Abstract
IN the course of the preparation of various chloroethylamines which are potential tumour growth-inhibitors we have examined 2-chloroethyl methane-sulphonate (I, X = Cl; CB 1506) as a reagent for the direct conversion of an amino-group into a chloroethylamino-group under mild conditions. It occurred to us that amino-groups in biological systems might be chloroethylated in vivo by this compound. For this reason the methanesulphonate (I, X = Cl) was tested against a number of transplanted animal tumours.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
HADDOW, A., Ross, W. Tumour Growth-inhibitory Alkyl Sulphonates. Nature 177, 995–996 (1956). https://doi.org/10.1038/177995a0
Issue Date:
DOI: https://doi.org/10.1038/177995a0
This article is cited by
-
N-acetyl-S-(2-hydroxyethyl)-L-cysteine as a potential tool in biological monitoring studies?
Archives of Toxicology (1989)
-
Correlation between Some Chemical and Biological Reactions of Ethyl Methanesulphonate
Nature (1963)
-
Mode of Action of Alkylating Agents: Formation of S-Ethylcysteine from Ethyl Methanesulphonate In Vivo
Nature (1957)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.