Results 101 to 110 of about 2,969 (182)
During aerobic myeloperoxidase-catalysed oxidation of isoniazid at pH 7.8, compound III was generated. Oxidation of isoniazid or hydrazine sulphate at pH valu7es of 6.5 or 7.8 in a myeloperoxidase-H2O2 system caused considerable haem loss, which was ...
J. V. van Zyl +3 more
semanticscholar +2 more sources
Thyronines (THs) and thyronamines (TAMs) are two groups of endogenous iodine-containing signaling molecules whose representatives differ from each other only regarding the number and/or the position of the iodine atoms.
S. Piehl +4 more
semanticscholar +2 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Inhibition of low density lipoprotein oxidation by thyronines and probucol.
Biochemical Pharmacology, 1993Oxidation of low density lipoproteins (LDL) results in increased macrophage uptake of LDL which may contribute to the formation of macrophage-derived foam cells in the early atherosclerotic lesion. In this study we show that thyroxine (T4), its optical antipodes, certain desiodo analogs and probucol inhibited cupric sulfate-catalyzed oxidation of human
A. N. Hanna +3 more
semanticscholar +3 more sources
Thyroidal Thyronine and Non-Thyronine Iodine Secretion in Euthyroid Subjects
The Journal of Clinical Endocrinology & Metabolism, 1971ABSTRACT Thyroidal non-thyronine iodine secretion was quantified in 22 euthyroid adult Arkansas subjects by measuring, simultaneously, thyroidal iodine accumulation A, thyroxine iodine turnover H4 and triiodothyronine iodine turnover H3. Non-thyronine iodine secretion was calculated as A-H4-H3.
D A, Fisher, T H, Oddie, C S, Thompson
openaire +2 more sources
Thyronin‐ und thyroxinähnliche Aminoalkohole, II
Archiv der Pharmazie, 1966AbstractEs werden drei Wege zur Synthese des D,L‐threo‐1‐[4′(p‐Hydroxyphenoxy)‐phenyl]‐1‐hydroxy‐2‐amino‐propans beschrieben, die eine stereospezifische Reduktion der Ausgangsketone nach verschiedenen Methoden gemeinsam haben: Racem. p‐Hydroxyphenoxy‐α‐phthalimidopropiophenon bildet bei einer modifizierten, racem.
H. K. Müller, G. Rieck
openaire +1 more source
Some biological actions of iodo-L-thyronines.
Journal of Endocrinology, 1960SUMMARY Six iodo-l-thyronines, viz. 3:3′:5′-triiodo-, 3:5-diiodo-, 3:3′-diiodo-, 3′:5′-diiodo-, 3-monoiodo-, and 3′-monoiodo-l-thyronine, have been compared with 3:5:3′-triiodo-l-thyronine, in mice by an anoxia method and in rats for antigoitrogenic activities and effects on rate of oxygen consumption.
E. Tomich, E. A. Woollett, M. A. Pratt
semanticscholar +3 more sources
THE ROLE OF THYRONINE IN THYROID HORMONE METABOLISM
The Journal of Clinical Endocrinology & Metabolism, 1979Thryonine (T0) has been identified in human urine using gas chromatography-mass fragmentography (G.C.M.F.). In 22 normal individuals urinary T0 concentration was found to range between 8--25 nmol/24h. Assuming the mean normal thyroxine (T4) production rate to be approximately 100 nmol/24h, our findings indicate that less than 20% of this could be ...
P, Willetts +3 more
openaire +2 more sources
THE THYROMIMETIC EFFECTS OF D-TRICHLOR-THYRONINE
Journal of Endocrinology, 1964SUMMARY Various aspects of thyroid activity of a non-iodine-containing thyroid analogue, 3:5:3′-trichloro-d-thyronine (d-trichlor-thyronine = d-ClT3) have been studied and compared with those of 3:5:3′-triiodo-l-thyronine (l-triiodo-thyronine = l-T3).
N W, OAKLEY, K, ADADEVEOH, P, WISE
openaire +2 more sources

