度骨化醇, 维生素 D 受体激动剂

维生素D2类似物,VDR激动剂
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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
D408749-1ml
1ml 现货 Stock Image
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Compound libraries (12332)

基本描述

英文别名 1α-hydroxyvitamin D2 | (1R,3S,E)-5-((E)-2-((1R,3aS,7aR)-1-((2R,5S,E)-5,6-dimethylhept-3-en-2-yl)-7a-methyl-octahydroinden-4-ylidene)ethylidene)-4-methylenecyclohexane-1,3-diol
规格或纯度 Moligand™, 10mM in DMSO
英文名称 Doxercalciferol
生化机理 多钙化醇(1α-羟基维生素 D2)是一种合成维生素 D2 类似物,可抑制甲状旁腺的合成和分泌,用于治疗继发性甲状旁腺功能亢进症和代谢性骨病。
储存温度 -80℃储存
运输条件 超低温冰袋运输
作用类型 激动剂
作用机制 维生素 D 受体激动剂
产品介绍


Information

Doxercalciferol (1α-hydroxyvitamin D2) is a syntheticvitamin D2analog, suppressing parathyroid synthesis and secretion, used to treat secondary hyperparathyroidism and metabolic bone disease.
In vitro


In vivo

Doxercalciferol (100 or 300 pg/g b.w.) normalizes serum calcium and parathyroid hormone (PTH) levels in nephrectomy treated mice. Doxercalciferol (300 pg/g b.w.) significantly reduces osteitis fibrosa in nephrectomy treated mice. Doxercalciferol results in significant decrease in cardiac hypertrophy and improves cardiac function in rats fed a high salt (HS) diet. Doxercalciferol treatment leads to a significant decrease in plasma brain natriuretic peptide (BNP) level and tissue atrial natriuretic factor (ANF) mRNA level in rats fed a high salt (HS) diet. Doxercalciferol also significantly reduces the level of protein kinase C-α (PKCα) suggesting that PKC-mediated cardiac hypertrophy may be associated with vitamin D deficiency. Doxercalciferol decreases proteinuria, podocyte injury, mesangial expansion, and extracellular matrix protein accumulation in Diet-induced obesity (DIO) mice. Doxercalciferol also decreases macrophage infiltration, oxidative stress, proinflammatory cytokines, and profibrotic growth factors in DIO mice. Doxercalciferol also prevents the activation of the renin-angiotensin-aldosterone system including the angiotensin II type 1 receptor and the mineralocorticoid receptor in DIO mice. Doxercalciferol combined with Losartan most effectively prevents albuminuria, restored glomerular filtration barrier structure, and dramatically reduces glomerulosclerosis in a dose-dependent manner in mice. Doxercalciferol combined with Losartan virtually prevents morphological and molecular changes in diabetic kidneys of mice.
Cell Data

cell lines:

Concentrations:

Incubation Time:

Powder Purity:≥99%

关联靶点(人)

VDR Tclin 维生素 D3 受体(Vitamin D3 receptor) (0 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

名称和识别符

Canonical SMILES CC(C)C(C)/C=C/C(C)C1CCC2C(/CCCC12C)=C/C=C/3CC(O)CC(O)C3=C
分子量 412.65

安全和危险性(GHS)

技术规格说明书

Concentration 9-11(mmol/L)
NMR Spectrum 1H Conforms to Structure

质检证书(CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:

溶液计算器

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