BIOMAT Database Logo BIOMAT Database Logo

[Enzymatic deiodination of thyroxin and its derivatives. II. Products formed and mechanism of the reaction]. 1961

S LISSITZKY, and M T BENEVENT, and M ROQUES

UI MeSH Term Description Entries
D004798 Enzymes Biological molecules that possess catalytic activity. They may occur naturally or be synthetically created. Enzymes are usually proteins, however CATALYTIC RNA and CATALYTIC DNA molecules have also been identified. Biocatalyst,Enzyme,Biocatalysts
D013974 Thyroxine The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (MONOIODOTYROSINE) and the coupling of iodotyrosines (DIIODOTYROSINE) in the THYROGLOBULIN. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form TRIIODOTHYRONINE which exerts a broad spectrum of stimulatory effects on cell metabolism. L-Thyroxine,Levothyroxine,T4 Thyroid Hormone,3,5,3',5'-Tetraiodothyronine,Berlthyrox,Dexnon,Eferox,Eltroxin,Eltroxine,Euthyrox,Eutirox,L-3,5,3',5'-Tetraiodothyronine,L-Thyrox,L-Thyroxin Henning,L-Thyroxin beta,L-Thyroxine Roche,Levo-T,Levothroid,Levothyroid,Levothyroxin Deladande,Levothyroxin Delalande,Levothyroxine Sodium,Levoxine,Levoxyl,Lévothyrox,Novothyral,Novothyrox,O-(4-Hydroxy-3,5-diiodophenyl) 3,5-diiodo-L-tyrosine,O-(4-Hydroxy-3,5-diiodophenyl)-3,5-diiodotyrosine,Oroxine,Sodium Levothyroxine,Synthroid,Synthrox,Thevier,Thyrax,Thyroxin,Tiroidine,Tiroxina Leo,Unithroid,L Thyrox,L Thyroxin Henning,L Thyroxin beta,L Thyroxine,L Thyroxine Roche,Levo T,Thyroid Hormone, T4
D054879 Halogenation Covalent attachment of HALOGENS to other compounds. Bromination,Chlorination,Fluorination,Iodination,Iodation

Related Publications

S LISSITZKY, and M T BENEVENT, and M ROQUES
Sensitized photooxidation of histidine and its derivatives. Products and mechanism of the reaction.
December 1969, Biochemistry,
S LISSITZKY, and M T BENEVENT, and M ROQUES
Products of enzymatic hydrolysis of cellulose and its derivatives.
May 1951, Archives of biochemistry and biophysics,
S LISSITZKY, and M T BENEVENT, and M ROQUES
[Deiodination of L-thyroxine and its derivatives. V. Comparative study of L-thyroxine deiodination by mitochondria or their extracts and rabbit liver microsomes in the presence of different co-factors. Mechanism of the deiodination reaction].
January 1965, Bulletin de la Societe de chimie biologique,
S LISSITZKY, and M T BENEVENT, and M ROQUES
[On the intermediate products and mechanism of deiodination of thyroid hormones].
June 1963, General and comparative endocrinology,
S LISSITZKY, and M T BENEVENT, and M ROQUES
Enzymatic synthesis of folylpolyglutamates. Characterization of the reaction and its products.
June 1980, The Journal of biological chemistry,
S LISSITZKY, and M T BENEVENT, and M ROQUES
[IN VITRO DEIODINATION OF THYROXIN BY THE HUMAN PLACENTA].
January 1964, Annales d'endocrinologie,
S LISSITZKY, and M T BENEVENT, and M ROQUES
[In vitro deiodination of thyroxin in different rat tissues].
January 1957, Schweizerische medizinische Wochenschrift,
S LISSITZKY, and M T BENEVENT, and M ROQUES
[Effectors and products of enzymatic diiodotyrosine deiodination by a plasmatic fraction from pig liver].
January 1981, Acta biologica et medica Germanica,
S LISSITZKY, and M T BENEVENT, and M ROQUES
[DEIODINATION IN VIVO OF H-3- AND I-125-3,5-THYROXIN].
January 1964, Comptes rendus des seances de la Societe de biologie et de ses filiales,
S LISSITZKY, and M T BENEVENT, and M ROQUES
[DEIODINATION IN VIVO OF H-3- AND I-125-3,5-THYROXIN].
January 1964, Comptes rendus des seances de la Societe de biologie et de ses filiales,
Copied contents to your clipboard!