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Liothyronine sodium/三碘代甲状腺素钠盐 {[allProObj[0].p_purity_real_show]}

货号:A103275 同义名: Triiodothyronine sodium; 3,3',5-Triiodo-L-thyronine sodium

Liothyronine sodium 是三碘甲状腺原氨酸(T3)的合成左旋异构体,对 hTRα 和 hTRβ 的 Ki 值均为 2.33 nM,常用于甲状腺功能减退的研究。

Liothyronine sodium/三碘代甲状腺素钠盐 化学结构 CAS号:55-06-1
Liothyronine sodium/三碘代甲状腺素钠盐 化学结构
CAS号:55-06-1
Liothyronine sodium/三碘代甲状腺素钠盐 3D分子结构
CAS号:55-06-1
Liothyronine sodium/三碘代甲状腺素钠盐 化学结构 CAS号:55-06-1
Liothyronine sodium/三碘代甲状腺素钠盐 3D分子结构 CAS号:55-06-1
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Liothyronine sodium/三碘代甲状腺素钠盐 纯度/质量文件 产品仅供科研

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Liothyronine sodium/三碘代甲状腺素钠盐 生物活性

描述 Liothyronine Sodium is the sodium salt form of liothyronine, a synthetic form of the levorotatory isomer of the naturally occurring thyroid hormone triiodothyronine (T3). Liothyronine (Sodium) is an active form of thyroid hormone, which binds to β1 thyroid hormone receptor (TRβ1), and activates its activity. Liothyronine (T3, 100 nM) stimulates the proliferation of hepatocarcinema cells in which TRβ1 is overexpressed[3]. High T(3) (triiodothyronine) levels induce a low TRalpha1:TRalpha2 ratio which could protect the cell from excessive T(3)-induced gene expression[4]. Expression of a mutant receptor with impaired triiodothyronine (T(3)) binding and dominant negative activity affected cerebellar development and motor performance. TRs are also involved in adult brain function. TRalpha1 deletion, or expression of a dominant negative mutant receptor, induces consistent behavioral changes in adult mice, leading to severe anxiety and morphological changes in the hippocampus[5].

Liothyronine sodium/三碘代甲状腺素钠盐 细胞实验

Cell Line
Concentration Treated Time Description References
MDA-MB-468 100 nM 3 hours To investigate the effect of T3 on mitochondrial Ca2+ uptake, results showed that T3 significantly enhanced mitochondrial Ca2+ uptake in MDA-MB-468 cells. Cell Commun Signal. 2024 Nov 6;22(1):533
hTERT-HME1 100 nM 3 hours To investigate the effect of T3 on mitochondrial Ca2+ uptake, results showed that T3 did not significantly affect mitochondrial Ca2+ uptake in hTERT-HME1 cells. Cell Commun Signal. 2024 Nov 6;22(1):533
PC3 100 nM 3 hours To investigate the effect of T3 on mitochondrial Ca2+ uptake, results showed that T3 did not significantly affect mitochondrial Ca2+ uptake in PC3 cells. Cell Commun Signal. 2024 Nov 6;22(1):533
MCF7 100 nM 3 hours To investigate the effect of T3 on mitochondrial Ca2+ uptake, results showed that T3 significantly enhanced mitochondrial Ca2+ uptake in MCF7 cells. Cell Commun Signal. 2024 Nov 6;22(1):533
SVF cells 100 nM Various time points To evaluate the time-dependent effect of T3 on Myc protein expression, results showed that T3 treatment time-dependently increased Myc protein expression. Nat Commun. 2022 Jun 13;13(1):3394
Brown adipocyte precursor cell line (BAC) 100 nM 24 hours To evaluate the effect of T3 on Myc protein expression, results showed that T3 treatment increased Myc protein expression. Nat Commun. 2022 Jun 13;13(1):3394
mBAP-9 cell line 10 nM 24 hours To study the effect of T3 on mitophagy using mito-RFP/GFP plasmid transfection, results showed increased red puncta, indicating enhanced mitophagy. Autophagy. 2019 Jan;15(1):131-150
primary brown adipocytes 10 nM 24 hours To investigate the effect of T3 on autophagic flux, results showed increased MAP1LC3B-II levels, indicating enhanced autophagic flux. Autophagy. 2019 Jan;15(1):131-150
iPSC-derived hepatocytes (iHEPs) 1 nM, 10 nM, 100 nM 24 hours To investigate the regulatory role of T3 via THRβ1 on metabolic pathways in human hepatocytes, including gluconeogenesis, lipid oxidation, fatty acid synthesis, and fatty acid uptake. Results showed that T3 significantly upregulated G6PC and PCK1 expression, downregulated FBP1 expression, and increased glucose production through THRβ1. Mol Metab. 2024 Dec;90:102057
human islets 10 nM 72 hours To study the effects of T3 and glucose on the expression of ChREBPα and ChREBPβ in human islet cells, similar effects were observed as in INS-1 cells. Mol Metab. 2022 Dec;66:101646
INS-1 832/13 rat insulinoma cells 10 nM 48 hours To investigate the effects of T3 and glucose on the expression of ChREBPα and ChREBPβ, it was found that ChREBPα expression was induced in the presence of T3, while ChREBPβ expression was induced at high glucose concentrations and reached higher levels in the presence of T3. Mol Metab. 2022 Dec;66:101646
HEK cells 100 μM 3 minutes Evaluate the inhibitory effect of Liothyronine on GAT1, results showed Liothyronine significantly inhibited the uptake of radiolabeled GABA J Med Chem. 2015 Mar 12;58(5):2149-58

Liothyronine sodium/三碘代甲状腺素钠盐 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Male mice Hypothyroid mouse model Intraperitoneal injection 0.25 μg/g body weight (standard dose) Once daily for 2-6 days To evaluate the effect of T3 on thermogenic capacity and hyperplasia of iBAT, results showed that long-term T3 treatment increased thermogenic capacity and hyperplasia of iBAT. Nat Commun. 2022 Jun 13;13(1):3394
Mice Hyperthyroid mouse model Intraperitoneal injection 10 μg/100 g body weight Daily for 10 days To investigate the effect of T3 on autophagy and mitochondrial biogenesis in BAT, results showed increased autophagic flux and mitochondrial protein expression. Autophagy. 2019 Jan;15(1):131-150

Liothyronine sodium/三碘代甲状腺素钠盐 参考文献

[1]Bernal J. Thyroid hormone receptors in brain development and function. Nat Clin Pract Endocrinol Metab. 2007 Mar;3(3):249-59.

[2]Timmer DC, Bakker O, Wiersinga WM. Triiodothyronine affects the alternative splicing of thyroid hormone receptor alpha mRNA. J Endocrinol. 2003 Nov;179(2):217-25.

[3]Lin KH, Lin YW, Parkison C, Cheng SY. Stimulation of proliferation by 3,3',5-triiodo-L-thyronine in poorly differentiated human hepatocarcinoma cells overexpressing beta 1 thyroid hormone receptor. Cancer Lett. 1994 Oct 14;85(2):189-94

[4]Timmer DC, Bakker O, Wiersinga WM. Triiodothyronine affects the alternative splicing of thyroid hormone receptor alpha mRNA. J Endocrinol. 2003 Nov;179(2):217-25

[5]Bernal J. Thyroid hormone receptors in brain development and function. Nat Clin Pract Endocrinol Metab. 2007 Mar;3(3):249-59

Liothyronine sodium/三碘代甲状腺素钠盐 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.49mL

0.30mL

0.15mL

7.43mL

1.49mL

0.74mL

14.86mL

2.97mL

1.49mL

Liothyronine sodium/三碘代甲状腺素钠盐 技术信息

CAS号55-06-1
分子式C15H11I3NNaO4
分子量 672.96
SMILES Code O=C([O-])[C@@H](N)CC1=CC(I)=C(OC2=CC=C(O)C(I)=C2)C(I)=C1.[Na+]
MDL No. MFCD00002594
别名 Triiodothyronine sodium; 3,3',5-Triiodo-L-thyronine sodium; Cytomel; T3 sodium
运输蓝冰
InChI Key SBXXSUDPJJJJLC-YDALLXLXSA-M
Pubchem ID 23666110
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry,2-8°C

溶解方案

DMSO: 4 mg/mL(5.94 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

0.1 M NaOH: 10 mg/mL(14.86 mM),配合低频超声,并调节pH至11

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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