-
1
-
-
80053005317
-
Thioredoxin 1-mediated post-translational modifications: Reduction, transnitrosylation, denitrosylation, and related proteomics methodologies
-
Wu, C.; Parrott, A. M.; Fu, C.; Liu, T.; Marino, S. M.; Gladyshev, V. N.; Jain, M. R.; Baykal, A. T.; Li, Q.; Oka, S.; Sadoshima, J.; Beuve, A.; Simmons, W. J.; Li, H. Thioredoxin 1-mediated post-translational modifications: Reduction, transnitrosylation, denitrosylation, and related proteomics methodologies Antioxid. Redox Signaling 2011, 15, 2565-2604
-
(2011)
Antioxid. Redox Signaling
, vol.15
, pp. 2565-2604
-
-
Wu, C.1
Parrott, A.M.2
Fu, C.3
Liu, T.4
Marino, S.M.5
Gladyshev, V.N.6
Jain, M.R.7
Baykal, A.T.8
Li, Q.9
Oka, S.10
Sadoshima, J.11
Beuve, A.12
Simmons, W.J.13
Li, H.14
-
2
-
-
0033544915
-
Thioredoxin-dependent redox regulation of p53-mediated p21 activation
-
Ueno, M.; Masutani, H.; Arai, R. J.; Yamauchi, A.; Hirota, K.; Sakai, T.; Inamoto, T.; Yamaoka, Y.; Yodoi, J.; Nikaido, T. Thioredoxin-dependent redox regulation of p53-mediated p21 activation J. Biol. Chem. 1999, 274, 35809-35815
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 35809-35815
-
-
Ueno, M.1
Masutani, H.2
Arai, R.J.3
Yamauchi, A.4
Hirota, K.5
Sakai, T.6
Inamoto, T.7
Yamaoka, Y.8
Yodoi, J.9
Nikaido, T.10
-
3
-
-
58149352993
-
Thioredoxin system inhibitors as mediators of apoptosis for cancer therapy
-
Tonissen, K. F.; Di Trapani, G. Thioredoxin system inhibitors as mediators of apoptosis for cancer therapy Mol. Nutr. Food Res. 2009, 53, 87-103
-
(2009)
Mol. Nutr. Food Res.
, vol.53
, pp. 87-103
-
-
Tonissen, K.F.1
Di Trapani, G.2
-
4
-
-
0035029131
-
Properties and biological activities of thioredoxins
-
Powis, G.; Montfort, W. R. Properties and biological activities of thioredoxins Annu. Rev. Pharmacol. Toxicol. 2001, 41, 261-295
-
(2001)
Annu. Rev. Pharmacol. Toxicol.
, vol.41
, pp. 261-295
-
-
Powis, G.1
Montfort, W.R.2
-
5
-
-
0037036358
-
Reversible inactivation of the tumor suppressor PTEN by H2O2
-
Lee, S. R.; Yang, K. S.; Kwon, J.; Lee, C.; Jeong, W.; Rhee, S. G. Reversible inactivation of the tumor suppressor PTEN by H2O2 J. Biol. Chem. 2002, 277, 20336-20342
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 20336-20342
-
-
Lee, S.R.1
Yang, K.S.2
Kwon, J.3
Lee, C.4
Jeong, W.5
Rhee, S.G.6
-
6
-
-
0041323072
-
Catalytic and chemical competence of regulation of cdc25 phosphatase by oxidation/reduction
-
Sohn, J.; Rudolph, J. Catalytic and chemical competence of regulation of cdc25 phosphatase by oxidation/reduction Biochemistry 2003, 42, 10060-10070
-
(2003)
Biochemistry
, vol.42
, pp. 10060-10070
-
-
Sohn, J.1
Rudolph, J.2
-
8
-
-
0030585429
-
Crystal structures of reduced, oxidized, and mutated human thioredoxins: Evidence for a regulatory homodimer
-
Weichsel, A.; Gasdaska, J. R.; Powis, G.; Montfort, W. R. Crystal structures of reduced, oxidized, and mutated human thioredoxins: evidence for a regulatory homodimer Structure 1996, 4, 735-751
-
(1996)
Structure
, vol.4
, pp. 735-751
-
-
Weichsel, A.1
Gasdaska, J.R.2
Powis, G.3
Montfort, W.R.4
-
9
-
-
0000962563
-
Three-dimensional structure of Escherichia coli thioredoxin-S2 to 2.8 A resolution
-
Holmgren, A.; Soderberg, B. O.; Eklund, H.; Branden, C. I. Three-dimensional structure of Escherichia coli thioredoxin-S2 to 2.8 A resolution Proc. Natl. Acad. Sci. U.S.A. 1975, 72, 2305-2309
-
(1975)
Proc. Natl. Acad. Sci. U.S.A.
, vol.72
, pp. 2305-2309
-
-
Holmgren, A.1
Soderberg, B.O.2
Eklund, H.3
Branden, C.I.4
-
10
-
-
0025909444
-
High-resolution three-dimensional structure of reduced recombinant human thioredoxin in solution
-
Forman-Kay, J. D.; Clore, G. M.; Wingfield, P. T.; Gronenborn, A. M. High-resolution three-dimensional structure of reduced recombinant human thioredoxin in solution Biochemistry 1991, 30, 2685-2698
-
(1991)
Biochemistry
, vol.30
, pp. 2685-2698
-
-
Forman-Kay, J.D.1
Clore, G.M.2
Wingfield, P.T.3
Gronenborn, A.M.4
-
11
-
-
0019163962
-
Differential reactivity of the functional sulfhydryl groups of cysteine-32 and cysteine-35 present in the reduced form of thioredoxin from Escherichia coli
-
Kallis, G. B.; Holmgren, A. Differential reactivity of the functional sulfhydryl groups of cysteine-32 and cysteine-35 present in the reduced form of thioredoxin from Escherichia coli J. Biol. Chem. 1980, 255, 10261-10265
-
(1980)
J. Biol. Chem.
, vol.255
, pp. 10261-10265
-
-
Kallis, G.B.1
Holmgren, A.2
-
12
-
-
79960322216
-
Crystal structure of the human thioredoxin reductase-thioredoxin complex
-
Fritz-Wolf, K.; Kehr, S.; Stumpf, M.; Rahlfs, S.; Becker, K. Crystal structure of the human thioredoxin reductase-thioredoxin complex Nat. Commun. 2011, 2, 383
-
(2011)
Nat. Commun.
, vol.2
, pp. 383
-
-
Fritz-Wolf, K.1
Kehr, S.2
Stumpf, M.3
Rahlfs, S.4
Becker, K.5
-
13
-
-
44949114211
-
Thioredoxin reductase inhibition by antitumor quinols: A quinol pharmacophore effect correlating to antiproliferative activity
-
Chew, E. H.; Lu, J.; Bradshaw, T. D.; Holmgren, A. Thioredoxin reductase inhibition by antitumor quinols: A quinol pharmacophore effect correlating to antiproliferative activity FASEB J. 2008, 22, 2072-2083
-
(2008)
FASEB J.
, vol.22
, pp. 2072-2083
-
-
Chew, E.H.1
Lu, J.2
Bradshaw, T.D.3
Holmgren, A.4
-
14
-
-
4244218956
-
Cyclic oxidation and reduction of protein methionine residues is an important antioxidant mechanism
-
Stadtman, E. R.; Moskovitz, J.; Berlett, B. S.; Levine, R. L. Cyclic oxidation and reduction of protein methionine residues is an important antioxidant mechanism Mol. Cell. Biochem. 2002, 234-235, 3-9
-
(2002)
Mol. Cell. Biochem.
, vol.234-235
, pp. 3-9
-
-
Stadtman, E.R.1
Moskovitz, J.2
Berlett, B.S.3
Levine, R.L.4
-
15
-
-
0034703631
-
Thioredoxin, a singlet oxygen quencher and hydroxyl radical scavenger: Redox independent functions
-
Das, K. C.; Das, C. K. Thioredoxin, a singlet oxygen quencher and hydroxyl radical scavenger: redox independent functions Biochem. Biophys. Res. Commun. 2000, 277, 443-447
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.277
, pp. 443-447
-
-
Das, K.C.1
Das, C.K.2
-
16
-
-
44449119080
-
Regulated protein denitrosylation by cytosolic and mitochondrial thioredoxins
-
Benhar, M.; Forrester, M. T.; Hess, D. T.; Stamler, J. S. Regulated protein denitrosylation by cytosolic and mitochondrial thioredoxins Science 2008, 320, 1050-1054
-
(2008)
Science
, vol.320
, pp. 1050-1054
-
-
Benhar, M.1
Forrester, M.T.2
Hess, D.T.3
Stamler, J.S.4
-
17
-
-
0032080283
-
Mammalian thioredoxin is a direct inhibitor of apoptosis signal-regulating kinase (ASK) 1
-
Saitoh, M.; Nishitoh, H.; Fujii, M.; Takeda, K.; Tobiume, K.; Sawada, Y.; Kawabata, M.; Miyazono, K.; Ichijo, H. Mammalian thioredoxin is a direct inhibitor of apoptosis signal-regulating kinase (ASK) 1 EMBO J. 1998, 17, 2596-2606
-
(1998)
EMBO J.
, vol.17
, pp. 2596-2606
-
-
Saitoh, M.1
Nishitoh, H.2
Fujii, M.3
Takeda, K.4
Tobiume, K.5
Sawada, Y.6
Kawabata, M.7
Miyazono, K.8
Ichijo, H.9
-
18
-
-
34547427294
-
Thioredoxin is required for S-nitrosation of procaspase-3 and the inhibition of apoptosis in Jurkat cells
-
Mitchell, D. A.; Morton, S. U.; Fernhoff, N. B.; Marletta, M. A. Thioredoxin is required for S-nitrosation of procaspase-3 and the inhibition of apoptosis in Jurkat cells Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 11609-11614
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 11609-11614
-
-
Mitchell, D.A.1
Morton, S.U.2
Fernhoff, N.B.3
Marletta, M.A.4
-
19
-
-
24644441050
-
The thioredoxin reductase/thioredoxin system: Novel redox targets for cancer therapy
-
Biaglow, J. E.; Miller, R. A. The thioredoxin reductase/thioredoxin system: Novel redox targets for cancer therapy Cancer Biol. Ther. 2005, 4, 6-13
-
(2005)
Cancer Biol. Ther.
, vol.4
, pp. 6-13
-
-
Biaglow, J.E.1
Miller, R.A.2
-
20
-
-
0034797926
-
Thioredoxin expression is associated with lymph node status and prognosis in early operable non-small cell lung cancer
-
Kakolyris, S.; Giatromanolaki, A.; Koukourakis, M.; Powis, G.; Souglakos, J.; Sivridis, E.; Georgoulias, V.; Gatter, K. C.; Harris, A. L. Thioredoxin expression is associated with lymph node status and prognosis in early operable non-small cell lung cancer Clin. Cancer Res. 2001, 7, 3087-3091
-
(2001)
Clin. Cancer Res.
, vol.7
, pp. 3087-3091
-
-
Kakolyris, S.1
Giatromanolaki, A.2
Koukourakis, M.3
Powis, G.4
Souglakos, J.5
Sivridis, E.6
Georgoulias, V.7
Gatter, K.C.8
Harris, A.L.9
-
21
-
-
0042991494
-
Increased expression of thioredoxin-1 in human colorectal cancer is associated with decreased patient survival
-
Raffel, J.; Bhattacharyya, A. K.; Gallegos, A.; Cui, H.; Einspahr, J. G.; Alberts, D. S.; Powis, G. Increased expression of thioredoxin-1 in human colorectal cancer is associated with decreased patient survival J. Lab. Clin. Med. 2003, 142, 46-51
-
(2003)
J. Lab. Clin. Med.
, vol.142
, pp. 46-51
-
-
Raffel, J.1
Bhattacharyya, A.K.2
Gallegos, A.3
Cui, H.4
Einspahr, J.G.5
Alberts, D.S.6
Powis, G.7
-
22
-
-
0032562519
-
Thioredoxin redox control of cell growth and death and the effects of inhibitors
-
Powis, G.; Kirkpatrick, D. L.; Angulo, M.; Baker, A. Thioredoxin redox control of cell growth and death and the effects of inhibitors Chem.-Biol. Interact. 1998, 111-112, 23-34
-
(1998)
Chem.-Biol. Interact.
, vol.111-112
, pp. 23-34
-
-
Powis, G.1
Kirkpatrick, D.L.2
Angulo, M.3
Baker, A.4
-
23
-
-
0036735392
-
The redox protein thioredoxin-1 (Trx-1) increases hypoxia-inducible factor 1alpha protein expression: Trx-1 overexpression results in increased vascular endothelial growth factor production and enhanced tumor angiogenesis
-
Welsh, S. J.; Bellamy, W. T.; Briehl, M. M.; Powis, G. The redox protein thioredoxin-1 (Trx-1) increases hypoxia-inducible factor 1alpha protein expression: Trx-1 overexpression results in increased vascular endothelial growth factor production and enhanced tumor angiogenesis Cancer Res. 2002, 62, 5089-5095
-
(2002)
Cancer Res.
, vol.62
, pp. 5089-5095
-
-
Welsh, S.J.1
Bellamy, W.T.2
Briehl, M.M.3
Powis, G.4
-
24
-
-
0034832095
-
Thioredoxin alters the matrix metalloproteinase/tissue inhibitors of metalloproteinase balance and stimulates human SK-N-SH neuroblastoma cell invasion
-
Farina, A. R.; Tacconelli, A.; Cappabianca, L.; Masciulli, M. P.; Holmgren, A.; Beckett, G. J.; Gulino, A.; Mackay, A. R. Thioredoxin alters the matrix metalloproteinase/tissue inhibitors of metalloproteinase balance and stimulates human SK-N-SH neuroblastoma cell invasion Eur. J. Biochem. 2001, 268, 405-413
-
(2001)
Eur. J. Biochem.
, vol.268
, pp. 405-413
-
-
Farina, A.R.1
Tacconelli, A.2
Cappabianca, L.3
Masciulli, M.P.4
Holmgren, A.5
Beckett, G.J.6
Gulino, A.7
MacKay, A.R.8
-
25
-
-
28544450990
-
High thioredoxin expression is associated with resistance to docetaxel in primary breast cancer
-
Kim, S. J.; Miyoshi, Y.; Taguchi, T.; Tamaki, Y.; Nakamura, H.; Yodoi, J.; Kato, K.; Noguchi, S. High thioredoxin expression is associated with resistance to docetaxel in primary breast cancer Clin. Cancer Res. 2005, 11, 8425-8430
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 8425-8430
-
-
Kim, S.J.1
Miyoshi, Y.2
Taguchi, T.3
Tamaki, Y.4
Nakamura, H.5
Yodoi, J.6
Kato, K.7
Noguchi, S.8
-
26
-
-
0030956591
-
Possible roles of an adult T-cell leukemia (ATL)-derived factor/thioredoxin in the drug resistance of ATL to adriamycin
-
Wang, J.; Kobayashi, M.; Sakurada, K.; Imamura, M.; Moriuchi, T.; Hosokawa, M. Possible roles of an adult T-cell leukemia (ATL)-derived factor/thioredoxin in the drug resistance of ATL to adriamycin Blood 1997, 89, 2480-2487
-
(1997)
Blood
, vol.89
, pp. 2480-2487
-
-
Wang, J.1
Kobayashi, M.2
Sakurada, K.3
Imamura, M.4
Moriuchi, T.5
Hosokawa, M.6
-
27
-
-
0029938958
-
Increased expression of thioredoxin/adult T-cell leukemia-derived factor in cisplatin-resistant human cancer cell lines
-
Yamada, M.; Tomida, A.; Yoshikawa, H.; Taketani, Y.; Tsuruo, T. Increased expression of thioredoxin/adult T-cell leukemia-derived factor in cisplatin-resistant human cancer cell lines Clin. Cancer Res. 1996, 2, 427-432
-
(1996)
Clin. Cancer Res.
, vol.2
, pp. 427-432
-
-
Yamada, M.1
Tomida, A.2
Yoshikawa, H.3
Taketani, Y.4
Tsuruo, T.5
-
28
-
-
0029051872
-
Cellular levels of thioredoxin associated with drug sensitivity to cisplatin, mitomycin C, doxorubicin, and etoposide
-
Yokomizo, A.; Ono, M.; Nanri, H.; Makino, Y.; Ohga, T.; Wada, M.; Okamoto, T.; Yodoi, J.; Kuwano, M.; Kohno, K. Cellular levels of thioredoxin associated with drug sensitivity to cisplatin, mitomycin C, doxorubicin, and etoposide Cancer Res. 1995, 55, 4293-4296
-
(1995)
Cancer Res.
, vol.55
, pp. 4293-4296
-
-
Yokomizo, A.1
Ono, M.2
Nanri, H.3
Makino, Y.4
Ohga, T.5
Wada, M.6
Okamoto, T.7
Yodoi, J.8
Kuwano, M.9
Kohno, K.10
-
29
-
-
0032055646
-
Mechanisms of inhibition of the thioredoxin growth factor system by antitumor 2-imidazolyl disulfides
-
Kirkpatrick, D. L.; Kuperus, M.; Dowdeswell, M.; Potier, N.; Donald, L. J.; Kunkel, M.; Berggren, M.; Angulo, M.; Powis, G. Mechanisms of inhibition of the thioredoxin growth factor system by antitumor 2-imidazolyl disulfides Biochem. Pharmacol. 1998, 55, 987-994
-
(1998)
Biochem. Pharmacol.
, vol.55
, pp. 987-994
-
-
Kirkpatrick, D.L.1
Kuperus, M.2
Dowdeswell, M.3
Potier, N.4
Donald, L.J.5
Kunkel, M.6
Berggren, M.7
Angulo, M.8
Powis, G.9
-
30
-
-
0142144338
-
The thioredoxin redox inhibitors 1-methylpropyl 2-imidazolyl disulfide and pleurotin inhibit hypoxia-induced factor 1alpha and vascular endothelial growth factor formation
-
Welsh, S. J.; Williams, R. R.; Birmingham, A.; Newman, D. J.; Kirkpatrick, D. L.; Powis, G. The thioredoxin redox inhibitors 1-methylpropyl 2-imidazolyl disulfide and pleurotin inhibit hypoxia-induced factor 1alpha and vascular endothelial growth factor formation Mol. Cancer Ther. 2003, 2, 235-243
-
(2003)
Mol. Cancer Ther.
, vol.2
, pp. 235-243
-
-
Welsh, S.J.1
Williams, R.R.2
Birmingham, A.3
Newman, D.J.4
Kirkpatrick, D.L.5
Powis, G.6
-
31
-
-
34247507112
-
A Phase i pharmacokinetic and pharmacodynamic study of PX-12, a novel inhibitor of thioredoxin-1, in patients with advanced solid tumors
-
Ramanathan, R. K.; Kirkpatrick, D. L.; Belani, C. P.; Friedland, D.; Green, S. B.; Chow, H. H.; Cordova, C. A.; Stratton, S. P.; Sharlow, E. R.; Baker, A.; Dragovich, T. A Phase I pharmacokinetic and pharmacodynamic study of PX-12, a novel inhibitor of thioredoxin-1, in patients with advanced solid tumors Clin. Cancer Res. 2007, 13, 2109-2114
-
(2007)
Clin. Cancer Res.
, vol.13
, pp. 2109-2114
-
-
Ramanathan, R.K.1
Kirkpatrick, D.L.2
Belani, C.P.3
Friedland, D.4
Green, S.B.5
Chow, H.H.6
Cordova, C.A.7
Stratton, S.P.8
Sharlow, E.R.9
Baker, A.10
Dragovich, T.11
-
32
-
-
33645466124
-
Molecular pharmacology and antitumor activity of palmarumycin-based inhibitors of thioredoxin reductase
-
Powis, G.; Wipf, P.; Lynch, S. M.; Birmingham, A.; Kirkpatrick, D. L. Molecular pharmacology and antitumor activity of palmarumycin-based inhibitors of thioredoxin reductase Mol. Cancer Ther. 2006, 5, 630-636
-
(2006)
Mol. Cancer Ther.
, vol.5
, pp. 630-636
-
-
Powis, G.1
Wipf, P.2
Lynch, S.M.3
Birmingham, A.4
Kirkpatrick, D.L.5
-
33
-
-
0035829182
-
New inhibitors of the thioredoxin-thioredoxin reductase system based on a naphthoquinone spiroketal natural product lead
-
Wipf, P.; Hopkins, T. D.; Jung, J. K.; Rodriguez, S.; Birmingham, A.; Southwick, E. C.; Lazo, J. S.; Powis, G. New inhibitors of the thioredoxin-thioredoxin reductase system based on a naphthoquinone spiroketal natural product lead Bioorg. Med. Chem. Lett. 2001, 11, 2637-2641
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2637-2641
-
-
Wipf, P.1
Hopkins, T.D.2
Jung, J.K.3
Rodriguez, S.4
Birmingham, A.5
Southwick, E.C.6
Lazo, J.S.7
Powis, G.8
-
34
-
-
1642452655
-
Mitochondrial thioredoxin reductase inhibition by gold(I) compounds and concurrent stimulation of permeability transition and release of cytochrome c
-
Rigobello, M. P.; Scutari, G.; Folda, A.; Bindoli, A. Mitochondrial thioredoxin reductase inhibition by gold(I) compounds and concurrent stimulation of permeability transition and release of cytochrome c Biochem. Pharmacol. 2004, 67, 689-696
-
(2004)
Biochem. Pharmacol.
, vol.67
, pp. 689-696
-
-
Rigobello, M.P.1
Scutari, G.2
Folda, A.3
Bindoli, A.4
-
35
-
-
0037331676
-
Thioredoxin reductase and cancer cell growth inhibition by organotellurium antioxidants
-
Engman, L.; Al-Maharik, N.; McNaughton, M.; Birmingham, A.; Powis, G. Thioredoxin reductase and cancer cell growth inhibition by organotellurium antioxidants Anticancer Drugs 2003, 14, 153-161
-
(2003)
Anticancer Drugs
, vol.14
, pp. 153-161
-
-
Engman, L.1
Al-Maharik, N.2
McNaughton, M.3
Birmingham, A.4
Powis, G.5
-
36
-
-
20944439854
-
Elucidation of thioredoxin as a molecular target for antitumor quinols
-
Bradshaw, T. D.; Matthews, C. S.; Cookson, J.; Chew, E. H.; Shah, M.; Bailey, K.; Monks, A.; Harris, E.; Westwell, A. D.; Wells, G.; Laughton, C. A.; Stevens, M. F. Elucidation of thioredoxin as a molecular target for antitumor quinols Cancer Res. 2005, 65, 3911-3919
-
(2005)
Cancer Res.
, vol.65
, pp. 3911-3919
-
-
Bradshaw, T.D.1
Matthews, C.S.2
Cookson, J.3
Chew, E.H.4
Shah, M.5
Bailey, K.6
Monks, A.7
Harris, E.8
Westwell, A.D.9
Wells, G.10
Laughton, C.A.11
Stevens, M.F.12
-
37
-
-
0037015071
-
The histone deacetylase inhibitor SAHA arrests cancer cell growth, up-regulates thioredoxin-binding protein-2, and down-regulates thioredoxin
-
Butler, L. M.; Zhou, X.; Xu, W. S.; Scher, H. I.; Rifkind, R. A.; Marks, P. A.; Richon, V. M. The histone deacetylase inhibitor SAHA arrests cancer cell growth, up-regulates thioredoxin-binding protein-2, and down-regulates thioredoxin Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 11700-11705
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 11700-11705
-
-
Butler, L.M.1
Zhou, X.2
Xu, W.S.3
Scher, H.I.4
Rifkind, R.A.5
Marks, P.A.6
Richon, V.M.7
-
38
-
-
21644477778
-
Thioredoxin reductase is irreversibly modified by curcumin: A novel molecular mechanism for its anticancer activity
-
Fang, J.; Lu, J.; Holmgren, A. Thioredoxin reductase is irreversibly modified by curcumin: A novel molecular mechanism for its anticancer activity J. Biol. Chem. 2005, 280, 25284-25290
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 25284-25290
-
-
Fang, J.1
Lu, J.2
Holmgren, A.3
-
39
-
-
2942700238
-
Natural product based inhibitors of the thioredoxin-thioredoxin reductase system
-
Wipf, P.; Lynch, S. M.; Birmingham, A.; Tamayo, G.; Jimenez, A.; Campos, N.; Powis, G. Natural product based inhibitors of the thioredoxin-thioredoxin reductase system Org. Biomol. Chem. 2004, 2, 1651-1658
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 1651-1658
-
-
Wipf, P.1
Lynch, S.M.2
Birmingham, A.3
Tamayo, G.4
Jimenez, A.5
Campos, N.6
Powis, G.7
-
40
-
-
0141922903
-
Induction of apoptosis without redox catastrophe by thioredoxin- inhibitory compounds
-
Pallis, M.; Bradshaw, T. D.; Westwell, A. D.; Grundy, M.; Stevens, M. F.; Russell, N. Induction of apoptosis without redox catastrophe by thioredoxin-inhibitory compounds Biochem. Pharmacol. 2003, 66, 1695-1705
-
(2003)
Biochem. Pharmacol.
, vol.66
, pp. 1695-1705
-
-
Pallis, M.1
Bradshaw, T.D.2
Westwell, A.D.3
Grundy, M.4
Stevens, M.F.5
Russell, N.6
-
41
-
-
10744226522
-
Mechanism-based inactivation of thioredoxin reductase from Plasmodium falciparum by Mannich bases. Implication for cytotoxicity
-
Davioud-Charvet, E.; McLeish, M. J.; Veine, D. M.; Giegel, D.; Arscott, L. D.; Andricopulo, A. D.; Becker, K.; Muller, S.; Schirmer, R. H.; Williams, C. H., Jr.; Kenyon, G. L. Mechanism-based inactivation of thioredoxin reductase from Plasmodium falciparum by Mannich bases. Implication for cytotoxicity Biochemistry 2003, 42, 13319-13330
-
(2003)
Biochemistry
, vol.42
, pp. 13319-13330
-
-
Davioud-Charvet, E.1
McLeish, M.J.2
Veine, D.M.3
Giegel, D.4
Arscott, L.D.5
Andricopulo, A.D.6
Becker, K.7
Muller, S.8
Schirmer, R.H.9
Williams Jr., C.H.10
Kenyon, G.L.11
-
42
-
-
84855843872
-
-
PCT Int. Appl. WO 2000006088 A2 20000210
-
PCT Int. Appl. WO 2000006088 A2 20000210, 2000.
-
(2000)
-
-
-
43
-
-
0018728098
-
Reduction of disulfides by thioredoxin. Exceptional reactivity of insulin and suggested functions of thioredoxin in mechanism of hormone action
-
Holmgren, A. Reduction of disulfides by thioredoxin. Exceptional reactivity of insulin and suggested functions of thioredoxin in mechanism of hormone action J. Biol. Chem. 1979, 254, 9113-9119
-
(1979)
J. Biol. Chem.
, vol.254
, pp. 9113-9119
-
-
Holmgren, A.1
-
44
-
-
0028038601
-
Peptidomimetics-Tailored enzyme inhibitors
-
Gante, J. Peptidomimetics-Tailored enzyme inhibitors Angew. Chem., Int. Ed. 1994, 33, 1699-1720
-
(1994)
Angew. Chem., Int. Ed.
, vol.33
, pp. 1699-1720
-
-
Gante, J.1
-
45
-
-
77649210502
-
Studies of the synthesis of all stereoisomers of MG-132 proteasome inhibitors in the tumor targeting approach
-
Mroczkiewicz, M.; Winkler, K.; Nowis, D.; Placha, G.; Golab, J.; Ostaszewski, R. Studies of the synthesis of all stereoisomers of MG-132 proteasome inhibitors in the tumor targeting approach J. Med. Chem. 2010, 53, 1509-1518
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1509-1518
-
-
Mroczkiewicz, M.1
Winkler, K.2
Nowis, D.3
Placha, G.4
Golab, J.5
Ostaszewski, R.6
-
46
-
-
0345010930
-
An attempted total synthesis if lysergic acid via an alkene/N- sulfonylimine cyclization
-
Ralbovsky, L. J.; Scola, M. P.; Sugino, E.; Burgos-Garcia, C.; Weinreb, M. S.; Parves, M. An attempted total synthesis if lysergic acid via an alkene/N-sulfonylimine cyclization Heterocycles 1996, 43, 1497-1512
-
(1996)
Heterocycles
, vol.43
, pp. 1497-1512
-
-
Ralbovsky, L.J.1
Scola, M.P.2
Sugino, E.3
Burgos-Garcia, C.4
Weinreb, M.S.5
Parves, M.6
-
47
-
-
85005647840
-
Isocyanide synthesis with phosphoryl chloride and diisopropylamine
-
Obrecht, R.; Herrmann, R.; Ugi, I. Isocyanide synthesis with phosphoryl chloride and diisopropylamine Synthesis 1985, 4, 400-402
-
(1985)
Synthesis
, vol.4
, pp. 400-402
-
-
Obrecht, R.1
Herrmann, R.2
Ugi, I.3
-
48
-
-
0018468568
-
Reagents for the crosslinking of proteins by equilibrium transfer alkylation
-
Mitra, S.; Lawton, R. G. Reagents for the crosslinking of proteins by equilibrium transfer alkylation J. Am. Chem. Soc. 1979, 101, 3097-3110
-
(1979)
J. Am. Chem. Soc.
, vol.101
, pp. 3097-3110
-
-
Mitra, S.1
Lawton, R.G.2
-
49
-
-
33845647216
-
Rapid combinatorial access to macrocyclic ansapeptoids and ansapeptides with natural-product-like core structures
-
Greef de, M.; Abeln, S.; Belkasmi, K.; Dömling, A.; Orru, V. A. R.; Wessjohann, A. L. Rapid combinatorial access to macrocyclic ansapeptoids and ansapeptides with natural-product-like core structures Synthesis 2006, 23, 3997-4004
-
(2006)
Synthesis
, vol.23
, pp. 3997-4004
-
-
De, G.M.1
Abeln, S.2
Belkasmi, K.3
Dömling, A.4
Orru, V.A.R.5
Wessjohann, A.L.6
-
50
-
-
0028264433
-
In vivo inhibition of cathepsin B by peptidyl (acyloxy)methyl ketones
-
Wagner, B. M.; Smith, R. A.; Coles, P. J.; Copp, L. J.; Ernest, M. J.; Krantz, A. In vivo inhibition of cathepsin B by peptidyl (acyloxy)methyl ketones J. Med. Chem. 1994, 37, 1833-1840
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1833-1840
-
-
Wagner, B.M.1
Smith, R.A.2
Coles, P.J.3
Copp, L.J.4
Ernest, M.J.5
Krantz, A.6
-
51
-
-
0026602786
-
Synthesis and evaluation of imidazolyl disulfides for selective cytotoxicity to hypoxic EMT6 tumor cells in vitro
-
Kirkpatrick, D. L.; Jimale, M. L.; King, K. M.; Chen, T. Synthesis and evaluation of imidazolyl disulfides for selective cytotoxicity to hypoxic EMT6 tumor cells in vitro Eur. J. Med. Chem. 1992, 27, 33-37
-
(1992)
Eur. J. Med. Chem.
, vol.27
, pp. 33-37
-
-
Kirkpatrick, D.L.1
Jimale, M.L.2
King, K.M.3
Chen, T.4
-
52
-
-
0142039915
-
The Staphostatin-staphopain complex: A forward binding inhibitor in complex with its target cysteine protease
-
Filipek, R.; Rzychon, M.; Oleksy, A.; Gruca, M.; Dubin, A.; Potempa, J.; Bochtler, M. The Staphostatin-staphopain complex: A forward binding inhibitor in complex with its target cysteine protease J. Biol. Chem. 2003, 278, 40959-40966
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 40959-40966
-
-
Filipek, R.1
Rzychon, M.2
Oleksy, A.3
Gruca, M.4
Dubin, A.5
Potempa, J.6
Bochtler, M.7
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