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FGFR4-IN-8
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Catalog No. T73121Cas No. 2765240-52-4
FGFR4-IN-8 (Compound 7v) is an ATP-competitive inhibitor that covalently and selectively targets both wild-type and gatekeeper mutant forms of FGFR4. It exhibits inhibitory potency with IC50 values of 0.5 nM for FGFR4, 0.25 nM for FGFR4 V550L, 1.6 nM for FGFR4 V550M, and 931 nM for FGFR4 C552S. Additionally, FGFR4-IN-8 shows potent antiproliferative effects on Hep3B hepatocellular carcinoma cells (IC50 of 29 nM) and demonstrates moderate antitumor efficacy in vivo in a Huh-7 xenograft model in nude mice [1].
FGFR4-IN-8
😃Good
Catalog No. T73121Cas No. 2765240-52-4
FGFR4-IN-8 (Compound 7v) is an ATP-competitive inhibitor that covalently and selectively targets both wild-type and gatekeeper mutant forms of FGFR4. It exhibits inhibitory potency with IC50 values of 0.5 nM for FGFR4, 0.25 nM for FGFR4 V550L, 1.6 nM for FGFR4 V550M, and 931 nM for FGFR4 C552S. Additionally, FGFR4-IN-8 shows potent antiproliferative effects on Hep3B hepatocellular carcinoma cells (IC50 of 29 nM) and demonstrates moderate antitumor efficacy in vivo in a Huh-7 xenograft model in nude mice [1].
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 25 mg | 1.586 € | 8-10 weeks | |
| 50 mg | 2.071 € | 8-10 weeks | |
| 100 mg | 2.660 € | 8-10 weeks |
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Product Introduction
Bioactivity
Chemical Properties
| Description | FGFR4-IN-8 (Compound 7v) is an ATP-competitive inhibitor that covalently and selectively targets both wild-type and gatekeeper mutant forms of FGFR4. It exhibits inhibitory potency with IC50 values of 0.5 nM for FGFR4, 0.25 nM for FGFR4 V550L, 1.6 nM for FGFR4 V550M, and 931 nM for FGFR4 C552S. Additionally, FGFR4-IN-8 shows potent antiproliferative effects on Hep3B hepatocellular carcinoma cells (IC50 of 29 nM) and demonstrates moderate antitumor efficacy in vivo in a Huh-7 xenograft model in nude mice [1]. |
| Molecular Weight | 654.56 |
| Formula | C32H34Cl2FN7O3 |
| Cas No. | 2765240-52-4 |
Storage & Solubility Information
| Storage | 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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