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How to Cite 1. For In-Text Citation (Materials & Methods): 2. For Key Resources Table: |
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| Formula | C46H47ClN8O9S |
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| Molecular Weight | 923.43 | CAS No. | 1818885-28-7 | ||||
| Solubility (25°C)* | In vitro | DMSO | 100 mg/mL (108.29 mM) | ||||
| Ethanol | 3 mg/mL (3.24 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 | ARV-825 is a BRD4 Inhibitor that recruits BRD4 to the E3 ubiquitin ligase cereblon, leading to fast, efficient, and prolonged degradation of BRD4 and sustained down-regulation of MYC. | ||||
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| In vitro | Compared with the BRD4 inhibitors, ARV-825 treatment results in a strikingly more pronounced effect on the levels of c-MYC, and downstream cell proliferation and apoptosis induction in BL (Burkitt’s Lymphoma) cell lines. The IC50s of this compound for all tested cell lines and primary AML cells at 72 hours are in the low nanomolar range (2-50 nM). This treatment reduces PIM1 levels and phosphorylation of CXCR4 in AML cells while overexpression of PIM1 or Myc reverses the phenomena. |
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| In vivo | In a mouse model of human leukemia, the leukemia burdens are significantly lower in the ARV-825 treated mice as confirmed by luciferase imaging, flow cytometry, spleen size and survived longer compared to control mice. |
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| Pharmacological inhibition of bromodomain and extra-terminal proteins induces an NRF-2-mediated antiviral state that is subverted by SARS-CoV-2 infection [ PLOS Pathogens, September 25, 2023, e1011657] | PubMed: 37747932 |
| Loss of BRD4 induces cell senescence in HSC/HPCs by deregulating histone H3 clipping [ EMBO Reports, October 09, 2023, e57032] | |
| Single-cell analysis of neoplastic plasma cells identifies myeloma pathobiology mediators and potential targets [ Cell Reports Medicine, February 18, 2025, 101925] | PubMed: nan |
| Induction of MNK Kinase-dependent eIF4E Phosphorylation by Inhibitors Targeting BET Proteins Limits Efficacy of BET Inhibitors [ Molecular Cancer Therapeutics, February 04, 2019, 235-244] | PubMed: 30446586 |
| Single-cell analysis of neoplastic plasma cells identifies myeloma pathobiology mediators and potential targets [ Cell Rep Med, 2025, S2666-3791(24)00696-7] | PubMed: 39855192 |
| Single-cell morphology encodes functional subtypes of senescence in aging human dermal fibroblasts [ Sci Adv, 2025, 11(17):eads1875] | PubMed: 40279419 |
| Dual Inhibition of CDK4/6 and XPO1 Induces Senescence With Acquired Vulnerability to CRBN-Based PROTAC Drugs [ Gastroenterology, 2024, S0016-5085(24)00062-3] | PubMed: 38262581 |
| Single-cell morphology encodes functional subtypes of senescence in aging human dermal fibroblasts [ bioRxiv, 2024, 2024.05.10.593637] | PubMed: 38798365 |
| Pharmacological inhibition of bromodomain and extra-terminal proteins induces an NRF-2-mediated antiviral state that is subverted by SARS-CoV-2 infection [ PLoS Pathog, 2023, 19(9):e1011657] | PubMed: 37747932 |
| BET proteins inhibitor JQ1 impairs GM-CSF-promoted peritoneal macrophage self-renewal and IL-4-induced alternative polarization [ International Immunopharmacology, 2023, 110954] | PubMed: 37716160 |
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