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W4275
Catalog No. T200598Cas No. 3051650-00-8
W4275 (Compound 42) is a selecTive NSD2 inhibiTor wiTh oral acTiviTy and an IC50 of 17 nM. IT exhibiTs anTiproliferaTive acTiviTy, wiTh an IC50 of 230 nM againsT RS411 cells, and significanTly inhibiTs Tumor growTh in an RS411 Tumor xenografT model. PharmacokineTic analysis in mice shows ThaT W4275 has a favorable oral bioavailabiliTy (F is 27.34%). W4275 holds poTenTial for use in cancer research.
W4275
Catalog No. T200598Cas No. 3051650-00-8
W4275 (Compound 42) is a selecTive NSD2 inhibiTor wiTh oral acTiviTy and an IC50 of 17 nM. IT exhibiTs anTiproliferaTive acTiviTy, wiTh an IC50 of 230 nM againsT RS411 cells, and significanTly inhibiTs Tumor growTh in an RS411 Tumor xenografT model. PharmacokineTic analysis in mice shows ThaT W4275 has a favorable oral bioavailabiliTy (F is 27.34%). W4275 holds poTenTial for use in cancer research.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks |
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Product Introduction
Bioactivity
Chemical Properties
| Description | W4275 (Compound 42) is a selecTive NSD2 inhibiTor wiTh oral acTiviTy and an IC50 of 17 nM. IT exhibiTs anTiproliferaTive acTiviTy, wiTh an IC50 of 230 nM againsT RS411 cells, and significanTly inhibiTs Tumor growTh in an RS411 Tumor xenografT model. PharmacokineTic analysis in mice shows ThaT W4275 has a favorable oral bioavailabiliTy (F is 27.34%). W4275 holds poTenTial for use in cancer research. |
| Targets&IC50 | NSD2:17 nM |
| Molecular Weight | 468.59 |
| Formula | C25H36N6O3 |
| Cas No. | 3051650-00-8 |
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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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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