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BAY-805
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Catalog No. T73461Cas No. 2925481-88-3
BAY-805 is a selective, high-affinity inhibitor of the ubiquitin-specific protease USP21 and an in vitro chemical probe. It possesses low nanomolar affinity and enhances NF-κB levels.
BAY-805
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Purity: 99.49%
Catalog No. T73461Cas No. 2925481-88-3
BAY-805 is a selective, high-affinity inhibitor of the ubiquitin-specific protease USP21 and an in vitro chemical probe. It possesses low nanomolar affinity and enhances NF-κB levels.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $117 | - | In Stock | |
| 5 mg | $283 | - | In Stock | |
| 10 mg | $419 | - | In Stock | |
| 25 mg | $700 | - | In Stock | |
| 50 mg | $1,120 | - | In Stock | |
| 100 mg | $1,920 | - | 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:99.49%
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Product Introduction
Bioactivity
Chemical Properties
| Description | BAY-805 is a selective, high-affinity inhibitor of the ubiquitin-specific protease USP21 and an in vitro chemical probe. It possesses low nanomolar affinity and enhances NF-κB levels. |
| In vitro | BAY-805 exhibits inhibitory effects on both hUSP21 HTRF and hUSP21 Ub-Rhod activities, with corresponding IC₅₀ values of 6 nM and 2 nM, respectively [1]. BAY-805 (10 µM) can induce NF-κB activation (EC₅₀=17 nM) [1]. BAY-805 (10 µM and 50 µM) significantly inhibits USP21 activity while demonstrating weak inhibitory effects on USP22 and USP10 [1]. Additionally, BAY-805 (0.0001-1000000 nM) shows selective inhibition against USP21 [1]. |
| Molecular Weight | 507.57 |
| Formula | C24H28F3N5O2S |
| Cas No. | 2925481-88-3 |
| Smiles | C(N[C@@H](C(NC=1SC(CC2=CC=C(C#N)C=C2)=NN1)=O)CC(C)C)(=O)C3(C(F)(F)F)CCCCC3 |
| Color | White |
| Appearance | Solid |
Storage & Solubility Information
| 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: ≥ 160 mg/mL, Sonication is recommended. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor 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。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor 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 clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
Dose Conversion
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Tech Support
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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