-
1
-
-
0002160618
-
Nicotinamide mononucleotide activation of new DNA-dependent polyadenylic acid synthesizing nuclear enzyme
-
Chambon, P.; Weill, J. D.; Mandel, P. Nicotinamide mononucleotide activation of new DNA-dependent polyadenylic acid synthesizing nuclear enzyme. Biochem. Biophys. Res. Commun., 1963, 11, 39-43.
-
(1963)
Biochem. Biophys. Res. Commun
, vol.11
, pp. 39-43
-
-
Chambon, P.1
Weill, J.D.2
Mandel, P.3
-
2
-
-
0014218010
-
Polymerization of the adenosine 5'-diphosphate-ribose moiety of nicotinamide-adenine dinucleotide by nuclear enzyme. I. Enzymatic reactions
-
Fujimura, S.; Hasegawa, S.; Shimizu, Y.; Sugimura, T. Polymerization of the adenosine 5'-diphosphate-ribose moiety of nicotinamide-adenine dinucleotide by nuclear enzyme. I. Enzymatic reactions. Biochim. Biophys. Acta, 1967, 145(2), 247-259.
-
(1967)
Biochim. Biophys. Acta
, vol.145
, Issue.2
, pp. 247-259
-
-
Fujimura, S.1
Hasegawa, S.2
Shimizu, Y.3
Sugimura, T.4
-
3
-
-
0014198717
-
Studies on the polymer of adenosine diphosphate ribose. I. Enzymic formation from nicotinamide adenine dinuclotide in mammalian nuclei
-
Nishizuka, Y.; Ueda, K.; Nakazawa, K.; Hayaishi, O. Studies on the polymer of adenosine diphosphate ribose. I. Enzymic formation from nicotinamide adenine dinuclotide in mammalian nuclei. J. Biol. Chem., 1967, 242(13), 3164-3171.
-
(1967)
J. Biol. Chem
, vol.242
, Issue.13
, pp. 3164-3171
-
-
Nishizuka, Y.1
Ueda, K.2
Nakazawa, K.3
Hayaishi, O.4
-
4
-
-
77951023118
-
Toward a unified nomenclature for mammalian ADPribosyltransferases
-
Hottiger, M. O.; Hassa, P. O.; Lüscher, B.; Schüler, H.; Koch-Nolte, F. Toward a unified nomenclature for mammalian ADPribosyltransferases. Trends Biochem. Sci., 2010, 35(4), 208-219.
-
(2010)
Trends Biochem. Sci
, vol.35
, Issue.4
, pp. 208-219
-
-
Hottiger, M.O.1
Hassa, P.O.2
Lüscher, B.3
Schüler, H.4
Koch-Nolte, F.5
-
5
-
-
38449088040
-
The diverse biological roles of mammalian PARPS, a small but powerful family of poly-ADPribose polymerases
-
Hassa, P. O.; Hottiger, M. O. The diverse biological roles of mammalian PARPS, a small but powerful family of poly-ADPribose polymerases. Front. Biosci., 2008, 13, 3046-3082.
-
(2008)
Front. Biosci
, vol.13
, pp. 3046-3082
-
-
Hassa, P.O.1
Hottiger, M.O.2
-
6
-
-
33745867638
-
Poly(ADPribose): Novel functions for an old molecule
-
Schreiber, V.; Dantzer, F.; Ame, J. C.; de Murcia, G. Poly(ADPribose): novel functions for an old molecule. Nat. Rev. Mol. Cell Biol., 2006, 7(7), 517-528.
-
(2006)
Nat. Rev. Mol. Cell Biol
, vol.7
, Issue.7
, pp. 517-528
-
-
Schreiber, V.1
Dantzer, F.2
Ame, J.C.3
de Murcia, G.4
-
7
-
-
77950023283
-
PARP inhibition: PARP1 and beyond
-
Rouleau, M.; Patel, A.; Hendzel, M. J.; Kaufmann, S. H.; Poirier, G. G. PARP inhibition: PARP1 and beyond. Nat. Rev. Cancer, 2010, 10(4), 293-301.
-
(2010)
Nat. Rev. Cancer
, vol.10
, Issue.4
, pp. 293-301
-
-
Rouleau, M.1
Patel, A.2
Hendzel, M.J.3
Kaufmann, S.H.4
Poirier, G.G.5
-
8
-
-
0032518339
-
DNA repair: PARP-another guardian angel?
-
Jeggo, P. A. DNA repair: PARP-another guardian angel? Curr. Biol., 1998, 8(2), 49-51.
-
(1998)
Curr. Biol
, vol.8
, Issue.2
, pp. 49-51
-
-
Jeggo, P.A.1
-
9
-
-
84857891632
-
On PAR with PARP: Cellular stress signaling through poly(ADP-ribose) and PARP-1
-
Luo, X.; Kraus, W. L. On PAR with PARP: cellular stress signaling through poly(ADP-ribose) and PARP-1. Genes Dev., 2012, 26(5), 417-432.
-
(2012)
Genes Dev
, vol.26
, Issue.5
, pp. 417-432
-
-
Luo, X.1
Kraus, W.L.2
-
10
-
-
77956648852
-
The roles of PARP1 in gene control and cell differentiation
-
Ji, Y.; Tulin, A. V. The roles of PARP1 in gene control and cell differentiation. Curr. Opin. Genet. Dev., 2010, 20(5), 512-518.
-
(2010)
Curr. Opin. Genet. Dev
, vol.20
, Issue.5
, pp. 512-518
-
-
Ji, Y.1
Tulin, A.V.2
-
11
-
-
44649130038
-
Transcriptional control by PARP-1: Chromatin modulation, enhancer-binding, coregulation, and insulation
-
Kraus, W. L. Transcriptional control by PARP-1: chromatin modulation, enhancer-binding, coregulation, and insulation. Curr. Opin. Cell Biol., 2008, 20(3), 294-302.
-
(2008)
Curr. Opin. Cell Biol
, vol.20
, Issue.3
, pp. 294-302
-
-
Kraus, W.L.1
-
12
-
-
40949092052
-
Genomic maintenance: The p53 poly(ADPribosyl) ation connection
-
Alvarez-Gonzalez, R. Genomic maintenance: the p53 poly(ADPribosyl) ation connection. Sci. STKE, 2007, 2007(415), pe68.
-
(2007)
Sci. STKE
, vol.2007
, Issue.415
-
-
Alvarez-Gonzalez, R.1
-
13
-
-
84865731753
-
The role of PARP-1 and PARP-2 enzymes in metabolic regulation and disease
-
Bai, P.; Canto, C. The role of PARP-1 and PARP-2 enzymes in metabolic regulation and disease. Cell Metab., 2012, 16(3), 290-295.
-
(2012)
Cell Metab
, vol.16
, Issue.3
, pp. 290-295
-
-
Bai, P.1
Canto, C.2
-
14
-
-
84862758175
-
New insights into the molecular and cellular functions of poly(ADP-ribose) and PARPs
-
Gibson, B. A.; Kraus, W. L. New insights into the molecular and cellular functions of poly(ADP-ribose) and PARPs. Nat. Rev. Mol. Cell Biol., 2012, 13(7), 411-424.
-
(2012)
Nat. Rev. Mol. Cell Biol
, vol.13
, Issue.7
, pp. 411-424
-
-
Gibson, B.A.1
Kraus, W.L.2
-
15
-
-
34250370941
-
Poly(ADP-ribose) polymerase as a drug target for cardiovascular disease and cancer: An update
-
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(3), 171-181.
-
(2007)
Drug News Perspect
, vol.20
, Issue.3
, pp. 171-181
-
-
Horvath, E.M.1
Szabo, C.2
-
16
-
-
34247324385
-
Poly(ADPribose) polymerase inhibitors: New pharmacological functions and potential clinical implications
-
de la Lastra, C. A.; Villegas, I.; Sanchez-Fidalgo, S. Poly(ADPribose) polymerase inhibitors: new pharmacological functions and potential clinical implications. Curr. Pharm. Des., 2007, 13(9), 933-962.
-
(2007)
Curr. Pharm. Des
, vol.13
, Issue.9
, pp. 933-962
-
-
de la Lastra, C.A.1
Villegas, I.2
Sanchez-Fidalgo, S.3
-
17
-
-
17244375049
-
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase
-
Bryant, H. E.; Schultz, N.; Thomas, H. D.; Parker, K. M.; Flower, D.; Lopez, E.; Kyle, S.; Meuth, M.; Curtin, N. J.; Helleday, T. Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase. Nature, 2005, 434(7035), 913-917.
-
(2005)
Nature
, vol.434
, Issue.7035
, pp. 913-917
-
-
Bryant, H.E.1
Schultz, N.2
Thomas, H.D.3
Parker, K.M.4
Flower, D.5
Lopez, E.6
Kyle, S.7
Meuth, M.8
Curtin, N.J.9
Helleday, T.10
-
18
-
-
17244373777
-
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
-
Farmer, H.; McCabe, N.; Lord, C. J.; Tutt, A. N.; Johnson, D. A.; Richardson, T. B.; Santarosa, M.; Dillon, K. J.; Hickson, I.; Knights, C.; Martin, N. M.; Jackson, S. P.; Smith, G. C.; Ashworth, A. Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature, 2005, 434(7035), 917-921.
-
(2005)
Nature
, vol.434
, Issue.7035
, pp. 917-921
-
-
Farmer, H.1
McCabe, N.2
Lord, C.J.3
Tutt, A.N.4
Johnson, D.A.5
Richardson, T.B.6
Santarosa, M.7
Dillon, K.J.8
Hickson, I.9
Knights, C.10
Martin, N.M.11
Jackson, S.P.12
Smith, G.C.13
Ashworth, A.14
-
19
-
-
67650471685
-
Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers
-
Fong, P. C.; Boss, D. S.; Yap, T. A.; Tutt, A.; Wu, P.; Mergui-Roelvink, M.; Mortimer, P.; Swaisland, H.; Lau, A.; O'Connor, M. J.; Ashworth, A.; Carmichael, J.; Kaye, S. B.; Schellens, J. H.; de Bono, J. S. Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers. N. Engl. J. Med., 2009, 361(2), 123-134.
-
(2009)
N. Engl. J. Med
, vol.361
, Issue.2
, pp. 123-134
-
-
Fong, P.C.1
Boss, D.S.2
Yap, T.A.3
Tutt, A.4
Wu, P.5
Mergui-Roelvink, M.6
Mortimer, P.7
Swaisland, H.8
Lau, A.9
O'Connor, M.J.10
Ashworth, A.11
Carmichael, J.12
Kaye, S.B.13
Schellens, J.H.14
de Bono, J.S.15
-
20
-
-
84859864552
-
Targeting the DNA damage response in oncology: Past, present and future perspectives
-
Basu, B.; Yap, T. A.; Molife, L. R.; de Bono, J. S. Targeting the DNA damage response in oncology: past, present and future perspectives. Curr. Opin. Oncol. 2012, 24(3), 316-324.
-
(2012)
Curr. Opin. Oncol
, vol.24
, Issue.3
, pp. 316-324
-
-
Basu, B.1
Yap, T.A.2
Molife, L.R.3
de Bono, J.S.4
-
21
-
-
38649092421
-
Poly(ADP-ribose)polymerase 1 (PARP-1) and postischemic brain damage
-
Moroni, F. Poly(ADP-ribose)polymerase 1 (PARP-1) and postischemic brain damage. Curr. Opin. Pharmacol., 2008, 8(1), 96-103.
-
(2008)
Curr. Opin. Pharmacol
, vol.8
, Issue.1
, pp. 96-103
-
-
Moroni, F.1
-
22
-
-
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.; Pieper, A.; Wang, Z. Q.; Dawson, T. M.; Snyder, S. H.; Dawson, V. L. Poly(ADP-ribose) polymerase gene disruption renders mice resistant to cerebral ischemia. Nat. Med., 1997, 3(10), 1089-1095.
-
(1997)
Nat. Med
, vol.3
, Issue.10
, 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
Pieper, A.7
Wang, Z.Q.8
Dawson, T.M.9
Snyder, S.H.10
Dawson, V.L.11
-
23
-
-
19444364781
-
Poly(ADP-ribosyl)ation and stroke
-
Chiarugi, A. Poly(ADP-ribosyl)ation and stroke. Pharmacol. Res. 2005, 52(1), 15-24.
-
(2005)
Pharmacol. Res
, vol.52
, Issue.1
, pp. 15-24
-
-
Chiarugi, A.1
-
24
-
-
0036499892
-
Poly(ADP-ribose) polymerase: Killer or conspirator? The 'suicide hypothesis' revisited
-
Chiarugi, A. Poly(ADP-ribose) polymerase: killer or conspirator? The 'suicide hypothesis' revisited. Trends Pharmacol. Sci., 2002, 23(3), 122-129.
-
(2002)
Trends Pharmacol. Sci
, vol.23
, Issue.3
, pp. 122-129
-
-
Chiarugi, A.1
-
25
-
-
79251564088
-
A review of PARP inhibitors: From bench to bedside
-
Underhill, C.; Toulmonde, M.; Bonnefoi, H. A review of PARP inhibitors: from bench to bedside. Ann. Oncol., 2011, 22(2), 268-279.
-
(2011)
Ann. Oncol
, vol.22
, Issue.2
, pp. 268-279
-
-
Underhill, C.1
Toulmonde, M.2
Bonnefoi, H.3
-
26
-
-
80052379415
-
PARP inhibitors in cancer: Moving beyond BRCA
-
Telli, M. L. PARP inhibitors in cancer: moving beyond BRCA. Lancet Oncol., 2011, 12(9), 827-828.
-
(2011)
Lancet Oncol
, vol.12
, Issue.9
, pp. 827-828
-
-
Telli, M.L.1
-
27
-
-
77953764486
-
Evolution of poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors. From concept to clinic
-
Ferraris, D. V. Evolution of poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors. From concept to clinic. J. Med. Chem., 2010, 53(12), 4561-4584.
-
(2010)
J. Med. Chem
, vol.53
, Issue.12
, pp. 4561-4584
-
-
Ferraris, D.V.1
-
28
-
-
84865737317
-
Role of PARP inhibitors in cancer biology and therapy
-
Davar, D.; Beumer, J. H.; Hamieh, L.; Tawbi, H. Role of PARP inhibitors in cancer biology and therapy. Curr. Med. Chem., 2012, 19(23), 3907-3921.
-
(2012)
Curr. Med. Chem
, vol.19
, Issue.23
, pp. 3907-3921
-
-
Davar, D.1
Beumer, J.H.2
Hamieh, L.3
Tawbi, H.4
-
29
-
-
77955019276
-
Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and advanced breast cancer: A proof-of-concept trial
-
Tutt, A.; Robson, M.; Garber, J. E.; Domchek, S. M.; Audeh, M. W.; Weitzel, J. N.; Friedlander, M.; Arun, B.; Loman, N.; Schmutzler, R. K.; Wardley, A.; Mitchell, G.; Earl, H.; Wickens, M.; Carmichael, J. Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and advanced breast cancer: a proof-of-concept trial. Lancet, 2010, 376(9737), 235-244.
-
(2010)
Lancet
, vol.376
, Issue.9737
, pp. 235-244
-
-
Tutt, A.1
Robson, M.2
Garber, J.E.3
Domchek, S.M.4
Audeh, M.W.5
Weitzel, J.N.6
Friedlander, M.7
Arun, B.8
Loman, N.9
Schmutzler, R.K.10
Wardley, A.11
Mitchell, G.12
Earl, H.13
Wickens, M.14
Carmichael, J.15
-
30
-
-
77955039099
-
Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer: A proof-of-concept trial
-
Audeh, M. W.; Carmichael, J.; Penson, R. T.; Friedlander, M.; Powell, B.; Bell-McGuinn, K. M.; Scott, C.; Weitzel, J. N.; Oaknin, A.; Loman, N.; Lu, K.; Schmutzler, R. K.; Matulonis, U.; Wickens, M.; Tutt, A. Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer: a proof-of-concept trial. Lancet, 2010, 376(9737), 245-251.
-
(2010)
Lancet
, vol.376
, Issue.9737
, pp. 245-251
-
-
Audeh, M.W.1
Carmichael, J.2
Penson, R.T.3
Friedlander, M.4
Powell, B.5
Bell-McGuinn, K.M.6
Scott, C.7
Weitzel, J.N.8
Oaknin, A.9
Loman, N.10
Lu, K.11
Schmutzler, R.K.12
Matulonis, U.13
Wickens, M.14
Tutt, A.15
-
31
-
-
80052535308
-
PARP inhibitors stumble in breast cancer
-
Guha, M. PARP inhibitors stumble in breast cancer. Nat. Biotechnol., 2011, 29(5), 373-374.
-
(2011)
Nat. Biotechnol
, vol.29
, Issue.5
, pp. 373-374
-
-
Guha, M.1
-
32
-
-
83255165692
-
Re-evaluating PARP1 inhibitor in cancer
-
Tulin, A. Re-evaluating PARP1 inhibitor in cancer. Nat. Biotechnol., 2011, 29(12), 1078-1079.
-
(2011)
Nat. Biotechnol
, vol.29
, Issue.12
, pp. 1078-1079
-
-
Tulin, A.1
-
33
-
-
84856004336
-
Stumbling blocks on the path to personalized medicine in breast cancer: The case of PARP inhibitors for BRCA1/2-associated cancers
-
Balmana, J.; Domchek, S. M.; Tutt, A.; Garber, J. E. Stumbling blocks on the path to personalized medicine in breast cancer: the case of PARP inhibitors for BRCA1/2-associated cancers. Cancer Discov., 2011, 1(1), 29-34.
-
(2011)
Cancer Discov
, vol.1
, Issue.1
, pp. 29-34
-
-
Balmana, J.1
Domchek, S.M.2
Tutt, A.3
Garber, J.E.4
-
34
-
-
77956477049
-
Drug profiling: Knowing where it hits
-
Merino, A.; Bronowska, A. K.; Jackson, D. B.; Cahill, D. J. Drug profiling: knowing where it hits. Drug Discov. Today, 2010, 15(17-18), 749-756.
-
(2010)
Drug Discov. Today
, vol.15
, Issue.17-18
, pp. 749-756
-
-
Merino, A.1
Bronowska, A.K.2
Jackson, D.B.3
Cahill, D.J.4
-
35
-
-
77955333346
-
Rational approaches to targeted polypharmacology: Creating and navigating protein-ligand interaction networks
-
Metz, J. T.; Hajduk, P. J. Rational approaches to targeted polypharmacology: creating and navigating protein-ligand interaction networks. Curr. Opin. Chem. Biol., 2010, 14(4), 498-504.
-
(2010)
Curr. Opin. Chem. Biol
, vol.14
, Issue.4
, pp. 498-504
-
-
Metz, J.T.1
Hajduk, P.J.2
-
36
-
-
70449634957
-
Predicting new molecular targets for known drugs
-
Keiser, M. J.; Setola, V.; Irwin, J. J.; Laggner, C.; Abbas, A. I.; Hufeisen, S. J.; Jensen, N. H.; Kuijer, M. B.; Matos, R. C.; Tran, T. B.; Whaley, R.; Glennon, R. A.; Hert, J.; Thomas, K. L.; Edwards, D. D.; Shoichet, B. K.; Roth, B. L. Predicting new molecular targets for known drugs. Nature, 2009, 462(7270), 175-181.
-
(2009)
Nature
, vol.462
, Issue.7270
, pp. 175-181
-
-
Keiser, M.J.1
Setola, V.2
Irwin, J.J.3
Laggner, C.4
Abbas, A.I.5
Hufeisen, S.J.6
Jensen, N.H.7
Kuijer, M.B.8
Matos, R.C.9
Tran, T.B.10
Whaley, R.11
Glennon, R.A.12
Hert, J.13
Thomas, K.L.14
Edwards, D.D.15
Shoichet, B.K.16
Roth, B.L.17
-
37
-
-
33846876695
-
Relating protein pharmacology by ligand chemistry
-
Keiser, M. J.; Roth, B. L.; Armbruster, B. N.; Ernsberger, P.; Irwin, J. J.; Shoichet, B. K. Relating protein pharmacology by ligand chemistry. Nat. Biotechnol., 2007, 25(2), 197-206.
-
(2007)
Nat. Biotechnol
, vol.25
, Issue.2
, pp. 197-206
-
-
Keiser, M.J.1
Roth, B.L.2
Armbruster, B.N.3
Ernsberger, P.4
Irwin, J.J.5
Shoichet, B.K.6
-
38
-
-
33746156959
-
Global mapping of pharmacological space
-
Paolini, G. V.; Shapland, R. H.; van Hoorn, W. P.; Mason, J. S.; Hopkins, A. L. Global mapping of pharmacological space. Nat. Biotechnol., 2006, 24(7), 805-815.
-
(2006)
Nat. Biotechnol
, vol.24
, Issue.7
, pp. 805-815
-
-
Paolini, G.V.1
Shapland, R.H.2
van Hoorn, W.P.3
Mason, J.S.4
Hopkins, A.L.5
-
39
-
-
79952171625
-
Probing the links between in vitro potency, ADMET and physicochemical parameters
-
Gleeson, M. P.; Hersey, A.; Montanari, D.; Overington, J. Probing the links between in vitro potency, ADMET and physicochemical parameters. Nat. Rev. Drug Discov., 2011, 10(3), 197-208.
-
(2011)
Nat. Rev. Drug Discov
, vol.10
, Issue.3
, pp. 197-208
-
-
Gleeson, M.P.1
Hersey, A.2
Montanari, D.3
Overington, J.4
-
40
-
-
51349085387
-
Data completeness-the Achilles heel of drug-target networks
-
Mestres, J.; Gregori-Puigjane, E.; Valverde, S.; Sole, R. V. Data completeness-the Achilles heel of drug-target networks. Nat. Biotechnol., 2008, 26(9), 983-984.
-
(2008)
Nat. Biotechnol
, vol.26
, Issue.9
, pp. 983-984
-
-
Mestres, J.1
Gregori-Puigjane, E.2
Valverde, S.3
Sole, R.V.4
-
41
-
-
77954052283
-
Systems approaches to polypharmacology and drug discovery
-
Boran, A. D.; Iyengar, R. Systems approaches to polypharmacology and drug discovery. Curr. Opin. Drug Discov. Devel., 2010, 13(3), 297-309.
-
(2010)
Curr. Opin. Drug Discov. Devel
, vol.13
, Issue.3
, pp. 297-309
-
-
Boran, A.D.1
Iyengar, R.2
-
42
-
-
32344446028
-
Can we rationally design promiscuous drugs?
-
Hopkins, A. L.; Mason, J. S.; Overington, J. P. Can we rationally design promiscuous drugs? Curr. Opin. Struct. Biol., 2006, 16(1), 127-136.
-
(2006)
Curr. Opin. Struct. Biol
, vol.16
, Issue.1
, pp. 127-136
-
-
Hopkins, A.L.1
Mason, J.S.2
Overington, J.P.3
-
43
-
-
33846574259
-
Fragments, network biology and designing multiple ligands
-
Morphy, R.; Rankovic, Z. Fragments, network biology and designing multiple ligands. Drug Discov. Today, 2007, 12(3-4), 156-160.
-
(2007)
Drug Discov. Today
, vol.12
, Issue.3-4
, pp. 156-160
-
-
Morphy, R.1
Rankovic, Z.2
-
44
-
-
35248817286
-
Modeling promiscuity based on in vitro safety pharmacology profiling data
-
Azzaoui, K.; Hamon, J.; Faller, B.; Whitebread, S.; Jacoby, E.; Bender, A.; Jenkins, J. L.; Urban, L. Modeling promiscuity based on in vitro safety pharmacology profiling data. Chem. Med. Chem., 2007, 2(6), 874-880.
-
(2007)
Chem. Med. Chem
, vol.2
, Issue.6
, pp. 874-880
-
-
Azzaoui, K.1
Hamon, J.2
Faller, B.3
Whitebread, S.4
Jacoby, E.5
Bender, A.6
Jenkins, J.L.7
Urban, L.8
-
45
-
-
31344462177
-
Conformational diversity of ligands bound to proteins
-
Stockwell, G. R.; Thornton, J. M. Conformational diversity of ligands bound to proteins. J. Mol. Biol., 2006, 356(4), 928-944.
-
(2006)
J. Mol. Biol
, vol.356
, Issue.4
, pp. 928-944
-
-
Stockwell, G.R.1
Thornton, J.M.2
-
46
-
-
2342586724
-
Conformational analysis of drug-like molecules bound to proteins: An extensive study of ligand reorganization upon binding
-
Perola, E.; Charifson, P. S. Conformational analysis of drug-like molecules bound to proteins: an extensive study of ligand reorganization upon binding. J. Med. Chem., 2004, 47(10), 2499-2510.
-
(2004)
J. Med. Chem
, vol.47
, Issue.10
, pp. 2499-2510
-
-
Perola, E.1
Charifson, P.S.2
-
47
-
-
79955554738
-
Quantifying structure and performance diversity for sets of small molecules comprising small-molecule screening collections
-
Clemons, P. A.; Wilson, J. A.; Dancik, V.; Muller, S.; Carrinski, H. A.; Wagner, B. K.; Koehler, A. N.; Schreiber, S. L. Quantifying structure and performance diversity for sets of small molecules comprising small-molecule screening collections. Proc. Natl. Acad. Sci. USA, 2011, 108(17), 6817-6822.
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, Issue.17
, pp. 6817-6822
-
-
Clemons, P.A.1
Wilson, J.A.2
Dancik, V.3
Muller, S.4
Carrinski, H.A.5
Wagner, B.K.6
Koehler, A.N.7
Schreiber, S.L.8
-
48
-
-
84866638168
-
Structural insights into the molecular basis of the ligand promiscuity
-
Sturm, N.; Desaphy, J.; Quinn, R. J.; Rognan, D.; Kellenberger, E. Structural insights into the molecular basis of the ligand promiscuity. J. Chem. Inf. Model., 2012, 52(9), 2410-2421.
-
(2012)
J. Chem. Inf. Model
, vol.52
, Issue.9
, pp. 2410-2421
-
-
Sturm, N.1
Desaphy, J.2
Quinn, R.J.3
Rognan, D.4
Kellenberger, E.5
-
49
-
-
35748934487
-
The influence of drug-like concepts on decision-making in medicinal chemistry
-
Leeson, P. D.; Springthorpe, B. The influence of drug-like concepts on decision-making in medicinal chemistry. Nat. Rev. Drug Discov., 2007, 6(11), 881-890.
-
(2007)
Nat. Rev. Drug Discov
, vol.6
, Issue.11
, pp. 881-890
-
-
Leeson, P.D.1
Springthorpe, B.2
-
50
-
-
59849106371
-
Protein promiscuity and its implications for biotechnology
-
Nobeli, I.; Favia, A. D.; Thornton, J. M. Protein promiscuity and its implications for biotechnology. Nat. Biotechnol., 2009, 27(2), 157-167.
-
(2009)
Nat. Biotechnol
, vol.27
, Issue.2
, pp. 157-167
-
-
Nobeli, I.1
Favia, A.D.2
Thornton, J.M.3
-
51
-
-
1942517756
-
Promiscuity: What protects us, perplexes us
-
Redinbo, M. R. Promiscuity: what protects us, perplexes us. Drug Discov. Today, 2004, 9(10), 431-432.
-
(2004)
Drug Discov. Today
, vol.9
, Issue.10
, pp. 431-432
-
-
Redinbo, M.R.1
-
52
-
-
64849101493
-
Protein dynamism and evolvability
-
Tokuriki, N.; Tawfik, D. S. Protein dynamism and evolvability. Science, 2009, 324(5924), 203-207.
-
(2009)
Science
, vol.324
, Issue.5924
, pp. 203-207
-
-
Tokuriki, N.1
Tawfik, D.S.2
-
53
-
-
77949880028
-
What makes an enzyme promiscuous?
-
Babtie, A.; Tokuriki, N.; Hollfelder, F. What makes an enzyme promiscuous? Curr. Opin. Chem. Biol., 2010, 14(2), 200-207.
-
(2010)
Curr. Opin. Chem. Biol
, vol.14
, Issue.2
, pp. 200-207
-
-
Babtie, A.1
Tokuriki, N.2
Hollfelder, F.3
-
54
-
-
35448981499
-
Connecting small molecules to nuclear receptor pathways
-
Hettne, K.; Cases, M.; Boyer, S.; Mestres, J. Connecting small molecules to nuclear receptor pathways. Curr. Top. Med. Chem., 2007, 7(15), 1530-1536.
-
(2007)
Curr. Top. Med. Chem
, vol.7
, Issue.15
, pp. 1530-1536
-
-
Hettne, K.1
Cases, M.2
Boyer, S.3
Mestres, J.4
-
55
-
-
84857939963
-
Family wide chemical profiling and structural analysis of PARP and Tankyrase inhibitors
-
Wahlberg, E.; Karlberg, T.; Kouznetsova, E.; Markova, N.; Macchiarulo, A.; Thorsell, A. G.; Pol, E.; Frostell, Å.; Ekblad, T.; Öncü, D.; Kull, B.; Robertson, G. M.; Pellicciari, R.; Schüler, H.; Weigelt, J. Family wide chemical profiling and structural analysis of PARP and Tankyrase inhibitors. Nature Biotechnol., 2012, 30(3), 283-288.
-
(2012)
Nature Biotechnol
, vol.30
, Issue.3
, pp. 283-288
-
-
Wahlberg, E.1
Karlberg, T.2
Kouznetsova, E.3
Markova, N.4
Macchiarulo, A.5
Thorsell, A.G.6
Pol, E.7
Frostell, A.8
Ekblad, T.9
Öncü, D.10
Kull, B.11
Robertson, G.M.12
Pellicciari, R.13
Schüler, H.14
Weigelt, J.15
-
56
-
-
0035289536
-
Protective effects of PJ34, a novel, potent inhibitor of poly(ADP-ribose) polymerase (PARP) in in vitro and in vivo models of stroke
-
Abdelkarim, G. E.; Gertz, K.; Harms, C.; Katchanov, J.; Dirnagl, U.; Szabo, C.; Endres, M. Protective effects of PJ34, a novel, potent inhibitor of poly(ADP-ribose) polymerase (PARP) in in vitro and in vivo models of stroke. Int. J. Mol. Med. 2001, 7(3), 255-260.
-
(2001)
Int. J. Mol. Med
, vol.7
, Issue.3
, pp. 255-260
-
-
Abdelkarim, G.E.1
Gertz, K.2
Harms, C.3
Katchanov, J.4
Dirnagl, U.5
Szabo, C.6
Endres, M.7
-
57
-
-
0035136240
-
Diabetic endothelial dysfunction: The role of poly(ADP-ribose) polymerase activation
-
Garcia Soriano, F.; Virag, L.; Jagtap, P.; Szabo, E.; Mabley, J. G.; Liaudet, L.; Marton, A.; Hoyt, D. G.; Murthy, K. G.; Salzman, A. L.; Southan, G. J.; Szabo, C. Diabetic endothelial dysfunction: the role of poly(ADP-ribose) polymerase activation. Nat. Med., 2001, 7(1), 108-113.
-
(2001)
Nat. Med
, vol.7
, Issue.1
, pp. 108-113
-
-
Garcia Soriano, F.1
Virag, L.2
Jagtap, P.3
Szabo, E.4
Mabley, J.G.5
Liaudet, L.6
Marton, A.7
Hoyt, D.G.8
Murthy, K.G.9
Salzman, A.L.10
Southan, G.J.11
Szabo, C.12
-
58
-
-
84864342499
-
Administration of the PARP inhibitor Pj34 ameliorates the impaired vascular function associated with eNOS(-/-) mice
-
English, F. A.; McCarthy, F. P.; Andersson, I. J.; Stanley, J. L.; Davidge, S. T.; Baker, P. N.; Walsh, S. K.; Kenny, L. C. Administration of the PARP inhibitor Pj34 ameliorates the impaired vascular function associated with eNOS(-/-) mice. Reprod. Sci., 2012, 19(8), 806-813.
-
(2012)
Reprod. Sci
, vol.19
, Issue.8
, pp. 806-813
-
-
English, F.A.1
McCarthy, F.P.2
Andersson, I.J.3
Stanley, J.L.4
Davidge, S.T.5
Baker, P.N.6
Walsh, S.K.7
Kenny, L.C.8
-
59
-
-
0036159367
-
Myocardial protection by PJ34, a novel potent poly (ADP-ribose) synthetase inhibitor
-
Faro, R.; Toyoda, Y.; McCully, J. D.; Jagtap, P.; Szabo, E.; Virag, L.; Bianchi, C.; Levitsky, S.; Szabo, C.; Sellke, F. W. Myocardial protection by PJ34, a novel potent poly (ADP-ribose) synthetase inhibitor. Ann. Thorac. Surg., 2002, 73(2), 575-781.
-
(2002)
Ann. Thorac. Surg
, vol.73
, Issue.2
, pp. 575-781
-
-
Faro, R.1
Toyoda, Y.2
McCully, J.D.3
Jagtap, P.4
Szabo, E.5
Virag, L.6
Bianchi, C.7
Levitsky, S.8
Szabo, C.9
Sellke, F.W.10
-
60
-
-
42149104494
-
PJ34, a poly adenosine diphosphate-ribose polymerase inhibitor, attenuates chromate-induced nephrotoxicity
-
Yam-Canul, P.; Chirino, Y. I.; Sanchez-Gonzalez, D. J.; Martinez-Martinez, C. M.; Cruz, C.; Pedraza-Chaverri, J. PJ34, a poly adenosine diphosphate-ribose polymerase inhibitor, attenuates chromate-induced nephrotoxicity. Basic Clin. Pharmacol. Toxicol., 2008, 102(5), 483-488.
-
(2008)
Basic Clin. Pharmacol. Toxicol
, vol.102
, Issue.5
, pp. 483-488
-
-
Yam-Canul, P.1
Chirino, Y.I.2
Sanchez-Gonzalez, D.J.3
Martinez-Martinez, C.M.4
Cruz, C.5
Pedraza-Chaverri, J.6
-
61
-
-
20744452940
-
Synthesis and in vivo evaluation of [11C]PJ34, a potential radiotracer for imaging the role of PARP-1 in necrosis
-
Tu, Z.; Chu, W.; Zhang, J.; Dence, C. S.; Welch, M. J.; Mach, R. H. Synthesis and in vivo evaluation of [11C]PJ34, a potential radiotracer for imaging the role of PARP-1 in necrosis. Nucl. Med. Biol., 2005, 32(5), 437-443.
-
(2005)
Nucl. Med. Biol
, vol.32
, Issue.5
, pp. 437-443
-
-
Tu, Z.1
Chu, W.2
Zhang, J.3
Dence, C.S.4
Welch, M.J.5
Mach, R.H.6
-
62
-
-
84873410910
-
Poly (ADP-ribose) polymerase 14 and its enzyme activity regulates T(H)2 differentiation and allergic airway disease
-
Mehrotra, P.; Hollenbeck, A.; Riley, J. P.; Li, F.; Patel, R. J.; Akhtar, N.; Goenka, S. Poly (ADP-ribose) polymerase 14 and its enzyme activity regulates T(H)2 differentiation and allergic airway disease. J. Allergy Clin. Immunol., 2013, 131(2), 521-531.
-
(2013)
J. Allergy Clin. Immunol
, vol.131
, Issue.2
, pp. 521-531
-
-
Mehrotra, P.1
Hollenbeck, A.2
Riley, J.P.3
Li, F.4
Patel, R.J.5
Akhtar, N.6
Goenka, S.7
-
63
-
-
84862233980
-
PARP16/ARTD15 is a novel endoplasmic-reticulumassociated mono-ADP-ribosyltransferase that interacts with, and modifies karyopherin-ss1
-
Di Paola, S.; Micaroni, M.; Di Tullio, G.; Buccione, R.; Di Girolamo, M. PARP16/ARTD15 is a novel endoplasmic-reticulumassociated mono-ADP-ribosyltransferase that interacts with, and modifies karyopherin-ss1. PLoS One, 2012, 7(6), e37352.
-
(2012)
PLoS One
, vol.7
, Issue.6
-
-
Di Paola, S.1
Micaroni, M.2
Di Tullio, G.3
Buccione, R.4
Di Girolamo, M.5
-
64
-
-
68549097788
-
Inhibition of matrix metalloproteinase-2 by PARP inhibitors
-
Nicolescu, A. C.; Holt, A.; Kandasamy, A. D.; Pacher, P.; Schulz, R. Inhibition of matrix metalloproteinase-2 by PARP inhibitors. Biochem. Biophys. Res. Commun., 2009, 387(4), 646-650.
-
(2009)
Biochem. Biophys. Res. Commun
, vol.387
, Issue.4
, pp. 646-650
-
-
Nicolescu, A.C.1
Holt, A.2
Kandasamy, A.D.3
Pacher, P.4
Schulz, R.5
-
65
-
-
81155162490
-
The PARP inhibitor PJ34 causes a PARP1-independent, p21 dependent mitotic arrest
-
Madison, D. L.; Stauffer, D.; Lundblad, J. R. The PARP inhibitor PJ34 causes a PARP1-independent, p21 dependent mitotic arrest. DNA Repair, 2011, 10(10), 1003-1013.
-
(2011)
DNA Repair
, vol.10
, Issue.10
, pp. 1003-1013
-
-
Madison, D.L.1
Stauffer, D.2
Lundblad, J.R.3
-
66
-
-
80053343176
-
A phenanthrene derived PARP inhibitor is an extra-centrosomes de-clustering agent exclusively eradicating human cancer cells
-
Castiel, A.; Visochek, L.; Mittelman, L.; Dantzer, F.; Izraeli, S.; Cohen-Armon, M. A phenanthrene derived PARP inhibitor is an extra-centrosomes de-clustering agent exclusively eradicating human cancer cells. BMC Cancer, 2011, 11, 412.
-
(2011)
BMC Cancer
, vol.11
, pp. 412
-
-
Castiel, A.1
Visochek, L.2
Mittelman, L.3
Dantzer, F.4
Izraeli, S.5
Cohen-Armon, M.6
-
67
-
-
84871588981
-
Identification of pim kinases as novel targets for PJ34 with confounding effects in PARP biology
-
Antolin, A. A.; Jalencas, X.; Yelamos, J.; Mestres, J. Identification of pim kinases as novel targets for PJ34 with confounding effects in PARP biology. ACS Chem. Biol., 2012, 7(12), 1962-1967.
-
(2012)
ACS Chem. Biol
, vol.7
, Issue.12
, pp. 1962-1967
-
-
Antolin, A.A.1
Jalencas, X.2
Yelamos, J.3
Mestres, J.4
-
68
-
-
84862022770
-
Unusual increase in lumbar network excitability of the rat spinal cord evoked by the PARP-1 inhibitor PJ-34 through inhibition of glutamate uptake
-
Nasrabady, S. E.; Kuzhandaivel, A.; Akrami, A.; Bianchetti, E.; Milanese, M.; Bonanno, G.; Nistri, A. Unusual increase in lumbar network excitability of the rat spinal cord evoked by the PARP-1 inhibitor PJ-34 through inhibition of glutamate uptake. Neuropharmacology, 2012, 63(3), 415-426.
-
(2012)
Neuropharmacology
, vol.63
, Issue.3
, pp. 415-426
-
-
Nasrabady, S.E.1
Kuzhandaivel, A.2
Akrami, A.3
Bianchetti, E.4
Milanese, M.5
Bonanno, G.6
Nistri, A.7
-
69
-
-
84868208375
-
Differential anti-proliferative activities of poly(ADP-ribose) polymerase (PARP) inhibitors in triple-negative breast cancer cells
-
Chuang, H. C.; Kapuriya, N.; Kulp, S. K.; Chen, C. S.; Shapiro, C. L. Differential anti-proliferative activities of poly(ADP-ribose) polymerase (PARP) inhibitors in triple-negative breast cancer cells. Breast Cancer Res. Treat., 2012, 134(2), 649-659.
-
(2012)
Breast Cancer Res. Treat
, vol.134
, Issue.2
, pp. 649-659
-
-
Chuang, H.C.1
Kapuriya, N.2
Kulp, S.K.3
Chen, C.S.4
Shapiro, C.L.5
-
70
-
-
0034685885
-
Characterization of sPARP-1. An alternative product of PARP-1 gene with poly(ADP-ribose) polymerase activity independent of DNA strand breaks
-
Sallmann, F. R.; Vodenicharov, M. D.; Wang, Z. Q.; Poirier, G. G. Characterization of sPARP-1. An alternative product of PARP-1 gene with poly(ADP-ribose) polymerase activity independent of DNA strand breaks. J. Biol. Chem., 2000, 275(20), 15504-15511.
-
(2000)
J. Biol. Chem
, vol.275
, Issue.20
, pp. 15504-15511
-
-
Sallmann, F.R.1
Vodenicharov, M.D.2
Wang, Z.Q.3
Poirier, G.G.4
-
71
-
-
77957743077
-
Evolutionary history of the poly(ADP-ribose) polymerase gene family in eukaryotes
-
Citarelli, M.; Teotia, S.; Lamb, R. S. Evolutionary history of the poly(ADP-ribose) polymerase gene family in eukaryotes. BMC Evol. Biol., 2010, 10, 308.
-
(2010)
BMC Evol. Biol
, vol.10
, pp. 308
-
-
Citarelli, M.1
Teotia, S.2
Lamb, R.S.3
-
72
-
-
26644446700
-
B-aggressive lymphoma family proteins have unique domains that modulate transcription and exhibit poly(ADP-ribose) polymerase activity
-
Aguiar, R. C.; Takeyama, K.; He, C.; Kreinbrink, K.; Shipp, M. A. B-aggressive lymphoma family proteins have unique domains that modulate transcription and exhibit poly(ADP-ribose) polymerase activity. J. Biol. Chem., 2005, 280(40), 33756-33765.
-
(2005)
J. Biol. Chem
, vol.280
, Issue.40
, pp. 33756-33765
-
-
Aguiar, R.C.1
Takeyama, K.2
He, C.3
Kreinbrink, K.4
Shipp, M.A.5
-
73
-
-
58149102549
-
Assessment of chemical coverage of kinome space and its implications for kinase drug discovery
-
Bamborough, P.; Drewry, D.; Harper, G.; Smith, G. K.; Schneider, K. Assessment of chemical coverage of kinome space and its implications for kinase drug discovery. J. Med. Chem., 2008, 51(24), 7898-7914.
-
(2008)
J. Med. Chem
, vol.51
, Issue.24
, pp. 7898-7914
-
-
Bamborough, P.1
Drewry, D.2
Harper, G.3
Smith, G.K.4
Schneider, K.5
-
74
-
-
0025923294
-
Destabilization of Zn2+ coordination in ADP-ribose transferase (polymerizing) by 6-nitroso-1, 2-benzopyrone coincidental with inactivation of the polymerase but not the DNA binding function
-
Buki, K. G.; Bauer, P. I.; Mendeleyev, J.; Hakam, A.; Kun, E. Destabilization of Zn2+ coordination in ADP-ribose transferase (polymerizing) by 6-nitroso-1, 2-benzopyrone coincidental with inactivation of the polymerase but not the DNA binding function. FEBS Lett., 1991, 290(1-2), 181-185.
-
(1991)
FEBS Lett
, vol.290
, Issue.1-2
, pp. 181-185
-
-
Buki, K.G.1
Bauer, P.I.2
Mendeleyev, J.3
Hakam, A.4
Kun, E.5
-
75
-
-
0012702917
-
Prevention of tumorigenesis of oncogene-transformed rat fibroblasts with DNA site inhibitors of poly(ADP ribose) polymerase
-
Tseng, A., Jr.; Lee, W. M.; Jakobovits, E. B.; Kirsten, E.; Hakam, A.; McLick, J.; Buki, K.; Kun, E. Prevention of tumorigenesis of oncogene-transformed rat fibroblasts with DNA site inhibitors of poly(ADP ribose) polymerase. Proc. Natl. Acad. Sci. USA, 1987, 84(4), 1107-1111.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, Issue.4
, pp. 1107-1111
-
-
Tseng Jr., A.1
Lee, W.M.2
Jakobovits, E.B.3
Kirsten, E.4
Hakam, A.5
McLick, J.6
Buki, K.7
Kun, E.8
-
76
-
-
84868221110
-
Trapping of PARP1 and PARP2 by Clinical PARP Inhibitors
-
Murai, J.; Huang, S. Y.; Das, B. B.; Renaud, A.; Zhang, Y.; Doroshow, J. H.; Ji, J.; Takeda, S.; Pommier, Y. Trapping of PARP1 and PARP2 by Clinical PARP Inhibitors. Cancer Res., 2012, 72(21), 5588-5599.
-
(2012)
Cancer Res
, vol.72
, Issue.21
, pp. 5588-5599
-
-
Murai, J.1
Huang, S.Y.2
Das, B.B.3
Renaud, A.4
Zhang, Y.5
Doroshow, J.H.6
Ji, J.7
Takeda, S.8
Pommier, Y.9
-
77
-
-
84856890540
-
Structure of human tankyrase 1 in complex with small-molecule inhibitors PJ34 and XAV939
-
Kirby, C. A.; Cheung, A.; Fazal, A.; Shultz, M. D.; Stams, T. Structure of human tankyrase 1 in complex with small-molecule inhibitors PJ34 and XAV939. Acta Crystallogr. Sect. F Struct. Biol. Cryst. Commun., 2012, 68(Pt2), 115-118.
-
(2012)
Acta Crystallogr. Sect. F Struct. Biol. Cryst. Commun
, vol.68
, Issue.PART 2
, pp. 115-118
-
-
Kirby, C.A.1
Cheung, A.2
Fazal, A.3
Shultz, M.D.4
Stams, T.5
-
78
-
-
65649119760
-
Structural basis for inhibitor specificity in human poly(ADP-ribose) polymerase-3
-
Lehtio, L.; Jemth, A. S.; Collins, R.; Loseva, O.; Johansson, A.; Markova, N.; Hammarstrom, M.; Flores, A.; Holmberg-Schiavone, L.; Weigelt, J.; Helleday, T.; Schuler, H.; Karlberg, T. Structural basis for inhibitor specificity in human poly(ADP-ribose) polymerase-3. J. Med. Chem., 2009, 52(9), 3108-3111.
-
(2009)
J. Med. Chem
, vol.52
, Issue.9
, pp. 3108-3111
-
-
Lehtio, L.1
Jemth, A.S.2
Collins, R.3
Loseva, O.4
Johansson, A.5
Markova, N.6
Hammarstrom, M.7
Flores, A.8
Holmberg-Schiavone, L.9
Weigelt, J.10
Helleday, T.11
Schuler, H.12
Karlberg, T.13
-
79
-
-
58249122326
-
Small molecule-mediated disruption of Wntdependent signaling in tissue regeneration and cancer
-
Chen, B.; Dodge, M. E.; Tang, W.; Lu, J.; Ma, Z.; Fan, C. W.; Wei, S.; Hao, W.; Kilgore, J.; Williams, N. S.; Roth, M. G.; Amatruda, J. F.; Chen, C.; Lum, L. Small molecule-mediated disruption of Wntdependent signaling in tissue regeneration and cancer. Nat. Chem. Biol., 2009, 5(2), 100-107.
-
(2009)
Nat. Chem. Biol
, vol.5
, Issue.2
, pp. 100-107
-
-
Chen, B.1
Dodge, M.E.2
Tang, W.3
Lu, J.4
Ma, Z.5
Fan, C.W.6
Wei, S.7
Hao, W.8
Kilgore, J.9
Williams, N.S.10
Roth, M.G.11
Amatruda, J.F.12
Chen, C.13
Lum, L.14
-
80
-
-
70349695861
-
Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling
-
Huang, S. M.; Mishina, Y. M.; Liu, S.; Cheung, A.; Stegmeier, F.; Michaud, G. A.; Charlat, O.; Wiellette, E.; Zhang, Y.; Wiessner, S.; Hild, M.; Shi, X.; Wilson, C. J.; Mickanin, C.; Myer, V.; Fazal, A.; Tomlinson, R.; Serluca, F.; Shao, W.; Cheng, H.; Shultz, M.; Rau, C.; Schirle, M.; Schlegl, J.; Ghidelli, S.; Fawell, S.; Lu, C.; Curtis, D.; Kirschner, M. W.; Lengauer, C.; Finan, P. M.; Tallarico, J. A.; Bouwmeester, T.; Porter, J. A.; Bauer, A.; Cong, F. Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling. Nature, 2009, 461(7264), 614-620.
-
(2009)
Nature
, vol.461
, Issue.7264
, pp. 614-620
-
-
Huang, S.M.1
Mishina, Y.M.2
Liu, S.3
Cheung, A.4
Stegmeier, F.5
Michaud, G.A.6
Charlat, O.7
Wiellette, E.8
Zhang, Y.9
Wiessner, S.10
Hild, M.11
Shi, X.12
Wilson, C.J.13
Mickanin, C.14
Myer, V.15
Fazal, A.16
Tomlinson, R.17
Serluca, F.18
Shao, W.19
Cheng, H.20
Shultz, M.21
Rau, C.22
Schirle, M.23
Schlegl, J.24
Ghidelli, S.25
Fawell, S.26
Lu, C.27
Curtis, D.28
Kirschner, M.W.29
Lengauer, C.30
Finan, P.M.31
Tallarico, J.A.32
Bouwmeester, T.33
Porter, J.A.34
Bauer, A.35
Cong, F.36
more..
-
81
-
-
84876230312
-
Structural Basis and SAR for G007-LK, a Lead Stage 1, 2, 4-Triazole Based Specific Tankyrase 1/2 Inhibitor
-
Voronkov, A.; Holsworth, D. D.; Waaler, J.; Wilson, S. R.; Ekblad, B.; Perdreau-Dahl, H.; Dinh, H.; Drewes, G.; Hopf, C.; Morth, J. P.; Krauss, S. Structural Basis and SAR for G007-LK, a Lead Stage 1, 2, 4-Triazole Based Specific Tankyrase 1/2 Inhibitor. J. Med. Chem., 2013, 56(7), 3012-3023.
-
(2013)
J. Med. Chem
, vol.56
, Issue.7
, pp. 3012-3023
-
-
Voronkov, A.1
Holsworth, D.D.2
Waaler, J.3
Wilson, S.R.4
Ekblad, B.5
Perdreau-Dahl, H.6
Dinh, H.7
Drewes, G.8
Hopf, C.9
Morth, J.P.10
Krauss, S.11
-
82
-
-
33745457705
-
Minocycline inhibits poly(ADP-ribose) polymerase-1 at nanomolar concentrations
-
Alano, C. C.; Kauppinen, T. M.; Valls, A. V.; Swanson, R. A. Minocycline inhibits poly(ADP-ribose) polymerase-1 at nanomolar concentrations. Proc. Natl. Acad. Sci. USA, 2006, 103(25), 9685-9690.
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, Issue.25
, pp. 9685-9690
-
-
Alano, C.C.1
Kauppinen, T.M.2
Valls, A.V.3
Swanson, R.A.4
-
83
-
-
78751643428
-
Minocycline protects cardiac myocytes against simulated ischemiareperfusion injury by inhibiting poly(ADP-ribose) polymerase-1
-
Tao, R.; Kim, S. H.; Honbo, N.; Karliner, J. S.; Alano, C. C. Minocycline protects cardiac myocytes against simulated ischemiareperfusion injury by inhibiting poly(ADP-ribose) polymerase-1. J. Cardiovasc. Pharmacol., 2010, 56(6), 659-668.
-
(2010)
J. Cardiovasc. Pharmacol
, vol.56
, Issue.6
, pp. 659-668
-
-
Tao, R.1
Kim, S.H.2
Honbo, N.3
Karliner, J.S.4
Alano, C.C.5
-
84
-
-
77954699101
-
Repurposing an old drug to improve the use and safety of tissue plasminogen activator for acute ischemic stroke: Minocycline
-
Hess, D. C.; Fagan, S. C. Repurposing an old drug to improve the use and safety of tissue plasminogen activator for acute ischemic stroke: minocycline. Pharmacotherapy, 2010, 30(7 Pt 2), 55-61S.
-
(2010)
Pharmacotherapy
, vol.30
, Issue.7 PART 2
, pp. 55-61
-
-
Hess, D.C.1
Fagan, S.C.2
-
85
-
-
28644435115
-
Pharmacological actions of Cordyceps, a prized folk medicine
-
Ng, T. B.; Wang, H. X. Pharmacological actions of Cordyceps, a prized folk medicine. J. Pharm. Pharmacol., 2005, 57(12), 1509-1519.
-
(2005)
J. Pharm. Pharmacol
, vol.57
, Issue.12
, pp. 1509-1519
-
-
Ng, T.B.1
Wang, H.X.2
-
86
-
-
84857168046
-
Cordycepin blocks lung injury-associated inflammation and promotes BRCA1-deficient breast cancer cell killing by effectively inhibiting PARP
-
Kim, H.; Naura, A. S.; Errami, Y.; Ju, J.; Boulares, A. H. Cordycepin blocks lung injury-associated inflammation and promotes BRCA1-deficient breast cancer cell killing by effectively inhibiting PARP. Mol. Med., 2011, 17(9-10), 893-900.
-
(2011)
Mol. Med
, vol.17
, Issue.9-10
, pp. 893-900
-
-
Kim, H.1
Naura, A.S.2
Errami, Y.3
Ju, J.4
Boulares, A.H.5
-
87
-
-
84867887068
-
The nucleoside antagonist cordycepin causes DNA double strand breaks in breast cancer cells
-
Lee, H. J.; Burger, P.; Vogel, M.; Friese, K.; Bruning, A. The nucleoside antagonist cordycepin causes DNA double strand breaks in breast cancer cells. Invest. New Drugs, 2012, 30(5), 1917-1925.
-
(2012)
Invest. New Drugs
, vol.30
, Issue.5
, pp. 1917-1925
-
-
Lee, H.J.1
Burger, P.2
Vogel, M.3
Friese, K.4
Bruning, A.5
-
88
-
-
84868130864
-
Natural inhibitors of poly(ADP-ribose) polymerase-1
-
Banasik, M.; Stedeford, T.; Strosznajder, R. P. Natural inhibitors of poly(ADP-ribose) polymerase-1. Mol. Neurobiol., 2012, 46(1), 55-63.
-
(2012)
Mol. Neurobiol
, vol.46
, Issue.1
, pp. 55-63
-
-
Banasik, M.1
Stedeford, T.2
Strosznajder, R.P.3
-
89
-
-
64849111005
-
Sending signals dynamically
-
Smock, R. G.; Gierasch, L. M. Sending signals dynamically. Science. 2009, 324(5924), 198-203.
-
(2009)
Science
, vol.324
, Issue.5924
, pp. 198-203
-
-
Smock, R.G.1
Gierasch, L.M.2
-
90
-
-
12844260196
-
Docking studies on PARP-1 inhibitors: Insights into the role of a binding pocket water molecule
-
Bellocchi, D.; Macchiarulo, A.; Costantino, G.; Pellicciari, R. Docking studies on PARP-1 inhibitors: insights into the role of a binding pocket water molecule. Bioorg. Med. Chem., 2005, 13(4), 1151-1157.
-
(2005)
Bioorg. Med. Chem
, vol.13
, Issue.4
, pp. 1151-1157
-
-
Bellocchi, D.1
Macchiarulo, A.2
Costantino, G.3
Pellicciari, R.4
-
91
-
-
79959265786
-
Discovery and characterization of novel potent PARP-1 inhibitors endowed with neuroprotective properties: From TIQ-A to HYDAMTIQ
-
Pellicciari, R.; Camaioni, E.; Gilbert, A. M.; Macchiarulo, A.; Bikker, J. A.; Shah, F.; Bard, J.; Costantino, G.; Gioiello, A.; Robertson, G. M.; Sabbatini, P.; Venturoni, F.; Liscio, P.; Carotti, A.; Bellocchi, D.; Cozzi, A.; Wood, A.; Gonzales, C.; Zaleska, M. M.; Ellingboe, J. W.; Moroni, F. Discovery and characterization of novel potent PARP-1 inhibitors endowed with neuroprotective properties: From TIQ-A to HYDAMTIQ. Med. Chem. Commun., 2011, 2, 559-565.
-
(2011)
Med. Chem. Commun
, vol.2
, pp. 559-565
-
-
Pellicciari, R.1
Camaioni, E.2
Gilbert, A.M.3
Macchiarulo, A.4
Bikker, J.A.5
Shah, F.6
Bard, J.7
Costantino, G.8
Gioiello, A.9
Robertson, G.M.10
Sabbatini, P.11
Venturoni, F.12
Liscio, P.13
Carotti, A.14
Bellocchi, D.15
Cozzi, A.16
Wood, A.17
Gonzales, C.18
Zaleska, M.M.19
Ellingboe, J.W.20
Moroni, F.21
more..
-
92
-
-
31044446976
-
Discovery of potent and selective PARP-1 and PARP-2 inhibitors: SBDD analysis via a combination of X-ray structural study and homology modeling
-
Ishida, J.; Yamamoto, H.; Kido, Y.; Kamijo, K.; Murano, K.; Miyake, H.; Ohkubo, M.; Kinoshita, T.; Warizaya, M.; Iwashita, A.; Mihara, K.; Matsuoka, N.; Hattori, K. Discovery of potent and selective PARP-1 and PARP-2 inhibitors: SBDD analysis via a combination of X-ray structural study and homology modeling. Bioorg. Med. Chem., 2006, 14(5), 1378-1390.
-
(2006)
Bioorg. Med. Chem
, vol.14
, Issue.5
, pp. 1378-1390
-
-
Ishida, J.1
Yamamoto, H.2
Kido, Y.3
Kamijo, K.4
Murano, K.5
Miyake, H.6
Ohkubo, M.7
Kinoshita, T.8
Warizaya, M.9
Iwashita, A.10
Mihara, K.11
Matsuoka, N.12
Hattori, K.13
-
93
-
-
57349119185
-
Imidazoquinolinone, imidazopyridine, and isoquinolindione derivatives as novel and potent inhibitors of the poly(ADP-ribose) polymerase (PARP): A comparison with standard PARP inhibitors
-
Eltze, T.; Boer, R.; Wagner, T.; Weinbrenner, S.; McDonald, M. C.; Thiemermann, C.; Burkle, A.; Klein, T. Imidazoquinolinone, imidazopyridine, and isoquinolindione derivatives as novel and potent inhibitors of the poly(ADP-ribose) polymerase (PARP): a comparison with standard PARP inhibitors. Mol. Pharmacol., 2008, 74(6), 1587-1598.
-
(2008)
Mol. Pharmacol
, vol.74
, Issue.6
, pp. 1587-1598
-
-
Eltze, T.1
Boer, R.2
Wagner, T.3
Weinbrenner, S.4
McDonald, M.C.5
Thiemermann, C.6
Burkle, A.7
Klein, T.8
-
94
-
-
48149115729
-
On the way to selective PARP-2 inhibitors. Design, synthesis, and preliminary evaluation of a series of isoquinolinone derivatives
-
Pellicciari, R.; Camaioni, E.; Costantino, G.; Formentini, L.; Sabbatini, P.; Venturoni, F.; Eren, G.; Bellocchi, D.; Chiarugi, A.; Moroni, F. On the way to selective PARP-2 inhibitors. Design, synthesis, and preliminary evaluation of a series of isoquinolinone derivatives. ChemMedChem, 2008, 3(6), 914-923.
-
(2008)
ChemMedChem
, vol.3
, Issue.6
, pp. 914-923
-
-
Pellicciari, R.1
Camaioni, E.2
Costantino, G.3
Formentini, L.4
Sabbatini, P.5
Venturoni, F.6
Eren, G.7
Bellocchi, D.8
Chiarugi, A.9
Moroni, F.10
-
95
-
-
79953790546
-
5-Benzamidoisoquinolin-1-ones and 5-(omegacarboxyalkyl) isoquinolin-1-ones as isoform-selective inhibitors of poly(ADP-ribose) polymerase 2 (PARP-2)
-
Sunderland, P. T.; Woon, E. C.; Dhami, A.; Bergin, A. B.; Mahon, M. F.; Wood, P. J.; Jones, L. A.; Tully, S. R.; Lloyd, M. D.; Thompson, A. S.; Javaid, H.; Martin, N. M.; Threadgill, M. D. 5-Benzamidoisoquinolin-1-ones and 5-(omegacarboxyalkyl) isoquinolin-1-ones as isoform-selective inhibitors of poly(ADP-ribose) polymerase 2 (PARP-2). J. Med. Chem., 2011, 54(7), 2049-2059.
-
(2011)
J. Med. Chem
, vol.54
, Issue.7
, pp. 2049-2059
-
-
Sunderland, P.T.1
Woon, E.C.2
Dhami, A.3
Bergin, A.B.4
Mahon, M.F.5
Wood, P.J.6
Jones, L.A.7
Tully, S.R.8
Lloyd, M.D.9
Thompson, A.S.10
Javaid, H.11
Martin, N.M.12
Threadgill, M.D.13
-
96
-
-
74349126956
-
Identification and SAR of novel pyrrolo[1, 2-a]pyrazin-1(2H)-one derivatives as inhibitors of poly(ADP-ribose) polymerase-1 (PARP-1)
-
Pescatore, G.; Branca, D.; Fiore, F.; Kinzel, O.; Bufi, L. L.; Muraglia, E.; Orvieto, F.; Rowley, M.; Toniatti, C.; Torrisi, C.; Jones, P. Identification and SAR of novel pyrrolo[1, 2-a]pyrazin-1(2H)-one derivatives as inhibitors of poly(ADP-ribose) polymerase-1 (PARP-1). Bioorg. Med. Chem. Lett., 2010, 20(3), 1094-1099.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.3
, pp. 1094-1099
-
-
Pescatore, G.1
Branca, D.2
Fiore, F.3
Kinzel, O.4
Bufi, L.L.5
Muraglia, E.6
Orvieto, F.7
Rowley, M.8
Toniatti, C.9
Torrisi, C.10
Jones, P.11
-
97
-
-
74049143159
-
Development of substituted 6-[4-fluoro-3-(piperazin-1-ylcarbonyl)benzyl]-4, 5-dimethylpyridazin-3(2H)-ones as potent poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors active in BRCA deficient cells
-
Ferrigno, F.; Branca, D.; Kinzel, O.; Lillini, S.; Llauger Bufi, L.; Monteagudo, E.; Muraglia, E.; Rowley, M.; Schultz-Fademrecht, C.; Toniatti, C.; Torrisi, C.; Jones, P. Development of substituted 6-[4-fluoro-3-(piperazin-1-ylcarbonyl)benzyl]-4, 5-dimethylpyridazin-3(2H)-ones as potent poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors active in BRCA deficient cells. Bioorg. Med. Chem. Lett., 2010, 20(3), 1100-1105.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.3
, pp. 1100-1105
-
-
Ferrigno, F.1
Branca, D.2
Kinzel, O.3
Lillini, S.4
Llauger Bufi, L.5
Monteagudo, E.6
Muraglia, E.7
Rowley, M.8
Schultz-Fademrecht, C.9
Toniatti, C.10
Torrisi, C.11
Jones, P.12
-
98
-
-
72249092276
-
Discovery and SAR of novel, potent and selective hexahydrobenzonaphthyridinone inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1)
-
Torrisi, C.; Bisbocci, M.; Ingenito, R.; Ontoria, J. M.; Rowley, M.; Schultz-Fademrecht, C.; Toniatti, C.; Jones, P. Discovery and SAR of novel, potent and selective hexahydrobenzonaphthyridinone inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1). Bioorg. Med. Chem. Lett., 2010, 20(2), 448-452.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.2
, pp. 448-452
-
-
Torrisi, C.1
Bisbocci, M.2
Ingenito, R.3
Ontoria, J.M.4
Rowley, M.5
Schultz-Fademrecht, C.6
Toniatti, C.7
Jones, P.8
-
99
-
-
72249100571
-
Synthesis and biological evaluation of substituted 2-phenyl-2Hindazole-7-carboxamides as potent poly(ADP-ribose) polymerase (PARP) inhibitors
-
Scarpelli, R.; Boueres, J. K.; Cerretani, M.; Ferrigno, F.; Ontoria, J. M.; Rowley, M.; Schultz-Fademrecht, C.; Toniatti, C.; Jones, P. Synthesis and biological evaluation of substituted 2-phenyl-2Hindazole-7-carboxamides as potent poly(ADP-ribose) polymerase (PARP) inhibitors. Bioorg. Med. Chem. Lett., 2010, 20(2), 488-492.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.2
, pp. 488-492
-
-
Scarpelli, R.1
Boueres, J.K.2
Cerretani, M.3
Ferrigno, F.4
Ontoria, J.M.5
Rowley, M.6
Schultz-Fademrecht, C.7
Toniatti, C.8
Jones, P.9
-
100
-
-
67649971602
-
Identification of aminoethyl pyrrolo dihydroisoquinolinones as novel poly(ADP-ribose) polymerase-1 inhibitors
-
Branca, D.; Cerretani, M.; Jones, P.; Koch, U.; Orvieto, F.; Palumbi, M. C.; Rowley, M.; Toniatti, C.; Muraglia, E. Identification of aminoethyl pyrrolo dihydroisoquinolinones as novel poly(ADP-ribose) polymerase-1 inhibitors. Bioorg. Med. Chem. Lett., 2009, 19(15), 4042-4045.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.15
, pp. 4042-4045
-
-
Branca, D.1
Cerretani, M.2
Jones, P.3
Koch, U.4
Orvieto, F.5
Palumbi, M.C.6
Rowley, M.7
Toniatti, C.8
Muraglia, E.9
-
101
-
-
67649971777
-
Identification of substituted pyrazolo[1, 5-a]quinazolin-5(4H)-one as potent poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors
-
Orvieto, F.; Branca, D.; Giomini, C.; Jones, P.; Koch, U.; Ontoria, J. M.; Palumbi, M. C.; Rowley, M.; Toniatti, C.; Muraglia, E. Identification of substituted pyrazolo[1, 5-a]quinazolin-5(4H)-one as potent poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors. Bioorg. Med. Chem. Lett., 2009, 19(15), 4196-4200.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.15
, pp. 4196-4200
-
-
Orvieto, F.1
Branca, D.2
Giomini, C.3
Jones, P.4
Koch, U.5
Ontoria, J.M.6
Palumbi, M.C.7
Rowley, M.8
Toniatti, C.9
Muraglia, E.10
-
102
-
-
70949086814
-
Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): A novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and-2 mutant tumors
-
Jones, P.; Altamura, S.; Boueres, J.; Ferrigno, F.; Fonsi, M.; Giomini, C.; Lamartina, S.; Monteagudo, E.; Ontoria, J. M.; Orsale, M. V.; Palumbi, M. C.; Pesci, S.; Roscilli, G.; Scarpelli, R.; Schultz-Fademrecht, C.; Toniatti, C.; Rowley, M. Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): a novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and-2 mutant tumors. J. Med. Chem., 2009, 52(22), 7170-7185.
-
(2009)
J. Med. Chem
, vol.52
, Issue.22
, pp. 7170-7185
-
-
Jones, P.1
Altamura, S.2
Boueres, J.3
Ferrigno, F.4
Fonsi, M.5
Giomini, C.6
Lamartina, S.7
Monteagudo, E.8
Ontoria, J.M.9
Orsale, M.V.10
Palumbi, M.C.11
Pesci, S.12
Roscilli, G.13
Scarpelli, R.14
Schultz-Fademrecht, C.15
Toniatti, C.16
Rowley, M.17
-
103
-
-
84875890173
-
Poly (ADP-Ribose) Polymerase Inhibitor MK-4827 together with Radiation as a Novel Therapy for Metastatic Neuroblastoma
-
Mueller, S.; Bhargava, S.; Molinaro, A. M.; Yang, X.; Kolkowitz, I.; Olow, A.; Wehmeijer, N.; Orbach, S.; Chen, J.; Matthay, K. K.; Haas-Kogan, D. A. Poly (ADP-Ribose) Polymerase Inhibitor MK-4827 together with Radiation as a Novel Therapy for Metastatic Neuroblastoma. Anticancer Res., 2013, 33(3), 755-762.
-
(2013)
Anticancer Res
, vol.33
, Issue.3
, pp. 755-762
-
-
Mueller, S.1
Bhargava, S.2
Molinaro, A.M.3
Yang, X.4
Kolkowitz, I.5
Olow, A.6
Wehmeijer, N.7
Orbach, S.8
Chen, J.9
Matthay, K.K.10
Haas-Kogan, D.A.11
-
104
-
-
84875423694
-
MK-4827, a PARP-1/-2 inhibitor, strongly enhances response of human lung and breast cancer xenografts to radiation
-
Wang, L.; Mason, K. A.; Ang, K. K.; Buchholz, T.; Valdecanas, D.; Mathur, A.; Buser-Doepner, C.; Toniatti, C.; Milas, L. MK-4827, a PARP-1/-2 inhibitor, strongly enhances response of human lung and breast cancer xenografts to radiation. Invest. New Drugs, 2012, 30(6), 2113-2120.
-
(2012)
Invest. New Drugs
, vol.30
, Issue.6
, pp. 2113-2120
-
-
Wang, L.1
Mason, K.A.2
Ang, K.K.3
Buchholz, T.4
Valdecanas, D.5
Mathur, A.6
Buser-Doepner, C.7
Toniatti, C.8
Milas, L.9
-
105
-
-
54549103449
-
4-[3-(4-cyclopropanecarbonylpiperazine-1-carbonyl)-4-fluorobenzyl]-2H-phthalazin-1-one: A novel bioavailable inhibitor of poly(ADP-ribose) polymerase-1
-
Menear, K. A.; Adcock, C.; Boulter, R.; Cockcroft, X. L.; Copsey, L.; Cranston, A.; Dillon, K. J.; Drzewiecki, J.; Garman, S.; Gomez, S.; Javaid, H.; Kerrigan, F.; Knights, C.; Lau, A.; Loh, V. M., Jr.; Matthews, I. T.; Moore, S.; O'Connor, M. J.; Smith, G. C.; Martin, N. M. 4-[3-(4-cyclopropanecarbonylpiperazine-1-carbonyl)-4-fluorobenzyl]-2H-phthalazin-1-one: a novel bioavailable inhibitor of poly(ADP-ribose) polymerase-1. J. Med. Chem., 2008, 51(20), 6581-6591.
-
(2008)
J. Med. Chem
, vol.51
, Issue.20
, pp. 6581-6591
-
-
Menear, K.A.1
Adcock, C.2
Boulter, R.3
Cockcroft, X.L.4
Copsey, L.5
Cranston, A.6
Dillon, K.J.7
Drzewiecki, J.8
Garman, S.9
Gomez, S.10
Javaid, H.11
Kerrigan, F.12
Knights, C.13
Lau, A.14
Loh Jr., V.M.15
Matthews, I.T.16
Moore, S.17
O'Connor, M.J.18
Smith, G.C.19
Martin, N.M.20
more..
-
106
-
-
84856879500
-
Structural basis of selective inhibition of human tankyrases
-
Narwal, M.; Venkannagari, H.; Lehtio, L. Structural basis of selective inhibition of human tankyrases. J. Med. Chem., 2012, 55(3), 1360-1367.
-
(2012)
J. Med. Chem
, vol.55
, Issue.3
, pp. 1360-1367
-
-
Narwal, M.1
Venkannagari, H.2
Lehtio, L.3
-
107
-
-
34249006299
-
ABT-888, an orally active poly(ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models
-
Donawho, C. K.; Luo, Y.; Luo, Y.; Penning, T. D.; Bauch, J. L.; Bouska, J. J.; Bontcheva-Diaz, V. D.; Cox, B. F.; DeWeese, T. L.; Dillehay, L. E.; Ferguson, D. C.; Ghoreishi-Haack, N. S.; Grimm, D. R.; Guan, R.; Han, E. K.; Holley-Shanks, R. R.; Hristov, B.; Idler, K. B.; Jarvis, K.; Johnson, E. F.; Kleinberg, L. R.; Klinghofer, V.; Lasko, L. M.; Liu, X.; Marsh, K. C.; McGonigal, T. P.; Meulbroek, J. A.; Olson, A. M.; Palma, J. P.; Rodriguez, L. E.; Shi, Y.; Stavropoulos, J. A.; Tsurutani, A. C.; Zhu, G. D.; Rosenberg, S. H.; Giranda, V. L.; Frost, D. J. ABT-888, an orally active poly(ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models. Clin. Cancer Res., 2007, 13(9), 2728-2737.
-
(2007)
Clin. Cancer Res
, vol.13
, Issue.9
, pp. 2728-2737
-
-
Donawho, C.K.1
Luo, Y.2
Luo, Y.3
Penning, T.D.4
Bauch, J.L.5
Bouska, J.J.6
Bontcheva-Diaz, V.D.7
Cox, B.F.8
DeWeese, T.L.9
Dillehay, L.E.10
Ferguson, D.C.11
Ghoreishi-Haack, N.S.12
Grimm, D.R.13
Guan, R.14
Han, E.K.15
Holley-Shanks, R.R.16
Hristov, B.17
Idler, K.B.18
Jarvis, K.19
Johnson, E.F.20
Kleinberg, L.R.21
Klinghofer, V.22
Lasko, L.M.23
Liu, X.24
Marsh, K.C.25
McGonigal, T.P.26
Meulbroek, J.A.27
Olson, A.M.28
Palma, J.P.29
Rodriguez, L.E.30
Shi, Y.31
Stavropoulos, J.A.32
Tsurutani, A.C.33
Zhu, G.D.34
Rosenberg, S.H.35
Giranda, V.L.36
Frost, D.J.37
more..
-
108
-
-
47549095368
-
Discovery and SAR of 2-(1-propylpiperidin-4-yl)-1H-benzimidazole-4-carboxamide: A potent inhibitor of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer
-
Penning, T. D.; Zhu, G. D.; Gandhi, V. B.; Gong, J.; Thomas, S.; Lubisch, W.; Grandel, R.; Wernet, W.; Park, C. H.; Fry, E. H.; Liu, X.; Shi, Y.; Klinghofer, 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, V. L. Discovery and SAR of 2-(1-propylpiperidin-4-yl)-1H-benzimidazole-4-carboxamide: A potent inhibitor of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer. Bioorg. Med. Chem., 2008, 16(14), 6965-6975.
-
(2008)
Bioorg. Med. Chem
, vol.16
, Issue.14
, pp. 6965-6975
-
-
Penning, T.D.1
Zhu, G.D.2
Gandhi, V.B.3
Gong, J.4
Thomas, S.5
Lubisch, W.6
Grandel, R.7
Wernet, W.8
Park, C.H.9
Fry, E.H.10
Liu, X.11
Shi, Y.12
Klinghofer, V.13
Johnson, E.F.14
Donawho, C.K.15
Frost, D.J.16
Bontcheva-Diaz, V.17
Bouska, J.J.18
Olson, A.M.19
Marsh, K.C.20
Luo, Y.21
Rosenberg, S.H.22
Giranda, V.L.23
more..
-
109
-
-
58149263490
-
Preclinical modeling of a phase 0 clinical trial: Qualification of a pharmacodynamic assay of poly (ADP-ribose) polymerase in tumor biopsies of mouse xenografts
-
National Cancer Institute Phase 0 Clinical Trials, T
-
Kinders, R. J.; Hollingshead, M.; Khin, S.; Rubinstein, L.; Tomaszewski, J. E.; Doroshow, J. H.; Parchment, R. E.; National Cancer Institute Phase 0 Clinical Trials, T. Preclinical modeling of a phase 0 clinical trial: qualification of a pharmacodynamic assay of poly (ADP-ribose) polymerase in tumor biopsies of mouse xenografts. Clin. Cancer Res., 2008, 14(21), 6877-6885.
-
(2008)
Clin. Cancer Res
, vol.14
, Issue.21
, pp. 6877-6885
-
-
Kinders, R.J.1
Hollingshead, M.2
Khin, S.3
Rubinstein, L.4
Tomaszewski, J.E.5
Doroshow, J.H.6
Parchment, R.E.7
-
110
-
-
77954709179
-
Structural basis for the interaction between tankyrase-2 and a potent Wnt-signaling inhibitor
-
Karlberg, T.; Markova, N.; Johansson, I.; Hammarstrom, M.; Schutz, P.; Weigelt, J.; Schuler, H. Structural basis for the interaction between tankyrase-2 and a potent Wnt-signaling inhibitor. J. Med. Chem., 2010, 53(14), 5352-5355.
-
(2010)
J. Med. Chem
, vol.53
, Issue.14
, pp. 5352-5355
-
-
Karlberg, T.1
Markova, N.2
Johansson, I.3
Hammarstrom, M.4
Schutz, P.5
Weigelt, J.6
Schuler, H.7
-
111
-
-
42749090879
-
Zinc binding catalytic domain of human tankyrase 1
-
Lehtio, L.; Collins, R.; van den Berg, S.; Johansson, A.; Dahlgren, L. G.; Hammarstrom, M.; Helleday, T.; Holmberg-Schiavone, L.; Karlberg, T.; Weigelt, J. Zinc binding catalytic domain of human tankyrase 1. J. Mol. Biol., 2008, 379(1), 136-145.
-
(2008)
J. Mol. Biol
, vol.379
, Issue.1
, pp. 136-145
-
-
Lehtio, L.1
Collins, R.2
van den Berg, S.3
Johansson, A.4
Dahlgren, L.G.5
Hammarstrom, M.6
Helleday, T.7
Holmberg-Schiavone, L.8
Karlberg, T.9
Weigelt, J.10
-
112
-
-
84861843671
-
A novel tankyrase inhibitor decreases canonical Wnt signaling in colon carcinoma cells and reduces tumor growth in conditional APC mutant mice
-
Waaler, J.; Machon, O.; Tumova, L.; Dinh, H.; Korinek, V.; Wilson, S. R.; Paulsen, J. E.; Pedersen, N. M.; Eide, T. J.; Machonova, O.; Gradl, D.; Voronkov, A.; von Kries, J. P.; Krauss, S. A novel tankyrase inhibitor decreases canonical Wnt signaling in colon carcinoma cells and reduces tumor growth in conditional APC mutant mice. Cancer Res., 2012, 72(11), 2822-2832.
-
(2012)
Cancer Res
, vol.72
, Issue.11
, pp. 2822-2832
-
-
Waaler, J.1
Machon, O.2
Tumova, L.3
Dinh, H.4
Korinek, V.5
Wilson, S.R.6
Paulsen, J.E.7
Pedersen, N.M.8
Eide, T.J.9
Machonova, O.10
Gradl, D.11
Voronkov, A.12
von Kries, J.P.13
Krauss, S.14
-
113
-
-
84863116261
-
[1, 2, 4]triazol-3-ylsulfanylmethyl)-3-phenyl-[1, 2, 4]oxadiazoles: Antagonists of the Wnt pathway that inhibit tankyrases 1 and 2 via novel adenosine pocket binding
-
Shultz, M. D.; Kirby, C. A.; Stams, T.; Chin, D. N.; Blank, J.; Charlat, O.; Cheng, H.; Cheung, A.; Cong, F.; Feng, Y.; Fortin, P. D.; Hood, T.; Tyagi, V.; Xu, M.; Zhang, B.; Shao, W. [1, 2, 4]triazol-3-ylsulfanylmethyl)-3-phenyl-[1, 2, 4]oxadiazoles: antagonists of the Wnt pathway that inhibit tankyrases 1 and 2 via novel adenosine pocket binding. J. Med. Chem., 2012, 55(3), 1127-1136.
-
(2012)
J. Med. Chem
, vol.55
, Issue.3
, pp. 1127-1136
-
-
Shultz, M.D.1
Kirby, C.A.2
Stams, T.3
Chin, D.N.4
Blank, J.5
Charlat, O.6
Cheng, H.7
Cheung, A.8
Cong, F.9
Feng, Y.10
Fortin, P.D.11
Hood, T.12
Tyagi, V.13
Xu, M.14
Zhang, B.15
Shao, W.16
-
114
-
-
78651385875
-
Novel synthetic antagonists of canonical Wnt signaling inhibit colorectal cancer cell growth
-
Waaler, J.; Machon, O.; von Kries, J. P.; Wilson, S. R.; Lundenes, E.; Wedlich, D.; Gradl, D.; Paulsen, J. E.; Machonova, O.; Dembinski, J. L.; Dinh, H.; Krauss, S. Novel synthetic antagonists of canonical Wnt signaling inhibit colorectal cancer cell growth. Cancer Res., 2011, 71(1), 197-205.
-
(2011)
Cancer Res
, vol.71
, Issue.1
, pp. 197-205
-
-
Waaler, J.1
Machon, O.2
von Kries, J.P.3
Wilson, S.R.4
Lundenes, E.5
Wedlich, D.6
Gradl, D.7
Paulsen, J.E.8
Machonova, O.9
Dembinski, J.L.10
Dinh, H.11
Krauss, S.12
-
115
-
-
84877720042
-
A Novel Tankyrase Smallmolecule Inhibitor Suppresses APC Mutation-driven Colorectal Tumor Growth
-
Lau, T.; Chan, E.; Callow, M.; Waaler, J.; Boggs, J.; Blake, R. A.; Magnuson, S.; Sambrone, A.; Schutten, M.; Firestein, R.; Machon, O.; Korinek, V.; Choo, E.; Diaz, D.; Merchant, M.; Polakis, P.; Holsworth, D. D.; Krauss, S.; Costa, M. A Novel Tankyrase Smallmolecule Inhibitor Suppresses APC Mutation-driven Colorectal Tumor Growth. Cancer Res., 2013, 73(10), 3132-3144.
-
(2013)
Cancer Res
, vol.73
, Issue.10
, pp. 3132-3144
-
-
Lau, T.1
Chan, E.2
Callow, M.3
Waaler, J.4
Boggs, J.5
Blake, R.A.6
Magnuson, S.7
Sambrone, A.8
Schutten, M.9
Firestein, R.10
Machon, O.11
Korinek, V.12
Choo, E.13
Diaz, D.14
Merchant, M.15
Polakis, P.16
Holsworth, D.D.17
Krauss, S.18
Costa, M.19
-
116
-
-
84873910351
-
Discovery of a class of novel tankyrase inhibitors that bind to both the nicotinamide pocket and the induced pocket
-
Bregman, H.; Gunaydin, H.; Gu, Y.; Schneider, S.; Wilson, C.; DiMauro, E. F.; Huang, X. Discovery of a class of novel tankyrase inhibitors that bind to both the nicotinamide pocket and the induced pocket. J. Med. Chem., 2013, 56(3), 1341-1345.
-
(2013)
J. Med. Chem
, vol.56
, Issue.3
, pp. 1341-1345
-
-
Bregman, H.1
Gunaydin, H.2
Gu, Y.3
Schneider, S.4
Wilson, C.5
DiMauro, E.F.6
Huang, X.7
-
117
-
-
84858383452
-
Novel binding mode of a potent and selective tankyrase inhibitor
-
Gunaydin, H.; Gu, Y.; Huang, X. Novel binding mode of a potent and selective tankyrase inhibitor. PLoS One, 2012, 7(3), e33740.
-
(2012)
PLoS One
, vol.7
, Issue.3
-
-
Gunaydin, H.1
Gu, Y.2
Huang, X.3
-
118
-
-
77249142404
-
The art of the chemical probe
-
Frye, S. V. The art of the chemical probe. Nat. Chem. Biol., 2010, 6(3), 159-161.
-
(2010)
Nat. Chem. Biol
, vol.6
, Issue.3
, pp. 159-161
-
-
Frye, S.V.1
|