Abstract |
In tissue cultures of C-57 black mouse heart and sarcoma T-241, beta-2-thienyl-DL-alanine acts specifically as a phenylalanine antagonist. Heart cultures can transaminate between beta-2-thienyl-DL-alanine and phenylpyruvate to form L-phenylalanine and thus block the toxic action of the remaining beta-2-thienyl-DL-alanine, whereas sarcoma T-241 cultures cannot. Of eleven mouse tumors and four rat tumors tested for their ability to perform this reaction, nine tumors had little or no activity. The beta-2-thienylpyruvic acid resulting from transamination further reacts to form a red compound the exact structure of which is not yet known.
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Authors | J A JACQUEZ, R K BARCLAY, C C STOCK |
Journal | The Journal of experimental medicine
(J Exp Med)
Vol. 96
Issue 5
Pg. 499-512
(Nov 1952)
ISSN: 0022-1007 [Print] United States |
PMID | 13000060
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Alanine
(analogs & derivatives)
- Animals
- In Vitro Techniques
- Mice
- Neoplasms, Experimental
- Rats
- beta-Alanine
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