L-Thyroxine structure, CAS 51-48-9

L-Thyroxine

CAS Number51-48-9

SynonymsThyroxine (VAN); b-((3,5-Diiodo-4-hydroxyphenoxy)-3,5-diiodophenyl)alanine; EINECS 200-101-1; (-)-3-[4-(4-Hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]alanine; 3,3',5,5''-Tetraiodo-L-thyronine; O-(4-Hydroxy-3,5-diiodophenyl)-3,5-diiodo-L-tyrosine; 3-[4-(4-Hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]-L-alanine; Thyroxine; L-3,5,3',5'-Tetraiodothyronine; thyroxine-binding globulin; (-)-Thyroxine; thyroxin; T4; L-Thyroxine; Tetraiodothyronine; THX; transthyretin; L-Thyroxin; Thyrax; l-t4; Levothyroxine; 3,5,3',5'-Tetraiodothyronine; O-(4-Hydroxy-3,5-diidophenyl)-3,5-diiodo-L-tyrosine; 4-14-00-02373 (Beilstein Handbook Reference); thyroxinal; L-thyroxine zwitterion; (2S)-2-Amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoic acid; Henning; MFCD00002596

Molecular FormulaHOC6H2(I)2OC6H2(I)2CH2CH(NH2)CO2H

Molecular Weight776.87

Purity≥98 (HPLC)%

Density2.6±0.1 g/cm3

Boiling Point576.3±50.0 °C at 760 mmHg

Melting Point223 °C (dec.) (lit.)

Flash Point

Appearancepowder

EINECS200-101-1

MSDSChineseEnglish

Symbol6.1

Signal WordWarning

Cat. No.: 2A-9016607 Purity: ≥98 (HPLC)%
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Quality Control of [ 51-48-9 ] Purity: ≥98 (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number51-48-9
Catalog No.2A-9016607
Chinese Name左旋甲状腺素
SynonymsThyroxine (VAN); b-((3,5-Diiodo-4-hydroxyphenoxy)-3,5-diiodophenyl)alanine; EINECS 200-101-1; (-)-3-[4-(4-Hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]alanine; 3,3',5,5''-Tetraiodo-L-thyronine; O-(4-Hydroxy-3,5-diiodophenyl)-3,5-diiodo-L-tyrosine; 3-[4-(4-Hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]-L-alanine; Thyroxine; L-3,5,3',5'-Tetraiodothyronine; thyroxine-binding globulin; (-)-Thyroxine; thyroxin; T4; L-Thyroxine; Tetraiodothyronine; THX; transthyretin; L-Thyroxin; Thyrax; l-t4; Levothyroxine; 3,5,3',5'-Tetraiodothyronine; O-(4-Hydroxy-3,5-diidophenyl)-3,5-diiodo-L-tyrosine; 4-14-00-02373 (Beilstein Handbook Reference); thyroxinal; L-thyroxine zwitterion; (2S)-2-Amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoic acid; Henning; MFCD00002596
Molecular FormulaHOC6H2(I)2OC6H2(I)2CH2CH(NH2)CO2H
Molecular Weight776.87
Purity≥98 (HPLC)
Density2.6±0.1 g/cm3
Boiling Point576.3±50.0 °C at 760 mmHg
Melting Point223 °C (dec.) (lit.)
Appearancepowder
Water Solubilityinsoluble
Storage ConditionIt should be sealed with argon gas and stored in a
ApplicationL-Thyroxine (Levothyroxine; T4) is a synthetic thyroid hormone used to treat hypothyroidism. The DIO enzyme converts L-Thyroxine (T4) into the biologically active triiodothyronine (T3).
EINECS200-101-1
HTC2942000000
PubChem ID24900033
MDL NumberMFCD00002595
SMILESN[C@@H](Cc1cc(I)c(Oc2cc(I)c(O)c(I)c2)c(I)c1)C(O)=O
InChI1S/C15H11I4NO4/c16-8-4-7(5-9(17)13(8)21)24-14-10(18)1-6(2-11(14)19)3-12(20)15(22)23/h1-2,4-5,12,21H,3,20H2,(H,22,23)/t12-/m0/s1
InChI KeyXUIIKFGFIJCVMT-LBPRGKRZSA-N
Beilstein/REAXYS2228515
NACRES CodeNA.32
eCl@ss32190102
UNSPSC51111800
Hazard Symbols6.1
Safety DescriptionS24/25
MSDSmsds/16607_1_51_48_9.pdf
BioactivityL-Thyroxine (Levothyroxine; T4) is a synthetic hormone in the treatment of hypothyroidism. DIO enzymes convert biologically active thyroid hormone (Triiodothyronine,T3) from L-Thyroxine (T4). Related Catalog Signaling Pathways >> Others >> Thyroid Hormone Receptor Research Areas >> Endocrinology Natural Products >> Others Target Human Endogenous Metabolite In Vivo Deiodinases (DIOs), which catalyse the conversion of thyroxine (pro-hormone) to the active thyroid hormone, are associated with thyroid stimulating hormone (TSH) levels. DIO1 and DIO2 catalyze activation of thyroid hormone secretion in contrast to DIO3 playing role inactivation of the secretion. Activities of DIO1 and DIO2 play pivotal role in the negative feedback regulation of pituitary TSH secretion[1]. L-Thyroxine (T4) and Triiodothyronine (T3) hormones are known to modulate the expression of ionic channels, pumps and regulatory contractile proteins. Moreover, thyroid hormones have been shown to influence calcium homeostasis and flux responsible for excitation and contractility, with L-Thyroxine and Triiodothyronine modulating its pharmacological control and secretion. In rats fed 12 weeks with the iodine-free diet, a significant decrease in the levels of both Triiodothyronine and L-Thyroxine is observed when compared to the control group fed with standard diet (p<0.001). In the group treated with low doses of L-Thyroxine, an increase in L-Thyroxine levels is observed (p=0.02) while Triiodothyronine levels remain virtually similar to the control group (p=0.19). Rats treated with high doses of L-Thyroxine display a significant increase in both Triiodothyronine and L-Thyroxine circulating concentrations compared to the non-treated hypothyroid group (p<0.001 and p=0.004, respectively) and a significant increase in L-Thyroxine levels when compared to the control values (p=0.03)[2]. Animal Admin Rats[2] Sprague-Dawley female rats (N=22) are used. Non-pregnant rats are divided into four groups: 1) control, 2) hypothyroidism, 3) hypothyroidism treated with low doses of L-Thyroxine (20 μg/kg/day) and 4) with high doses of L-Thyroxine (100 μg/kg/day). Control rats (group 1) are fed with standard diet, while the intervention rats are fed with iodine-free diet for 12 weeks to induce hypothyroidism (groups 2-4) which is continued for four more weeks to allow screening of hypothyroid status and L-Thyroxine-treatment. Food and water (iodine-free diet) are available ad libitum. The hypothyroid group treated with low (group 3) or high doses of L-Thyroxine (group 4) are injected intraperitoneally every 24 h with respectively 20 μg/kg/day and 100 μg/kg/day. Blood samples are collected for thyroid function screening at week 12 and 16 following the initiation of either the control or iodine-free diet. Hysterectomy is performed under general anesthesia (isoflurane 2%) at the end of the treatment and the two uterine horns are placed in physiological Krebs' solution until isometric tension measurements within no more than 1 h. References [1]. Arici M, et al. Association between genetic polymorphism and levothyroxine bioavailability in hypothyroid patients. Endocr J. 2018 Jan 11. [2]. Corriveau S, et al. Levothyroxine treatment generates an abnormal uterine contractility patterns in an in vitro animalmodel. J Clin Transl Endocrinol. 2015 Sep 9;2(4):144-149. Chemical & Physical Properties Density 2.6±0.1 g/cm3 Boiling Point 576.3±50.0 °C at 760 mmHg Melting Point 235 °C Molecular Formula C15H11I4NO4 Molecular Weight 776.870 Flash Point 302.3±30.1 °C Exact Mass 776.686646 PSA 92.78000 LogP 5.93 Vapour Pressure 0.0±1.7 mmHg at 25°C Index of Refraction 1.795 InChIKey XUIIKFGFIJCVMT-LBPRGKRZSA-N SMILES NC(Cc1cc(I)c(Oc2cc(I)c(O)c(I)c2)c(I)c1)C(=O)O Storage condition 2~8°C Water Solubility insoluble
Use ofL-Thyroxine (Levothyroxine; T4) is a synthetic hormone in the treatment of hypothyroidism. DIO enzymes convert biologically active thyroid hormone (Triiodothyronine,T3) from L-Thyroxine (T4). Properties Articles475 Name L-thyroxine Synonym More Synonyms L-thyroxine Biological Activity Description L-Thyroxine (Levothyroxine; T4) is a synthetic hormone in the treatment of hypothyroidism. DIO enzymes convert biologically active thyroid hormone (Triiodothyronine,T3) from L-Thyroxine (T4). Related Catalog Signaling Pathways >> Others >> Thyroid Hormone Receptor Research Areas >> Endocrinology Natural Products >> Others Human Endogenous Metabolite Animal Admin Rats[2] Sprague-Dawley female rats (N=22) are used. Non-pregnant rats are divided into four groups: 1) control, 2) hypothyroidism, 3) hypothyroidism treated with low doses of L-Thyroxine (20 μg/kg/day) and 4) with high doses of L-Thyroxine (100 μg/kg/day). Control rats (group 1) are fed with standard diet, while the intervention rats are fed with iodine-free diet for 12 weeks to induce hypothyroidism (groups 2-4) which is continued for four more weeks to allow screening of hypothyroid status and L-Thyroxine-treatment. Food and water (iodine-free diet) are available ad libitum. The hypothyroid group treated with low (group 3) or high doses of L-Thyroxine (group 4) are injected intraperitoneally every 24 h with respectively 20 μg/kg/day and 100 μg/kg/day. Blood samples are collected for thyroid function screening at week 12 and 16 following the initiation of either the control or iodine-free diet. Hysterectomy is performed under general anesthesia (isoflurane 2%) at the end of the treatment and the two uterine horns are placed in physiological Krebs' solution until isometric tension measurements within no more than 1 h. References [1]. Arici M, et al. Association between genetic polymorphism and levothyroxine bioavailability in hypothyroid patients. Endocr J. 2018 Jan 11. [2]. Corriveau S, et al. Levothyroxine treatment generates an abnormal uterine contractility patterns in an in vitro animalmodel. J Clin Transl Endocrinol. 2015 Sep 9;2(4):144-149. Chemical & Physical Properties Molecular Formula C15H11I4NO4 Exact Mass 776.686646 PSA 92.78000 Index of Refraction 1.795 InChIKey XUIIKFGFIJCVMT-LBPRGKRZSA-N Water Solubility insoluble
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