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VL285 Phenol
VL285 Phenol is an analogue of VL285 featuring a Phenol group. As a small molecule VHL ligand, VL285 serves as a degrader in HaloPROTAC3 synthesis, effectively degrading HaloTag7 fusion proteins (IC 50 = 0.34 μM) [1].
Catalog No. T87622Cas No. 1448188-69-9
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VL285 Phenol
Catalog No. T87622Cas No. 1448188-69-9
VL285 Phenol is an analogue of VL285 featuring a Phenol group. As a small molecule VHL ligand, VL285 serves as a degrader in HaloPROTAC3 synthesis, effectively degrading HaloTag7 fusion proteins (IC 50 = 0.34 μM) [1].
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose. | Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks |
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Bioactivity
Chemical Properties
| Description | VL285 Phenol is an analogue of VL285 featuring a Phenol group. As a small molecule VHL ligand, VL285 serves as a degrader in HaloPROTAC3 synthesis, effectively degrading HaloTag7 fusion proteins (IC 50 = 0.34 μM) [1]. |
| In vitro | VL285 (100 μM; 24 hours) reduces the ability of HaloPROTAC3 to induce degradation of GFP-HaloTag7 [1]. |
| Molecular Weight | 548.65 |
| Formula | C29H32N4O5S |
| Cas No. | 1448188-69-9 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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% 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 μLddH2O 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 μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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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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