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PMID: 12127512 Published · ppublish English Journal Article

Synthesis and biological evaluation of N-(7-indolyl)-3-pyridinesulfonamide derivatives as potent antitumor agents.

Bioorganic & medicinal chemistry letters ·Vol. 12 ·No. 16 ·2002-08-19 ·Pages 2097-100

Owa T, Yoshino H, Okauchi T, Okabe T, Ozawa Y, Hata Sugi N, Yoshimatsu K, Nagasu T, Koyanagi N, Kitoh K

Abstract

We herein report the synthesis and antitumor activity of E7070 analogues containing a 3-pyridinesulfonamide moiety. E7070 was selected from our sulfonamide-based compound collections, currently undergoing Phase II clinical trials because of its tolerable toxicity profile and some antitumor responses in the Phase I setting. Of the analogues examined, ER-35745, a 6-amino-3-pyridinesulfonamide derivative, demonstrated significant oral efficacy against the HCT116 human colon carcinoma xenograft in nude mice.

MeSH Terms
Animals Antineoplastic Agents/chemical synthesis,chemistry,pharmacology,therapeutic use Carcinoma/drug therapy,pathology Colon/pathology Colonic Neoplasms/drug therapy,pathology Humans Mice Mice, Nude Molecular Structure Structure-Activity Relationship Sulfonamides/chemical synthesis,chemistry,pharmacology,therapeutic use Tumor Cells, Cultured
Chemicals
Antineoplastic Agents Sulfonamides
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Owa Takashi
Tsukuba Research Laboratories, Eisai Co., Ltd., 5-1-3 Tokodai, Tsukuba, 300-2635, Ibaraki, Japan. [email protected]
Yoshino Hiroshi
Okauchi Tatsuo
Okabe Tadashi
Ozawa Yoichi
Hata Sugi Naoko
Yoshimatsu Kentaro
Nagasu Takeshi
Koyanagi Nozomu
Kitoh Kyosuke
Article Info
Journal
Bioorganic & medicinal chemistry letters
Abbr.
Bioorg Med Chem Lett
ISSN
0960-894X
Published
2002-08-19
Pages
2097-100
Language
English
Region
England
NLM ID
9107377
Subset
IM
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