Cancer Research Cancer Research Funding Available  EMT and Cancer Progression and Treatment
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 55, 1316-1320, March 15, 1995]
© 1995 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Arakawa, H.
Right arrow Articles by Nishimura, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Arakawa, H.
Right arrow Articles by Nishimura, S.

Novel Indolocarbazole Compound 6-N-Formylamino-12,13-dihydro-1,11-dihydroxy-13-(ß-D-glucopyranosyl)-5H-indolo[2,3-a]pyrro[3,4-c]carbazole-5,7(6H)-dione (NB-506): Its Potent Antitumor Activities in Mice

Hiroharu Arakawa1, Tomoko Iguchi, Masashi Morita, Tomoko Yoshinari, Katsuhisa Kojiri, Hiroyuki Suda, Akira Okura2 and Susumu Nishimura

Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories, Okubo 3, Tsukuba 300-33, Japan

NB-506 [6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(ß-D-glucopyranosyl)-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione] is a new antitumor indolocarbazole compound. The growths of murine M5076 and Ehrlich solid tumors were inhibited 76 and 96%, respectively, by i.v. injection at doses of 300 mg/m2. Furthermore, NB-506 caused regression of nodules of human PC-13 lung cancer and MKN-45 stomach cancer cells at i.v. doses of 90 mg/m2. Human HCT 116 and LS 180 colon cancers also regressed with injections of NB-506. Repeated injections of NB-506 had a stronger antitumor effect than intermittent injections in mice with MKN-45. The cumulative toxicity of NB-506 was low in terms of lethality in mice, i.e., the LD50s on single and 10 repeated i.v. injections into CDF1 mice were 990 and 810 mg/m2/injection, respectively. In conclusion, NB-506 is considered to be an interesting possible candidate as an anticancer drug for treatment of solid tumors in humans.

1 To whom requests for reprints should be addressed.

2 Deceased.

Received 10/18/94. Accepted 1/16/95.




This article has been cited by other articles:


Home page
Mol. Pharmacol.Home page
M. Facompre, C. Carrasco, P. Colson, C. Houssier, J. D. Chisholm, D. L. Van Vranken, and C. Bailly
DNA Binding and Topoisomerase I Poisoning Activities of Novel Disaccharide Indolocarbazoles
Mol. Pharmacol., November 1, 2002; 62(5): 1215 - 1227.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
N. Takenaga, M. Ishii, T. Kamei, and T. Yasumori
Structure-Activity Relationship in O-Glucuronidation of Indolocarbazole Analogs
Drug Metab. Dispos., May 1, 2002; 30(5): 494 - 497.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
B. Pilch, E. Allemand, M. Facompre, C. Bailly, J.-F. Riou, J. Soret, and J. Tazi
Specific Inhibition of Serine- and Arginine-rich Splicing Factors Phosphorylation, Spliceosome Assembly, and Splicing by the Antitumor Drug NB-506
Cancer Res., September 1, 2001; 61(18): 6876 - 6884.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
T. Yoshinari, M. Ohkubo, K. Fukasawa, S.-i. Egashira, Y. Hara, M. Matsumoto, K. Nakai, H. Arakawa, H. Morishima, and S. Nishimura
Mode of Action of a New Indolocarbazole Anticancer Agent, J-107088, Targeting Topoisomerase I
Cancer Res., September 1, 1999; 59(17): 4271 - 4275.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
S. Pollack, L. Young, J. Bilsland, N. Wilkie, S. Ellis, F. Hefti, H. Broughton, and S. Harper
The Staurosporine-Like Compound L-753,000 (NB-506) Potentiates the Neurotrophic Effects of Neurotrophin-3 by Acting Selectively at the TrkA Receptor
Mol. Pharmacol., July 1, 1999; 56(1): 185 - 195.
[Abstract] [Full Text]


Home page
Cancer Res.Home page
H. Komatani, M. Morita, N. Sakaizumi, K. Fukasawa, E. Yoshida, A. Okura, T. Yoshinari, and S. Nishimura
A New Mechanism of Acquisition of Drug Resistance by Partial Duplication of Topoisomerase I
Cancer Res., June 1, 1999; 59(11): 2701 - 2708.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
C. Bailly, L. Dassonneville, P. Colson, C. Houssier, K. Fukasawa, S. Nishimura, and T. Yoshinari
Intercalation into DNA Is Not Required for Inhibition of Topoisomerase I by Indolocarbazole Antitumor Agents
Cancer Res., June 1, 1999; 59(12): 2853 - 2860.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
N. Takenaga, M. Ishii, S. Nakajima, T. Hasegawa, R. Iwasa, H. Ishizaki, and T. Kamei
In Vivo Metabolism of a New Anticancer Agent, 6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(beta -D-glucopyranosil)5H-indolo [2,3-a]pyrrolo [3,4-c]carbazole-5,7(6H)-dione (NB-506) in Rats and Dogs: Pharmacokinetics, Isolation, Identification, and Quantification of Metabolites
Drug Metab. Dispos., February 1, 1999; 27(2): 205 - 212.
[Abstract] [Full Text]


Home page
Drug Metab. Dispos.Home page
N. Takenaga, T. Hasegawa, M. Ishii, H. Ishizaki, S. Hata, and T. Kamei
In Vitro Metabolism of a New Anticancer Agent, 6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(beta -D-glucopyranosil)5H-indolo [2,3-a]pyrrolo [3,4-c]carbazole-5,7(6H)-dione (NB-506), in Mice, Rats, Dogs, and Humans
Drug Metab. Dispos., February 1, 1999; 27(2): 213 - 220.
[Abstract] [Full Text]


Home page
Mol. Pharmacol.Home page
C. Bailly, X. Qu, F. Anizon, M. Prudhomme, J.-F. Riou, and J. B. Chaires
Enhanced Binding to DNA and Topoisomerase I Inhibition by an Analog of the Antitumor Antibiotic Rebeccamycin Containing an Amino Sugar Residue
Mol. Pharmacol., February 1, 1999; 55(2): 377 - 385.
[Abstract] [Full Text]


Home page
Cancer Res.Home page
E. Labourier, J.-F. Riou, M. Prudhomme, C. Carrasco, C. Bailly, and J. Tazi
Poisoning of Topoisomerase I by an Antitumor Indolocarbazole Drug: Stabilization of Topoisomerase I-DNA Covalent Complexes and Specific Inhibition of the Protein Kinase Activity
Cancer Res., January 1, 1999; 59(1): 52 - 55.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
C. Bailly, P. Colson, C. Houssier, E. Rodrigues-Pereira, M. Prudhomme, and M. J. Waring
Recognition of Specific Sequences in DNA by a Topoisomerase I Inhibitor Derived from the Antitumor Drug Rebeccamycin
Mol. Pharmacol., January 1, 1998; 53(1): 77 - 87.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1995 by the American Association for Cancer Research.