Abstract
THE preparation, and biological and preliminary chemical properties of trichothecin, an antifungal substance from Trichoihecium roseum Link, have been described1. From the data then available it was erroneously concluded that the compound was a lactone with the probable molecular formula C15H20O4. Further work has shown that trichothecin is an ester, C19H24O5, the components of which are isocrotonic acid and a ketonic alcohol, trichothecolone.
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
References
Freeman, G. G., and Morrison, R. I., (a) Nature, 162, 30 (1948); (b) Biochem. J., 44, 1 (1949); (c) J. Gen. Microbiol., 3, 60 (1949).
Purdie, T., and Marshall, W., J. Chem. Soc., 59, 476 (1891).
Michael, A., and Schulthess, J., J. prakt. Chem. (2), 46, 236 (1892).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
FREEMAN, G., GILL, J. Alkaline Hydrolysis of Trichothecin. Nature 166, 698–699 (1950). https://doi.org/10.1038/166698b0
Issue Date:
DOI: https://doi.org/10.1038/166698b0
This article is cited by
-
Enzymic Inactivation of Trichothecin and Crotocin
Nature (1961)
-
A New Trichothecin-like Antifungal Antibiotic
Nature (1959)
-
Onderzoekingen over een virusremstof voorkomend in Dianthus cariophyllus L. Werkingsspectrum, remmingsmechanisme en aard
Tijdschrift Over Plantenziekten (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.