-
1
-
-
0034306450
-
Specificity and mechanism of action of some commonly used protein kinase inhibitors
-
Davies, S. P.; Reddy, H.; Caivano, M.; Cohen, P. Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem. J. 2000, 351, 95-105.
-
(2000)
Biochem. J.
, vol.351
, pp. 95-105
-
-
Davies, S.P.1
Reddy, H.2
Caivano, M.3
Cohen, P.4
-
2
-
-
0005953097
-
Protein kinase activity associated with the avian sarcoma virus src gene product
-
Collett, M. S.; Erikson, R. L. Protein kinase activity associated with the avian sarcoma virus src gene product. Proc. Natl. Acad. Sci. U.S.A. 1978, 75, 2021-2024.
-
(1978)
Proc. Natl. Acad. Sci. U.S.A.
, vol.75
, pp. 2021-2024
-
-
Collett, M.S.1
Erikson, R.L.2
-
3
-
-
0036527429
-
Protein kinases-the major drug targets of the twenty-first century?
-
Cohen, P. Protein kinases-the major drug targets of the twenty-first century? Nat. Rev. Drug Discovery 2002, 1, 309-315.
-
(2002)
Nat. Rev. Drug Discovery
, vol.1
, pp. 309-315
-
-
Cohen, P.1
-
4
-
-
0034699382
-
A chemical switch for inhibitor-sensitive alleles of any protein kinase
-
Bishop, A. C.; Ubersax, J. A.; Petsch, D. T.; Matheos, D. P.; Gray, N. S.; Blethrow, J.; Shimizu, E.; Tsien, J. Z.; Schultz, P. G.; Rose, M. D.; Wood, J. L.; Morgan, D. O.; Shokat, K. M. A chemical switch for inhibitor-sensitive alleles of any protein kinase. Nature 2000, 407, 395-401.
-
(2000)
Nature
, vol.407
, pp. 395-401
-
-
Bishop, A.C.1
Ubersax, J.A.2
Petsch, D.T.3
Matheos, D.P.4
Gray, N.S.5
Blethrow, J.6
Shimizu, E.7
Tsien, J.Z.8
Schultz, P.G.9
Rose, M.D.10
Wood, J.L.11
Morgan, D.O.12
Shokat, K.M.13
-
5
-
-
0032563315
-
Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors
-
Gray, N. S.; Wodicka, L.; Thunnissen, A. M.; Norman, T. C.; Kwon, S.; Espinoza, F. H.; Morgan, D. O.; Barnes, G.; LeClerc, S.; Meijer, L.; Kim, S. H.; Lockhart, D. J.; Schultz, P. G. Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors. Science 1998, 281, 533-538.
-
(1998)
Science
, vol.281
, pp. 533-538
-
-
Gray, N.S.1
Wodicka, L.2
Thunnissen, A.M.3
Norman, T.C.4
Kwon, S.5
Espinoza, F.H.6
Morgan, D.O.7
Barnes, G.8
LeClerc, S.9
Meijer, L.10
Kim, S.H.11
Lockhart, D.J.12
Schultz, P.G.13
-
6
-
-
0036010705
-
Coupling structure-based design with combinatorial chemistry: Application of active site derived pharmacophores with informative library design
-
Eksterowicz, J. E.; Evensen, E.; Lemmen, C.; Brady, G. P.; Lanctot, J. K.; Bradley, E. K.; Saiah, E.; Robinson, L. A.; Grootenhuis, P. D.; Blaney, J. M. Coupling structure-based design with combinatorial chemistry: application of active site derived pharmacophores with informative library design. J. Mol. Graphics Modell. 2002, 20, 469-477.
-
(2002)
J. Mol. Graphics Modell
, vol.20
, pp. 469-477
-
-
Eksterowicz, J.E.1
Evensen, E.2
Lemmen, C.3
Brady, G.P.4
Lanctot, J.K.5
Bradley, E.K.6
Saiah, E.7
Robinson, L.A.8
Grootenhuis, P.D.9
Blaney, J.M.10
-
7
-
-
0023885305
-
The protein kinase family: Conserved features and deduced phylogeny of the catalytic domains
-
Hanks, S. K.; Quinn, A. M.; Hunter, T. The protein kinase family: conserved features and deduced phylogeny of the catalytic domains. Science 1988, 241, 42-52.
-
(1988)
Science
, vol.241
, pp. 42-52
-
-
Hanks, S.K.1
Quinn, A.M.2
Hunter, T.3
-
8
-
-
0034640214
-
Inhibition of voltage-dependent sodium channels by Ro 31-8220, a "specific" protein kinase C inhibitor
-
Lingameneni, R.; Vysotskaya, T. N.; Duch, D. S.; Hemmings, H. C., Jr. Inhibition of voltage-dependent sodium channels by Ro 31-8220, a "specific" protein kinase C inhibitor. FEBS Lett. 2000, 473, 265-268.
-
(2000)
FEBS Lett.
, vol.473
, pp. 265-268
-
-
Lingameneni, R.1
Vysotskaya, T.N.2
Duch, D.S.3
Hemmings H.C., Jr.4
-
9
-
-
0037013196
-
Flavonoid inhibition of sodium-dependent vitamin C transporter 1 (SVCT1) and glucose transporter isoform 2 (GLUT2), intestinal transporters for vitamin C and glucose
-
Song, J.; Kwon, O.; Chen, S.; Daruwala, R.; Eck, P.; Park, J. B.; Levine, M. Flavonoid inhibition of sodium-dependent vitamin C transporter 1 (SVCT1) and glucose transporter isoform 2 (GLUT2), intestinal transporters for vitamin C and glucose. J. Biol. Chem. 2002, 277, 15252-15260.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 15252-15260
-
-
Song, J.1
Kwon, O.2
Chen, S.3
Daruwala, R.4
Eck, P.5
Park, J.B.6
Levine, M.7
-
10
-
-
0035931322
-
Phytoestrogens inhibit human 17beta-hydroxysteroid dehydrogenase type 5
-
Krazeisen, A.; Breitling, R.; Moller, G.; Adamski, J. Phytoestrogens inhibit human 17beta-hydroxysteroid dehydrogenase type 5. Mol. Cell. Endocrinol. 2001, 171, 151-162.
-
(2001)
Mol. Cell. Endocrinol.
, vol.171
, pp. 151-162
-
-
Krazeisen, A.1
Breitling, R.2
Moller, G.3
Adamski, J.4
-
11
-
-
0035851112
-
Rottlerin is a mitochondrial uncoupler that decreases cellular ATP levels and indirectly blocks protein kinase Cdelta tyrosine phosphorylation
-
Soltoff, S. P. Rottlerin is a mitochondrial uncoupler that decreases cellular ATP levels and indirectly blocks protein kinase Cdelta tyrosine phosphorylation. J. Biol. Chem. 2001, 276, 37986-37992.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 37986-37992
-
-
Soltoff, S.P.1
-
12
-
-
0035957082
-
Protein kinase C effectors bind to multidrug ABC transporters and inhibit their activity
-
Conseil, G.; Perez-Victoria, J. M.; Jault, J. M.; Gamarro, F.; Goffeau, A.; Hofmann, J.; Di Pietro, A. Protein kinase C effectors bind to multidrug ABC transporters and inhibit their activity. Biochemistry 2001, 40, 2564-2571.
-
(2001)
Biochemistry
, vol.40
, pp. 2564-2571
-
-
Conseil, G.1
Perez-Victoria, J.M.2
Jault, J.M.3
Gamarro, F.4
Goffeau, A.5
Hofmann, J.6
Di Pietro, A.7
-
13
-
-
0000714445
-
Structure-activity relationships in a series of substituted indolocarbazoles: Topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties
-
Pereira, E. R.; Belin, L.; Sancelme, M.; Prudhomme, M.; Ollier, M.; Rapp, M.; Severe, D.; Riou, J. F.; Fabbro, D.; Meyer, T. Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. J. Med. Chem. 1996, 39, 4471-4477.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 4471-4477
-
-
Pereira, E.R.1
Belin, L.2
Sancelme, M.3
Prudhomme, M.4
Ollier, M.5
Rapp, M.6
Severe, D.7
Riou, J.F.8
Fabbro, D.9
Meyer, T.10
-
14
-
-
0033945117
-
Allosteric interactions of staurosporine and other indolocarbazoles with N-[methyl-(3)-H]scopolamine and acetylcholine at muscarinic receptor subtypes: Identification ofa second allosteric site
-
Lazareno, S.; Popham, A.; Birdsall, N. J. Allosteric interactions of staurosporine and other indolocarbazoles with N-[methyl-(3)-H]scopolamine and acetylcholine at muscarinic receptor subtypes: identification ofa second allosteric site. Mol. Pharmacol. 2000, 58, 194-207.
-
(2000)
Mol. Pharmacol.
, vol.58
, pp. 194-207
-
-
Lazareno, S.1
Popham, A.2
Birdsall, N.J.3
-
15
-
-
0037061628
-
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening
-
McGovern, S. L.; Caselli, E.; Grigorieff, N.; Shoichet, B. K. A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening. J. Med. Chem. 2002, 45, 1712-1722.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 1712-1722
-
-
McGovern, S.L.1
Caselli, E.2
Grigorieff, N.3
Shoichet, B.K.4
-
16
-
-
0028339457
-
Rottlerin, a novel protein kinase inhibitor
-
Gschwendt, M.; Muller, H. J.; Kielbassa, K.; Zang, R.; Kittstein, W.; Rincke, G.; Marks, F. Rottlerin, a novel protein kinase inhibitor. Biochem. Biophys. Res. Commun. 1994, 199, 93-98.
-
(1994)
Biochem. Biophys. Res. Commun.
, vol.199
, pp. 93-98
-
-
Gschwendt, M.1
Muller, H.J.2
Kielbassa, K.3
Zang, R.4
Kittstein, W.5
Rincke, G.6
Marks, F.7
-
17
-
-
0026726483
-
The inhibition of phosphatidylinositol 3-kinase by quercetin and analogs
-
Matter, W. F.; Brown, R. F.; Vlahos, C. J. The inhibition of phosphatidylinositol 3-kinase by quercetin and analogs. Biochem. Biophys. Res. Commun. 1992, 186, 624-631.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.186
, pp. 624-631
-
-
Matter, W.F.1
Brown, R.F.2
Vlahos, C.J.3
-
18
-
-
0027298410
-
Suramin: A novel antineoplastic agent with multiple potential mechanisms of action
-
Stein, C. A. Suramin: a novel antineoplastic agent with multiple potential mechanisms of action. Cancer Res. 1993, 53, 2239-2248.
-
(1993)
Cancer Res.
, vol.53
, pp. 2239-2248
-
-
Stein, C.A.1
-
19
-
-
0035957844
-
Study of protein adsorption on indigo particles confirms the existence of enzyme-indigo interaction sites in cellulase molecules
-
Gusakov, A. V.; Sinitsyn, A. P.; Markov, A. V.; Sinitsyna, O. A.; Ankudimova, N. V.; Berlin, A. G. Study of protein adsorption on indigo particles confirms the existence of enzyme-indigo interaction sites in cellulase molecules. J. Biotechnol. 2001, 87, 83-90.
-
(2001)
J. Biotechnol.
, vol.87
, pp. 83-90
-
-
Gusakov, A.V.1
Sinitsyn, A.P.2
Markov, A.V.3
Sinitsyna, O.A.4
Ankudimova, N.V.5
Berlin, A.G.6
-
20
-
-
0037011890
-
Development of a virtual screening method for identification of "Frequent Hitters" in compound libraries
-
Roche, O.; Schneider, P.; Zuegge, J.; Guba, W.; Kansy, M.; Alanine, A.; Bleicher, K.; Danel, F.; Gutknecht, E. M.; Rogers-Evans, M.; Neidhart, W.; Stalder, H.; Dillon, M.; Sjogren, E.; Fotouhi, N.; Gillespie, P.; Goodnow, R.; Harris, W.; Jones, P.; Taniguchi, M.; Tsujii, S.; von Der Saal, W.; Zimmermann, G.; Schneider, G. Development of a Virtual Screening Method for Identification of "Frequent Hitters" in Compound Libraries. J Med. Chem. 2002, 45, 137-142.
-
(2002)
J Med. Chem.
, vol.45
, pp. 137-142
-
-
Roche, O.1
Schneider, P.2
Zuegge, J.3
Guba, W.4
Kansy, M.5
Alanine, A.6
Bleicher, K.7
Danel, F.8
Gutknecht, E.M.9
Rogers-Evans, M.10
Neidhart, W.11
Stalder, H.12
Dillon, M.13
Sjogren, E.14
Fotouhi, N.15
Gillespie, P.16
Goodnow, R.17
Harris, W.18
Jones, P.19
Taniguchi, M.20
Tsujii, S.21
Von Der Saal, W.22
Zimmermann, G.23
Schneider, G.24
more..
-
21
-
-
0030756360
-
Reactive compounds and in vitro false positives in HTS
-
Rishton, G. M. Reactive compounds and in vitro false positives in HTS. Drug Discovery Today 1997, 2, 382-384.
-
(1997)
Drug Discovery Today
, vol.2
, pp. 382-384
-
-
Rishton, G.M.1
-
22
-
-
0035821596
-
Simple selection criteria for drug-like chemical matter
-
Muegge, I.; Heald, S. L.; Brittelli, D. Simple selection criteria for drug-like chemical matter. J. Med. Chem. 2001, 44, 1841-1846.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 1841-1846
-
-
Muegge, I.1
Heald, S.L.2
Brittelli, D.3
-
23
-
-
0031024171
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Delivery Rev. 1997, 23, 3-25.
-
(1997)
Adv. Drug Delivery Rev.
, vol.23
, pp. 3-25
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
25
-
-
0033634827
-
Structural determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin, and staurosporine
-
Walker, E. H.; Pacold, M. E.; Perisic, O.; Stephens, L.; Hawkins, P. T.; Wymann, M. P.; Williams, R. L. Structural determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin, and staurosporine. Mol. Cell 2000, 6, 909-919.
-
(2000)
Mol. Cell
, vol.6
, pp. 909-919
-
-
Walker, E.H.1
Pacold, M.E.2
Perisic, O.3
Stephens, L.4
Hawkins, P.T.5
Wymann, M.P.6
Williams, R.L.7
-
26
-
-
0031034930
-
Crystal structure of the Src family tyrosine kinase Hck
-
Sicheri, F.; Moarefi, I.; Kuriyan, J. Crystal structure of the Src family tyrosine kinase Hck. Nature 1997, 385, 602-609.
-
(1997)
Nature
, vol.385
, pp. 602-609
-
-
Sicheri, F.1
Moarefi, I.2
Kuriyan, J.3
-
27
-
-
0032287160
-
Supramolecular ligands: Monomer structure and protein ligation capability
-
Stopa, B.; Gorny, M.; Konieczny, L.; Piekarska, B.; Rybarska, J.; Skowronek, M.; Roterman, I. Supramolecular ligands: monomer structure and protein ligation capability. Biochimie 1998, 80, 963-968.
-
(1998)
Biochimie
, vol.80
, pp. 963-968
-
-
Stopa, B.1
Gorny, M.2
Konieczny, L.3
Piekarska, B.4
Rybarska, J.5
Skowronek, M.6
Roterman, I.7
-
28
-
-
0032487847
-
Structure-based enhancement of boronic acid-based inhibitors of AmpC β-lactamase
-
Weston, G. S.; Blazquez, J.; Baquero, F.; Shoichet, B. K. Structure-based enhancement of boronic acid-based inhibitors of AmpC β-lactamase. J. Med. Chem. 1998, 41, 4577-4586.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 4577-4586
-
-
Weston, G.S.1
Blazquez, J.2
Baquero, F.3
Shoichet, B.K.4
-
29
-
-
0030598861
-
Enhancement of the turnover number of thermostable malate dehydrogenase by deleting hydrogen bonds around the catalytic site
-
Nishiyama, M.; Kinoshita, M.; Kudo, H.; Horinouchi, S.; Tanokura, M. Enhancement of the turnover number of thermostable malate dehydrogenase by deleting hydrogen bonds around the catalytic site. Biochem. Biophys. Res. Commun. 1996, 225, 844-848.
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.225
, pp. 844-848
-
-
Nishiyama, M.1
Kinoshita, M.2
Kudo, H.3
Horinouchi, S.4
Tanokura, M.5
-
30
-
-
0013223828
-
A FRET-based assay platform for ultra-high density drug screening of protein kinases and phosphatases
-
Rodems, S. M.; Hamman, B. D.; Lin, C.; Zhao, J.; Shah, S.; Heidary, D.; Makings, L.; Stack, J. H.; Pollok, B. A. A FRET-based assay platform for ultra-high density drug screening of protein kinases and phosphatases. Assay Drug Dev. Technol. 2002, 1, 9-19.
-
(2002)
Assay Drug Dev. Technol.
, vol.1
, pp. 9-19
-
-
Rodems, S.M.1
Hamman, B.D.2
Lin, C.3
Zhao, J.4
Shah, S.5
Heidary, D.6
Makings, L.7
Stack, J.H.8
Pollok, B.A.9
-
31
-
-
0027665732
-
Protein kinase C inhibitors; Structure-activity relationships in K252c-related compounds
-
Fabre, S.; Prudhomme, M.; Rapp, M. Protein kinase C inhibitors; structure-activity relationships in K252c-related compounds. Bioorg. Med. Chem. 1993, 1, 193-196.
-
(1993)
Bioorg. Med. Chem.
, vol.1
, pp. 193-196
-
-
Fabre, S.1
Prudhomme, M.2
Rapp, M.3
-
32
-
-
0025942516
-
The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C
-
Toullec, D.; Pianetti, P.; Coste, H.; Bellevergue, P.; Grand-Perret, T.; Ajakane, M.; Baudet, V.; Boissin, P.; Boursier, E.; Loriolle, F.; et al. The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C. J. Biol. Chem. 1991, 266, 15771-15781.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 15771-15781
-
-
Toullec, D.1
Pianetti, P.2
Coste, H.3
Bellevergue, P.4
Grand-Perret, T.5
Ajakane, M.6
Baudet, V.7
Boissin, P.8
Boursier, E.9
Loriolle, F.10
-
33
-
-
0033128165
-
Indirubin, the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases
-
Hoessel, R.; Leclerc, S.; Endicott, J. A.; Nobel, M. E.; Lawrie, A.; Tunnah, P.; Leost, M.; Damiens, E.; Marie, D.; Marko, D.; Niederberger, E.; Tang, W.; Eisenbrand, G.; Meijer, L. Indirubin, the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases. Nat. Cell Biol. 1999, 1, 60-67.
-
(1999)
Nat. Cell Biol.
, vol.1
, pp. 60-67
-
-
Hoessel, R.1
Leclerc, S.2
Endicott, J.A.3
Nobel, M.E.4
Lawrie, A.5
Tunnah, P.6
Leost, M.7
Damiens, E.8
Marie, D.9
Marko, D.10
Niederberger, E.11
Tang, W.12
Eisenbrand, G.13
Meijer, L.14
-
34
-
-
0029166667
-
A synthetic inhibitor of the mitogen-activated protein kinase cascade
-
Dudley, D. T.; Pang, L.; Decker, S. J.; Bridges, A. J.; Saltiel, A. R. A synthetic inhibitor of the mitogen-activated protein kinase cascade. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 7686-7689.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 7686-7689
-
-
Dudley, D.T.1
Pang, L.2
Decker, S.J.3
Bridges, A.J.4
Saltiel, A.R.5
-
35
-
-
0028884033
-
PD 098059 is a specific inhibitor of the activation of mitogen-activated protein kinase kinase in vitro and in vivo
-
Alessi, D. R.; Cuenda, A.; Cohen, P.; Dudley, D. T.; Saltiel, A. R. PD 098059 is a specific inhibitor of the activation of mitogen-activated protein kinase kinase in vitro and in vivo. J. Biol. Chem. 1995, 270, 27489-27494.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 27489-27494
-
-
Alessi, D.R.1
Cuenda, A.2
Cohen, P.3
Dudley, D.T.4
Saltiel, A.R.5
-
36
-
-
0032582678
-
Direct inhibition of cyclooxygenase-1 and -2 by the kinase inhibitors SB 203580 and PD 98059. SB 203580 also inhibits thromboxane synthase
-
Borsch-Haubold, A. G.; Pasquet, S.; Watson, S. P. Direct inhibition of cyclooxygenase-1 and -2 by the kinase inhibitors SB 203580 and PD 98059. SB 203580 also inhibits thromboxane synthase. J. Biol. Chem. 1998, 273, 28766-28772.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 28766-28772
-
-
Borsch-Haubold, A.G.1
Pasquet, S.2
Watson, S.P.3
-
37
-
-
0030951146
-
p38 mitogen-activated protein kinase down-regulates nitric oxide and up-regulates prostaglandin E2 biosynthesis stimulated by interleukin-lbeta
-
Guan, Z.; Baier, L. D.; Morrison, A. R. p38 mitogen-activated protein kinase down-regulates nitric oxide and up-regulates prostaglandin E2 biosynthesis stimulated by interleukin-lbeta. J. Biol. Chem. 1997, 272, 8083-8089.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 8083-8089
-
-
Guan, Z.1
Baier, L.D.2
Morrison, A.R.3
-
38
-
-
0030656619
-
Calcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension
-
Uehata, M.; Ishizaki, T.; Satoh, H.; Ono, T.; Kawahara, T.; Morishita, T.; Tamakawa, H.; Yamagami, K.; Inui, J.; Maekawa, M.; Narumiya, S. Calcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension. Nature 1997, 389, 990-994.
-
(1997)
Nature
, vol.389
, pp. 990-994
-
-
Uehata, M.1
Ishizaki, T.2
Satoh, H.3
Ono, T.4
Kawahara, T.5
Morishita, T.6
Tamakawa, H.7
Yamagami, K.8
Inui, J.9
Maekawa, M.10
Narumiya, S.11
-
39
-
-
0025250131
-
Effects of suramin, an anti-human immunodeficiency virus reverse transcriptase agent, on protein kinase C. Differential activation and inhibition of protein kinase C isozymes
-
Mahoney, C. W.; Azzi, A.; Huang, K. P. Effects of suramin, an anti-human immunodeficiency virus reverse transcriptase agent, on protein kinase C. Differential activation and inhibition of protein kinase C isozymes. J. Biol. Chem. 1990, 265, 5424-5428.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 5424-5428
-
-
Mahoney, C.W.1
Azzi, A.2
Huang, K.P.3
-
40
-
-
85047696478
-
Phosphorothioate oligonucleotides, suramin and heparin inhibit DNA-dependent protein kinase activity
-
Hosoi, Y.; Matsumoto, Y.; Tomita, M.; Enomoto, A.; Morita, A.; Sakai, K.; Umeda, N.; Zhao, H. J.; Nakagawa, K.; Ono, T.; Suzuki, N. Phosphorothioate oligonucleotides, suramin and heparin inhibit DNA-dependent protein kinase activity. Br. J. Cancer 2002, 86, 1143-1149.
-
(2002)
Br. J. Cancer
, vol.86
, pp. 1143-1149
-
-
Hosoi, Y.1
Matsumoto, Y.2
Tomita, M.3
Enomoto, A.4
Morita, A.5
Sakai, K.6
Umeda, N.7
Zhao, H.J.8
Nakagawa, K.9
Ono, T.10
Suzuki, N.11
-
41
-
-
0033527745
-
The COOH terminus of Rho-kinase negatively regulates rho-kinase activity
-
Amano, M.; Chihara, K.; Nakamura, N.; Kaneko, T.; Matsuura, Y.; Kaibuchi, K. The COOH terminus of Rho-kinase negatively regulates rho-kinase activity. J. Biol. Chem. 1999, 274, 32418-32424.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 32418-32424
-
-
Amano, M.1
Chihara, K.2
Nakamura, N.3
Kaneko, T.4
Matsuura, Y.5
Kaibuchi, K.6
-
42
-
-
0027432424
-
Wortmannin is a potent phosphatidylinositol 3-kinase inhibitor: The role of phosphatidylinositol 3,4,5-trisphosphate in neutrophil responses
-
Arcaro, A.; Wymann, M. P. Wortmannin is a potent phosphatidylinositol 3-kinase inhibitor: the role of phosphatidylinositol 3,4,5-trisphosphate in neutrophil responses. Biochem. J. 1993, 296, 297-301.
-
(1993)
Biochem. J.
, vol.296
, pp. 297-301
-
-
Arcaro, A.1
Wymann, M.P.2
-
43
-
-
0026793938
-
Wortmannin, a microbial product inhibitor of myosin light chain kinase
-
Nakanishi, S.; Kakita, S.; Takahashi, I.; Kawahara, K.; Tsukuda, E.; Sano, T.; Yamada, K.; Yoshida, M.; Kase, H.; Matsuda, Y.; et al. Wortmannin, a microbial product inhibitor of myosin light chain kinase. J. Biol. Chem. 1992, 267, 2157-2163.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 2157-2163
-
-
Nakanishi, S.1
Kakita, S.2
Takahashi, I.3
Kawahara, K.4
Tsukuda, E.5
Sano, T.6
Yamada, K.7
Yoshida, M.8
Kase, H.9
Matsuda, Y.10
|