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Formula | C21H19FN4O |
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Molecular Weight | 362.4 | CAS No. | 1396841-57-8 | ||||
Solubility (25°C)* | In vitro | DMSO | 72 mg/mL (198.67 mM) | ||||
Water | Insoluble | ||||||
Ethanol | 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.) |
Description | RGFP966 is an HDAC3 inhibitor with IC50 of 0.08 μM in cell-free assay, exhibits > 200-fold selectivity over other HDAC. | ||
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Targets |
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In vitro | RGFP966 is a slow-on/slow-off, competitive tight-binding HDAC inhibitor, with an IC50 of 0.08μM for HDAC3 and no effective inhibition of any other HDAC at concentrations up to 15μM. [1] RGFP966 treatment on two CTCL cell lines for 24 hours prior to western blot analysis resulted in increased acetylation at H3K9/K14, H3K27, and H4K5, but not H3K56ac. RGFP966 decreases cell growth in CTCL (cutaneous T cell lymphoma) cell lines due to increased apoptosis that is associated with DNA damage and impaired S phase progression. RGFP966 causes a significant reduction in DNA replication fork velocity within the first hour of drug treatment. [2] | ||
In vivo | RGFP966 treatment (10 mg/kg) enhances long-term memory for object memory. RGFP966 (3 or 10 mg/kg, s.c.) facilitates extinction and prevents reinstatement of cocaine- conditioned place preference. [1] |
Kinase Assay:[1] |
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Cell Assay:[2] |
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Animal Study:[1] |
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Data from [Data independently produced by , , Leukemia, 2017, 31(12):2761-2770]
Data from [Data independently produced by , , J Invest Dermatol, 2017, 137(9):1935-1944]
Data from [Data independently produced by , , Front Mol Neurosci, 2016, 9:131]
Data from [Data independently produced by , , J Immunol, 2015, 195(11):5421-31]
HDAC3 integrates TGF-β and microbial cues to program tuft cell biogenesis and diurnal rhythms in mucosal immune surveillance [ Sci Immunol, 2024, 9(99):eadk7387] | PubMed: 39331726 |
Unbiased screening identifies regulators of cell-cell adhesion and treatment options in pemphigus [ Nat Commun, 2024, 15(1):8044] | PubMed: 39271654 |
The lysine methyltransferase SMYD2 facilitates neointimal hyperplasia by regulating the HDAC3-SRF axis [ Acta Pharm Sin B, 2024, 14(2):712-728] | PubMed: 38322347 |
Kaempferol alleviates myocardial ischemia injury by reducing oxidative stress via the HDAC3-mediated Nrf2 signaling pathway [ J Adv Res, 2024, S2090-1232(24)00491-0] | PubMed: 39505146 |
Extracellular CIRP induces abnormal activation of fibroblast-like synoviocytes from patients with RA via the TLR4-mediated HDAC3 pathways [ Int Immunopharmacol, 2024, 128:111525] | PubMed: 38218010 |
LINC01021 Attenuates Expression and Affects Alternative Splicing of a Subset of p53-Regulated Genes [ Cancers (Basel), 2024, 16(9)1639] | PubMed: 38730591 |
Deficiency of histone deacetylases 3 in macrophage alleviates monosodium urate crystals-induced gouty inflammation in mice [ Arthritis Res Ther, 2024, 26(1):96] | PubMed: 38711064 |
LncRNA CHROMR/miR-27b-3p/MET axis promotes the proliferation, invasion, and contributes to rituximab resistance in diffuse large B-cell lymphoma [ J Biol Chem, 2024, 300(3):105762] | PubMed: 38367665 |
Afatinib or Bevacizumab in combination with Osimertinib efficiently control tumor development in orthotopic murine models of non-small lung cancer [ PLoS One, 2024, 19(6):e0304914] | PubMed: 38935790 |
Macrophagic HDAC3 inhibition ameliorates Dextran Sulfate Sodium induced inflammatory bowel disease through GBP5-NLRP3 pathway [ Int J Med Sci, 2024, 21(8):1385-1398] | PubMed: 38903915 |
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