Model reactions for the biosynthesis of thyroxine: X. Non-enzymic formation of thyroxine and 3,3′,5′-triiodothyronine residues in thyroglobulin
- 8 March 1965
- journal article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - General Subjects
- Vol. 97 (3), 523-531
- https://doi.org/10.1016/0304-4165(65)90165-0
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
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- Model Reactions for the Biosynthesis of Thyroxine. V. Reaction of 4-Hydroxy-3-iodophenylpyruvic Acid and of 4-Hydroxy-3,5-diiodophenylpyruvic Acid with L-Tyrosine or Its Iodinated Congeners. A Novel Synthesis of 3,3',5'-Triiodo-L-thyronine1,2The Journal of Organic Chemistry, 1964
- Nonenzymic synthesis of thyroxine residues in thyroglobulinBiochimica et Biophysica Acta, 1963
- The Properties of ThyroglobulinJournal of Biological Chemistry, 1962
- Synthesis of Thyroxine by L-Amino Acid OxidaseEndocrinology, 1962
- Synthesis of Specifically Iodine-131- and Carbon-14-Labeled Thyroxine1The Journal of Organic Chemistry, 1962
- Conversion of 3,5-diiodotyrosine to thyroxine by rattlesnake venomBiochimica et Biophysica Acta, 1962
- Reaction of 4-Hydroxy-3,5-diiodophenylpyruvic Acid with 3,5-DiiodotyrosineThe Journal of Organic Chemistry, 1961
- Notizen: Zum Mechanismus der Biosynthese des ThyroxinsZeitschrift für Naturforschung B, 1956
- Sur deux nouveaux constituants hormonaux du corps thyroïde, la 3:3′-diiodothyronine et la 3:3′:5′-triiodothyronineBiochimica et Biophysica Acta, 1956