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PLX-3618
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Catalog No. T88470Cas No. 2851986-76-8
Alias PLX3618, PLX 3618
PLX-3618 is an effective BRD4 molecular glue degrader (DC50=12.2 nM) that recruits the E3 ligase substrate receptor DCAF11, promoting BRD4 polyubiquitination and proteasomal degradation to induce apoptosis in AML cells.
PLX-3618
😃Good
Purity: 99.71%
Catalog No. T88470Alias PLX3618, PLX 3618Cas No. 2851986-76-8
PLX-3618 is an effective BRD4 molecular glue degrader (DC50=12.2 nM) that recruits the E3 ligase substrate receptor DCAF11, promoting BRD4 polyubiquitination and proteasomal degradation to induce apoptosis in AML cells.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | - | In Stock | |
| 50 mg | $1,980 | - | In Stock | |
| 100 mg | $2,500 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.71%
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | PLX-3618 is an effective BRD4 molecular glue degrader (DC50=12.2 nM) that recruits the E3 ligase substrate receptor DCAF11, promoting BRD4 polyubiquitination and proteasomal degradation to induce apoptosis in AML cells. |
| Targets&IC50 | BRD4:12.2 nM (DC50) |
| Synonyms | PLX3618, PLX 3618 |
| Molecular Weight | 601.68 |
| Formula | C32H27N9O2S |
| Cas No. | 2851986-76-8 |
| Smiles | CC=1C2=C(N3C([C@H](CC(N)=O)N=C2C4=CC=C(C=C4)C5=CC(NC(=O)C6=C7N(N=C6)C=CC=N7)=CC=C5)=NN=C3C)SC1C |
| Color | White |
| Appearance | Solid |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (132.96 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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Calculator
In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。Stock solution preparation method: 2 mg of drug dissolved in 50 μL DMSO (stock solution concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(stock solution concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyThe above example illustrates how to use "In Vivo Formulation Calculator" and does not represent a recommended formulation for any specific compound. Please select an appropriate dissolution method based on your experimental animals and route of administration.
Dose Conversion
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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