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How to Cite 1. For In-Text Citation (Materials & Methods): 2. For Key Resources Table: |
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| Formula | C30H34N2O3 |
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| Molecular Weight | 470.60 | CAS No. | 198481-32-2 | ||||||||||||
| Solubility (25°C)* | In vitro | DMSO | 94 mg/mL (199.74 mM) | ||||||||||||
| Ethanol | 24 mg/mL (50.99 mM) | ||||||||||||||
| Water | Insoluble | ||||||||||||||
| In vivo (Add solvents to the product individually and in order) |
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
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| Description | Bazedoxifene (TSE-424) is a selective estrogen receptor modulator that binds to and activates ERα and ERβ with IC50 values of 26 nM and 99 nM, respectively. It also inhibits IL-6/GP130 interactions, suppresses STAT3 signaling, induces apoptosis, and reduces tumor growth, viability, and colony formation in cancer models, while being studied for effects on bone density, uterine health, and CNS vasomotor responses. |
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| Effects of Combination of Estradiol with Selective Progesterone Receptor Modulators (SPRMs) on Human Breast Cancer Cells In Vitro and In Vivo [ PLOS One, March 24, 2016, e0151182] | PubMed: 27011208 |
| The Interleukin-11/IL-11 Receptor Promotes Glioblastoma Survival and Invasion under Glucose-Starved Conditions through Enhanced Glutaminolysis [ International Journal of Molecular Sciences, February 08, 2023, 3356] | PubMed: 36834778 |
| Repurposing the selective estrogen receptor modulator bazedoxifene to suppress gastrointestinal cancer growth [ EMBO Molecular Medicine, 2019 Apr, e9539] | PubMed: 30885958 |
| Effects of Combination of Estradiol with Selective Progesterone Receptor Modulators (SPRMs) on Human Breast Cancer Cells In Vitro and In Vivo [ PLoS One, 2016 Mar 24, e0151182] | PubMed: 27011208 |
| Drug Design Targeting Protein–Protein Interactions (PPIs) Using Multiple Ligand Simultaneous Docking (MLSD) and Drug Repositioning: Discovery of Raloxifene and Bazedoxifene as Novel Inhibitors of IL-6/GP130 Interface [ Journal of Medicinal Chemistry, 2014 Feb 13, 632-641] | PubMed: 24456369 |
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