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EB 1089 is a VDR (vitamin D receptor) agonist, serving as an analog of 1,25 dihydroxyvitamin D. Its role as an agonist allows it to effectively reverse hypercalcemia and inhibit PTH-rP (parathyroid hormone-related peptide, PTHRP) in vitro. Notably, in studies using a squamous cancer cell line, EB 1089 demonstrated the ability to reverse hypercalcemia. Moreover, it displayed downregulation of PTHRP expression in a prostate cancer cell line, C4-2, and promoted anchorage-independent cell growth in vitro. Furthermore, EB 1089 has exhibited inhibitory effects on the proliferation of HEp-2 cell lines, with p57 playing a significant role in this inhibition. Additionally, it acts as a mitogen for neonatal rat lung fibroblasts. Its activation of the vitamin D receptor (VDR) regulates the expression of genes associated with cell growth and differentiation. Moreover, EB 1089 interacts with various proteins, including nuclear factor-kappa B (NF-kB), peroxisome proliferator-activated receptor gamma (PPAR-γ), and cyclic AMP response element binding protein (CREB). These interactions are believed to underlie the anti-inflammatory, anti-apoptotic, and anti-proliferative effects exhibited by EB 1089 in vitro.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
EB 1089, 500 µg | sc-358831A | 500 µg | $161.00 | |||
EB 1089, 1 mg | sc-358831 | 1 mg | $212.00 | |||
EB 1089, 5 mg | sc-358831B | 5 mg | $941.00 |