyamoto, M.1    Murphy, T.H.2    Schnaar, R.L.3    Coyle, J.T.4
  • 48
    • 50049133588 scopus 로고    scopus 로고
    • Glutathione peroxidase 4 senses and translates oxidative stress into 12/15-lipoxygenase dependent- and AIF-mediated cell death
    • COI: 1:CAS:528:DC%2BD1cXhtFeju77K
    • Seiler, A. et al. Glutathione peroxidase 4 senses and translates oxidative stress into 12/15-lipoxygenase dependent- and AIF-mediated cell death. Cell Metabol. 8, 237–248 (2008).
    • (2008) Cell Metabol. , vol.8 , pp. 237-248
    • Seiler, A.1
  • 49
    • 40849085503 scopus 로고    scopus 로고
    • Synthetic lethal screening identifies compounds activating iron-dependent, nonapoptotic cell death in oncogenic-RAS-harboring cancer cells
    • COI: 1:CAS:528:DC%2BD1cXjs1Klsrs%3D
    • Yang, W. S. & Stockwell, B. R. Synthetic lethal screening identifies compounds activating iron-dependent, nonapoptotic cell death in oncogenic-RAS-harboring cancer cells. Chem. Biol. 15, 234–245 (2008).
    • (2008) Chem. Biol. , vol.15 , pp. 234-245
    • Yang, W.S.1    Stockwell, B.R.2
  • 50
    • 85036572148 scopus 로고    scopus 로고
    • A next generation connectivity map: L1000 platform and the first 1,000,000 profiles
    • COI: 1:CAS:528:DC%2BC2sXhvFWmsbrE
    • Subramanian, A. et al. A next generation connectivity map: L1000 platform and the first 1,000,000 profiles. Cell 171, 1437–1452 (2017).
    • (2017) Cell , vol.171 , pp. 1437-1452
    • Subramanian, A.1
  • 51
    • 84901323900 scopus 로고    scopus 로고
    • Pharmacological inhibition of cystine–glutamate exchange induces endoplasmic reticulum stress and ferroptosis
    • Dixon, S. J. et al. Pharmacological inhibition of cystine–glutamate exchange induces endoplasmic reticulum stress and ferroptosis. eLife 3, e02523 (2014).
    • (2014) eLife , vol.3
    • Dixon, S.J.1
  • 52
    • 84874024997 scopus 로고    scopus 로고
    • 1,3,5-Triazine as a modular scaffold for covalent inhibitors with streamlined target identification
    • COI: 1:CAS:528:DC%2BC3sXhvFalu7o%3D
    • Banerjee, R., Pace, N. J., Brown, D. R. & Weerapana, E. 1,3,5-Triazine as a modular scaffold for covalent inhibitors with streamlined target identification. J. Am. Chem. Soc. 135, 2497–2500 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 2497-2500
    • Banerjee, R.1    Pace, N.J.2    Brown, D.R.3    Weerapana, E.4
  • 53
    • 0029644246 scopus 로고
    • Thioredoxin structure and mechanism: conformational changes on oxidation of the active-site sulfhydryls to a disulfide
    • COI: 1:CAS:528:DyaK2MXksFyntLs%3D
    • Holmgren, A. Thioredoxin structure and mechanism: conformational changes on oxidation of the active-site sulfhydryls to a disulfide. Structure 3, 239–243 (1995).
    • (1995) Structure , vol.3 , pp. 239-243
    • Holmgren, A.1
  • 54
    • 0035584857 scopus 로고    scopus 로고
    • Reactive oxygen species, antioxidants and the mammalian thioredoxin system
    • COI: 1:CAS:528:DC%2BD3MXos1Knu7w%3D
    • Nordberg, J. & Arnér, E. S. J. Reactive oxygen species, antioxidants and the mammalian thioredoxin system. Free Radic. Biol. Med. 31, 1287–1312 (2001).
    • (2001) Free Radic. Biol. Med. , vol.31 , pp. 1287-1312
    • Nordberg, J.1    Arnér, E.S.J.2
  • 55
    • 34547920652 scopus 로고    scopus 로고
    • A cellular and molecular investigation of the action of PMX464, a putative thioredoxin inhibitor, in normal and colorectal cancer cell lines
    • COI: 1:CAS:528:DC%2BD2sXovFehsL8%3D
    • Mukherjee, A. et al. A cellular and molecular investigation of the action of PMX464, a putative thioredoxin inhibitor, in normal and colorectal cancer cell lines. Br. J. Pharmacol. 151, 1167–1175 (2007).
    • (2007) Br. J. Pharmacol. , vol.151 , pp. 1167-1175
    • Mukherjee, A.1
  • 56
    • 31944432877 scopus 로고    scopus 로고
    • The antitumor thioredoxin-1 inhibitor PX-12 (1-methylpropyl 2-imidazolyl disulfide) decreases thioredoxin-1 and VEGF levels in cancer patient plasma
    • COI: 1:CAS:528:DC%2BD28XhtFShu7w%3D
    • Baker, A. F. et al. The antitumor thioredoxin-1 inhibitor PX-12 (1-methylpropyl 2-imidazolyl disulfide) decreases thioredoxin-1 and VEGF levels in cancer patient plasma. J. Lab. Clin. Med. 147, 83–90 (2006).
    • (2006) J. Lab. Clin. Med. , vol.147 , pp. 83-90
    • Baker, A.F.1
  • 57
    • 0032055646 scopus 로고    scopus 로고
    • Mechanisms of inhibition of the thioredoxin growth factor system by antitumor 2-imidazolyl disulfides
    • COI: 1:CAS:528:DyaK1cXit12ru7o%3D
    • Kirkpatrick, D. L. et al. Mechanisms of inhibition of the thioredoxin growth factor system by antitumor 2-imidazolyl disulfides. Biochem. Pharmacol. 55, 987–994 (1998).
    • (1998) Biochem. Pharmacol. , vol.55 , pp. 987-994
    • Kirkpatrick, D.L.1
  • 58
    • 54949138058 scopus 로고    scopus 로고
    • Targeting airway inflammation: PMX464 and the epithelial bulls eye
    • COI: 1:CAS:528:DC%2BD1cXht12lsrnM
    • Sexton, D. W. Targeting airway inflammation: PMX464 and the epithelial bulls eye. Br. J. Pharmacol. 155, 620–622 (2008).
    • (2008) Br. J. Pharmacol. , vol.155 , pp. 620-622
    • Sexton, D.W.1
  • 59
    • 85032029609 scopus 로고    scopus 로고
    • Thioredoxin-1 actively maintains the pseudokinase MLKL in a reduced state to suppress disulfide bond-dependent MLKL polymer formation and necroptosis
    • COI: 1:CAS:528:DC%2BC2sXhs12lsrrM
    • Reynoso, E. et al. Thioredoxin-1 actively maintains the pseudokinase MLKL in a reduced state to suppress disulfide bond-dependent MLKL polymer formation and necroptosis. J. Biol. Chem. 292, 17514–17524 (2017).
    • (2017) J. Biol. Chem. , vol.292 , pp. 17514-17524
    • Reynoso, E.1
  • 60
    • 84891939128 scopus 로고    scopus 로고
    • PX-12 inhibits the growth of A549 lung cancer cells via G2/M phase arrest and ROS-dependent apoptosis
    • COI: 1:CAS:528:DC%2BC2cXptl2iu7c%3D
    • You, B. R., Shin, H. R. & Park, W. H. PX-12 inhibits the growth of A549 lung cancer cells via G2/M phase arrest and ROS-dependent apoptosis. Int. J. Oncol. 44, 301–308 (2014).
    • (2014) Int. J. Oncol. , vol.44 , pp. 301-308
    • You, B.R.1    Shin, H.R.2    Park, W.H.3
  • 61
    • 85020842503 scopus 로고    scopus 로고
    • Small molecule probes for cellular death machines
    • COI: 1:CAS:528:DC%2BC2sXhtVWqsb7N
    • Li, Y., Qian, L. & Yuan, J. Small molecule probes for cellular death machines. Curr. Opin. Chem. Biol. 39, 74–82 (2017).
    • (2017) Curr. Opin. Chem. Biol. , vol.39 , pp. 74-82
    • Li, Y.1    Qian, L.2    Yuan, J.3
  • 62
    • 85036533976 scopus 로고    scopus 로고
    • Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018
    • Galluzzi, L. et al. Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. Cell Death Differ. 25, 486–541 (2018).
    • (2018) Cell Death Differ. , vol.25 , pp. 486-541
    • Galluzzi, L.1
  • 63
    • 85021891297 scopus 로고    scopus 로고
    • Salinomycin kills cancer stem cells by sequestering iron in lysosomes
    • COI: 1:CAS:528:DC%2BC2sXnslKku7Y%3D
    • Mai, T. T. et al. Salinomycin kills cancer stem cells by sequestering iron in lysosomes. Nat. Chem. 9, 1025–1033 (2017).
    • (2017) Nat. Chem. , vol.9 , pp. 1025-1033
    • Mai, T.T.1
  • 64
    • 85047634715 scopus 로고    scopus 로고
    • Ferroptosis-inducing agents compromise in vitro human islet viability and function
    • Bruni, A. et al. Ferroptosis-inducing agents compromise in vitro human islet viability and function. Cell Death Dis. 9, 595–605 (2018).
    • (2018) Cell Death Dis. , vol.9 , pp. 595-605
    • Bruni, A.1


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