-
1
-
-
9844260513
-
Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group
-
Anizon F, Belin L, Moreau P, Sancelme M, Voldoire A, Prudhomme M, Ollier M, Sevère D, Riou JF, Bailly C, Fabbro D, and Meyer T (1997) Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. J Med Chem 40:3456-3465.
-
(1997)
J Med Chem
, vol.40
, pp. 3456-3465
-
-
Anizon, F.1
Belin, L.2
Moreau, P.3
Sancelme, M.4
Voldoire, A.5
Prudhomme, M.6
Ollier, M.7
Sevère, D.8
Riou, J.F.9
Bailly, C.10
Fabbro, D.11
Meyer, T.12
-
2
-
-
0042121548
-
Rebeccamycin analogues bearing amine substituents or other groups on the sugar moiety
-
Anizon F, Moreau P, Sancelme M, Laine W, Bailly C, and Prudhomme M (2003) Rebeccamycin analogues bearing amine substituents or other groups on the sugar moiety. Bioorg Med Chem 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
-
3
-
-
0030944043
-
DNA cleavage by topoisomerase I in the presence of indolocarbazole derivatives of rebeccamycin
-
Bailly C, Riou JF, Colson P, Houssier C, Rodrigues-Pereira E, and Prudhomme M (1997) DNA cleavage by topoisomerase I in the presence of indolocarbazole derivatives of rebeccamycin. Biochemistry 36:3917-3929.
-
(1997)
Biochemistry
, vol.36
, pp. 3917-3929
-
-
Bailly, C.1
Riou, J.F.2
Colson, P.3
Houssier, C.4
Rodrigues-Pereira, E.5
Prudhomme, M.6
-
4
-
-
0023178261
-
Production and biological activity of rebeccamycin, a novel antitumor agent
-
Bush JA, Long BH, Catino JJ, Bradner WT, and Tomita K (1987) Production and biological activity of rebeccamycin, a novel antitumor agent. J Antibiot 40:668-678.
-
(1987)
J Antibiot
, vol.40
, pp. 668-678
-
-
Bush, J.A.1
Long, B.H.2
Catino, J.J.3
Bradner, W.T.4
Tomita, K.5
-
5
-
-
0034306450
-
Specificity and mechanism of action of some commonly used protein kinase inhibitors
-
Davies SP, Reddy H, Caivano M, and Cohen P (2000) Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem J 351:95-105.
-
(2000)
Biochem J
, vol.351
, pp. 95-105
-
-
Davies, S.P.1
Reddy, H.2
Caivano, M.3
Cohen, P.4
-
6
-
-
34249104303
-
Phase I and pharmacokinetic study of 7-hydroxystaurosporine and carboplatin in advanced solid tumors
-
Edelman MJ, Bauer KS Jr, Wu S, Smith R, Bisacia S, and Dancey J (2007) Phase I and pharmacokinetic study of 7-hydroxystaurosporine and carboplatin in advanced solid tumors. Clin Cancer Res 13:2667-2674.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 2667-2674
-
-
Edelman, M.J.1
Bauer Jr, K.S.2
Wu, S.3
Smith, R.4
Bisacia, S.5
Dancey, J.6
-
7
-
-
0036947498
-
DNA targeting of two new antitumor rebeccamycin derivatives
-
Facompré M, Baldeyrou B, Bailly C, Anizon F, Marminon C, Prudhomme M, Colson P, and Houssier C (2002) DNA targeting of two new antitumor rebeccamycin derivatives. Eur J Med Chem 37:925-932.
-
(2002)
Eur J Med Chem
, vol.37
, pp. 925-932
-
-
Facompré, M.1
Baldeyrou, B.2
Bailly, C.3
Anizon, F.4
Marminon, C.5
Prudhomme, M.6
Colson, P.7
Houssier, C.8
-
8
-
-
35148834201
-
Synthesis and evaluation of substituted benzoisoquinolinones as potent inhibitors of Chk1 kinase
-
Garbaccio RM, Huang S, Tasber ES, Fraley ME, Yan Y, Munshi S, Ikuta M, Kuo L, Kreatsoulas C, Stirdivant S, et al. (2007) Synthesis and evaluation of substituted benzoisoquinolinones as potent inhibitors of Chk1 kinase. Bioorg Med Chem Lett 17:6280-6285.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 6280-6285
-
-
Garbaccio, R.M.1
Huang, S.2
Tasber, E.S.3
Fraley, M.E.4
Yan, Y.5
Munshi, S.6
Ikuta, M.7
Kuo, L.8
Kreatsoulas, C.9
Stirdivant, S.10
-
9
-
-
0034053130
-
The Chk1 protein kinase and the Cdc25C regulatory pathways are targets of the anticancer agent UCN-01
-
Graves PR, Yu L, Schwarz JK, Gales J, Sausville EA, O'Connor PM, and Piwnica-Worms H (2000) The Chk1 protein kinase and the Cdc25C regulatory pathways are targets of the anticancer agent UCN-01. J Biol Chem 275:5600-5605.
-
(2000)
J Biol Chem
, vol.275
, pp. 5600-5605
-
-
Graves, P.R.1
Yu, L.2
Schwarz, J.K.3
Gales, J.4
Sausville, E.A.5
O'Connor, P.M.6
Piwnica-Worms, H.7
-
10
-
-
0033975054
-
An indolocarbazole inhibitor of human checkpoint kinase (Chk1) abrogates cell cycle arrest caused by DNA damage
-
Jackson JR, Gilmartin A, Imburgia C, Winkler JD, Marshall LA, and Roshak A (2000) An indolocarbazole inhibitor of human checkpoint kinase (Chk1) abrogates cell cycle arrest caused by DNA damage. Cancer Res 60:566-572.
-
(2000)
Cancer Res
, vol.60
, pp. 566-572
-
-
Jackson, J.R.1
Gilmartin, A.2
Imburgia, C.3
Winkler, J.D.4
Marshall, L.A.5
Roshak, A.6
-
11
-
-
4444344407
-
G2 checkpoint abrogators as anticancer drugs
-
Kawabe T (2004) G2 checkpoint abrogators as anticancer drugs. Mol Cancer Ther 3:513-519.
-
(2004)
Mol Cancer Ther
, vol.3
, pp. 513-519
-
-
Kawabe, T.1
-
12
-
-
0035808457
-
Indirubins inhibit glycogen synthase kinase-3β and CDK5/p25, two kinases involved in abnormal tau phosphorylation in Alzheimer's disease: A property common to most CDK inhibitors?
-
Leclerc S, Garnier M, Hoessel R, Marko D, Bibb JA, Snyder GL, Greengard P, Biernat J, Wu YZ, Mandelkow EM, et al. (2001) Indirubins inhibit glycogen synthase kinase-3β and CDK5/p25, two kinases involved in abnormal tau phosphorylation in Alzheimer's disease: A property common to most CDK inhibitors? J Biol Chem 276:251-260.
-
(2001)
J Biol Chem
, vol.276
, pp. 251-260
-
-
Leclerc, S.1
Garnier, M.2
Hoessel, R.3
Marko, D.4
Bibb, J.A.5
Snyder, G.L.6
Greengard, P.7
Biernat, J.8
Wu, Y.Z.9
Mandelkow, E.M.10
-
13
-
-
39749185974
-
Defective p53 signaling in p53 wild-type tumors attenuates p21waf1 induction and cyclin B repression rendering them sensitive to Chk1 inhibitors that abrogate DNA damage-induced S and G2 arrest
-
Levesque AA, Fanous AA, Poh A, and Eastman A (2008) Defective p53 signaling in p53 wild-type tumors attenuates p21waf1 induction and cyclin B repression rendering them sensitive to Chk1 inhibitors that abrogate DNA damage-induced S and G2 arrest. Mol Cancer Ther 7:252-262.
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 252-262
-
-
Levesque, A.A.1
Fanous, A.A.2
Poh, A.3
Eastman, A.4
-
14
-
-
0037075811
-
Syntheses and antiproliferative activities of new rebeccamycin derivatives with the sugar unit linked to both indole nitrogens
-
Marminon C, Anizon F, Moreau P, Léonce S, Pierré A, Pfeiffer B, Renard P, and Prudhomme M (2002) Syntheses and antiproliferative activities of new rebeccamycin derivatives with the sugar unit linked to both indole nitrogens. J Med Chem 45:1330-1339.
-
(2002)
J Med Chem
, vol.45
, pp. 1330-1339
-
-
Marminon, C.1
Anizon, F.2
Moreau, P.3
Léonce, S.4
Pierré, A.5
Pfeiffer, B.6
Renard, P.7
Prudhomme, M.8
-
15
-
-
0037434589
-
Syntheses 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, and Prudhomme M (2003a) Syntheses and antiproliferative activities of 7-azarebeccamycin analogues bearing one 7-azaindole moiety. J Med Chem 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
-
16
-
-
0037355137
-
Syntheses and antiproliferative activities of rebeccamycin analogues bearing two 7-azaindole moieties
-
Marminon C, Pierré A, Pfeiffer B, Pérez V, Léonce S, Renard P, and Prudhomme M (2003b) Syntheses and antiproliferative activities of rebeccamycin analogues bearing two 7-azaindole moieties. Bioorg Med Chem 11:679-687.
-
(2003)
Bioorg Med Chem
, vol.11
, pp. 679-687
-
-
Marminon, C.1
Pierré, A.2
Pfeiffer, B.3
Pérez, V.4
Léonce, S.5
Renard, P.6
Prudhomme, M.7
-
17
-
-
0018846636
-
Sequencing end-labeled DNA with base-specific chemical cleavages
-
Maxam AM and Gilbert W (1980) Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol 65:499-560.
-
(1980)
Methods Enzymol
, vol.65
, pp. 499-560
-
-
Maxam, A.M.1
Gilbert, W.2
-
18
-
-
0242582505
-
Le cycle de division cellulaire et sa régulation.
-
Meijer L (2003) Le cycle de division cellulaire et sa régulation. Oncologie 5:311-316.
-
(2003)
Oncologie
, vol.5
, pp. 311-316
-
-
Meijer, L.1
-
19
-
-
0038207882
-
Non-camptothecin DNA topoisomerase I inhibitors in cancer therapy
-
Meng LH, Liao ZY, and Pommier Y (2003) Non-camptothecin DNA topoisomerase I inhibitors in cancer therapy. Curr Top Med Chem 3:305-320.
-
(2003)
Curr Top Med Chem
, vol.3
, pp. 305-320
-
-
Meng, L.H.1
Liao, Z.Y.2
Pommier, Y.3
-
20
-
-
2442687670
-
Synthesis of a staurosporine analogue possessing a 7-azaindole unit instead of an indole moiety
-
Messaoudi S, Anizon F, Pfeiffer B, Golsteyn R, and Prudhomme M (2004) Synthesis of a staurosporine analogue possessing a 7-azaindole unit instead of an indole moiety. Tetrahedron Lett 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
-
22
-
-
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, and Prudhomme M (2005b) 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 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
-
23
-
-
33749234576
-
Synthesis and biological activities of 7-aza rebeccamycin analogues bearing the sugar moiety on the nitrogen of the pyridine ring
-
Messaoudi S, Anizon F, Peixoto P, David-Cordonnier MH, Golsteyn RM, Léonce S, Pfeiffer B, and Prudhomme M (2006) Synthesis and biological activities of 7-aza rebeccamycin analogues bearing the sugar moiety on the nitrogen of the pyridine ring. Bioorg Med Chem 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
-
24
-
-
15144351325
-
Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle
-
Moreau P, Anizon F, Sancelme M, Prudhomme M, Bailly C, Carrasco C, Ollier M, Sevère D, Riou JF, Fabbro D, et al. (1998) Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. J Med Chem 41:1631-1640.
-
(1998)
J Med Chem
, vol.41
, pp. 1631-1640
-
-
Moreau, P.1
Anizon, F.2
Sancelme, M.3
Prudhomme, M.4
Bailly, C.5
Carrasco, C.6
Ollier, M.7
Sevère, D.8
Riou, J.F.9
Fabbro, D.10
-
25
-
-
0033602140
-
Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent
-
Moreau P, Anizon F, Sancelme M, Prudhomme M, Bailly C, Sevère D, Riou JF, Fabbro D, Meyer T, and Aubertin AM (1999a) Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. J Med Chem 42:584-592.
-
(1999)
J Med Chem
, vol.42
, pp. 584-592
-
-
Moreau, P.1
Anizon, F.2
Sancelme, M.3
Prudhomme, M.4
Bailly, C.5
Sevère, D.6
Riou, J.F.7
Fabbro, D.8
Meyer, T.9
Aubertin, A.M.10
-
26
-
-
0033587125
-
Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives
-
Moreau P, Anizon F, Sancelme M, Prudhomme M, Sevère D, Riou JF, Goossens JF, Hénichart JP, Bailly C, Labourier E, et al. (1999b) Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. J Med Chem 42:1816-1822.
-
(1999)
J Med Chem
, vol.42
, pp. 1816-1822
-
-
Moreau, P.1
Anizon, F.2
Sancelme, M.3
Prudhomme, M.4
Sevère, D.5
Riou, J.F.6
Goossens, J.F.7
Hénichart, J.P.8
Bailly, C.9
Labourier, E.10
-
27
-
-
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, et al. (2003) Semi-synthesis, topoisomerase I and kinases inhibitory properties, and antiproliferative activities of new rebeccamycin derivatives. Bioorg Med Chem 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
-
28
-
-
0000714445
-
Structure-activity relationships in a series of substituted indolocarbazoles : Topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties
-
Pereira ER, Belin L, Sancelme M, Prudhomme M, Ollier M, Rapp M, Sevère D, Riou JF, Fabbro D, and Meyer T (1996) Structure-activity relationships in a series of substituted indolocarbazoles : topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. J Med Chem 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
Sevère, D.7
Riou, J.F.8
Fabbro, D.9
Meyer, T.10
-
29
-
-
33746388284
-
Modulation of cell cycle progression in human tumors: A pharmacokinetic and tumor molecular pharmacodynamic study of cisplatin plus the Chk1 inhibitor UCN-01 (NCS 638850)
-
Perez RP, Lewis LD, Beelen AP, Olszanski AJ, Johnston N, Rhodes CH, Beaulieu B, Ernstoff MS, and Eastman A (2006) Modulation of cell cycle progression in human tumors: a pharmacokinetic and tumor molecular pharmacodynamic study of cisplatin plus the Chk1 inhibitor UCN-01 (NCS 638850). Clin Cancer Res 12:7079-7085.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 7079-7085
-
-
Perez, R.P.1
Lewis, L.D.2
Beelen, A.P.3
Olszanski, A.J.4
Johnston, N.5
Rhodes, C.H.6
Beaulieu, B.7
Ernstoff, M.S.8
Eastman, A.9
-
30
-
-
0030762374
-
Indolocarbazoles as anti-cancer agents
-
Prudhomme M (1997) Indolocarbazoles as anti-cancer agents. Curr Pharm Des 3:265-290.
-
(1997)
Curr Pharm Des
, vol.3
, pp. 265-290
-
-
Prudhomme, M.1
-
31
-
-
6444232494
-
Biological targets of antitumor indolocarbazoles bearing a sugar moiety
-
Prudhomme M (2004a) Biological targets of antitumor indolocarbazoles bearing a sugar moiety. Curr Med Chem-Anti-Cancer Agents 4:509-521.
-
(2004)
Curr Med Chem-Anti-Cancer Agents
, vol.4
, pp. 509-521
-
-
Prudhomme, M.1
-
32
-
-
4444228258
-
Combining DNA damaging agents and Chk1 inhibitors
-
Prudhomme M (2004b) Combining DNA damaging agents and Chk1 inhibitors. Curr Med Chem-Anti-Cancer Agents 4:435-438.
-
(2004)
Curr Med Chem-Anti-Cancer Agents
, vol.4
, pp. 435-438
-
-
Prudhomme, M.1
-
34
-
-
0023552288
-
UCN-01, a selective inhibitor of protein kinase C from Streptomyces
-
Takahashi I, Kobayashi E, Asano K, Yoshida M, and Nakano H (1987) UCN-01, a selective inhibitor of protein kinase C from Streptomyces. J Antibiot 40:1782-1784.
-
(1987)
J Antibiot
, vol.40
, pp. 1782-1784
-
-
Takahashi, I.1
Kobayashi, E.2
Asano, K.3
Yoshida, M.4
Nakano, H.5
-
36
-
-
33745856631
-
Chk1 inhibitors for novel cancer treatment
-
Tao ZF and Lin NH (2006) Chk1 inhibitors for novel cancer treatment. Anticancer Agents Med Chem 6:377-388.
-
(2006)
Anticancer Agents Med Chem
, vol.6
, pp. 377-388
-
-
Tao, Z.F.1
Lin, N.H.2
-
37
-
-
34147108049
-
Structure-based design, synthesis, and biological evaluation of potent and selective macrocyclic checkpoint kinase 1 inhibitors
-
Tao ZF, Wang L, Stewart KD, Chen Z, Gu W, Bui MH, Merta P, Zhang H, Kovar P, Johnson E, et al. (2007) Structure-based design, synthesis, and biological evaluation of potent and selective macrocyclic checkpoint kinase 1 inhibitors. J Med Chem 50:1514-1527.
-
(2007)
J Med Chem
, vol.50
, pp. 1514-1527
-
-
Tao, Z.F.1
Wang, L.2
Stewart, K.D.3
Chen, Z.4
Gu, W.5
Bui, M.H.6
Merta, P.7
Zhang, H.8
Kovar, P.9
Johnson, E.10
-
38
-
-
34547094373
-
UCN-01 in combination with topotecan in patients with advanced recurrent ovarian cancer: A study of the Princess Margaret Hospital phase II consortium
-
Welch S, Hirte HW, Carey MS, Hotte SJ, Tsao MS, Brown S, Pond GR, Dancey JE, and Oza AM (2007) UCN-01 in combination with topotecan in patients with advanced recurrent ovarian cancer: a study of the Princess Margaret Hospital phase II consortium. Gynecol Oncol 106:305-310.
-
(2007)
Gynecol Oncol
, vol.106
, pp. 305-310
-
-
Welch, S.1
Hirte, H.W.2
Carey, M.S.3
Hotte, S.J.4
Tsao, M.S.5
Brown, S.6
Pond, G.R.7
Dancey, J.E.8
Oza, A.M.9
-
39
-
-
0037484271
-
Chk1 mediates S and G2 arrests through Cdc25A degradation in response to DNA-damaging agents
-
Xiao Z, Chen Z, Gunasekera AH, Sowin TJ, Rosenberg SH, Fesik S, and Zhang H (2003) Chk1 mediates S and G2 arrests through Cdc25A degradation in response to DNA-damaging agents. J Biol Chem 278:21767-21773.
-
(2003)
J Biol Chem
, vol.278
, pp. 21767-21773
-
-
Xiao, Z.1
Chen, Z.2
Gunasekera, A.H.3
Sowin, T.J.4
Rosenberg, S.H.5
Fesik, S.6
Zhang, H.7
-
40
-
-
2242421834
-
Structural basis for Chk1 inhibition by UCN-01
-
Zhao B, Bower MJ, McDevitt PJ, Zhao H, Davis ST, Johanson KO, Green SM, Concha NO, and Zhou BBS (2002) Structural basis for Chk1 inhibition by UCN-01. J Biol Chem 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
Davis, S.T.5
Johanson, K.O.6
Green, S.M.7
Concha, N.O.8
Zhou, B.B.S.9
-
41
-
-
1542725073
-
Targeting the checkpoint kinases: Chemosensitization versus chemoprotection
-
Zhou BB and Bartek J (2004) Targeting the checkpoint kinases: chemosensitization versus chemoprotection. Nat Rev Cancer 4:216-225.
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 216-225
-
-
Zhou, B.B.1
Bartek, J.2
|