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Eldecalcitol/艾地骨化醇 {[allProObj[0].p_purity_real_show]}

货号:A586998 同义名: ED-71; 2-(3-hydroxypropoxy)-1,25-dihydroxyvitamin D3

Eldecalcitol 是一种维生素 D 类似物,用于骨质疏松相关机制研究。

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Eldecalcitol/艾地骨化醇 化学结构 CAS号:104121-92-8
Eldecalcitol/艾地骨化醇 化学结构
CAS号:104121-92-8
Eldecalcitol/艾地骨化醇 3D分子结构
CAS号:104121-92-8
Eldecalcitol/艾地骨化醇 化学结构 CAS号:104121-92-8
Eldecalcitol/艾地骨化醇 3D分子结构 CAS号:104121-92-8
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Eldecalcitol/艾地骨化醇 纯度/质量文件 产品仅供科研

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Eldecalcitol/艾地骨化醇 生物活性

描述 Eldecalcitol, an analog of vitamin D, is a drug used for the treatment of osteoporosis.

Eldecalcitol/艾地骨化醇 细胞实验

Cell Line
Concentration Treated Time Description References
CX3CR1-positive cells from CX3CR1-EGFP knockin mice 10^-9 to 10^-8 M 2 days Suppressed S1PR2 expression Proc Natl Acad Sci U S A. 2013 Apr 23;110(17):7009-13
CSF1R-positive cells from CSF1R-EGFP transgenic mice 10^-9 to 10^-8 M 2 days Suppressed S1PR2 expression Proc Natl Acad Sci U S A. 2013 Apr 23;110(17):7009-13
RAW264.7 cells 10^-9 to 10^-8 M 2 days Suppressed S1PR2 expression and enhanced chemotaxis to S1P Proc Natl Acad Sci U S A. 2013 Apr 23;110(17):7009-13
RAW264.7 cells 1 × 10–9 M 48 hours To evaluate the effect of ED-71 on RAW264.7 cell polarization, results showed that ED-71 alone promoted M2 macrophage polarization. Stem Cell Res Ther. 2022 Mar 21;13(1):113
CD4+ T cells 1 nM 48 hours To evaluate the effect of ED-71 on Treg cell differentiation under high glucose conditions, results showed ED-71 improved HG-inhibited Treg cell differentiation. Cell Mol Life Sci. 2024 Oct 5;81(1):423
Human gingival fibroblasts (HGFs) 0, 0.5, 5, 50 nM 24 hours To evaluate the inhibitory effect of ED-71 on LPS-induced cell death. Results showed that ED-71 pretreatment significantly reduced LPS-induced cell death. Drug Des Devel Ther. 2020 Nov 13;14:4901-4913
C2C12 cells 0.1, 1, and 10 nM 24 hours To investigate the effect of eldecalcitol on TNF-α-induced muscle atrophy. Eldecalcitol significantly inhibited the expression of MuRF-1 and Atrogin-1, increased the diameter of myotubes, and inhibited the NF-κB signaling pathway. Skelet Muscle. 2023 Dec 19;13(1):22

Eldecalcitol/艾地骨化醇 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6J male mice Tail suspension model Intraperitoneal injection 3.5 or 5 ng Twice a week for 3 weeks To investigate the effect of eldecalcitol on tail suspension-induced muscle atrophy and osteoporosis. Eldecalcitol significantly improved grip strength, restored muscle weight, improved bone microarchitecture, and restored the impaired oxidative defense system. Skelet Muscle. 2023 Dec 19;13(1):22
C57BLKS/J Iar-+ Leprdb/+ Leprdb mice Diabetic osteoporosis model Oral 0.25 μg/kg 3 times per week for 4 weeks To evaluate the effect of ED-71 on bone formation in diabetic osteoporosis mice, results showed that ED-71 significantly enhanced bone formation and promoted M2 macrophage polarization. Stem Cell Res Ther. 2022 Mar 21;13(1):113
Mice Glucocorticoid-induced osteoporosis model Oral gavage 50 ng/kg/d 5 times per week for 8 weeks Prevented GC-induced upregulation of atrogin1 and MuRF1 expression, preserved bone structure and function JCI Insight. 2024 Nov 8;9(21):e182664
Mice Type 2 diabetes model Oral 0.25 µg/kg 3 times per week for 4 weeks To evaluate the therapeutic effects of ED-71 on diabetic osteoporosis and glucolipid metabolic disorder, results showed ED-71 attenuated bone loss and marrow adiposity while improving glucolipid metabolism. Cell Mol Life Sci. 2024 Oct 5;81(1):423
Mice Ovariectomy-induced osteoporosis model Oral 50 ng/kg body weight Once daily for 4 weeks Prevented osteoporosis and suppressed S1PR2 expression in circulating monocytes Proc Natl Acad Sci U S A. 2013 Apr 23;110(17):7009-13
Rats Ovariectomized rat model Oral 30 or 90 ng/kg body weight Five times per week for 12 weeks To examine the effects of Eldecalcitol on bone in ovariectomized rats, showing that ELD increased bone volume and trabecular thickness, reduced osteoclast numbers, and preferentially induced minimodeling-based bone formation in the epiphyses. Int J Mol Sci. 2024 Apr 11;25(8):4257

Eldecalcitol/艾地骨化醇 参考文献

[1]Saito K, Miyakoshi N, et al. Eldecalcitol improves muscle strength and dynamic balance in postmenopausal women with osteoporosis: an open-label randomized controlled study. J Bone Miner Metab. 2016 Sep;34(5):547-54.

[2]Ito M, Nakamura T, et al. Effect of eldecalcitol, an active vitamin D analog, on hip structure and biomechanical properties: 3D assessment by clinical CT. Bone. 2011 Sep;49(3):328-34.

Eldecalcitol/艾地骨化醇 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.04mL

0.41mL

0.20mL

10.19mL

2.04mL

1.02mL

20.38mL

4.08mL

2.04mL

Eldecalcitol/艾地骨化醇 技术信息

CAS号104121-92-8
分子式C30H50O5
分子量 490.72
SMILES Code O[C@H]1[C@@H](OCCCO)[C@H](O)C(/C(C1)=C\C=C2[C@]3([H])CC[C@H]([C@H](C)CCCC(C)(O)C)[C@@]3(C)CCC\2)=C
MDL No. MFCD25977156
别名 ED-71; 2-(3-hydroxypropoxy)-1,25-dihydroxyvitamin D3; Edirol; 2-(3-Hydroxypropoxy)calcitriol; 1,25-dihydroxyvitamin D3
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry, store in freezer, under -20°C

溶解方案

DMSO: 3 mg/mL(6.11 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

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