Weight | 672.958 g/mol |
---|---|
Formula | C15H11I3NNaO4 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 5 |
LIOTHYRONINE SODIUM (55-06-1)
Triiodothyronine · Liothyronine · Cytomel
Score:
#460 in Neuroscience
,
#780 in Biochemistry
,
#2125 in Biology
,
#2608 in Chemistry
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- Depletion of L-3,5,3'-Triiodothyronine and L-Thyroxine in Euthyroid Calf Serum for Use in Cell Culture Studies of the Action of Thyroid Hormone* (Endocrinology, 1979)
- Tissue Differences in the Concentration of Triiodothyronine Nuclear Binding Sites in the Rat: Liver, Kidney, Pituitary, Heart, Brain, Spleen and Testis (Endocrinology, 1974)
- Reciprocal Changes in Serum Concentrations of 3,3,5-Triiodothyronine (Reverse T3) and 3,35-Triiodothyronine (T3) in Systemic Illnesses (The Journal of Clinical Endocrinology and Metabolism, 1975)
- Effects of thyroxine as compared with thyroxine plus triiodothyronine in patients with hypothyroidism. (The New England Journal of Medicine, 1999)
- High incidence of decreased serum triiodothyronine concentration in patients with nonthyroidal disease. (The Journal of Clinical Endocrinology and Metabolism, 1975)
- Adrenergic activation of triiodothyronine production in brown adipose tissue (Nature, 1983)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Triiodothyronine
- Liothyronine
- Cytomel
- T3 Thyroid Hormone
-
SMILESC1=CC(=C(C=C1OC2=C(C=C(C=C2I)CC(C(=O)[O-])N)I)I)O.[Na+]
-
InChIKeySBXXSUDPJJJJLC-UHFFFAOYSA-M
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