-
1
-
-
0037032835
-
-
Manning, G.; Whyte, D.B.; Martinez, R.; Hunter, Sudarsanam, T.S. The protein kinase complement of the human genome. Science 2002, 298, 1912-1934.
-
Manning, G.; Whyte, D.B.; Martinez, R.; Hunter, Sudarsanam, T.S. The protein kinase complement of the human genome. Science 2002, 298, 1912-1934.
-
-
-
-
2
-
-
0011672458
-
ATP site-directed competitive and irreversible inhibitors of protein kinases
-
Garcia-Echeverria, C.; Traxler, P.; Evans, D.B. ATP site-directed competitive and irreversible inhibitors of protein kinases. Med. Res. Rev. 2000, 20, 28-57.
-
(2000)
Med. Res. Rev
, vol.20
, pp. 28-57
-
-
Garcia-Echeverria, C.1
Traxler, P.2
Evans, D.B.3
-
3
-
-
0034642532
-
Cyclin-dependent kinase inhibitors: Useful targets in cell cycle regulation
-
Sielecki, T.M.; Boylan, J.F.; Benfield, P.A.; Trainor, G.L. Cyclin-dependent kinase inhibitors: useful targets in cell cycle regulation. J. Med. Chem. 2000, 43, 1-18.
-
(2000)
J. Med. Chem
, vol.43
, pp. 1-18
-
-
Sielecki, T.M.1
Boylan, J.F.2
Benfield, P.A.3
Trainor, G.L.4
-
4
-
-
0034788453
-
Tyrosine kinase inhibitors: From rational design to clinical trials
-
Traxler, P.; Bold, G.; Buchdunger, E.; Caravatti, G.; Furet, P.; Manley, P.; O'Reilly, T.; Wood, J.; Zimmermann, J. Tyrosine kinase inhibitors: from rational design to clinical trials. Med. Res. Rev. 2001, 21, 499-512.
-
(2001)
Med. Res. Rev
, vol.21
, pp. 499-512
-
-
Traxler, P.1
Bold, G.2
Buchdunger, E.3
Caravatti, G.4
Furet, P.5
Manley, P.6
O'Reilly, T.7
Wood, J.8
Zimmermann, J.9
-
5
-
-
75149197313
-
Cyclin-dependent kinase inhibitors for treating cancer
-
Toogood, P.L. Cyclin-dependent kinase inhibitors for treating cancer. Chem. Rev. 2001, 101, 2541-2572.
-
(2001)
Chem. Rev
, vol.101
, pp. 2541-2572
-
-
Toogood, P.L.1
-
6
-
-
0035413617
-
Chemical inhibitors of protein kinases
-
Bridges, A.J. Chemical inhibitors of protein kinases. Chem. Rev. 2001, 101, 2541-2572.
-
(2001)
Chem. Rev
, vol.101
, pp. 2541-2572
-
-
Bridges, A.J.1
-
7
-
-
0036591874
-
Structural biology in drug design: Selective protein kinase inhibitors
-
Scapin, G. Structural biology in drug design: selective protein kinase inhibitors. Drug Discov. 2001, 7, 601-611.
-
(2001)
Drug Discov
, vol.7
, pp. 601-611
-
-
Scapin, G.1
-
8
-
-
0034491146
-
Protein kinase as therapeutic targets
-
Sridhar, R.; Hanson-Painton, O.; Cooper, D.R. Protein kinase as therapeutic targets. Pharm. Res. 2000, 17, 1345-135
-
(2000)
Pharm. Res
, vol.17
, pp. 1345-2135
-
-
Sridhar, R.1
Hanson-Painton, O.2
Cooper, D.R.3
-
9
-
-
57749188299
-
Targeting cancer with small molecule kinase inhibitors
-
Zhang, J.; Yang, P.L.; Gray, N.S. Targeting cancer with small molecule kinase inhibitors. Nat. Rev. Cancer 2009, 9, 28-39.
-
(2009)
Nat. Rev. Cancer
, vol.9
, pp. 28-39
-
-
Zhang, J.1
Yang, P.L.2
Gray, N.S.3
-
10
-
-
0032567379
-
Granulatimide and isogranulatimide, aromatic alkaloids with G2 checkpoint inhibition activity isolated from the brazilian ascidian Didemnun granulatum: Structure elucidation and synthesis
-
Berlinck, R.G.S.; Britton, R.; Piers, E.; Lim, L.; Roberge, M.; Moreira da Rocha, R.; Andersen, R.J. Granulatimide and isogranulatimide, aromatic alkaloids with G2 checkpoint inhibition activity isolated from the brazilian ascidian Didemnun granulatum: structure elucidation and synthesis. J. Org. Chem. 1998, 63, 9850-9856.
-
(1998)
J. Org. Chem
, vol.63
, pp. 9850-9856
-
-
Berlinck, R.G.S.1
Britton, R.2
Piers, E.3
Lim, L.4
Roberge, M.5
Moreira da Rocha, R.6
Andersen, R.J.7
-
11
-
-
7444245571
-
Inhibition of Chk1 by the G2 DNA damage checkpoint inhibitor isogranulatimide
-
Jiang, X.; Zhao, B.; Britton, R.; Lim, L.Y.; Leong, D.; Sanghera, J.S.; Zhou, B.B.S.; Piers, E.; Andersen, R.J.; Roberge, M. Inhibition of Chk1 by the G2 DNA damage checkpoint inhibitor isogranulatimide. Mol. Cancer Ther. 2004, 3, 1221-1227.
-
(2004)
Mol. Cancer Ther
, vol.3
, pp. 1221-1227
-
-
Jiang, X.1
Zhao, B.2
Britton, R.3
Lim, L.Y.4
Leong, D.5
Sanghera, J.S.6
Zhou, B.B.S.7
Piers, E.8
Andersen, R.J.9
Roberge, M.10
-
12
-
-
0034713393
-
Functional link between ataxia-telangiectasia and nijmegen breakage syndrome gene products
-
Zhao, S.; Weng, Y.-C.; Yuan, S.-S. F.; Lin, Y.-T; Hsu, H.-C.; Lin, S.-C. J.; Gerbino, E.; Song, M.-H.; Zdzienicka, P. Functional link between ataxia-telangiectasia and nijmegen breakage syndrome gene products. Nature, 2000, 405, 473-476.
-
(2000)
Nature
, vol.405
, pp. 473-476
-
-
Zhao, S.1
Weng, Y.-C.2
Yuan, S.-S.F.3
Lin, Y.-T.4
Hsu, H.-C.5
Lin, S.-C.J.6
Gerbino, E.7
Song, M.-H.8
Zdzienicka, P.9
-
13
-
-
0242659422
-
Inhibition of the G2 DNA damage checkpoint and of protein kinases Chk1 and Chk2 by the marine sponge alkaloid debromohymenialdisine
-
Curman, D.; Cinel, B.; Williams, D.E.; Rundle, N.; Block, W.D.; Goodarzi, A.A.; Hutchins, J.R.; Clarke, P.R.; Zhou, B.-B.; Lees-Miller, S.P.; Andersen, R.J.; Roberge, M. Inhibition of the G2 DNA damage checkpoint and of protein kinases Chk1 and Chk2 by the marine sponge alkaloid debromohymenialdisine. J. Biol. Chem. 2001, 276, 17914-17919.
-
(2001)
J. Biol. Chem
, vol.276
, pp. 17914-17919
-
-
Curman, D.1
Cinel, B.2
Williams, D.E.3
Rundle, N.4
Block, W.D.5
Goodarzi, A.A.6
Hutchins, J.R.7
Clarke, P.R.8
Zhou, B.-B.9
Lees-Miller, S.P.10
Andersen, R.J.11
Roberge, M.12
-
14
-
-
2242421834
-
Structural basis for Chk1 inhibition by UCN-01
-
Zhao, B.; Bower, M.J.; McDevitt, P.J.; Zhao, H.; Davies, S.T.; Johanson, K.O.; Green, S.M.; Concha, N.O.; Zhou, B.B.S. Structural basis for Chk1 inhibition by UCN-01. J. Biol. Chem. 2002, 277, 46609-46615.
-
(2002)
J. Biol. Chem
, vol.277
, pp. 46609-46615
-
-
Zhao, B.1
Bower, M.J.2
McDevitt, P.J.3
Zhao, H.4
Davies, S.T.5
Johanson, K.O.6
Green, S.M.7
Concha, N.O.8
Zhou, B.B.S.9
-
15
-
-
52749086350
-
Pyrrolocarbazoles as checkpoint 1 kinase inhibitors
-
Hénon, H.; Conchon, E.; Hugon, B.; Messaoudi, S.; Golsteyn, R.M. Prudhomme. Pyrrolocarbazoles as checkpoint 1 kinase inhibitors. Anti-Cancer Agents Med. Chem. 2008, 8, 577-597.
-
(2008)
Anti-Cancer Agents Med. Chem
, vol.8
, pp. 577-597
-
-
Hénon, H.1
Conchon, E.2
Hugon, B.3
Messaoudi, S.4
Golsteyn5
Prudhomme, R.M.6
-
16
-
-
17444423644
-
High-throughput assay for G2 checkpoint inhibitors and identification of the structurally novel compound isogranulatimide
-
Roberge, M.; Berlinck, R.G.S.; Xu, L.; Anderson, H.J.; Lim, L.Y.; Curman, D.; Stringer, C.M.; Friend, S.H.; Davies, P.; Vincent, I.; Haggarty, S.J.; Kelly, M.T.; Britton, R.; Piers, E.; Andersen, R.J. High-throughput assay for G2 checkpoint inhibitors and identification of the structurally novel compound isogranulatimide. J. Cancer Res. 1998, 58, 5701-5706.
-
(1998)
J. Cancer Res
, vol.58
, pp. 5701-5706
-
-
Roberge, M.1
Berlinck, R.G.S.2
Xu, L.3
Anderson, H.J.4
Lim, L.Y.5
Curman, D.6
Stringer, C.M.7
Friend, S.H.8
Davies, P.9
Vincent, I.10
Haggarty, S.J.11
Kelly, M.T.12
Britton, R.13
Piers, E.14
Andersen, R.J.15
-
17
-
-
0032985884
-
A cyclised didemnimide alkaloid from the Caribbean ascidian Didemnum conchyliatum
-
Vervoort, H.C.; Fenical, W.; Keifer, P.A. A cyclised didemnimide alkaloid from the Caribbean ascidian Didemnum conchyliatum. J. Nat. Prod. 1999, 62, 389-391.
-
(1999)
J. Nat. Prod
, vol.62
, pp. 389-391
-
-
Vervoort, H.C.1
Fenical, W.2
Keifer, P.A.3
-
18
-
-
0030969780
-
-
Vervoort, H.C.; Richards-Gross, S.E.; Fenical, W. Didemnimides A-D: Novel predator-deterrent alkaloids from the carribean mangrove ascidian Didemnum conchyliatum. J. Org. Chem. 1997, 62, 1486-1490.
-
Vervoort, H.C.; Richards-Gross, S.E.; Fenical, W. Didemnimides A-D: Novel predator-deterrent alkaloids from the carribean mangrove ascidian Didemnum conchyliatum. J. Org. Chem. 1997, 62, 1486-1490.
-
-
-
-
19
-
-
0035089406
-
Granulatimide and 6-bromogranulatimide, minor alkaloids of the brazilian ascidian Didemnum granulatum
-
Britton, R.; de Oliveiras, J.H.H.L.; Andersen, R.J.; Berlinck, R.G.S. Granulatimide and 6-bromogranulatimide, minor alkaloids of the brazilian ascidian Didemnum granulatum. J. Nat. Prod. 2001, 64, 254-255.
-
(2001)
J. Nat. Prod
, vol.64
, pp. 254-255
-
-
Britton, R.1
de Oliveiras, J.H.H.L.2
Andersen, R.J.3
Berlinck, R.G.S.4
-
20
-
-
33846497955
-
-
Seleghim, M.H.R.; De Lira, S.P.; Campana, P.T.; Berlink, R.G.S.; Custodio, M.R. Localization of granulatimide alkaloids in the tissues of the ascidian Didemnum granulatum. Ma. Biol. 2007, 150, 967-975.
-
Seleghim, M.H.R.; De Lira, S.P.; Campana, P.T.; Berlink, R.G.S.; Custodio, M.R. Localization of granulatimide alkaloids in the tissues of the ascidian Didemnum granulatum. Ma. Biol. 2007, 150, 967-975.
-
-
-
-
21
-
-
0034723302
-
Improved synthesis of isogranulatimide, a G2 checkpoint inhibitor synthesis of didemnimide C, isodidemnimide A, neodidemnimide A, 17-methylgranulatimide, and isogranulatimide A-C
-
Piers, E.; Britton, R.; Andersen, R.J. Improved synthesis of isogranulatimide, a G2 checkpoint inhibitor synthesis of didemnimide C, isodidemnimide A, neodidemnimide A, 17-methylgranulatimide, and isogranulatimide A-C. J. Org. Chem. 2000, 65, 530-535.
-
(2000)
J. Org. Chem
, vol.65
, pp. 530-535
-
-
Piers, E.1
Britton, R.2
Andersen, R.J.3
-
22
-
-
0036596485
-
New synthetic route to granulatimide and its structural analogues
-
Yoshida, T.; Nishiyachi, M.; Nakashima, N.; Murase, M.; Kotani, E. New synthetic route to granulatimide and its structural analogues. Chem. Pharm. Bull. 2002, 50, 872-876.
-
(2002)
Chem. Pharm. Bull
, vol.50
, pp. 872-876
-
-
Yoshida, T.1
Nishiyachi, M.2
Nakashima, N.3
Murase, M.4
Kotani, E.5
-
23
-
-
0041520600
-
Synthesis of granulatimide positional analogues
-
Yoshida, T.; Nishiyachi, M.; Nakashima, N.; Murase, M.; Kotani, E. Synthesis of granulatimide positional analogues. Chem. Pharm. Bull. 2003, 51, 209-214.
-
(2003)
Chem. Pharm. Bull
, vol.51
, pp. 209-214
-
-
Yoshida, T.1
Nishiyachi, M.2
Nakashima, N.3
Murase, M.4
Kotani, E.5
-
24
-
-
0038065535
-
Synthesis of isogranulatimides A and B analogues possessing a 7-azaindole unit instead of an indole moiety
-
Hugon, B.; Pfeiffer, B.; Renard, P.; Prudhomme, M. Synthesis of isogranulatimides A and B analogues possessing a 7-azaindole unit instead of an indole moiety. Tetrahedron Lett. 2003, 44, 4607-4611.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 4607-4611
-
-
Hugon, B.1
Pfeiffer, B.2
Renard, P.3
Prudhomme, M.4
-
25
-
-
34447283531
-
Synthesis and biological activities of isogranulatimide analogues
-
Hugon, B.; Anizon, F.; Bailly, C.; Golsteyn, R. M.; Pierré, A.; Léonce, S.; Hickman, J.; Pfeiffer, B.; Prudhomme, M. Synthesis and biological activities of isogranulatimide analogues. Bioorg. Med. Chem. 2007, 15, 5965-5980.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 5965-5980
-
-
Hugon, B.1
Anizon, F.2
Bailly, C.3
Golsteyn, R.M.4
Pierré, A.5
Léonce, S.6
Hickman, J.7
Pfeiffer, B.8
Prudhomme, M.9
-
26
-
-
33845336481
-
Bis-imide granulatimide analogues as potent checkpoint 1 kinase inhibitors
-
Hénon, H.; Messaoudi, S.; Anizon, F.; Aboab, B.; Kucharczyk, N.; Léonce, S.; Golsteyn, R.M.; Pfeiffer, B.; Prudhomme, M. Bis-imide granulatimide analogues as potent checkpoint 1 kinase inhibitors. Eur. J. Pharm. 2007, 554, 106-112.
-
(2007)
Eur. J. Pharm
, vol.554
, pp. 106-112
-
-
Hénon, H.1
Messaoudi, S.2
Anizon, F.3
Aboab, B.4
Kucharczyk, N.5
Léonce, S.6
Golsteyn, R.M.7
Pfeiffer, B.8
Prudhomme, M.9
-
27
-
-
34648816236
-
Synthesis and biological activities of new checkpoint kinase 1 inhibitors structurally related to granulatimide
-
Conchon, E.; Anizon, F.; Aboab, B.; Prudhomme, M. Synthesis and biological activities of new checkpoint kinase 1 inhibitors structurally related to granulatimide. J. Med. Chem. 2007, 50, 4669-4680.
-
(2007)
J. Med. Chem
, vol.50
, pp. 4669-4680
-
-
Conchon, E.1
Anizon, F.2
Aboab, B.3
Prudhomme, M.4
-
28
-
-
42149187861
-
Synthesis, checkpoint kinase 1 inhibitory properties and in vitro antiproliferative activities of new pyrrolocarbazoles
-
Conchon, E.; Anizon, F.; Aboab, B.; Golsteyn, R.M.; Léonce, S.; Pfeiffer, B.; Prudhomme, M. Synthesis, checkpoint kinase 1 inhibitory properties and in vitro antiproliferative activities of new pyrrolocarbazoles. Bioorg. Med. Chem. 2008, 16, 4419-4430.
-
(2008)
Bioorg. Med. Chem
, vol.16
, pp. 4419-4430
-
-
Conchon, E.1
Anizon, F.2
Aboab, B.3
Golsteyn, R.M.4
Léonce, S.5
Pfeiffer, B.6
Prudhomme, M.7
-
29
-
-
30344446655
-
Synthesis and structure-activity relationships of novel poly(ADP-ribose) polymerase-1 inhibitors
-
Tao, M.; Park, C.H.; Bihovsky, R.; Wells, G.J.; Husten, J.; Ator, M.A.; Hudkins, R.L. Synthesis and structure-activity relationships of novel poly(ADP-ribose) polymerase-1 inhibitors. Bioorg. Med. Chem. Lett. 2006, 16, 938-942.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 938-942
-
-
Tao, M.1
Park, C.H.2
Bihovsky, R.3
Wells, G.J.4
Husten, J.5
Ator, M.A.6
Hudkins, R.L.7
-
30
-
-
31344433993
-
Synthesis and structure-activity relationships of novel pyrrolocarbazole lactam analogs as potent and cell-permeable inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1)
-
Wells, G.J.; Bihovsky, R.; Hudkins, R.L.; Ator, M.A.; Husten, J. Synthesis and structure-activity relationships of novel pyrrolocarbazole lactam analogs as potent and cell-permeable inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1). Bioorg. Med. Chem. Lett. 2006, 16, 1151-1155.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 1151-1155
-
-
Wells, G.J.1
Bihovsky, R.2
Hudkins, R.L.3
Ator, M.A.4
Husten, J.5
-
31
-
-
12444304196
-
Aryl[a]pyrrolo[3,4-c]carbazoles as selective Cyclyn D1-CDK4 inhibitors
-
Sanchez-Martinez, C.; Shih, C.; Faul, M.M.; Zhu, G.; Paal, M.; Somoza, C.; Li, T.; Kumrich, C. A.; Winneroski, L.L.; Xun, Z.; Brooks, H.B.; Patel, B.K.R.; Schultz, R.M.; DeHan, T.B.; Spencer, C.D.; Watkins, S.A.; Considine, E.; Dempsey, J.A.; Ogg, C.A.; Campbell, R.M.; Anderson, B.A.; Wagner, J. Aryl[a]pyrrolo[3,4-c]carbazoles as selective Cyclyn D1-CDK4 inhibitors. Bioorg. Med. Chem. Lett. 2003, 13, 3835-3839.
-
(2003)
Bioorg. Med. Chem. Lett
, vol.13
, pp. 3835-3839
-
-
Sanchez-Martinez, C.1
Shih, C.2
Faul, M.M.3
Zhu, G.4
Paal, M.5
Somoza, C.6
Li, T.7
Kumrich, C.A.8
Winneroski, L.L.9
Xun, Z.10
Brooks, H.B.11
Patel, B.K.R.12
Schultz, R.M.13
DeHan, T.B.14
Spencer, C.D.15
Watkins, S.A.16
Considine, E.17
Dempsey, J.A.18
Ogg, C.A.19
Campbell, R.M.20
Anderson, B.A.21
Wagner, J.22
more..
-
32
-
-
0001186193
-
A new efficient method for the synthesis of bisindolylmaleimides
-
Faul, M.M.; Winneroski, L.L.; Kumrich, C.A. A new efficient method for the synthesis of bisindolylmaleimides. J. Org. Chem. 1998, 63, 6053-6058.
-
(1998)
J. Org. Chem
, vol.63
, pp. 6053-6058
-
-
Faul, M.M.1
Winneroski, L.L.2
Kumrich, C.A.3
-
33
-
-
0033524732
-
A new one step synthesis of maleimides by condensation of glyoxylate esters with acetamides
-
Faul, M.M.; Winneroski, L.L.; Krumrich, C.A. A new one step synthesis of maleimides by condensation of glyoxylate esters with acetamides. Tetrahedron Lett. 1999, 40, 1109-1112.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 1109-1112
-
-
Faul, M.M.1
Winneroski, L.L.2
Krumrich, C.A.3
-
34
-
-
0037424693
-
Synthesis of quinolinyl/isoquinolinyl[a]pyrrolo[3,4-c]carbazoles as cyclin D1/CDK4 inhibitors
-
Zhu, G.; Conner, S.; Zhou, X.; Shih, C.; Brooks, H.B.; Considine, E.; Dempsey, J.A.; Ogg, C.; Patel, B.; Schultz, R.M.; Spencer, C.D.; Teicher, B.; Watkins, S.A. Synthesis of quinolinyl/isoquinolinyl[a]pyrrolo[3,4-c]carbazoles as cyclin D1/CDK4 inhibitors. Bioorg. Med. Chem. Lett. 2003, 13, 1231-1235.
-
(2003)
Bioorg. Med. Chem. Lett
, vol.13
, pp. 1231-1235
-
-
Zhu, G.1
Conner, S.2
Zhou, X.3
Shih, C.4
Brooks, H.B.5
Considine, E.6
Dempsey, J.A.7
Ogg, C.8
Patel, B.9
Schultz, R.M.10
Spencer, C.D.11
Teicher, B.12
Watkins, S.A.13
-
35
-
-
14944374500
-
Synthesis and biological evaluation of novel naphtocarbazoles as potential anticancer agents
-
Routier, S.; Peixoto, P.; Mérour, J.Y.; Coudert, G.; Dias, N.; Bailly, C.; Pierré, A.; Léonce, S.; Caignard, D.H. Synthesis and biological evaluation of novel naphtocarbazoles as potential anticancer agents. J. Med. Chem. 2005, 48, 1401-1413.
-
(2005)
J. Med. Chem
, vol.48
, pp. 1401-1413
-
-
Routier, S.1
Peixoto, P.2
Mérour, J.Y.3
Coudert, G.4
Dias, N.5
Bailly, C.6
Pierré, A.7
Léonce, S.8
Caignard, D.H.9
-
36
-
-
31544479559
-
Synthesis and biological evaluation of novel phenylcarbazoles as potential anticancer agents
-
Routier, S.; Mérour, J.-Y.; Dias, N.; Lansiaux, A.; Bailly, C.; Lozach, O.; Meijer, L. Synthesis and biological evaluation of novel phenylcarbazoles as potential anticancer agents. J. Med. Chem. 2006, 49, 789-799.
-
(2006)
J. Med. Chem
, vol.49
, pp. 789-799
-
-
Routier, S.1
Mérour, J.-Y.2
Dias, N.3
Lansiaux, A.4
Bailly, C.5
Lozach, O.6
Meijer, L.7
-
37
-
-
6444236961
-
An organometallic inhibitor for glycogen synthase kinase 3
-
Bregman, H.; Williams, D.S.; Atila, G.E.; Carroll, P.J.; Meggers, E. An organometallic inhibitor for glycogen synthase kinase 3. J. Am. Chem. Soc. 2004, 126, 13594-13595.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 13594-13595
-
-
Bregman, H.1
Williams, D.S.2
Atila, G.E.3
Carroll, P.J.4
Meggers, E.5
-
38
-
-
75149191889
-
Molecular cloning and expression of glycogen synthase kinase-3/factor A
-
Woodgett, J.R. Molecular cloning and expression of glycogen synthase kinase-3/factor A. EMBO J. 1990, 25, 923-929.
-
(1990)
EMBO J
, vol.25
, pp. 923-929
-
-
Woodgett, J.R.1
-
39
-
-
16844379913
-
Switching on a signalling pathway with an organoruthenium complex
-
Williams, D.S.; Atilla, G.E.; Bregman, H.; Arzoumanian, A.; Klein, P.S.; Meggers, E. Switching on a signalling pathway with an organoruthenium complex. Angew. Chem. Int. Ed. 2005, 44, 1984-1987.
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 1984-1987
-
-
Williams, D.S.1
Atilla, G.E.2
Bregman, H.3
Arzoumanian, A.4
Klein, P.S.5
Meggers, E.6
-
40
-
-
20644438252
-
Pyrido[2,3-a]pyrrolo[3,4-c] carbazole-5,7(6H)-diones: Synthesis, cyclometalation and protein kinase inhibition
-
Bregman, H.; Williams, D.S.; Meggers, W. Pyrido[2,3-a]pyrrolo[3,4-c] carbazole-5,7(6H)-diones: synthesis, cyclometalation and protein kinase inhibition. Synthesis 2005, 9, 1521-1527.
-
(2005)
Synthesis
, vol.9
, pp. 1521-1527
-
-
Bregman, H.1
Williams, D.S.2
Meggers, W.3
-
41
-
-
33748599842
-
Organometallic compounds with biological activity: A very selective and highly potent cellular inhibitor for glycogen synthase kinase 3
-
Atilla-Gokcumen, G.E.; Williams, D.S.; Bregman, H.; Pagano, N.; Meggers, E. Organometallic compounds with biological activity: a very selective and highly potent cellular inhibitor for glycogen synthase kinase 3. ChemBioChem 2006, 7, 1443-1450.
-
(2006)
ChemBioChem
, vol.7
, pp. 1443-1450
-
-
Atilla-Gokcumen, G.E.1
Williams, D.S.2
Bregman, H.3
Pagano, N.4
Meggers, E.5
-
42
-
-
33845976343
-
Ruthenium half-sandwich complexes as protein kinase inhibitors: An N-succinimidyl ester for rapid derivatizations of the cyclopentadienyl moiety
-
Bregman, H.; Meggers, E. Ruthenium half-sandwich complexes as protein kinase inhibitors: an N-succinimidyl ester for rapid derivatizations of the cyclopentadienyl moiety. Org. Lett. 2006, 24, 5465-5468.
-
(2006)
Org. Lett
, vol.24
, pp. 5465-5468
-
-
Bregman, H.1
Meggers, E.2
-
43
-
-
31444446334
-
Rapid access to unexplored chemical space by ligand scanning around a ruthenium center: Discovery of potent and selective protein kinase inhibitors
-
Bregman, H.; Carroll, P.J.; Meggers, E. Rapid access to unexplored chemical space by ligand scanning around a ruthenium center: discovery of potent and selective protein kinase inhibitors. J. Am. Chem. Soc. 2006, 128, 877-884.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 877-884
-
-
Bregman, H.1
Carroll, P.J.2
Meggers, E.3
-
44
-
-
59649119743
-
Extremely tigh binding of a ruthenium complex to glycogen synthase kinase 3
-
Atilla-Gokcumen, G.E.; Pagano, N.; Streu, C.; Maksimoska, J.; Filippakopoulos, P.; Knapp, S.; Meggers, E. Extremely tigh binding of a ruthenium complex to glycogen synthase kinase 3. ChemBioChem 2008, 9, 2933-2936.
-
(2008)
ChemBioChem
, vol.9
, pp. 2933-2936
-
-
Atilla-Gokcumen, G.E.1
Pagano, N.2
Streu, C.3
Maksimoska, J.4
Filippakopoulos, P.5
Knapp, S.6
Meggers, E.7
-
45
-
-
64349111699
-
Toward the development of a potent and selective organoruthenium mammalian sterile 20 kinase inhibitor
-
Anand, R.; Maksimoska, J.; Pagano, N.; Wong, E.Y.; Gimotty, P.A.; Diamond, S.L.; Meggers, E.; Marmorstein, R. Toward the development of a potent and selective organoruthenium mammalian sterile 20 kinase inhibitor. J. Med. Chem. 2009, 52, 1602-1611.
-
(2009)
J. Med. Chem
, vol.52
, pp. 1602-1611
-
-
Anand, R.1
Maksimoska, J.2
Pagano, N.3
Wong, E.Y.4
Gimotty, P.A.5
Diamond, S.L.6
Meggers, E.7
Marmorstein, R.8
-
46
-
-
0021816422
-
Isolation and structure of rebeccamycin a new antitumor antibiotic from nocardia aerocoligenes
-
Nettleton, D.E.; Doyle, T.W.; Kirshnan, B.; Matsumoto, G.K.; Clardy, J. Isolation and structure of rebeccamycin a new antitumor antibiotic from nocardia aerocoligenes. Tetrahedron Lett. 1985, 25, 4011-4014.
-
(1985)
Tetrahedron Lett
, vol.25
, pp. 4011-4014
-
-
Nettleton, D.E.1
Doyle, T.W.2
Kirshnan, B.3
Matsumoto, G.K.4
Clardy, J.5
-
47
-
-
0017395981
-
A new alkaloid AM-2282 of Streptomyces origin: Taxonomy, fermentation and preliminary characterization
-
Omura, S.; Iwai, Y.; Hirano, A.; Nakagawa, A.; Awaya, J.; Tsuchiva, H.; Takahashi, Y.; Masuma, R. A new alkaloid AM-2282 of Streptomyces origin: Taxonomy, fermentation and preliminary characterization. J. Antibiot. 1977, 30, 275-282.
-
(1977)
J. Antibiot
, vol.30
, pp. 275-282
-
-
Omura, S.1
Iwai, Y.2
Hirano, A.3
Nakagawa, A.4
Awaya, J.5
Tsuchiva, H.6
Takahashi, Y.7
Masuma, R.8
-
48
-
-
0029114101
-
Staurosporine, a potentially important gift from a microorganism
-
Omura, S.; Sasaki, Y.; Iwai, Y.; Takeshima, H. Staurosporine, a potentially important gift from a microorganism. J. Antibiot. 1995, 48, 535-548.
-
(1995)
J. Antibiot
, vol.48
, pp. 535-548
-
-
Omura, S.1
Sasaki, Y.2
Iwai, Y.3
Takeshima, H.4
-
49
-
-
0000714445
-
Structure-activity relationships in a series of substituted indolocarbazoles: Topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties
-
Rodrigues Pereira, E.; Belin, L.; Sancelme, M.; Prudhomme, M.; Ollier, M.; Rapp, D.; Sevère, 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
-
-
Rodrigues Pereira, E.1
Belin, L.2
Sancelme, M.3
Prudhomme, M.4
Ollier, M.5
Rapp, D.6
Sevère, D.7
Riou, J.F.8
Fabbro, D.9
Meyer, T.10
-
50
-
-
0344809977
-
ATP-Site directed inhibitors of cyclin-dependent kinases
-
Gray, N.; Détivaud, L.; Doerig, C.; Meijer, L. ATP-Site directed inhibitors of cyclin-dependent kinases. Curr. Med. Chem. 1999, 6, 859-875.
-
(1999)
Curr. Med. Chem
, vol.6
, pp. 859-875
-
-
Gray, N.1
Détivaud, L.2
Doerig, C.3
Meijer, L.4
-
51
-
-
0029015687
-
Production of the staurosporine aglycon K-252C with a blocked mutant of the staurosporine producer strain Streptomyces longisporoflavus and by biotransformation of staurosporine with Streptomyces mediddicm ATCC 13279
-
Goeke, K.; Hoehn, P.; Ghisalba, O. Production of the staurosporine aglycon K-252C with a blocked mutant of the staurosporine producer strain Streptomyces longisporoflavus and by biotransformation of staurosporine with Streptomyces mediddicm ATCC 13279. J. Antibiot. 1995, 48, 428-430.
-
(1995)
J. Antibiot
, vol.48
, pp. 428-430
-
-
Goeke, K.1
Hoehn, P.2
Ghisalba, O.3
-
52
-
-
0025841808
-
A new screening test for antimitotic compounds using the universal M phase-specific protein kinase, p34cdc2/cyclin Bcd13, affinity immobilized on p13suc1-coated microtitration plates
-
Rialet, V.; Meijer, L. A new screening test for antimitotic compounds using the universal M phase-specific protein kinase, p34cdc2/cyclin Bcd13, affinity immobilized on p13suc1-coated microtitration plates. Anticancer Res. 1991, 11, 1581.
-
(1991)
Anticancer Res
, vol.11
, pp. 1581
-
-
Rialet, V.1
Meijer, L.2
-
53
-
-
0034693811
-
Development of inhibitors for protein tyrosine kinases
-
Al-Obeidi, F.A.; Lam, K.S. Development of inhibitors for protein tyrosine kinases. Oncogene 2000, 19, 5690-5702.
-
(2000)
Oncogene
, vol.19
, pp. 5690-5702
-
-
Al-Obeidi, F.A.1
Lam, K.S.2
-
54
-
-
6444232494
-
Biological targets of antitumor indolocarbazoles bearing a sugar moiety
-
Prudhomme, M. Biological targets of antitumor indolocarbazoles bearing a sugar moiety. Curr. Med. Chem. Anticancer Agents 2004, 4, 509-521.
-
(2004)
Curr. Med. Chem. Anticancer Agents
, vol.4
, pp. 509-521
-
-
Prudhomme, M.1
-
55
-
-
33646026356
-
Staurosporine and structurally related indolocarbazoles as antitumor agents
-
Cragg, G.M, Gordon, M, Kingston, D.G.I, Newman, D.J, Eds, CRC Press: Boca Raton, FL, USA
-
Prudhomme, M. Staurosporine and structurally related indolocarbazoles as antitumor agents. In Anticancer Agents from Natural Products; Cragg, G.M., Gordon, M., Kingston, D.G.I., Newman, D.J., Eds.; CRC Press: Boca Raton, FL, USA, 2005; pp. 499-517.
-
(2005)
Anticancer Agents from Natural Products
, pp. 499-517
-
-
Prudhomme, M.1
-
56
-
-
19544366773
-
New cytotoxic bisindole alkaloids with protein tyrosine kinase inhibitory activity from a myxomycete Lycogala epidendrum
-
Hosoya, T.; Yamamoto, Y.; Uehara, Y.; Hayashi, M.; Komiyama, K.; Ishibashi, M. New cytotoxic bisindole alkaloids with protein tyrosine kinase inhibitory activity from a myxomycete Lycogala epidendrum. Bioorg. Med. Chem. Lett. 2005, 15, 2776-2780.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 2776-2780
-
-
Hosoya, T.1
Yamamoto, Y.2
Uehara, Y.3
Hayashi, M.4
Komiyama, K.5
Ishibashi, M.6
-
57
-
-
12444308937
-
-
Engler, T.A.; Furnee, K.; Malhotra, S.; Sanchez-Martinez, C.; Shih, C.; Xie, W.; Zhu, G.; Zhou, X.; Conner, S.; Faul, M.M.; Sullivan, K.A.; Kolis, S.P.; Brooks, H.B.; Patel, B.; Schultz, R.M.; DeHan, T.B.; Kirmani, K.; Spencer, C.D.; Watkins, S.A.; Considine, E.L.; Dempsey, J.A.; Ogg, C.A.; Stamm, N.B.; Anderson, B.D.; Campbell, R.M.. Vasudevan, V.; Lytle, M.L. Novel, potent and selective cyclin D1/CDK4 inhibitors: indolo[6,7-a]pyrrolo[3,4-c]carbazoles. Bioorg. Med. Chem. Lett. 2003, 13, 2261-2267.
-
Engler, T.A.; Furnee, K.; Malhotra, S.; Sanchez-Martinez, C.; Shih, C.; Xie, W.; Zhu, G.; Zhou, X.; Conner, S.; Faul, M.M.; Sullivan, K.A.; Kolis, S.P.; Brooks, H.B.; Patel, B.; Schultz, R.M.; DeHan, T.B.; Kirmani, K.; Spencer, C.D.; Watkins, S.A.; Considine, E.L.; Dempsey, J.A.; Ogg, C.A.; Stamm, N.B.; Anderson, B.D.; Campbell, R.M.. Vasudevan, V.; Lytle, M.L. Novel, potent and selective cyclin D1/CDK4 inhibitors: indolo[6,7-a]pyrrolo[3,4-c]carbazoles. Bioorg. Med. Chem. Lett. 2003, 13, 2261-2267.
-
-
-
-
58
-
-
11144354452
-
Synthetic approaches to indolo[6,7-α]pyrrolo[3,4-c]carbazoles: Potent cyclin D1/CDK4 inhibitors
-
Faul, M.M.; Engler, T.A.; Sullivan, K.A.; Grutsch, J.L.; Clayton, M.T.; Martinelli, M.J.; Pawlak, J.M.; LeTourneau, M.; Coffey, D.S.; Pedersen, S.W.; Kolis, S.P.; Furness, K.; Malhotra, S.; Alawar, R.S.; Ray, J.E. Synthetic approaches to indolo[6,7-α]pyrrolo[3,4-c]carbazoles: potent cyclin D1/CDK4 inhibitors. J. Org. Chem. 2004, 69, 2967-2975.
-
(2004)
J. Org. Chem
, vol.69
, pp. 2967-2975
-
-
Faul, M.M.1
Engler, T.A.2
Sullivan, K.A.3
Grutsch, J.L.4
Clayton, M.T.5
Martinelli, M.J.6
Pawlak, J.M.7
LeTourneau, M.8
Coffey, D.S.9
Pedersen, S.W.10
Kolis, S.P.11
Furness, K.12
Malhotra, S.13
Alawar, R.S.14
Ray, J.E.15
-
59
-
-
2442417541
-
Synthesis of 1,7-annulated indoles and their applications in the studies of cyclin dependant kinase inhibitors
-
Zhu, G.; Conner, S.E.; Zhou, X.; Chan, H.K.; Shih, C.; Engler, T.A.; Al-awar, R.S.; Brooks, H.B.; Watkins, S.A.; Spencer, C.D.; Schultz, R.M.; Dempsey, J.A.; Considine, E.L.; Patel, B.R.; Ogg, C.A.; Vasudevan, V.; Lytle, M.L. Synthesis of 1,7-annulated indoles and their applications in the studies of cyclin dependant kinase inhibitors. Bioorg. Med. Chem. Lett. 2004, 14, 3057-3061.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 3057-3061
-
-
Zhu, G.1
Conner, S.E.2
Zhou, X.3
Chan, H.K.4
Shih, C.5
Engler, T.A.6
Al-awar, R.S.7
Brooks, H.B.8
Watkins, S.A.9
Spencer, C.D.10
Schultz, R.M.11
Dempsey, J.A.12
Considine, E.L.13
Patel, B.R.14
Ogg, C.A.15
Vasudevan, V.16
Lytle, M.L.17
-
60
-
-
2442471732
-
1,7-Annulated indolocarbazoles as cyclin-dependent kinase inhibitors
-
Al-awar, R.S.; Ray, J.E.; Hecker, K.A.; Huang, J.; Waid, P.P.; Shih, C.; Brooks, H.B.; Spencer, C.D.; Watkins, S.A.; Patel, B.R.; Stamm, N.B.; Ogg, C.A.; Shultz, R.M.; Considine, E.L.; Faul, M.M.; Sullivan, K.A.; Kolis, S.P.; Grutsch, J.L.; Joseph, S. 1,7-Annulated indolocarbazoles as cyclin-dependent kinase inhibitors. Bioorg. Med. Chem. Lett. 2004, 14, 3217-3220.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 3217-3220
-
-
Al-awar, R.S.1
Ray, J.E.2
Hecker, K.A.3
Huang, J.4
Waid, P.P.5
Shih, C.6
Brooks, H.B.7
Spencer, C.D.8
Watkins, S.A.9
Patel, B.R.10
Stamm, N.B.11
Ogg, C.A.12
Shultz, R.M.13
Considine, E.L.14
Faul, M.M.15
Sullivan, K.A.16
Kolis, S.P.17
Grutsch, J.L.18
Joseph, S.19
-
61
-
-
0242361216
-
Semi-synthesis, topoisomerase I and kinases inhibitory properties and antiproliferative activities of new rebeccamycin derivatives
-
Moreau, P.; Gaillard, N.; Marminon, C.; Anizon, F.; Dias, N.; Baldeyrou, B.; Bailly, C.; Pierré, A.; Hickman, J.; Pfeiffer, B.; Renard, P.; Prudhomme, M. Semi-synthesis, topoisomerase I and kinases inhibitory properties and antiproliferative activities of new rebeccamycin derivatives. Bioorg. Med. Chem. 2003, 11, 4871-4879.
-
(2003)
Bioorg. Med. Chem
, vol.11
, pp. 4871-4879
-
-
Moreau, P.1
Gaillard, N.2
Marminon, C.3
Anizon, F.4
Dias, N.5
Baldeyrou, B.6
Bailly, C.7
Pierré, A.8
Hickman, J.9
Pfeiffer, B.10
Renard, P.11
Prudhomme, M.12
-
62
-
-
12144288796
-
-
Balasubramanian, B.N.; St. Laurent, D.R.; Saulnier, M.G.; Long, B.H.; Bachand, C.; Beaulieu, F.; Clarke, W.; Deshpande, M.; Eummer, J.; Fairchild, C.R.; Frennesson, D.B.; Kramer, R.; Lee, F. Y.; Mahler, M.; Martel, A.; Naidu, B.N.; Rose, W.C.; Russell, J.; Ruediger, E.; Solomon, C.; Stoffan, K.M.; Wong, H.; Zimmermann, K.; Vyas, D.M. Design and synthesis of a fluoroindolocarbazole series as selective topoisomerase I active agents. Discovery of water-soluble 3,9-difluoro-12,13H-benzo[b]-thienyl[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H) -dione (BMS-251873) with curative antitumor activity against xenograft tumor model. J. Med. Chem. 2004, 47, 1609-1612.
-
Balasubramanian, B.N.; St. Laurent, D.R.; Saulnier, M.G.; Long, B.H.; Bachand, C.; Beaulieu, F.; Clarke, W.; Deshpande, M.; Eummer, J.; Fairchild, C.R.; Frennesson, D.B.; Kramer, R.; Lee, F. Y.; Mahler, M.; Martel, A.; Naidu, B.N.; Rose, W.C.; Russell, J.; Ruediger, E.; Solomon, C.; Stoffan, K.M.; Wong, H.; Zimmermann, K.; Vyas, D.M. Design and synthesis of a fluoroindolocarbazole series as selective topoisomerase I active agents. Discovery of water-soluble 3,9-difluoro-12,13H-benzo[b]-thienyl[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H) -dione (BMS-251873) with curative antitumor activity against xenograft tumor model. J. Med. Chem. 2004, 47, 1609-1612.
-
-
-
-
63
-
-
20244372565
-
-
Saulnier, M.G.; Balasubramanian, B.N.; Long, B.H.; Frennesson, D.B.; Ruediger, E.; Zimmermann, K.; Eummer, J.T.; St. Laurent, D.R.; Stoffan, K.M.; Naidu, B.N.; Mahler, M.; Beaulieu, F.; Bachand, C.; Lee, F.Y.; Fairchild, C.R.; Stadnick, L.K.; Rose, W.C.; Solomon, C.; Wong, H.; Martel, A.; Wright, J.J.; Kramer, R.; Langley, D.R.; Vyas, D.M. Discovery of a fluoroindolo[2,3-α] carbazole clinical candidate with broad spectrum antitumor activity in preclinical tumor models superior to the marketed oncology drug, CPT-11. J. Med. Chem. 2005, 48, 2258-2261.
-
Saulnier, M.G.; Balasubramanian, B.N.; Long, B.H.; Frennesson, D.B.; Ruediger, E.; Zimmermann, K.; Eummer, J.T.; St. Laurent, D.R.; Stoffan, K.M.; Naidu, B.N.; Mahler, M.; Beaulieu, F.; Bachand, C.; Lee, F.Y.; Fairchild, C.R.; Stadnick, L.K.; Rose, W.C.; Solomon, C.; Wong, H.; Martel, A.; Wright, J.J.; Kramer, R.; Langley, D.R.; Vyas, D.M. Discovery of a fluoroindolo[2,3-α] carbazole clinical candidate with broad spectrum antitumor activity in preclinical tumor models superior to the marketed oncology drug, CPT-11. J. Med. Chem. 2005, 48, 2258-2261.
-
-
-
-
64
-
-
0042121548
-
Rebeccamycin analogues bearing amine substituents or other groups on the sugar moiety
-
Anizon, F.; Moreau, P.; Sancelme, M.; Laine, W.; Bailly, C.; Prudhomme, M. Rebeccamycin analogues bearing amine substituents or other groups on the sugar moiety. Bioorg. Med. Chem. 2003, 11, 3709-3722.
-
(2003)
Bioorg. Med. Chem
, vol.11
, pp. 3709-3722
-
-
Anizon, F.1
Moreau, P.2
Sancelme, M.3
Laine, W.4
Bailly, C.5
Prudhomme, M.6
-
65
-
-
0347022267
-
Synthesis of indolo[2,3-a]carbazole glycoside analogs of rebeccamycin: Inhibitors of cyclin D1-CDK4
-
Faul, M.M.; Sullivan, K.A.; Grutsch, J.L.; Winneroski, L.L.; Shih, C.; Sanchez-Martinez, C.; Cooper, J.T. Synthesis of indolo[2,3-a]carbazole glycoside analogs of rebeccamycin: inhibitors of cyclin D1-CDK4. Tetrahedron Lett. 2004, 45, 1095-1098.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 1095-1098
-
-
Faul, M.M.1
Sullivan, K.A.2
Grutsch, J.L.3
Winneroski, L.L.4
Shih, C.5
Sanchez-Martinez, C.6
Cooper, J.T.7
-
66
-
-
20244380623
-
Synthesis and biological activities of rebeccamycin analogues with uncommon sugars
-
Zhang, G.; Shen, J.; Cheng, H.; Fang, L.; Luo, S.; Muller, M.T.; Lee, G.E.; Wei, L.; Du, Y.; Sun, D.; Wang, P.G. Synthesis and biological activities of rebeccamycin analogues with uncommon sugars. J. Med. Chem. 2005, 48, 2600-2611.
-
(2005)
J. Med. Chem
, vol.48
, pp. 2600-2611
-
-
Zhang, G.1
Shen, J.2
Cheng, H.3
Fang, L.4
Luo, S.5
Muller, M.T.6
Lee, G.E.7
Wei, L.8
Du, Y.9
Sun, D.10
Wang, P.G.11
-
67
-
-
14944373194
-
Synthesis of 7-keto-Gö6976 (ICP-103)
-
Roy, S.; Eastman, A.; Gribble, G.W. Synthesis of 7-keto-Gö6976 (ICP-103). Synth. Commun. 2005, 35, 595-601.
-
(2005)
Synth. Commun
, vol.35
, pp. 595-601
-
-
Roy, S.1
Eastman, A.2
Gribble, G.W.3
-
68
-
-
33745596386
-
Synthesis of N-alkyl substituted bioactive indolocarbazoles related to Gö6979
-
Roy, S.; Eastman, A.; Gribble, G.W. Synthesis of N-alkyl substituted bioactive indolocarbazoles related to Gö6979. Tetrahedron 2006, 62, 7838-7845.
-
(2006)
Tetrahedron
, vol.62
, pp. 7838-7845
-
-
Roy, S.1
Eastman, A.2
Gribble, G.W.3
-
69
-
-
0001186193
-
A new efficient method for the synthesis of bisindolylmaleimides
-
b
-
Faul, M.M.; Winneroski, L.L.; Kumrich, C.A. A new efficient method for the synthesis of bisindolylmaleimides. J. Org. Chem. 1998, 63, 6053-6058. (b)
-
(1998)
J. Org. Chem
, vol.63
, pp. 6053-6058
-
-
Faul, M.M.1
Winneroski, L.L.2
Kumrich, C.A.3
-
70
-
-
0033524732
-
A new one step synthesis of maleimides by condensation of glyoxylate esters with acetamides
-
Faul, M.M.; Winneroski, L.L.; Krumrich, C.A. A new one step synthesis of maleimides by condensation of glyoxylate esters with acetamides. Tetrahedron Lett. 1999, 40, 1109-1112.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 1109-1112
-
-
Faul, M.M.1
Winneroski, L.L.2
Krumrich, C.A.3
-
71
-
-
33747883247
-
Synthesis of bisindolylmaleimides related to GF109203x and their efficient conversion to the bioactive indolocarbazoles
-
Roy, S.; Eastman, A.; Gribble, G.W. Synthesis of bisindolylmaleimides related to GF109203x and their efficient conversion to the bioactive indolocarbazoles. Org. Biomol. Chem. 2006, 4, 3228-3234.
-
(2006)
Org. Biomol. Chem
, vol.4
, pp. 3228-3234
-
-
Roy, S.1
Eastman, A.2
Gribble, G.W.3
-
72
-
-
0037067874
-
Synthesis and biological evaluation of 7-azaindolocarbazoles
-
Routier, S.; Ayerbe, N.; Mérour, J. Y.; Coudert, G.; Bailly, C.; Pierré, A.; Pfeiffer, B.; Caignard, D.H.; Renard, P. Synthesis and biological evaluation of 7-azaindolocarbazoles. Tetrahedron 2002, 58, 6621-6630.
-
(2002)
Tetrahedron
, vol.58
, pp. 6621-6630
-
-
Routier, S.1
Ayerbe, N.2
Mérour, J.Y.3
Coudert, G.4
Bailly, C.5
Pierré, A.6
Pfeiffer, B.7
Caignard, D.H.8
Renard, P.9
-
73
-
-
33845786925
-
-
Popowycz, F.; Routier, S.; Joseph, B.; Merour, J-Y. Synthesis and reactivity of 7-azaindole (1H-pyrrolo[2,3-b]pyridine). Tetrahedron 2007, 63, 1031-1064.
-
Popowycz, F.; Routier, S.; Joseph, B.; Merour, J-Y. Synthesis and reactivity of 7-azaindole (1H-pyrrolo[2,3-b]pyridine). Tetrahedron 2007, 63, 1031-1064.
-
-
-
-
74
-
-
0037434589
-
Synthesis and antiproliferative activities of 7-azarebeccamycin analogues bearing one 7-azaindole moiety
-
Marminon, C.; Pierré, A.; Pfeiffer, B.; Pérez, V.; Léonce, S.; Joubert, A.; Bailly, C.; Renard, P.; Hickman, J.; Prudhomme, M. Synthesis and antiproliferative activities of 7-azarebeccamycin analogues bearing one 7-azaindole moiety. J. Med. Chem. 2003, 46, 609-622.
-
(2003)
J. Med. Chem
, vol.46
, pp. 609-622
-
-
Marminon, C.1
Pierré, A.2
Pfeiffer, B.3
Pérez, V.4
Léonce, S.5
Joubert, A.6
Bailly, C.7
Renard, P.8
Hickman, J.9
Prudhomme, M.10
-
75
-
-
2442687670
-
Synthesis of a staurosporine analogue possessing a 7-azaindole unit instead of an indole moiety
-
Messaoudi, S.; Anizon, F.; Pfeiffer, B.; Golsteyn, R.; Prudhomme, M. Synthesis of a staurosporine analogue possessing a 7-azaindole unit instead of an indole moiety. Tetrahedron Lett. 2004, 45, 4643-4647.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 4643-4647
-
-
Messaoudi, S.1
Anizon, F.2
Pfeiffer, B.3
Golsteyn, R.4
Prudhomme, M.5
-
76
-
-
20544433629
-
Synthesis of bridged aza-rebeccamycin analogues
-
Messaoudi, S.; Anizon, F.; Pfeiffer, B.; Prudhomme, M. Synthesis of bridged aza-rebeccamycin analogues. Tetrahedron 2005, 61, 7304-7316.
-
(2005)
Tetrahedron
, vol.61
, pp. 7304-7316
-
-
Messaoudi, S.1
Anizon, F.2
Pfeiffer, B.3
Prudhomme, M.4
-
77
-
-
26444518787
-
Synthesis and cytotoxicities of 7-aza rebeccamycin analogues bearing various substituents on the sugar moiety, on the imide nitrogen and on the carbazole framework
-
Messaoudi, S.; Anizon, F.; Léonce, S.; Pierré, A.; Pfeiffer, B.; Prudhomme, M. Synthesis and cytotoxicities of 7-aza rebeccamycin analogues bearing various substituents on the sugar moiety, on the imide nitrogen and on the carbazole framework. Eur. J. Med. Chem. 2005, 40, 961-971.
-
(2005)
Eur. J. Med. Chem
, vol.40
, pp. 961-971
-
-
Messaoudi, S.1
Anizon, F.2
Léonce, S.3
Pierré, A.4
Pfeiffer, B.5
Prudhomme, M.6
-
78
-
-
33749234576
-
Synthesis and biological activities of 7-azarebeccamycin analogues bearing the sugar moiety on the nitrogen of the pyridine ring
-
Messaoudi, S.; Anizon, F.; Peixoto, P.; David-Cordonnier, M.H.; Golsteyn, R. M.; Léonce, S.; Pfeiffer, B.; Prudhomme, M. Synthesis and biological activities of 7-azarebeccamycin analogues bearing the sugar moiety on the nitrogen of the pyridine ring. Bioorg. Med. Chem. 2006, 14, 7551-7562.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 7551-7562
-
-
Messaoudi, S.1
Anizon, F.2
Peixoto, P.3
David-Cordonnier, M.H.4
Golsteyn, R.M.5
Léonce, S.6
Pfeiffer, B.7
Prudhomme, M.8
-
79
-
-
38949095649
-
-
Conchon, E.; Anizon, F.; Aboab, B.; Golsteyn, R. M.; Léonce, S.; Pfeiffer, B.; Prudhomme, M. Synthesis, in vitro antiproliferative activities, and Chk1 inhibitory properties of pyrrolo[3,4-a]carbazole-1,3-diones, pyrrolo[3,4-c]carbazole-1,3-diones, and 2-aminopyridazino[3,4-a]pyrrolo[3,4-c] carbazole-1,3,4,7-tetraone. Eur. J. Med. Chem. 2008, 43, 282-292.
-
Conchon, E.; Anizon, F.; Aboab, B.; Golsteyn, R. M.; Léonce, S.; Pfeiffer, B.; Prudhomme, M. Synthesis, in vitro antiproliferative activities, and Chk1 inhibitory properties of pyrrolo[3,4-a]carbazole-1,3-diones, pyrrolo[3,4-c]carbazole-1,3-diones, and 2-aminopyridazino[3,4-a]pyrrolo[3,4-c] carbazole-1,3,4,7-tetraone. Eur. J. Med. Chem. 2008, 43, 282-292.
-
-
-
-
80
-
-
19744365702
-
A small molecule-kinase interaction map for clinical kinase inhibitors
-
Fabian, M. A.; Biggs III, W.H.; Treiber, D.K.; Atteridge, C.E.; Azimioara, M.D.; Bendetti, M.G.; Carter, T.A.; Ciceri, P.; Edeen, P.T.; Floyd, M.; Ford, J.M.; Galvin, M.; Gerlach, J.L.; Grotzfeld, R.M.; Herrgard, S.; Insko, D.E.; Insko, M.A.; Lai, A.G.; Lelias, R.M.; Mehta, S.A.; Milanov, Z.V.; Velasco, A.M.; Wodicka, L.M.; Patel, H.K.; Zarrinkar, P.P.; Lockhardt, D.J. A small molecule-kinase interaction map for clinical kinase inhibitors. Nat. Biotechnol. 2005, 23, 329-336.
-
(2005)
Nat. Biotechnol
, vol.23
, pp. 329-336
-
-
Fabian, M.A.1
Biggs III, W.H.2
Treiber, D.K.3
Atteridge, C.E.4
Azimioara, M.D.5
Bendetti, M.G.6
Carter, T.A.7
Ciceri, P.8
Edeen, P.T.9
Floyd, M.10
Ford, J.M.11
Galvin, M.12
Gerlach, J.L.13
Grotzfeld, R.M.14
Herrgard, S.15
Insko, D.E.16
Insko, M.A.17
Lai, A.G.18
Lelias, R.M.19
Mehta, S.A.20
Milanov, Z.V.21
Velasco, A.M.22
Wodicka, L.M.23
Patel, H.K.24
Zarrinkar, P.P.25
Lockhardt, D.J.26
more..
-
81
-
-
38049018155
-
A quantitative analysis of kinase inhibitor selectivity
-
Karaman, M.W.; Herrgard, S.; Treiber, D.K.; Gallant, P.; Atteridge, C.E.; Campbell, B.T.; Chan, K.W.; Ciceri, P.; Davis, M.I.; Edeen, P.T.; Faraoni, R.; Floyd, M.; Hunt, J.P.; Lockhardt, D.J.; Milanov, Z.V.; Morrison, M.J.; Pallares, G.; Patel, H.K.; Pritchard, S.; Wodicka, L.M.; Zarrinkar, P.P. A quantitative analysis of kinase inhibitor selectivity. Nat. Biotechnol. 2008, 26, 127-132.
-
(2008)
Nat. Biotechnol
, vol.26
, pp. 127-132
-
-
Karaman, M.W.1
Herrgard, S.2
Treiber, D.K.3
Gallant, P.4
Atteridge, C.E.5
Campbell, B.T.6
Chan, K.W.7
Ciceri, P.8
Davis, M.I.9
Edeen, P.T.10
Faraoni, R.11
Floyd, M.12
Hunt, J.P.13
Lockhardt, D.J.14
Milanov, Z.V.15
Morrison, M.J.16
Pallares, G.17
Patel, H.K.18
Pritchard, S.19
Wodicka, L.M.20
Zarrinkar, P.P.21
more..
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