-
1
-
-
0028905348
-
Novel 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): Its potent antitumor activities in mice
-
Arakawa, H., Iguchi, T., Morita, M., Yoshinari, T., Kojiri, K., Suda, H., Okura, A., and Nishimura, S. Novel 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): its potent antitumor activities in mice. Cancer Res., 55: 1316-1320, 1995.
-
(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
-
2
-
-
0025788486
-
A new antitumor substance BE-13793C, produced by a streptomycete. Taxonomy, fermentation, isolation, structure determination and biological activity
-
Tokyo
-
Kojiri, K., Kondo, H., Yoshinari, T., Arakawa, H., Nakajima, S., Satoh, F., Kawamura, K., Okura, A., Suda, H., and Okanishi, M. A new antitumor substance BE-13793C, produced by a streptomycete. Taxonomy, fermentation, isolation, structure determination and biological activity. J. Antibiot. (Tokyo), 44: 723-728, 1991.
-
(1991)
J. Antibiot.
, vol.44
, pp. 723-728
-
-
Kojiri, K.1
Kondo, H.2
Yoshinari, T.3
Arakawa, H.4
Nakajima, S.5
Satoh, F.6
Kawamura, K.7
Okura, A.8
Suda, H.9
Okanishi, M.10
-
3
-
-
0027461273
-
Induction of topoisomerase 1-mediated DNA cleavage by a new indolocarbazole, ED-110
-
Yoshinari, T., Yamada, A., Uemura, D., Nomura, K., Arakawa, H., Kojiri, K., Yoshida, E., Suda, H., and Okura, A. Induction of topoisomerase 1-mediated DNA cleavage by a new indolocarbazole, ED-110. Cancer Res., 53: 490-494, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 490-494
-
-
Yoshinari, T.1
Yamada, A.2
Uemura, D.3
Nomura, K.4
Arakawa, H.5
Kojiri, K.6
Yoshida, E.7
Suda, H.8
Okura, A.9
-
4
-
-
0027297782
-
ED-110, a novel indolocarbazole, prevents the growth of experimental tumors in mice
-
Arakawa, H., Iguchi, T., Yoshinari, T., Kojiri, K., Suda, H., and Okura, A. ED-110, a novel indolocarbazole, prevents the growth of experimental tumors in mice. Jpn. J. Cancer Res., 84: 574-581, 1993.
-
(1993)
Jpn. J. Cancer Res.
, vol.84
, pp. 574-581
-
-
Arakawa, H.1
Iguchi, T.2
Yoshinari, T.3
Kojiri, K.4
Suda, H.5
Okura, A.6
-
5
-
-
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. 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.
-
(1995)
Cancer Res.
, vol.55
, pp. 2806-2813
-
-
Kanzawa, F.1
Nishio, K.2
Kubota, N.3
Saijo, N.4
-
6
-
-
0031297095
-
Cellular determinants of resistance to indolocarbazole analogue NB-506. A novel potent topoisomerase I inhibitor, in multidrug-resistant human tumor cells
-
Vanhoefer, U., Voigt, W., Hilger, R. A., Yin, M-B., Harstrick, A., Seeber, S., and Rustum, Y. M. Cellular determinants of resistance to indolocarbazole analogue NB-506. A novel potent topoisomerase I inhibitor, in multidrug-resistant human tumor cells. Oncol. Res., 9: 485-494, 1997.
-
(1997)
Oncol. Res.
, vol.9
, pp. 485-494
-
-
Vanhoefer, U.1
Voigt, W.2
Hilger, R.A.3
Yin, M.-B.4
Harstrick, A.5
Seeber, S.6
Rustum, Y.M.7
-
7
-
-
0003267271
-
Phase I and pharmacology study of 5-day infusion of NB-506
-
Ohe, Y., Tanigawara, Y., Fujii, H., Ohtsu, T., Wakita, H., Igarashi, T., Minami, H., Eguchi, K., Shinkai, T., Tamura, T., Kunotoh, H., Saijo, N., Okada, K., Ogino, H., and Sasaki, Y. Phase I and pharmacology study of 5-day infusion of NB-506. Proc. ACSO, 16: 199a, 1997.
-
(1997)
Proc. ACSO
, vol.16
-
-
Ohe, Y.1
Tanigawara, Y.2
Fujii, H.3
Ohtsu, T.4
Wakita, H.5
Igarashi, T.6
Minami, H.7
Eguchi, K.8
Shinkai, T.9
Tamura, T.10
Kunotoh, H.11
Saijo, N.12
Okada, K.13
Ogino, H.14
Sasaki, Y.15
-
8
-
-
0031965431
-
New chemotherapeutic agents for the treatment of non-small cell lung cancer
-
Saijo, N. New chemotherapeutic agents for the treatment of non-small cell lung cancer. Chest, 113: 17S-23S, 1998.
-
(1998)
Chest
, vol.113
-
-
Saijo, N.1
-
9
-
-
0026678588
-
Induction of mammalian DNA topoisomerase I-mediated DNA cleavage by antitumor indolocarbazole derivatives
-
Yamashita, Y., Fujii, N., Murakata, C., Ashizawa, T., Okabe, M., and Nakano, H. Induction of mammalian DNA topoisomerase I-mediated DNA cleavage by antitumor indolocarbazole derivatives. Biochemistry, 31: 12069-12075, 1992.
-
(1992)
Biochemistry
, vol.31
, pp. 12069-12075
-
-
Yamashita, Y.1
Fujii, N.2
Murakata, C.3
Ashizawa, T.4
Okabe, M.5
Nakano, H.6
-
10
-
-
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. 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. Cancer Res., 55: 1310-1315, 1995.
-
(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
-
11
-
-
9844260513
-
Syntheses and biological activity (topoisomerases inhibition, antitumoral and antimicrobial proper-ties) 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, J-F., Bailly, C., Fabbro, D., and Meyer, T. Syntheses and biological activity (topoisomerases inhibition, antitumoral and antimicrobial proper-ties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. J. Med. Chem., 40: 3456-3465, 1997.
-
(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
-
12
-
-
0030944043
-
DNA cleavage by topoisomerase I in the presence of indolocarbazole derivatives of rebeccamycin
-
Bailly, C., Riou, J-F., Colson, P., Houssier, C., Rodrigues-Pereira, E., and Prudhomme, M. DNA cleavage by topoisomerase I in the presence of indolocarbazole derivatives of rebeccamycin. Biochemistry, 36: 3917-3929, 1997.
-
(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
-
13
-
-
0031938920
-
Recognition of specific sequences in DNA by a topoisomerase I inhibitor derived from the antitumor drug rebeccamycin
-
Bailly, C., Colson, P., Houssier, C., Rodrigues-Pereira, E., Prudhomme, M., and Waring, M. J. Recognition of specific sequences in DNA by a topoisomerase I inhibitor derived from the antitumor drug rebeccamycin. Mol. Pharmacol., 53: 77-87, 1998.
-
(1998)
Mol. Pharmacol.
, vol.53
, pp. 77-87
-
-
Bailly, C.1
Colson, P.2
Houssier, C.3
Rodrigues-Pereira, E.4
Prudhomme, M.5
Waring, M.J.6
-
14
-
-
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, D. E., Prudhomme, M., and Chaires, J. B. 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.
-
(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
-
15
-
-
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, M., Sevère, D., Riou, J-F., and Fabbro, D. 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.
-
(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, M.6
Sevère, D.7
Riou, J.-F.8
Fabbro, D.9
-
16
-
-
0033602140
-
Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent
-
Moreau, P., Anizon, F., Sancelme, M., Prudhomme, M., Bailly, C., Ollier, M., Sevère, D., Riou, J-F., Fabbro, D., Meyer, T., and Aubertin, A-M. Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. J. Med. Chem., 42: 584-592, 1999.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 584-592
-
-
Moreau, P.1
Anizon, F.2
Sancelme, M.3
Prudhomme, M.4
Bailly, C.5
Ollier, M.6
Sevère, D.7
Riou, J.-F.8
Fabbro, D.9
Meyer, T.10
Aubertin, A.-M.11
-
17
-
-
0032168946
-
Synthese, biochemical and biological evaluation of staurosporine analogs from the microbial metabolite rebeccamycin
-
Anizon, F., Moreau, P., Sancelme, M., Voldoire, A., Prudhomme, M., Ollier, M., Sevère, D., Riou, J-F., Bailly, C., Fabbro, D., Meyer, T., and Aubertin, A-M. Synthese, biochemical and biological evaluation of staurosporine analogs from the microbial metabolite rebeccamycin. Bioorg. Med. Chem., 66: 1597-1604, 1998.
-
(1998)
Bioorg. Med. Chem.
, vol.66
, pp. 1597-1604
-
-
Anizon, F.1
Moreau, P.2
Sancelme, M.3
Voldoire, A.4
Prudhomme, M.5
Ollier, M.6
Sevère, D.7
Riou, J.-F.8
Bailly, C.9
Fabbro, D.10
Meyer, T.11
Aubertin, A.-M.12
-
18
-
-
0029973431
-
Practical synthesis of indolopyryrrolocarbazoles
-
Ohkubo, M., Nishimura, T., Jona, H., Honma, T., and Morishima. H. Practical synthesis of indolopyryrrolocarbazoles. Tetrahedron, 52: 8099-8112, 1996.
-
(1996)
Tetrahedron
, vol.52
, pp. 8099-8112
-
-
Ohkubo, M.1
Nishimura, T.2
Jona, H.3
Honma, T.4
Morishima, H.5
-
19
-
-
0030936079
-
Synthesis of dissymetric indolocarbazole glycosides using the Mitsunobu reaction at the glycosylation step
-
Ohkubo, M., Nishimura, T., Jona, H., Honma, T., Ito, S., and Morishima, H. Synthesis of dissymetric indolocarbazole glycosides using the Mitsunobu reaction at the glycosylation step. Tetrahedron, 53: 5937-5950, 1997.
-
(1997)
Tetrahedron
, vol.53
, pp. 5937-5950
-
-
Ohkubo, M.1
Nishimura, T.2
Jona, H.3
Honma, T.4
Ito, S.5
Morishima, H.6
-
20
-
-
0031032851
-
Synthesis of NB-506, a new anticancer agent
-
Ohkubo, M., Kawamoto, H., Ohno, T., Nakano, M., and Morishima, H. Synthesis of NB-506, a new anticancer agent. Tetrahedron, 53: 585-592, 1997.
-
(1997)
Tetrahedron
, vol.53
, pp. 585-592
-
-
Ohkubo, M.1
Kawamoto, H.2
Ohno, T.3
Nakano, M.4
Morishima, H.5
-
21
-
-
0019377693
-
Potential antitumor agent. 34. Quantitative relationships between DNA binding and molecular structure for 9-anilino-acridines substituted in the anilino ring
-
Baguley, B. C., Denny, W. A., Atwell, G. J., and Cain, B. F. Potential antitumor agent. 34. Quantitative relationships between DNA binding and molecular structure for 9-anilino-acridines substituted in the anilino ring. J. Med. Chem., 24: 170-177, 1981.
-
(1981)
J. Med. Chem.
, vol.24
, pp. 170-177
-
-
Baguley, B.C.1
Denny, W.A.2
Atwell, G.J.3
Cain, B.F.4
-
22
-
-
0012994651
-
Electro-optical instrumentation systems with their data acquisition and treatment
-
S. Krause (ed.), New York: Plenum Publishing Corporation
-
Houssier, C., and O'Konski, C. T. Electro-optical instrumentation systems with their data acquisition and treatment. In: S. Krause (ed.), Molecular Electro-Optics, pp. 309-339. New York: Plenum Publishing Corporation, 1981.
-
(1981)
Molecular Electro-optics
, pp. 309-339
-
-
Houssier, C.1
O'Konski, C.T.2
-
23
-
-
0001702435
-
Investigating nucleic acids, nucleoproteins, polynucleotides, and their interactions with small ligands by electro-optical systems
-
S. Krause (ed.), New York: Plenum Publishing Corporation
-
Houssier, C. Investigating nucleic acids, nucleoproteins, polynucleotides, and their interactions with small ligands by electro-optical systems. In: S. Krause (ed.), Molecular Electro-Optics, pp. 363-398. New York: Plenum Publishing Corporation, 1981.
-
(1981)
Molecular Electro-optics
, pp. 363-398
-
-
Houssier, C.1
-
24
-
-
0030053867
-
Electric linear dichroism as a new tool to study sequence preference in drug binding to DNA
-
Colson, P., Bailly, C., and Houssier, C. Electric linear dichroism as a new tool to study sequence preference in drug binding to DNA. Biophys. Chem., 58: 125-140, 1996.
-
(1996)
Biophys. Chem.
, vol.58
, pp. 125-140
-
-
Colson, P.1
Bailly, C.2
Houssier, C.3
-
25
-
-
0027035245
-
Drug-DNA sequence-dependent interactions analyzed by electric linear dichroism
-
Bailly, C., Hénichart, J-P., Colson, P., and Houssier, C. Drug-DNA sequence-dependent interactions analyzed by electric linear dichroism. J. Mol. Recognit., 5: 155-171, 1992.
-
(1992)
J. Mol. Recognit.
, vol.5
, pp. 155-171
-
-
Bailly, C.1
Hénichart, J.-P.2
Colson, P.3
Houssier, C.4
-
26
-
-
0028899328
-
Comparison of different footprinting methodologies for detecting binding sites for a small ligand on DNA
-
Bailly, C., and Waring, M. J. Comparison of different footprinting methodologies for detecting binding sites for a small ligand on DNA. J. Biomol. Struct. Dyn., 12: 869-898, 1995.
-
(1995)
J. Biomol. Struct. Dyn.
, vol.12
, pp. 869-898
-
-
Bailly, C.1
Waring, M.J.2
-
27
-
-
0023279028
-
DNA unwinding and inhibition of mouse leukemia L1210 DNA topoisomerase I by intercalators
-
Pommier, Y., Covey, J. M., Kerrigan, D., Markovits, J., and Pharm, R. DNA unwinding and inhibition of mouse leukemia L1210 DNA topoisomerase I by intercalators. Nucleic Acids Res., 15: 6713-6731, 1987.
-
(1987)
Nucleic Acids Res.
, vol.15
, pp. 6713-6731
-
-
Pommier, Y.1
Covey, J.M.2
Kerrigan, D.3
Markovits, J.4
Pharm, R.5
-
28
-
-
0022053771
-
Negative supercoiling induces spontaneous unwinding of bacterial promoter
-
Drew, H. R., Weeks, J. R., and Travers, A. A. Negative supercoiling induces spontaneous unwinding of bacterial promoter. EMBO J., 4: 1025-1032, 1985.
-
(1985)
EMBO J.
, vol.4
, pp. 1025-1032
-
-
Drew, H.R.1
Weeks, J.R.2
Travers, A.A.3
-
29
-
-
0027369170
-
The antileukemic alkaloid fagaronine is an inhibitor of DNA topoisomerases I and II
-
Larsen, A. K., Grondard, L., Couprie, J., Desoize, B., Comoe, L., Jardillier, J. C., and Riou, J. F. The antileukemic alkaloid fagaronine is an inhibitor of DNA topoisomerases I and II. Biochem. Pharmacol., 46: 1403-1412, 1993.
-
(1993)
Biochem. Pharmacol.
, vol.46
, pp. 1403-1412
-
-
Larsen, A.K.1
Grondard, L.2
Couprie, J.3
Desoize, B.4
Comoe, L.5
Jardillier, J.C.6
Riou, J.F.7
-
30
-
-
0025341331
-
New colorimetric cytotoxicity assay for anticancer-drug screening
-
Skehan, P., Storeng, R., Scudiero, D., Monks, A., MaMahon, J., Vistica, D., Warren, J. T., Bokesch, S., and Boyd, M. R. New colorimetric cytotoxicity assay for anticancer-drug screening. J. Natl. Cancer Inst., 82: 1107-1112, 1990.
-
(1990)
J. Natl. Cancer Inst.
, vol.82
, pp. 1107-1112
-
-
Skehan, P.1
Storeng, R.2
Scudiero, D.3
Monks, A.4
MaMahon, J.5
Vistica, D.6
Warren, J.T.7
Bokesch, S.8
Boyd, M.R.9
-
31
-
-
0025367455
-
Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against diverse panel of human tumor cell lines
-
Rubinstein, L. V., Shoemaker, R. H., Paull, K. D., Simon, R. M., Tosini, S., Skehan, P., Scudiero, D. A., Monks, A., and Boyd, M. R. Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against diverse panel of human tumor cell lines. J. Natl. Cancer Inst., 82: 1113-1118, 1990.
-
(1990)
J. Natl. Cancer Inst.
, vol.82
, pp. 1113-1118
-
-
Rubinstein, L.V.1
Shoemaker, R.H.2
Paull, K.D.3
Simon, R.M.4
Tosini, S.5
Skehan, P.6
Scudiero, D.A.7
Monks, A.8
Boyd, M.R.9
-
32
-
-
0032189683
-
Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme
-
Pommier, Y., Pourquier, P., Fan, Y., and Strumberg, D. Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme. Biochim. Biophys. Acta, 1400: 83-106, 1998.
-
(1998)
Biochim. Biophys. Acta
, vol.1400
, pp. 83-106
-
-
Pommier, Y.1
Pourquier, P.2
Fan, Y.3
Strumberg, D.4
-
33
-
-
0032033603
-
Diversity of DNA topoisomerases I and inhibitors
-
Pommier, Y. Diversity of DNA topoisomerases I and inhibitors. Biochimie, 80: 255-270, 1998.
-
(1998)
Biochimie
, vol.80
, pp. 255-270
-
-
Pommier, Y.1
-
34
-
-
0032484531
-
Sequence-selective cleavage by a topoisomerase I poison, NB-506
-
Fukasawa, K., Komatani, H., Hara, Y., Suda, H., Okura, A., Nishimura, S., and Yoshinari, T. Sequence-selective cleavage by a topoisomerase I poison, NB-506. Int. J. Cancer, 75: 145-150, 1998.
-
(1998)
Int. J. Cancer
, vol.75
, pp. 145-150
-
-
Fukasawa, K.1
Komatani, H.2
Hara, Y.3
Suda, H.4
Okura, A.5
Nishimura, S.6
Yoshinari, T.7
-
35
-
-
0032054504
-
DNA interaction of two clinical camptothecin drugs stabilize their active lactone forms
-
Yang, D., Strode, J. T., Spielmann, H. P., Wang, A. H-J., and Burke, T. G. DNA interaction of two clinical camptothecin drugs stabilize their active lactone forms. J. Am. Chem. Soc., 120: 2979-2980, 1998.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 2979-2980
-
-
Yang, D.1
Strode, J.T.2
Spielmann, H.P.3
Wang, A.H.-J.4
Burke, T.G.5
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