-
1
-
-
9844260513
-
Syntheses and biological activity (topoisomerases inhibition, antitumoral 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, Severe D, Riou JF, Bailly C, et al. (1997) Syntheses and biological activity (topoisomerases inhibition, antitumoral 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
Severe, D.8
Riou, J.F.9
Bailly, C.10
-
2
-
-
0028905348
-
Novel indolocarbazole compound 6-N-formylamino-12,13-dihydro-1, 11-dihydroxy-13-(β-D·- glucopyranosyl)-5H-indolo[2,3-apyrrolo-[3,4-c]carbazole-5,7-(6H)-dione (NB-506): Its potent antitumor activities in mice
-
Arakawa H, Iguchi T, Morita M, Yoshinari T, Kojiri K, Suda H, Okura A, and Nishimura S (1995) Novel indolocarbazole compound 6-N-formylamino-12,13-dihydro-1, 11-dihydroxy-13-(β-D·-glucopyranosyl)-5H-indolo[2, 3-apyrrolo-[3,4-c]carbazole-5,7-(6H)-dione (NB-506): Its potent antitumor activities in mice. Cancer Res 55:1316-1320.
-
(1995)
Cancer Res
, vol.55
, pp. 1316-1320
-
-
Arakawa, H.1
Iguchi, T.2
Morita, M.3
Yoshinari, T.4
Kojiri, K.5
Suda, H.6
Okura, A.7
Nishimura, S.8
-
3
-
-
0031277586
-
New developments in antitumor anthracyclines
-
Arcamone F, Animati F, Capranico G, Lombardi P, Pratesi G, Manzini S, Supino R, and Zunino F (1997) New developments in antitumor anthracyclines. Pharmacol Ther 76:117-124.
-
(1997)
Pharmacol Ther
, vol.76
, pp. 117-124
-
-
Arcamone, F.1
Animati, F.2
Capranico, G.3
Lombardi, P.4
Pratesi, G.5
Manzini, S.6
Supino, R.7
Zunino, F.8
-
4
-
-
0034736031
-
Formaldehyde cross-linking of a 2′-aminoglucose rebeccamycin derivative to both A·T and G·C base pairs in DNA
-
Bailly C, Goossens JF, Laine W, Anizon F, Prudhomme M, Ren J, and Chaires JB (2000) Formaldehyde cross-linking of a 2′-aminoglucose rebeccamycin derivative to both A·T and G·C base pairs in DNA. J Med Chem 43:4711-4720.
-
(2000)
J Med Chem
, vol.43
, pp. 4711-4720
-
-
Bailly, C.1
Goossens, J.F.2
Laine, W.3
Anizon, F.4
Prudhomme, M.5
Ren, J.6
Chaires, J.B.7
-
5
-
-
0033564429
-
Intercalation into DNA is not required for inhibition of topoisomerase I by indolocarbazole antitumor agents
-
Bailly C, Dassonneville L, Colson P, Houssier C, Fukasawa K, Nishimura S, and Yoshinari T (1999a) Intercalation into DNA is not required for inhibition of topoisomerase I by indolocarbazole antitumor agents. Cancer Res 59:2853-2860.
-
(1999)
Cancer Res
, vol.59
, pp. 2853-2860
-
-
Bailly, C.1
Dassonneville, L.2
Colson, P.3
Houssier, C.4
Fukasawa, K.5
Nishimura, S.6
Yoshinari, T.7
-
6
-
-
0025381502
-
Molecular recognition between oligopeptides and nucleic acids. DNA sequence specificity and binding properties of an acridine-linked netropsin hybrid ligand
-
Bailly C, Helbecque N, Hénichart JP, Colson P, Houssier C, Rao KE, Shea RG, and Lown JW (1990) Molecular recognition between oligopeptides and nucleic acids. DNA sequence specificity and binding properties of an acridine-linked netropsin hybrid ligand. J Mol Recognit 3:26-35.
-
(1990)
J Mol Recognit
, vol.3
, pp. 26-35
-
-
Bailly, C.1
Helbecque, N.2
Hénichart, J.P.3
Colson, P.4
Houssier, C.5
Rao, K.E.6
Shea, R.G.7
Lown, J.W.8
-
7
-
-
0033614922
-
Substitution at the F-ring N-imide of the indolocarbazole antitumor drug NB-506 increases the cytotoxicity, DNA binding and topoisomerase I inhibition activities
-
Bailly C, Qu X, Chaires JB, Colson P, Houssier C, Ohkubo M, Nishimura S, and Yoshinari T (1999b) Substitution at the F-ring N-imide of the indolocarbazole antitumor drug NB-506 increases the cytotoxicity, DNA binding and topoisomerase I inhibition activities. J Med Chem 42:2927-2935.
-
(1999)
J Med Chem
, vol.42
, pp. 2927-2935
-
-
Bailly, C.1
Qu, X.2
Chaires, J.B.3
Colson, P.4
Houssier, C.5
Ohkubo, M.6
Nishimura, S.7
Yoshinari, T.8
-
8
-
-
0033133944
-
Calories from carbohydrates. Energetic contribution of the carbohydrate moiety of rebeccamycin to DNA binding and the effect of its orientation on topoisomerase I inhibition
-
Bailly C, Qu X, Graves DE, Prudhomme M, and Chaires JB (1999c) Calories from carbohydrates. Energetic contribution of the carbohydrate moiety of rebeccamycin to DNA binding and the effect of its orientation on topoisomerase I inhibition. Chem Biol 6:277-286.
-
(1999)
Chem Biol
, vol.6
, pp. 277-286
-
-
Bailly, C.1
Qu, X.2
Graves, D.E.3
Prudhomme, M.4
Chaires, J.B.5
-
9
-
-
0034887619
-
DNA relaxation and cleavage assays to study topoisomerase I inhibitors
-
Bailly C (2001) DNA relaxation and cleavage assays to study topoisomerase I inhibitors. Methods Enzymol 340:610-623.
-
(2001)
Methods Enzymol
, vol.340
, pp. 610-623
-
-
Bailly, C.1
-
10
-
-
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
-
11
-
-
0028899328
-
Comparison of different footprinting methodologies for detecting binding sites for a small ligand on DNA
-
Bailly C and Waring MJ (1995) Comparison of different footprinting methodologies for detecting binding sites for a small ligand on DNA. J Biomol Struct Dyn 12:869-898.
-
(1995)
J Biomol Struct Dyn
, vol.12
, pp. 869-898
-
-
Bailly, C.1
Waring, M.J.2
-
12
-
-
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 (Tokyo) 40:668-678.
-
(1987)
J Antibiot (Tokyo)
, vol.40
, pp. 668-678
-
-
Bush, J.A.1
Long, B.H.2
Catino, J.J.3
Bradner, W.T.4
Tomita, K.5
-
13
-
-
0037089152
-
DNA sequence recognition by the indolocarbazole antitumor antibiotic AT2433-B1 and its diastereoisomer
-
Carrasco C, Facompré M, Chisholm JD, Van Vranken DL, Wilson WD, and Bailly C (2002) DNA sequence recognition by the indolocarbazole antitumor antibiotic AT2433-B1 and its diastereoisomer. Nucleic Acids Res 30:1774-0781.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 1774-0781
-
-
Carrasco, C.1
Facompré, M.2
Chisholm, J.D.3
Van Vranken, D.L.4
Wilson, W.D.5
Bailly, C.6
-
14
-
-
0033594499
-
A caveat in the application of the exciton chirality method to N,N-dialkyl amides. Synthesis and structural revision of AT2433-BB1
-
Chisholm JD, Golik J, Krishnan B, Matson JA, and Van Vranken DL (1999) A caveat in the application of the exciton chirality method to N,N-dialkyl amides. Synthesis and structural revision of AT2433-B1. J Am Chem Soc 121:3801-3802.
-
(1999)
J Am Chem Soc
, vol.121
, pp. 3801-3802
-
-
Chisholm, J.D.1
Golik, J.2
Krishnan, B.3
Matson, J.A.4
Van Vranken, D.L.5
-
15
-
-
0034602213
-
Regiocontrolled synthesis of the antitumor antibiotic AT2433-A1
-
Chisholm JD and Van Vranken DL (2000) Regiocontrolled synthesis of the antitumor antibiotic AT2433-A1. J Org Chem 65:7541-7553.
-
(2000)
J Org Chem
, vol.65
, pp. 7541-7553
-
-
Chisholm, J.D.1
Van Vranken, D.L.2
-
16
-
-
0030053867
-
Electric linear dichroism as a new tool to study sequence preference in drug binding to DNA
-
Colson P, Bailly C, and Houssier C (1996) Electric linear dichroism as a new tool to study sequence preference in drug binding to DNA. Biophys Chem 58:125-140.
-
(1996)
Biophys Chem
, vol.58
, pp. 125-140
-
-
Colson, P.1
Bailly, C.2
Houssier, C.3
-
17
-
-
0034633281
-
Determination of the refractive index increments of small molecules for correction of surface plasmon resonance data
-
Davis TM and Wilson WD (2000) Determination of the refractive index increments of small molecules for correction of surface plasmon resonance data. Anal Biochem 284:348-353.
-
(2000)
Anal Biochem
, vol.284
, pp. 348-353
-
-
Davis, T.M.1
Wilson, W.D.2
-
18
-
-
0028957974
-
Mutation at the catalytic site of topoisomerase I in CEM/C2, a human leukemia cell line resistant to camptothecin
-
Fujimori A, Harker WG, Kohlhagen G, Hoki Y, and Pommier Y (1995) Mutation at the catalytic site of topoisomerase I in CEM/C2, a human leukemia cell line resistant to camptothecin. Cancer Res 55:1339-1346.
-
(1995)
Cancer Res
, vol.55
, pp. 1339-1346
-
-
Fujimori, A.1
Harker, W.G.2
Kohlhagen, G.3
Hoki, Y.4
Pommier, Y.5
-
19
-
-
0024830687
-
AT2433-A1, AT2433-A2, AT2433-B1 and AT2433-B2 novel antitumor compounds produced by Actinomadura melliaura. II. Structure determination
-
Golik J, Doyle TW, Krishnan B, Dubay G, and Matson JA (1989) AT2433-A1, AT2433-A2, AT2433-B1 and AT2433-B2 novel antitumor compounds produced by Actinomadura melliaura. II. Structure determination. J Antibiot (Tokyo) 42:1784-1789.
-
(1989)
J Antibiot (Tokyo)
, vol.42
, pp. 1784-1789
-
-
Golik, J.1
Doyle, T.W.2
Krishnan, B.3
Dubay, G.4
Matson, J.A.5
-
20
-
-
0033064653
-
Topoisomerase poisoning activity of novel disaccharide anthracyclines
-
Guano F, Pourquier P, Tinelli S, Binaschi M, Bigioni M, Animati F, Manzini S, Zunino F, Kohlhagen G, Pommier Y, et al. (1999) Topoisomerase poisoning activity of novel disaccharide anthracyclines. Mol Pharmacol 67:77-84.
-
(1999)
Mol Pharmacol
, vol.67
, pp. 77-84
-
-
Guano, F.1
Pourquier, P.2
Tinelli, S.3
Binaschi, M.4
Bigioni, M.5
Animati, F.6
Manzini, S.7
Zunino, F.8
Kohlhagen, G.9
Pommier, Y.10
-
21
-
-
0024343095
-
Electric and flow linear dichroism of unfolded and condensed chromatin: A comparative study at low and intermediate ionic strength
-
Hagmar P, Marquet R, Colson P, Kubista M, Nielsen P, Norden B, and Houssier C (1989) Electric and flow linear dichroism of unfolded and condensed chromatin: A comparative study at low and intermediate ionic strength. J Biomol Struct Dyn 7:19-33.
-
(1989)
J Biomol Struct Dyn
, vol.7
, pp. 19-33
-
-
Hagmar, P.1
Marquet, R.2
Colson, P.3
Kubista, M.4
Nielsen, P.5
Norden, B.6
Houssier, C.7
-
22
-
-
0001702435
-
Investigating nucleic acids, nucleoproteins, polynucleotides and their interactions with small ligands by electro-optical systems
-
(Krause S ed.), Plenum Press, New York
-
Houssier C (1981) Investigating nucleic acids, nucleoproteins, polynucleotides and their interactions with small ligands by electro-optical systems, in Molecular Electro-Optics (Krause S ed.) pp. 363-398, Plenum Press, New York.
-
(1981)
Molecular Electro-Optics
, pp. 363-398
-
-
Houssier, C.1
-
23
-
-
0029035461
-
Antitumor activities of a new indolocarbazole substance, NB-506 and establishment of NB-506-resistant cell lines, SBC-3/NB
-
Kanzawa F, Nishio K, Kubota N, and Saijo N (1995) Antitumor activities of a new indolocarbazole substance, NB-506 and establishment of NB-506-resistant cell lines, SBC-3/NB. Cancer Res 55:2806-2813.
-
(1995)
Cancer Res
, vol.55
, pp. 2806-2813
-
-
Kanzawa, F.1
Nishio, K.2
Kubota, N.3
Saijo, N.4
-
24
-
-
0033881381
-
Apoptotic response of HL-60 human leukemia cells to the antitumor drug TAS-103
-
Kluza J, Lansiaux A, Wattez N, Mahieu C, Osheroff N, and Bailly C (2000) Apoptotic response of HL-60 human leukemia cells to the antitumor drug TAS-103. Cancer Res 60:4077-4084.
-
(2000)
Cancer Res
, vol.60
, pp. 4077-4084
-
-
Kluza, J.1
Lansiaux, A.2
Wattez, N.3
Mahieu, C.4
Osheroff, N.5
Bailly, C.6
-
25
-
-
0033152167
-
A new mechanism of acquisition of drug resistance by partial duplication of topoisomerase I
-
Komatani H, Morita M, Sakaizumi N, Fukasawa K, Yoshida E, Okura A, Yoshinari T, and Nishimura S (1999) A new mechanism of acquisition of drug resistance by partial duplication of topoisomerase I. Cancer Res 59:2701-2708.
-
(1999)
Cancer Res
, vol.59
, pp. 2701-2708
-
-
Komatani, H.1
Morita, M.2
Sakaizumi, N.3
Fukasawa, K.4
Yoshida, E.5
Okura, A.6
Yoshinari, T.7
Nishimura, S.8
-
26
-
-
0024333037
-
AT2433-A1, AT2433-A2, AT2433-B1 and AT2433-B2, novel antitumor antibiotic compounds produced by Actinomadura malliaura
-
Matson JA, Claridge C, Bush JA, Titus J, Bradner WT, Doyle TW, Horan AC, and Patel M (1989) AT2433-A1, AT2433-A2, AT2433-B1 and AT2433-B2, novel antitumor antibiotic compounds produced by Actinomadura malliaura. J Antibiot (Tokyo) 42:1547-1555.
-
(1989)
J Antibiot (Tokyo)
, vol.42
, pp. 1547-1555
-
-
Matson, J.A.1
Claridge, C.2
Bush, J.A.3
Titus, J.4
Bradner, W.T.5
Doyle, T.W.6
Horan, A.C.7
Patel, M.8
-
27
-
-
0021816422
-
Isolation and structure of rebeccamycin: A new antitumor antibiotic from Nocardia aerocolonigenes
-
Nettleton DE, Doyle TW, Krishnan B, Matsumoto GK, and Clardy J (1985) Isolation and structure of rebeccamycin: A new antitumor antibiotic from Nocardia aerocolonigenes. Tetrahedron Lett 26:4011-4014.
-
(1985)
Tetrahedron Lett
, vol.26
, pp. 4011-4014
-
-
Nettleton, D.E.1
Doyle, T.W.2
Krishnan, B.3
Matsumoto, G.K.4
Clardy, J.5
-
28
-
-
0030827993
-
Aclacinomycin A stabilizes topoisomerase I covalent complexes
-
Nitiss JL, Pourquier P, and Pommier Y (1997) Aclacinomycin A stabilizes topoisomerase I covalent complexes. Cancer Res 57:4564-4569.
-
(1997)
Cancer Res
, vol.57
, pp. 4564-4569
-
-
Nitiss, J.L.1
Pourquier, P.2
Pommier, Y.3
-
29
-
-
0033208192
-
Topoisomerase I inhibitors: Selectivity and cellular resistance
-
Pommier Y, Pourquier P, Urasaki Y, Wu J, and Laco GS (1999) Topoisomerase I inhibitors: Selectivity and cellular resistance. Drug Resist Updat 2:307-318.
-
(1999)
Drug Resist Updat
, vol.2
, pp. 307-318
-
-
Pommier, Y.1
Pourquier, P.2
Urasaki, Y.3
Wu, J.4
Laco, G.S.5
-
30
-
-
0033497816
-
A DNA-binding indolocarbazole disaccharide derivative remains highly cytotoxic without inhibiting topoisomerase I
-
Qu X, Chaires JB, Ohkubo M, Yoshinari T, Nishimura S, and Bailly C (2000) A DNA-binding indolocarbazole disaccharide derivative remains highly cytotoxic without inhibiting topoisomerase I. Anticancer Drug Des 14:433-442.
-
(2000)
Anticancer Drug Des
, vol.14
, pp. 433-442
-
-
Qu, X.1
Chaires, J.B.2
Ohkubo, M.3
Yoshinari, T.4
Nishimura, S.5
Bailly, C.6
-
31
-
-
0030836293
-
Differential poisoning of topoisomerases by menogaril and nogalamycin dictated by the minor groove-binding nogalose sugar
-
Sim SP, Gatto B, Yu C, Liu AA, Li TK, Pilch DS, LaVoie EJ, and Liu LF (1997) Differential poisoning of topoisomerases by menogaril and nogalamycin dictated by the minor groove-binding nogalose sugar. Biochemistry 36:13285-13291.
-
(1997)
Biochemistry
, vol.36
, pp. 13285-13291
-
-
Sim, S.P.1
Gatto, B.2
Yu, C.3
Liu, A.A.4
Li, T.K.5
Pilch, D.S.6
LaVoie, E.J.7
Liu, L.F.8
-
32
-
-
0035863393
-
Use of camptothecin-resistant mammalian cell lines to evaluate the role of topoisomerase I in the antiproliferative activity of the indolocarbazole, NB-506 and its topoisomerase I binding site
-
Urasaki Y, Laco G, Takebayashi Y, Bailly C, Kohlhagen G, and Pommier Y (2001) Use of camptothecin-resistant mammalian cell lines to evaluate the role of topoisomerase I in the antiproliferative activity of the indolocarbazole, NB-506 and its topoisomerase I binding site. Cancer Res 61:504-508.
-
(2001)
Cancer Res
, vol.61
, pp. 504-508
-
-
Urasaki, Y.1
Laco, G.2
Takebayashi, Y.3
Bailly, C.4
Kohlhagen, G.5
Pommier, Y.6
-
33
-
-
0037040269
-
Active site mutations in DNA topoisomerase I distinguish the cytotoxic activities of camptothecin of camptothecin and the indolocarbazole, rebeccamycin
-
Woo MH, Vance JR, Otero Marcos AR, Bailly C, and Bjornsti M-A (2002) Active site mutations in DNA topoisomerase I distinguish the cytotoxic activities of camptothecin of camptothecin and the indolocarbazole, rebeccamycin. J Biol Chem 277:3813-3822.
-
(2002)
J Biol Chem
, vol.277
, pp. 3813-3822
-
-
Woo, M.H.1
Vance, J.R.2
Otero Marcos, A.R.3
Bailly, C.4
Bjornsti, M.-A.5
-
34
-
-
0028931509
-
Novel antitumor indolocarbazole compound 6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(β· D-glucopyranosyl)-5H·indolo [2,3-a]pyrrolo-[3,4·c]carbazole-5,7-(6H)-dione (NB-506): Induction of topoisomerase I-mediated DNA cleavage and mechanisms of cell line-selective cytotoxicity
-
Yoshinari T, Matsumoto M, Arakawa H, Okada H, Noguchi K, Suda H, Okura A, and Nishimura S (1995) Novel antitumor indolocarbazole compound 6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(βmiddot; -D-glucopyranosyl)-5H-indolo-[2,3-a]pyrrolo-[3,4·c]carbazole-5, 7-(6H)-dione (NB-506): Induction of topoisomerase I-mediated DNA cleavage and mechanisms of cell line-selective cytotoxicity. Cancer Res 55:1310-1315.
-
(1995)
Cancer Res
, vol.55
, pp. 1310-1315
-
-
Yoshinari, T.1
Matsumoto, M.2
Arakawa, H.3
Okada, H.4
Noguchi, K.5
Suda, H.6
Okura, A.7
Nishimura, S.8
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