| Size | Price | Stock | Qty |
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| 5mg |
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| 10mg |
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| 25mg |
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| 50mg |
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| 100mg |
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| 250mg |
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Purity: ≥98%
INCB057643 is a novel, orally bioavailable BET inhibitor that has been tested in preclinical models of hematologic malignancies. INCB057643 is an analog of INCB054329 but with longer plasma half time which enables once a day dosing, while INCB054329 has to be dosed twice a day. INCB057643 inhibited binding of BRD2/BRD3/BRD4 to an acetylated histone H4 peptide in the low nM range, and was selective against other bromodomain containing proteins. In vitro analyses showed that INCB057643 inhibited proliferation of human AML, DLBCL, and multiple myeloma cell lines, with a corresponding decrease in MYC protein levels. Cell cycle analyses indicated that G1 arrest and a concentration-dependent increase in apoptosis were seen within 48 hours of treatment with INCB057643. Production of several cytokines, including IL-6, IL-10 and MIP-1α, was repressed by INCB057643 in human and mouse whole blood stimulated ex vivo with LPS. Consistent with these effects, analyses of gene expression in cells treated with INCB057643 revealed that pathways involved in cell cycle progression, apoptosis, and IL-6 were among the most significantly altered in vitro. Oral administration of INCB057643 resulted in significant anti-tumor efficacy in xenograft models of AML, myeloma, and DLBCL. Additionally, combining INCB057643 with standard of care agents used for the treatment of DLBCL including rituximab and bendamustine resulted in enhanced anti-tumor efficacy relative to that achieved with single agent therapies at doses that were well tolerated. In addition, many B cell malignancies are reliant on the PI3Kδ pathway for proliferation and survival, suggesting that the combination of INCB057643 with the clinical stage PI3Kδ specific inhibitor INCB050465 may be a rational therapeutic strategy for DLBCL. Compared with single agent BETi or PI3Kδi therapy, the combination significantly potentiated tumor growth inhibition in DLBCL models representative of the ABC subtype (HBL-1), and the double hit GCB subtype (WILL2). These data suggest that clinical exploration of INCB057643 as a monotherapy or in combination in hematologic malignancies is warranted.
| Targets |
Bromodomain and Extra-Terminal (BET) family proteins (BRD2, BRD3, BRD4); inhibits their binding to acetylated histone H4 peptide in the low nM range [1]
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| ln Vitro |
INCB-057643 is a new, orally accessible BET inhibitor. INCB-057643 inhibits binding of BRD2/BRD3/BRD4 to an acetylated histone H4 peptide in the low nM range, and is selective against other bromodomain containing proteins. In vitro tests demonstrate that INCB -057643 inhibits proliferation of human AML, DLBCL, and multiple myeloma cell lines, with a commensurate drop in MYC protein levels. Cell cycle studies suggest that G1 arrest and a concentration-dependent increase in apoptosis are detected within 48 hours of treatment with INCB- 057643[1].
INCB057643 inhibited the proliferation of human acute myeloid leukemia (AML), diffuse large B-cell lymphoma (DLBCL), and multiple myeloma cell lines, with a corresponding reduction in MYC protein levels [1] - Cell cycle analysis showed that treatment with INCB057643 induced G₁ phase arrest and a concentration-dependent increase in apoptosis within 48 hours [1] - In ex vivo LPS-stimulated human and mouse whole blood, INCB057643 repressed the production of pro-inflammatory cytokines including IL-6, IL-10, and MIP-1α [1] - Gene expression analysis of INCB057643-treated cells revealed significant alterations in pathways related to cell cycle progression, apoptosis, and IL-6 signaling [1] |
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| ln Vivo |
When LPS is induced ex vivo in human and mouse whole blood, INCB-057643 inhibits the production of many cytokines, including as IL-6, IL-10, and MIP-1α. In xenograft models of AML, myeloma, and DLBCL, oral treatment of INCB-057643 has a strong anti-tumor efficacious effect. Additionally, at well-tolerated doses, INCB-057643 enhances anti-tumor activity compared to single agent therapy when combined with standard of care medicines for the treatment of DLBCL, such as bendamustine and rituximab[1].
Oral administration of INCB057643 exerted significant anti-tumor efficacy in xenograft models of AML, multiple myeloma, and DLBCL [1] - Combination of INCB057643 with standard-of-care agents for DLBCL (rituximab and bendamustine) enhanced anti-tumor efficacy compared to single-agent therapy, with well-tolerated doses [1] - Co-administration of INCB057643 with the clinical-stage PI3Kδ inhibitor INCB050465 significantly potentiated tumor growth inhibition in DLBCL models (ABC subtype HBL-1 and double-hit GCB subtype WILL2), superior to single-agent INCB057643 or PI3Kδ inhibitor [1] |
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| Additional Infomation |
INCB-057643 is being investigated in the clinical trial NCT02959437 (azacitidine in combination with pembrolizumab and epapacress for the treatment of patients with advanced solid tumors (ECHO-206)). The BET inhibitor INCB057643 is an inhibitor of the brominated domain (BRD) and terminal extraterminal domain (BET) protein family with potential antitumor activity. After administration, INCB057643 binds to the acetylated lysine recognition motif in the BET protein BRD, thereby preventing the interaction between the BET protein and acetylated lysine on histones. This disrupts chromatin remodeling and gene expression. Inhibition of the expression of certain growth-promoting genes (e.g., c-Myc-dependent target genes) may lead to suppression of tumor cell growth. BET proteins are transcriptional regulators that are overexpressed in some tumor cells and play an important role in cell growth.
INCB057643 is a novel, orally bioavailable BET inhibitor[1] - BET family protein inhibitors regulate the expression of key genes involved in cell fate, cell cycle, and survival, including c-myc[1] - In preclinical models, BET inhibitors have shown significant efficacy in a variety of oncology indications, particularly in hematologic malignancies[1] - Many B-cell malignancies rely on the PI3Kδ pathway for proliferation and survival, which supports the rationale for combining INCB057643 with a PI3Kδ-specific inhibitor for the treatment of diffuse large B-cell lymphoma (DLBCL)[1] - It is necessary to conduct clinical trials of INCB057643 as a monotherapy or combination therapy for hematologic malignancies[1] |
| Molecular Formula |
C20H21N3O5S
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| Molecular Weight |
415.46284365654
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| Exact Mass |
415.12
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| CAS # |
1820889-23-3
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| Related CAS # |
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| PubChem CID |
118467751
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| Appearance |
White to off-white solid powder
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| LogP |
0.8
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| Hydrogen Bond Donor Count |
1
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| Hydrogen Bond Acceptor Count |
5
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| Rotatable Bond Count |
2
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| Heavy Atom Count |
29
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| Complexity |
862
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| Defined Atom Stereocenter Count |
0
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| SMILES |
O1C2=C(C3=CN(C)C(=O)C4NC=CC=43)C=C(S(C)(=O)=O)C=C2N(C)C(=O)C1(C)C
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| InChi Key |
VZSAMEOETVNDQH-UHFFFAOYSA-N
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| InChi Code |
InChI=1S/C20H21N3O5S/c1-20(2)19(25)23(4)15-9-11(29(5,26)27)8-13(17(15)28-20)14-10-22(3)18(24)16-12(14)6-7-21-16/h6-10,21H,1-5H3
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| Chemical Name |
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| Synonyms |
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| HS Tariff Code |
2934.99.9001
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| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
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| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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| Solubility (In Vitro) |
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| Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.08 mg/mL (5.01 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 20.8 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 2: ≥ 2.08 mg/mL (5.01 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 20.8 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution. View More
Solubility in Formulation 3: ≥ 2.08 mg/mL (5.01 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution. |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 2.4070 mL | 12.0349 mL | 24.0697 mL | |
| 5 mM | 0.4814 mL | 2.4070 mL | 4.8139 mL | |
| 10 mM | 0.2407 mL | 1.2035 mL | 2.4070 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration: mg/mL;
Method for preparing DMSO stock solution: mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation::Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O,mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.