Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Seocalcitol is an analog of vitamin D, binds vitamin D receptor protein from human osteosarcoma MG-63 cells(Kd : 0.27 nM).
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
500 μg | 35 days | $ 243.00 | |
1 mg | 35 days | $ 460.00 | |
5 mg | 35 days | $ 1,930.00 |
Description | Seocalcitol is an analog of vitamin D, binds vitamin D receptor protein from human osteosarcoma MG-63 cells(Kd : 0.27 nM). |
Targets&IC50 | Vitamin D receptor:(kd)0.27 nM |
In vitro | Seocalcitol is a stimulators of osteoclast recruitment in murine bone marrow cultures(EC50 at 0.1 nM). Seocalcitol stimulates bone resorption(EC50 of 0.03 nM)[1]. Seocalcitol elicites a dose-dependent induction of 24-hydroxylase mRNA in the kidney (EC50=0.4±0.13). In the kidney, Kd values for Seocalcitol is 0.48±0.04 nM. However, in the intestine, the Kd for Seocalcitol is 1.43±0.19 nM)[2]. Seocalcitol (0.1-10 nM) induces cell differentiation in a dosedependent manner. A higher differentiating activity is observed for 1 nM Seocalcitol than for 1 nM VD3. |
In vivo | Seocalcitol, a synthetic vitamin D analog, demonstrates lower hypercalcemic activity compared to 1,25(OH)2VD3. Its long-term intraperitoneal (IP) administration at 0.5 μg/kg body weight bi-daily significantly inhibits hepatocellular carcinoma (HCC) development in C3H/Sy mice[4]. Furthermore, when administered intraperitoneally to postnatal rats from days 4 to 12 at dosages of 0.38 or 1.25 μg/kg body weight per day, only the higher dosage (1.25 μg/kg) significantly attenuates weight gain, either as a standalone treatment or when combined with Dexamethasone, all-trans retinoic acid (RA), or retinoic acid[5]. |
Synonyms | EB 1089 |
Molecular Weight | 454.68 |
Formula | C30H46O3 |
CAS No. | 134404-52-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 50 mg/mL (109.97 mM)
You can also refer to dose conversion for different animals. More
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Seocalcitol 134404-52-7 Others EB 1089 EB1089 EB-1089 inhibitor inhibit