ID | 34207 |
FullText URL | |
Author |
Ali, Hamed I..
Tomita, Keiichiro
Akaho, Eiichi
Kambara, Hiroto
Miura, Shinji
Hayakawa, Hiroyuki
Ashida, Noriyuki
Kawashima, Yutaka
Yamagishi, Takehiro
Ikeya, Hisao
Yoneda, Fumio
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Abstract | Novel 2-deoxo-2-phenyl-5-deazaflavins and 2-deoxo-2-phenylflavin-5-oxides were prepared as a new class of antitumor agents and showed significant antitumor activities against NCI-H 460, HCT 116, A 431, CCRF-HSB-2, and KB cell lines. In vivo investigation, 2-deoxo-10-methyl-2-phenyl-5-deazaflavin exhibited the effective antitumor activity against A 431 human adenocarcinoma cells transplanted subcutaneously into nude mouse. Furthermore, AutoDock study has been done by binding of the flavin analogs into PTK pp60(c-src), where a good correlation between their IC50 and AutoDock binding free energy was exhibited. In particular, 2-deoxo-2-phenylflavin-5-oxides exhibited the highest potential binding affinity within the binding pocket of PTK.
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Keywords | antitumor activity
Flavin analog
AutoDock
protein tyrosine kinase
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Note | Published with permission from the copyright holder.
This is a author's copy,as published in Bioorganic & Medicinal Chemistry , 2007 Vol.15 Issue.1 pp.242-256 Publisher URL: http://dx.doi.org/10.1016/j.bmc.2006.09.063 Direct access to Thomson Web of Science record Copyright © 2007 by Elsevier Ltd. |
Published Date | 2007-01-01
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Publication Title |
Bioorganic & Medicinal Chemistry
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Volume | volume15
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Issue | issue1
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Publisher | Pergamon-Elsevier Science Ltd.
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Start Page | 242
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End Page | 256
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ISSN | 0968-0896
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NCID | AA10938083
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Content Type |
Journal Article
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language |
English
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Copyright Holders | Elsevier Ltd.
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File Version | author
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Refereed |
True
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DOI | |
PubMed ID | |
Web of Science KeyUT | |
Submission Path | organic_chemistry/11
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