Cancer Research Translational Cancer Medicine 2008: Cancer Clinical Trials and Personalized Medicine  Susan G. Komen for the Cure-AACR Outstanding Investigator Award for Breast Cancer Research
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 Cell Growth & Differentiation

[Cancer Research 24, 367-372, April 1, 1964]
© 1964 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 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 Petering, H. G.
Right arrow Articles by Underwood, G. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Petering, H. G.
Right arrow Articles by Underwood, G. E.

The Anti-Tumor Activity of 2-Keto-3-ethoxybutyraldehyde Bis(thiosemicarbazone) and Related Compounds*

H. G. Petering, H. H. Buskirk and G. E. Underwood

( The Biochemical Research Division of The Upjohn Company, Kalamazoo, Michigan)

2-Keto-3-ethoxybutyraldehyde bis(thiosemicarbazone) (KTS) has been shown to have marked carcinostatic and carcinolytic activity against several established rat tumors. Dose-response relationships have been established for its toxicity, tumor-inhibitory activity, and capability of causing regressions. The compound is more safely administered via the oral route than by intraperitoneal injection.

The activity of KTS is compared with several related compounds, and some indications of structural requirements for biological activity are noted.

* This paper was presented in part at the Meeting of the Federation of American Societies for Experimental Biology in Atlantic City, 1962.

Received 7/ 5/63.


This article has been cited by other articles:


Home page
Radiat Prot DosimetryHome page
K. Takakura, S. Yaguchi, Y. Kanansugi, K. Kobayashi, R. Okayasu, and Y. Fujibayashi
Enhancement of chromosomal aberrations in tumor cells with a non-labeled Cu-PTSM and irradiation with Cu K-shell monochromatic X rays
Radiat Prot Dosimetry, December 1, 2006; 122(1-4): 188 - 194.
[Abstract] [Full Text] [PDF]




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 Cell Growth & Differentiation
Copyright © 1964 by the American Association for Cancer Research.