-
2
-
-
0036447366
-
Potential Clinical Applications of Poly(ADP-ribose) Polymerase PARP Inhibitors
-
Tentori, C.; Portarena, I.; Graziani, G. Potential Clinical Applications of Poly(ADP-ribose) Polymerase PARP Inhibitors. Pharamcol. Res. 2002, 45, 73-85.
-
(2002)
Pharamcol. Res
, vol.45
, pp. 73-85
-
-
Tentori, C.1
Portarena, I.2
Graziani, G.3
-
3
-
-
0003401121
-
-
de Murcia, C, Shall, S, Eds, Oxford University Press: Oxford, U.K
-
de Murcia, C., Shall, S., Eds. From DNA Damage and Stress Signalling to Cell Death. Poly ADP-Ribolysation Reactions; Oxford University Press: Oxford, U.K., 2000.
-
(2000)
From DNA Damage and Stress Signalling to Cell Death. Poly ADP-Ribolysation Reactions
-
-
-
4
-
-
0030842946
-
Poly(ADP-ribose) polymerase gene disruption renders mice resistant to cerebral ischemia
-
Eliasson, M. J.; Sampei, K.; Mandir, A. S.; Hurn, P. D.; Traystman, R. J.; Bao, J.; Piper, A.; Wang, Z. Q.; Dawson, T. M.; Snyder, S. H.; Davson, V. L. Poly(ADP-ribose) polymerase gene disruption renders mice resistant to cerebral ischemia. Nat. Med. 1997, 3, 1089-1095.
-
(1997)
Nat. Med
, vol.3
, pp. 1089-1095
-
-
Eliasson, M.J.1
Sampei, K.2
Mandir, A.S.3
Hurn, P.D.4
Traystman, R.J.5
Bao, J.6
Piper, A.7
Wang, Z.Q.8
Dawson, T.M.9
Snyder, S.H.10
Davson, V.L.11
-
5
-
-
0034697060
-
The neuroprotective effect of cerebral poly(ADP-ribose) poly-merase inhibition in a rat model of global ischemia
-
(a) Plascke, K.; Kopitz, J.; Weigand, M. A.; Martin, E.; Bardenheuer, H. J. The neuroprotective effect of cerebral poly(ADP-ribose) poly-merase inhibition in a rat model of global ischemia. Neurosci. Lett. 2000, 248, 109-112.
-
(2000)
Neurosci. Lett
, vol.248
, pp. 109-112
-
-
Plascke, K.1
Kopitz, J.2
Weigand, M.A.3
Martin, E.4
Bardenheuer, H.J.5
-
6
-
-
33744790313
-
In vitro effect of the potent poly(ADP-ribose) polymerase (PARP) inhibitor INO-1001 alone and in combination with aspirin, eptifibatide, tirofiban, enoxaparin or alteplase on haemostatic parameters
-
(b) Tóth, O.; Szabó, C.; Kecskés, M.; Pótó, L.; Nagy, A.; Losonczy, H. In vitro effect of the potent poly(ADP-ribose) polymerase (PARP) inhibitor INO-1001 alone and in combination with aspirin, eptifibatide, tirofiban, enoxaparin or alteplase on haemostatic parameters. Life Sci. 2006, 79, 317-323.
-
(2006)
Life Sci
, vol.79
, pp. 317-323
-
-
Tóth, O.1
Szabó, C.2
Kecskés, M.3
Pótó, L.4
Nagy, A.5
Losonczy, H.6
-
7
-
-
0033954867
-
BGP-15, a nicotinic amidoxime derivate protecting heart from ischemia reper- fusion injury through modulation of poly(ADP-ribose) polymerase
-
Szabados, E.; Literati-Nagy, P.; Farkas, B.; Sumegi, B. BGP-15, a nicotinic amidoxime derivate protecting heart from ischemia reper- fusion injury through modulation of poly(ADP-ribose) polymerase. Biochem. Pharmacol. 2000, 59, 937-945.
-
(2000)
Biochem. Pharmacol
, vol.59
, pp. 937-945
-
-
Szabados, E.1
Literati-Nagy, P.2
Farkas, B.3
Sumegi, B.4
-
8
-
-
0032539957
-
+ binding to poly(ADP-ribose) polymerase as derived from crystal structures and homology modeling
-
+ binding to poly(ADP-ribose) polymerase as derived from crystal structures and homology modeling. Biochemistry 1998, 37, 3893-3900.
-
(1998)
Biochemistry
, vol.37
, pp. 3893-3900
-
-
Ruf, A.1
DeMurcia, G.2
Schulz, G.E.3
-
9
-
-
0035829430
-
Modelling of poly(ADP-ribose)polymerase (PARP) inhibitors. Docking of ligands and quantitative structure-activity relationship analysis
-
(b) Costantino, G.; Macchiarulo, A.; Camaioni, E.; Pellicciari, R. Modelling of poly(ADP-ribose)polymerase (PARP) inhibitors. Docking of ligands and quantitative structure-activity relationship analysis. J. Med. Chem. 2001, 44, 3786-3794.
-
(2001)
J. Med. Chem
, vol.44
, pp. 3786-3794
-
-
Costantino, G.1
Macchiarulo, A.2
Camaioni, E.3
Pellicciari, R.4
-
10
-
-
0026601666
-
Specific inhibitors of poly(ADP-ribose) synthetase and mono(ADP-ribosyl)transferase
-
Banasik, M.; Komura, H.; Shimoyama, M.; Ueda, K. Specific inhibitors of poly(ADP-ribose) synthetase and mono(ADP-ribosyl)transferase. J. Biol. Chem. 1992, 267, 1569-1575.
-
(1992)
J. Biol. Chem
, vol.267
, pp. 1569-1575
-
-
Banasik, M.1
Komura, H.2
Shimoyama, M.3
Ueda, K.4
-
11
-
-
0036733355
-
The therapeutic potential of poly(ADP-ribose) polymerase inhibitors
-
(a) Virag, L.; Szabo, C. The therapeutic potential of poly(ADP-ribose) polymerase inhibitors. Pharmacol. Rev. 2002, 54, 375-429.
-
Pharmacol. Re
, vol.2002
, Issue.54
, pp. 375-429
-
-
Virag, L.1
Szabo, C.2
-
12
-
-
12844264683
-
Life or death decisions: The case of poly(ADP-ribose) polymerase (PARP) as a therapeutic target for brain ischaemia
-
(b) Pellicciari, R.; Camaioni, E.; Costantino, G. Life or death decisions: the case of poly(ADP-ribose) polymerase (PARP) as a therapeutic target for brain ischaemia. Prog. Med. Chem. 2004, 42, 125-169.
-
(2004)
Prog. Med. Chem
, vol.42
, pp. 125-169
-
-
Pellicciari, R.1
Camaioni, E.2
Costantino, G.3
-
13
-
-
20644450130
-
-
Peukert, S.; Schwahn, U.; Güssregen, S.; Schreuder, H. E.; Hofmeister, A. Poly(ADP-ribose) polymerase (PARP-1) inhibitors based on tetrahydro-1(2H)-isoquinoline scaffold: synthesis, biological evaluation and X-ray crystal structure. Synthesis 2005, 1550-1554.
-
(c) Peukert, S.; Schwahn, U.; Güssregen, S.; Schreuder, H. E.; Hofmeister, A. Poly(ADP-ribose) polymerase (PARP-1) inhibitors based on tetrahydro-1(2H)-isoquinoline scaffold: synthesis, biological evaluation and X-ray crystal structure. Synthesis 2005, 1550-1554.
-
-
-
-
14
-
-
24944544025
-
Poly(ADP-ribose)polymerase inhibition-where now?
-
(d) Woon, E. C.; Threadqill, M. D. Poly(ADP-ribose)polymerase inhibition-where now? Curr. Med. Chem. 2005, 12, 2373-2392.
-
(2005)
Curr. Med. Chem
, vol.12
, pp. 2373-2392
-
-
Woon, E.C.1
Threadqill, M.D.2
-
15
-
-
18944390248
-
Poly(ADP-ribose) polymerase and the therapeutic effects of its inhibitors
-
(e) Jagtap, P.; Szabó, C. Poly(ADP-ribose) polymerase and the therapeutic effects of its inhibitors. Nat. Rev. Drug Discovery 2005, 4, 421-440.
-
(2005)
Nat. Rev. Drug Discovery
, vol.4
, pp. 421-440
-
-
Jagtap, P.1
Szabó, C.2
-
16
-
-
34250370941
-
Poly(ADP-ribose) polymerase as a drug target for cardiovascular disease and cancer: An update
-
(f) Horvath, E. M.; Szabo, C. Poly(ADP-ribose) polymerase as a drug target for cardiovascular disease and cancer: an update. Drug News Perspect. 2007, 20, 171-181.
-
(2007)
Drug News Perspect
, vol.20
, pp. 171-181
-
-
Horvath, E.M.1
Szabo, C.2
-
17
-
-
0034597569
-
Resistance-modifying agents. 9. Synthesis and biological properties of benzimidazole inhibitors of the DNA repair enzyme poly(ADR-ribose) polymerase
-
White, A. W.; Almassy, R.; Calvert, A. H.; Curtin, N. J.; Griffin, R. J.; Hostomsky, Z.; Maegley, K.; Newell, D. R.; Srinivasan, S.; Golding, B. T. Resistance-modifying agents. 9. Synthesis and biological properties of benzimidazole inhibitors of the DNA repair enzyme poly(ADR-ribose) polymerase. J. Med. Chem. 2000, 43, 4084-4097.
-
(2000)
J. Med. Chem
, vol.43
, pp. 4084-4097
-
-
White, A.W.1
Almassy, R.2
Calvert, A.H.3
Curtin, N.J.4
Griffin, R.J.5
Hostomsky, Z.6
Maegley, K.7
Newell, D.R.8
Srinivasan, S.9
Golding, B.T.10
-
18
-
-
19444362951
-
Clinical perspectives of PARP inhibitors
-
Graziani, G.; Szaboa, C. Clinical perspectives of PARP inhibitors. Pharmacol. Res. 2005, 52, 109-118.
-
(2005)
Pharmacol. Res
, vol.52
, pp. 109-118
-
-
Graziani, G.1
Szaboa, C.2
-
19
-
-
0033779864
-
A pyrroline derivative of mexiletine offers marked protection against ischemia/reperfusion-induced myocardial contractile dysfunction
-
Li, H.; Xu, K. Y.; Zhou, L.; Kalai, T.; Zweier, J. L.; Hideg, K.; Kuppusamy, P. A pyrroline derivative of mexiletine offers marked protection against ischemia/reperfusion-induced myocardial contractile dysfunction. J. Pharmacol. Exp. Ther. 2000, 295, 563-571.
-
(2000)
J. Pharmacol. Exp. Ther
, vol.295
, pp. 563-571
-
-
Li, H.1
Xu, K.Y.2
Zhou, L.3
Kalai, T.4
Zweier, J.L.5
Hideg, K.6
Kuppusamy, P.7
-
20
-
-
14844299446
-
-
Kálai, T.; Várbíró, G.; Bognár, Z.; Pálfi, A.; Hantó, K.; Bognár, B.; O″sz, E.; Sümegi, B.; Hideg, K. Synthesis and evaluation of the permeability transition inhibitory characteristics of paramagnetic and diamagnetic amiodarone derivatives. Bioorg. Med. Chem. 2005, 13, 2629-2636.
-
(a) Kálai, T.; Várbíró, G.; Bognár, Z.; Pálfi, A.; Hantó, K.; Bognár, B.; (O″sz, E.; Sümegi, B.; Hideg, K. Synthesis and evaluation of the permeability transition inhibitory characteristics of paramagnetic and diamagnetic amiodarone derivatives. Bioorg. Med. Chem. 2005, 13, 2629-2636.
-
-
-
-
21
-
-
33746682437
-
A novel SOD- mimetic permeability transition inhibitor agent protects ischemic heart by inhibiting both apoptotic and nectrotic cell death
-
(b) Bognár, Z.; Kálai, T.; Pálfi, A.; Hantó, K.; Bognár, B.; Márk, L.; Szabó, Z.; Tapodi, A.; Radnai, B.; Sárszegi, Zs.; Szántó, Á., Jr.; Gallyas, F.; Hideg, K.; Sumegi, B.; Várbíró, G. A novel SOD- mimetic permeability transition inhibitor agent protects ischemic heart by inhibiting both apoptotic and nectrotic cell death. Free Radical Biol. Med. 2006, 41, 835-848.
-
(2006)
Free Radical Biol. Med
, vol.41
, pp. 835-848
-
-
Bognár, Z.1
Kálai, T.2
Pálfi, A.3
Hantó, K.4
Bognár, B.5
Márk, L.6
Szabó, Z.7
Tapodi, A.8
Radnai, B.9
Sárszegi, Z.10
Szántó Jr., A.11
Gallyas, F.12
Hideg, K.13
Sumegi, B.14
Várbíró, G.15
-
22
-
-
33745600577
-
Structure- activity studies on the protection of trimetazidine derivatives modified with nitroxides and their precursor from myocardial ischemia-reperfusion injury
-
(a) Kailai, T.; Khan, M.; Balog, M.; Kutala, K. V.; Kuppusamy, P.; Hideg, K. Structure- activity studies on the protection of trimetazidine derivatives modified with nitroxides and their precursor from myocardial ischemia-reperfusion injury. Bioorg. Med. Chem. 2006, 14, 5510-5516.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 5510-5516
-
-
Kailai, T.1
Khan, M.2
Balog, M.3
Kutala, K.V.4
Kuppusamy, P.5
Hideg, K.6
-
23
-
-
33646814422
-
Attenuation of myocardial ischemia- reperfusion injury by trimetazidine derivatives functionalized with antioxidant properties
-
(b) Kutala, V. K.; Khan, M.; Mandal, R.; Ganesan, L. P.; Tridandapani, S.; Kálai, T.; Hideg, K.; Kuppusamy, P. Attenuation of myocardial ischemia- reperfusion injury by trimetazidine derivatives functionalized with antioxidant properties. J. Pharmacol. Exp. Ther. 2006, 317, 921-928.
-
(2006)
J. Pharmacol. Exp. Ther
, vol.317
, pp. 921-928
-
-
Kutala, V.K.1
Khan, M.2
Mandal, R.3
Ganesan, L.P.4
Tridandapani, S.5
Kálai, T.6
Hideg, K.7
Kuppusamy, P.8
-
24
-
-
3242794178
-
From magic bullets to designed multiple ligands
-
Morphy, R.; Kay, C.; Rankovic, Z. From magic bullets to designed multiple ligands. Drug Discovery Today 2004, 9, 641-651.
-
(2004)
Drug Discovery Today
, vol.9
, pp. 641-651
-
-
Morphy, R.1
Kay, C.2
Rankovic, Z.3
-
25
-
-
57449113590
-
Nitric oxide and nitroxides can act as efficient scavengers of protein- derived free radicals
-
Lam, A. M.; Pattison, D. I.; Bottle, S. E.; Keddie, J. D.; Davies, J. M. Nitric oxide and nitroxides can act as efficient scavengers of protein- derived free radicals. Chem. Res. Toxicol. 2008, 21, 2111-2119.
-
(2008)
Chem. Res. Toxicol
, vol.21
, pp. 2111-2119
-
-
Lam, A.M.1
Pattison, D.I.2
Bottle, S.E.3
Keddie, J.D.4
Davies, J.M.5
-
26
-
-
0029860317
-
·- or as SOD mimics?
-
·- or as SOD mimics? J. Biol. Chem. 1996, 271, 26026-26031.
-
(1996)
J. Biol. Chem
, vol.271
, pp. 26026-26031
-
-
Krishna, M.C.1
Russo, A.2
Mitchell, J.B.3
Goldstein, S.4
Hafni, H.5
Samuni, A.6
-
27
-
-
0034953441
-
Structure-activity relationship studies of protective function of nitroxides in Fenton system
-
Glebska, J.; Pulaski, L.; Gwozdzinski, K.; Kolimowski, J. Structure-activity relationship studies of protective function of nitroxides in Fenton system. BioMetals 2001, 14, 159-170.
-
(2001)
BioMetals
, vol.14
, pp. 159-170
-
-
Glebska, J.1
Pulaski, L.2
Gwozdzinski, K.3
Kolimowski, J.4
-
28
-
-
0031029545
-
Direct evidence for in vivo nitroxide free radical production from a new antiarrhythmic drug by EPR spectroscopy
-
Twomey, P.; Taira, J.; DeGraff, W.; Mitchell, J. B.; Russo, A.; Krishna, M. C.; Hankovszky, H. O.; Frank, L.; Hideg, K. Direct evidence for in vivo nitroxide free radical production from a new antiarrhythmic drug by EPR spectroscopy. Free Radical Biol. Med. 1997, 22, 909-916.
-
(1997)
Free Radical Biol. Med
, vol.22
, pp. 909-916
-
-
Twomey, P.1
Taira, J.2
DeGraff, W.3
Mitchell, J.B.4
Russo, A.5
Krishna, M.C.6
Hankovszky, H.O.7
Frank, L.8
Hideg, K.9
-
29
-
-
33845932682
-
Reversible reduction of nitroxides to hydroxilamines: Roles of ascorbate and glutathione
-
Bobko, A.; Kirilyuk, I. A.; Grigor'ev, I. A.; Zweier, J. L.; Khramtsov, V. V. Reversible reduction of nitroxides to hydroxilamines: roles of ascorbate and glutathione. Free Radical Biol. Med. 2007, 42, 404-412.
-
(2007)
Free Radical Biol. Med
, vol.42
, pp. 404-412
-
-
Bobko, A.1
Kirilyuk, I.A.2
Grigor'ev, I.A.3
Zweier, J.L.4
Khramtsov, V.V.5
-
30
-
-
18144450769
-
Synthesis and study of new 4-quinazolinone inhibitors of the DNA repair enzyme poly(ADP-ribose) polymerase (PARP)
-
Kulcsár, Gy.; Kalai, T.; O″sz, E.; Sár, C. P.; Jeko″, J.; Sümegi, B.; Hideg, K. Synthesis and study of new 4-quinazolinone inhibitors of the DNA repair enzyme poly(ADP-ribose) polymerase (PARP). ARKIVOC 2003, (Part iv), 121-131.
-
(2003)
ARKIVOC
, Issue.PART IV
, pp. 121-131
-
-
Kulcsár, G.1
Kalai, T.2
O″sz, E.3
Sár, C.P.4
Jeko″, J.5
Sümegi, B.6
Hideg, K.7
-
31
-
-
10744224018
-
Inhibition of ADP-evoked platelet aggregation by selected poly(ADP-ribose) polymerase Inhibitors
-
Alexy, T.; Tóth, A.; Marton, Z.; Horváth, B.; Koltai, K.; Fehér, G.; Kesmarky, G.; Kálai, T.; Hideg, K.; Sümegi, B.; Tóth, K. Inhibition of ADP-evoked platelet aggregation by selected poly(ADP-ribose) polymerase Inhibitors. J. Cardiovasc. Pharmacol. 2004, 43, 423-431.
-
(2004)
J. Cardiovasc. Pharmacol
, vol.43
, pp. 423-431
-
-
Alexy, T.1
Tóth, A.2
Marton, Z.3
Horváth, B.4
Koltai, K.5
Fehér, G.6
Kesmarky, G.7
Kálai, T.8
Hideg, K.9
Sümegi, B.10
Tóth, K.11
-
32
-
-
34547873881
-
Process development for ABT-472, a benzimidazole PARP inhibitor
-
Barkalow, J. H.; Breting, J.; Gaede, J. B.; Haight, R. A.; Henry, R.; Kotecki, B.; Mei, J.; Pearl, K. B.; Tedrow, J. S.; Viswanath, S. K. Process development for ABT-472, a benzimidazole PARP inhibitor. Org. Process Res. Dev. 2007, 11, 693-698.
-
(2007)
Org. Process Res. Dev
, vol.11
, pp. 693-698
-
-
Barkalow, J.H.1
Breting, J.2
Gaede, J.B.3
Haight, R.A.4
Henry, R.5
Kotecki, B.6
Mei, J.7
Pearl, K.B.8
Tedrow, J.S.9
Viswanath, S.K.10
-
33
-
-
49649087204
-
Synthesis of benzimidazoles condensed with, or linked to, nitroxides or heterocyclic N-oxides
-
Bognár, B.; Kálai, T.; Hideg, K. Synthesis of benzimidazoles condensed with, or linked to, nitroxides or heterocyclic N-oxides. Synthesis 2008, 2439-2445.
-
(2008)
Synthesis
, pp. 2439-2445
-
-
Bognár, B.1
Kálai, T.2
Hideg, K.3
-
34
-
-
0029097661
-
Selective reduction of nitrones and nitroxides to functionalized secondary amines
-
Sár, P. C.; Kálai, T.; Bárácz, M. N.; Jerkovich, Gy.; Hideg, K. Selective reduction of nitrones and nitroxides to functionalized secondary amines. Synth. Commun. 1995, 25, 2929-2940.
-
(1995)
Synth. Commun
, vol.25
, pp. 2929-2940
-
-
Sár, P.C.1
Kálai, T.2
Bárácz, M.N.3
Jerkovich, G.4
Hideg, K.5
-
35
-
-
0035191889
-
Short synthesis of the PARP inhibitor 2-(4-trifluoromethylphenyl)benzimidizal-4-carboxamide (NU1077)
-
Austen, S. C.; Kane, J. M. A. Short synthesis of the PARP inhibitor 2-(4-trifluoromethylphenyl)benzimidizal-4-carboxamide (NU1077). J Heterocycl. Chem. 2001, 38, 979-980.
-
(2001)
J Heterocycl. Chem
, vol.38
, pp. 979-980
-
-
Austen, S.C.1
Kane, J.M.A.2
-
36
-
-
64349090906
-
-
Hideg, K.; Hankovszky, H. O.; Lex, L.; Kulcsár, Gy. Nitroxyls. VI. Synthesis and reactions of 3-hydroxymethyl-2,2,5,5-tetramethyl-2,5- dihydropyrrole-1-oxyl and 3-formyl derivatives. Synthesis 1980, 91, 1914.
-
Hideg, K.; Hankovszky, H. O.; Lex, L.; Kulcsár, Gy. Nitroxyls. VI. Synthesis and reactions of 3-hydroxymethyl-2,2,5,5-tetramethyl-2,5- dihydropyrrole-1-oxyl and 3-formyl derivatives. Synthesis 1980, 91, 1914.
-
-
-
-
37
-
-
0038221668
-
Synthesis and reactions of symmetric paramagnetic pyrrolidine diene
-
Kálai, T.; Balog, M.; Jeko″, J.; Hideg, K. Synthesis and reactions of symmetric paramagnetic pyrrolidine diene. Synthesis 1999, 973-980.
-
(1999)
Synthesis
, pp. 973-980
-
-
Kálai, T.1
Balog, M.2
Jeko″, J.3
Hideg, K.4
-
38
-
-
0031784474
-
3-Substituted-2,2,5,5- tetramethyl-2,5-dihydro-1H-pyrrol-1-yloxyl radicals as versatile synthones for synthesis of new paramagnetic heterocycles
-
Kálai, T.; Balog, M.; Jeko″, J.; Hideg, K. 3-Substituted-2,2,5,5- tetramethyl-2,5-dihydro-1H-pyrrol-1-yloxyl radicals as versatile synthones for synthesis of new paramagnetic heterocycles. Synthesis 1998, 1476-1482.
-
(1998)
Synthesis
, pp. 1476-1482
-
-
Kálai, T.1
Balog, M.2
Jeko″, J.3
Hideg, K.4
-
39
-
-
0037884075
-
Palladium catalysed coupling reactions of paramagnetic vinyl halides
-
Kálai, T.; Balog, M.; Jeko″, J.; Hubbell, W. L.; Hideg, K. Palladium catalysed coupling reactions of paramagnetic vinyl halides. Synthesis 2002, 2365-2372.
-
(2002)
Synthesis
, pp. 2365-2372
-
-
Kálai, T.1
Balog, M.2
Jeko″, J.3
Hubbell, W.L.4
Hideg, K.5
-
40
-
-
64349097858
-
-
Cseko, J.; Hankovszky, H. O.; Hideg, K. Synthesis of novel, highly reactive 1-oxyl-2,2,6,6-tetramethyl-1,2,5,6-tetrahydropyridine derivatives. Can. J. Chem. 1985, 63, 940-943.
-
Cseko, J.; Hankovszky, H. O.; Hideg, K. Synthesis of novel, highly reactive 1-oxyl-2,2,6,6-tetramethyl-1,2,5,6-tetrahydropyridine derivatives. Can. J. Chem. 1985, 63, 940-943.
-
-
-
-
41
-
-
0021114886
-
A spin-label study of the disposition of the Fe-S cluster with respect to the active center of aconitase
-
Dreyer, J. L.; Beinert, H.; Keana, J. F. W.; Hankovszky, H. O.; Hideg, K.; Eaton, S. S.; Eaton, G. R. A spin-label study of the disposition of the Fe-S cluster with respect to the active center of aconitase. Biochim. Biovhvs. Acta 1983, 745, 229-236.
-
(1983)
Biochim. Biovhvs. Acta
, vol.745
, pp. 229-236
-
-
Dreyer, J.L.1
Beinert, H.2
Keana, J.F.W.3
Hankovszky, H.O.4
Hideg, K.5
Eaton, S.S.6
Eaton, G.R.7
-
42
-
-
0032572831
-
Studies of structure-activity relationship of nitroxide free radicals and their precursors as modifiers against oxidative damage
-
Krishna, M. C.; Degraff, W.; Hankovszky, H. O.; Sár, P. C.; Kálai, T.; Jekó́, J.; Russo, A.; Mitchell, J. B.; Hideg, K. Studies of structure-activity relationship of nitroxide free radicals and their precursors as modifiers against oxidative damage. J. Med. Chem. 1998, 41, 3477-3492.
-
(1998)
J. Med. Chem
, vol.41
, pp. 3477-3492
-
-
Krishna, M.C.1
Degraff, W.2
Hankovszky, H.O.3
Sár, P.C.4
Kálai, T.5
Jekó́, J.6
Russo, A.7
Mitchell, J.B.8
Hideg, K.9
-
43
-
-
0034236760
-
Synthesis, single crystal X-ray structure and W-band (95 GHz) EPR spectroscopy of a new anionic isoindoline aminoxyl: Synthesis and characterisation of some derivatives
-
Bottle, S. E.; Gillies, D. G.; Hughes, D. L.; Micallef, A. S.; Smirnov, A. I.; Sutcliffe, L. H. Synthesis, single crystal X-ray structure and W-band (95 GHz) EPR spectroscopy of a new anionic isoindoline aminoxyl: synthesis and characterisation of some derivatives. J. Chem. Soc., Perkin Trans. 2000, 2, 1285-1291.
-
(2000)
J. Chem. Soc., Perkin Trans
, vol.2
, pp. 1285-1291
-
-
Bottle, S.E.1
Gillies, D.G.2
Hughes, D.L.3
Micallef, A.S.4
Smirnov, A.I.5
Sutcliffe, L.H.6
-
44
-
-
33646864749
-
Conformational dynamics of loop 267-274 in G- and F-actin
-
Shvetsov, A.; Stamm, J. D.; Phillips, M.; Warshaviak, D.; Altenbach, C.; Rubenstein, P. A.; Hideg, K.; Hubbell, W. L.; Reisler, E. Conformational dynamics of loop 267-274 in G- and F-actin. Biochemistry 2006, 45, 6541-6549.
-
(2006)
Biochemistry
, vol.45
, pp. 6541-6549
-
-
Shvetsov, A.1
Stamm, J.D.2
Phillips, M.3
Warshaviak, D.4
Altenbach, C.5
Rubenstein, P.A.6
Hideg, K.7
Hubbell, W.L.8
Reisler, E.9
-
45
-
-
0038560332
-
Synthesis of pyrroline nitroxide annulated carbocycles and heterocycles
-
Kálai, T.; Jekó́, J.; Hideg, K. Synthesis of pyrroline nitroxide annulated carbocycles and heterocycles. Synthesis 2000, 831-837.
-
(2000)
Synthesis
, pp. 831-837
-
-
Kálai, T.1
Jekó́, J.2
Hideg, K.3
-
46
-
-
84915070406
-
VII. Synthesis and reactions of highly reactive 1-oxyl-2,2,5,5-tetramethyl-2,5-dihydro- pyrrole-3-ylmethyl sulfonates
-
Hankovszky, H. O.; Hideg, K.; Lex, L. Nitroxyls. VII. Synthesis and reactions of highly reactive 1-oxyl-2,2,5,5-tetramethyl-2,5-dihydro- pyrrole-3-ylmethyl sulfonates. Synthesis 1980, 914-916.
-
(1980)
Synthesis
, pp. 914-916
-
-
Hankovszky, H.O.1
Hideg, K.2
Lex3
Nitroxyls, L.4
-
47
-
-
20144371717
-
Checkpoint kinase inhibitors: SAR and radioprotective properties of a series of 2-arylbenzimidazoles
-
Arienti, K. L.; Brunmark, A.; Axe, F. U.; McClure, K.; Lee, A.; Blevitt, J.; Neff, K. D.; Huang, L.; Crawford, S.; Pandit, C. R.; Karlsson, L.; Breitenbucher, J. G. Checkpoint kinase inhibitors: SAR and radioprotective properties of a series of 2-arylbenzimidazoles. J. Med. Chem. 2005, 48, 1873-1885.
-
(2005)
J. Med. Chem
, vol.48
, pp. 1873-1885
-
-
Arienti, K.L.1
Brunmark, A.2
Axe, F.U.3
McClure, K.4
Lee, A.5
Blevitt, J.6
Neff, K.D.7
Huang, L.8
Crawford, S.9
Pandit, C.R.10
Karlsson, L.11
Breitenbucher, J.G.12
-
48
-
-
0032189180
-
Characterization of redox activity in resting and activated mast cells by reduction and reoxidation of lipophylic nitroxides
-
(a) Nishimura-Suzuki, T.; Swartz, H. M. Characterization of redox activity in resting and activated mast cells by reduction and reoxidation of lipophylic nitroxides. Gen. Pharmacol. 1998, 3, 617-623.
-
(1998)
Gen. Pharmacol
, vol.3
, pp. 617-623
-
-
Nishimura-Suzuki, T.1
Swartz, H.M.2
-
49
-
-
0031424177
-
Quantification of superoxide radicals and peroxinitrite in vascular cells using oxidation of sterically hindered hydroxylamines and electron spin resonance
-
(b) Dikalov, S.; Skatchkov, M.; Fink, B.; Bassenge, E. Quantification of superoxide radicals and peroxinitrite in vascular cells using oxidation of sterically hindered hydroxylamines and electron spin resonance. Nitric Oxide: Biol. Chem. 1997, 1, 423-431.
-
(1997)
Nitric Oxide: Biol. Chem
, vol.1
, pp. 423-431
-
-
Dikalov, S.1
Skatchkov, M.2
Fink, B.3
Bassenge, E.4
-
50
-
-
1242328673
-
-
Saito, K.; Takeshita, K.; Anzai, K.; Ozawa, T. Pharmacokinetic study of acyl-protected hydroxylamine probe, 1-acetoxy-3-carbabamoyl-2,2,5,5- tetramethylpyrrolidine, for in vivo measurements of reactive oxygen species. Free Radical Biol. Med. 2004, 36, 517-525.
-
Saito, K.; Takeshita, K.; Anzai, K.; Ozawa, T. Pharmacokinetic study of acyl-protected hydroxylamine probe, 1-acetoxy-3-carbabamoyl-2,2,5,5- tetramethylpyrrolidine, for in vivo measurements of reactive oxygen species. Free Radical Biol. Med. 2004, 36, 517-525.
-
-
-
-
51
-
-
64349086656
-
New Alicyclic-Amine- Substituted 4-Carboxamidobenzimidazoles as PARP-Inhibitors and Antioxidants
-
Patent WO/096793 A1, 2004
-
Hideg, K.; Kálai, T.; Sümegi, B. New Alicyclic-Amine- Substituted 4-Carboxamidobenzimidazoles as PARP-Inhibitors and Antioxidants. Patent WO2004/096793 A1, 2004.
-
(2004)
-
-
Hideg, K.1
Kálai, T.2
Sümegi, B.3
-
52
-
-
47549095368
-
-
Pennign, D. T.; Zhu, G.-D.; Gandhi, V. B.; Gong, J.; Thomas, S.; Luzbisch, W.; Grandel, R.; Wernet, W.; Park, C. H.; Fry, E. H.; Liu, X.; Shi, Y.; Kléinghofer, V.; Johnson, E. F.; Donawho, C. K.; Frost, D. J.; Bontcheva-Diaz, V.; Bouska, J. J.; Olson, A. M.; Marsh, K. C.; Luo, Y.; Rosenberg, S. H.; Giranda, L. V. Discovery and SAR of 2(-1-propynilpiperidin-4- yl)-1//-benzirmdazole-4-carboxarnide: a potent inhibitor of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer. Bioorg. Med. Chem. 2008, 16, 6965-6975.
-
Pennign, D. T.; Zhu, G.-D.; Gandhi, V. B.; Gong, J.; Thomas, S.; Luzbisch, W.; Grandel, R.; Wernet, W.; Park, C. H.; Fry, E. H.; Liu, X.; Shi, Y.; Kléinghofer, V.; Johnson, E. F.; Donawho, C. K.; Frost, D. J.; Bontcheva-Diaz, V.; Bouska, J. J.; Olson, A. M.; Marsh, K. C.; Luo, Y.; Rosenberg, S. H.; Giranda, L. V. Discovery and SAR of 2(-1-propynilpiperidin-4- yl)-1//-benzirmdazole-4-carboxarnide: a potent inhibitor of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer. Bioorg. Med. Chem. 2008, 16, 6965-6975.
-
-
-
-
53
-
-
0029028545
-
Methods for biochemical study of poly(ADP-ribose) metabolism in vitro and in vivo
-
Shah, G. M.; Poirier, D.; Duchaine, C.; Brochu, G.; Desnoyers, S.; Lagueux, J.; Verreault, A.; Hoflack, J. C.; Kirkland, J. B.; Poirier, G. G. Methods for biochemical study of poly(ADP-ribose) metabolism in vitro and in vivo. Anal. Biochem. 1995, 227, 1-13.
-
(1995)
Anal. Biochem
, vol.227
, pp. 1-13
-
-
Shah, G.M.1
Poirier, D.2
Duchaine, C.3
Brochu, G.4
Desnoyers, S.5
Lagueux, J.6
Verreault, A.7
Hoflack, J.C.8
Kirkland, J.B.9
Poirier, G.G.10
-
54
-
-
0030048479
-
Modulation of superoxide-dependent oxidation and hydroxylation reactions by nitric oxide
-
Miles, A. M.; Bohle, D. S.; Glassbrenner, P. A.; Hansert, B.; Wink, D. A.; Grisham, M. B. Modulation of superoxide-dependent oxidation and hydroxylation reactions by nitric oxide. J. Biol. Chem. 1996, 277, 40-47.
-
(1996)
J. Biol. Chem
, vol.277
, pp. 40-47
-
-
Miles, A.M.1
Bohle, D.S.2
Glassbrenner, P.A.3
Hansert, B.4
Wink, D.A.5
Grisham, M.B.6
|