货号:A462601
同义名:
1-hydroxycholecalciferol; 1.alpha.-Hydroxyvitamin D3
Alfacalcidol是一种维生素 D3 的衍生物,非选择性地激活维生素 D 受体 (VDR) ,用于骨质疏松相关的研究。
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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+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
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| 描述 | Alfacalcidol is a non-selective VDR activator medication[3]. Alfacalcidol possesses immunoregulatory effects in vitro and in vivo by inhibiting the cytokines IL-1, IL-6, TNF-alpha and particularly IL-12. Therapy with alfacalcidol results in increased production of Th2 helper cells which produce bone protective cytokines like IL-4 and IL-10. Alfacalcidol retards corticosteroid-induced bone loss in contrast to plain vitamin D. Due to its immunomodulating properties, alfacalcidol is particularly suitable for RA(rheumatoid arthritis)-induced bone loss and for the prevention of transplantation osteoporosis, and an adjuvant contribution to the disease-modifying therapy of RA and to the immunosuppressive therapy after transplantation can not be excluded[4]. Alfacalcidol (0.025-0.1 mg/kg; p.o.; five times a week; for 3 months) exerts bone-protective effects independently of its Ca-related effects, and is in this respect superior to vitamin D(3), and that the skeletal actions of alfacalcidol take place, at least in part, independently of suppression of PTH(parathyroid hormone)[5]. |
| Concentration | Treated Time | Description | References | |
| Huh7 cells | 5.00 μM | 6 days | To evaluate the inhibitory effect of Alfacalcidol on SFTSV-induced cytopathic effect (CPE). The results showed that the EC50 value of Alfacalcidol was 1.59 ± 0.35 μM, indicating a dose-dependent protective effect against SFTSV infection. | Virol Sin. 2024 Oct;39(5):802-811. |
| Huh7 cells | 1.59 ± 0.35 μM(EC50) | 6 days | To evaluate the inhibitory effect of Alfacalcidol on SFTSV-induced cytopathic effect (CPE). The results showed that Alfacalcidol significantly inhibited SFTSV-induced CPE in a dose-dependent manner. | Virol Sin. 2024 Oct;39(5):802-811. |
| Administration | Dosage | Frequency | Description | References | ||
| ICR suckling mice | Lethal SFTSV infection model | Intraperitoneal injection | 0.6 or 0.3 μg/kg | Daily for 8 days | To evaluate the therapeutic effect of Alfacalcidol on SFTSV-infected ICR suckling mice. The results showed that Alfacalcidol (0.6 μg/kg) provided 64% protection, significantly improving the survival rate of infected mice. | Virol Sin. 2024 Oct;39(5):802-811. |
| ICR suckling mice | SFTSV lethal infection model | Intraperitoneal injection | 0.6 or 0.3 μg/kg | Once daily for 8 days | To evaluate the therapeutic effect of Alfacalcidol on SFTSV-infected ICR suckling mice. The results showed that Alfacalcidol (0.6 μg/kg/d) provided 64% protection, significantly improving the survival rate of infected mice. | Virol Sin. 2024 Oct;39(5):802-811. |
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
| NCT02069886 | Thalassemia (Transfusion Delen... 展开 >>dent) 收起 << | Phase 4 | Withdrawn | December 2018 | - |
| NCT03483441 | Basal Cell Nevus Syndrome ... 展开 >> Basal Cell Carcinoma 收起 << | Phase 1 | Recruiting | May 1, 2023 | United States, Arizona ... 展开 >> University of Arizona College of Medicine Not yet recruiting Phoenix, Arizona, United States, 85004 Contact: Nathalie Zeitouni, MD 602-406-8222 Nathalie.Zeitouni@dignityhealth.org Sub-Investigator: Nathalie Zeitouni, MD United States, Ohio Cleveland Clinic Recruiting Cleveland, Ohio, United States, 44195 Contact: Jeff Negrey, MA 216-636-5504 negreyj2@ccf.org Principal Investigator: Edward Maytin, MD Sub-Investigator: Christine Warren, MD 收起 << |
| NCT02542865 | Growth and Development | Not Applicable | Completed | - | India ... 展开 >> GSK Investigational Site Pune, India, 411001 收起 << |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.50mL 0.50mL 0.25mL |
12.48mL 2.50mL 1.25mL |
24.96mL 4.99mL 2.50mL |
|
| CAS号 | 41294-56-8 |
| 分子式 | C27H44O2 |
| 分子量 | 400.64 |
| SMILES Code | C=C1[C@H](C[C@@H](C/C1=C/C=C2[C@]3([C@@](C)([C@H](CC3)[C@@H](CCCC(C)C)C)CCC/2)[H])O)O |
| MDL No. | MFCD00868328 |
| 别名 | 1-hydroxycholecalciferol; 1.alpha.-Hydroxyvitamin D3; EB 644; alpha-Calcidol; Alpha D 3; Alfarol; Tevabone; Oxydevit; Etalpha; Bondiol; 1-hydroxy Vitamin D3 |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, store in freezer, under -20°C |
| 溶解方案 |
DMSO: 50 mg/mL(124.8 mM),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 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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