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GX-674
🥰Excellent
Catalog No. T22829Cas No. 1432913-36-4
GX-674 is a highly potent and selective voltage-gated sodium channel 1.7 (Nav1.7) antagonist with an IC50 value of 0.1 nM measured at -40 mV for the study of inflammatory and neuropathic pain.
GX-674
🥰Excellent
Purity: 98.60%
Catalog No. T22829Cas No. 1432913-36-4
GX-674 is a highly potent and selective voltage-gated sodium channel 1.7 (Nav1.7) antagonist with an IC50 value of 0.1 nM measured at -40 mV for the study of inflammatory and neuropathic pain.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $64 | In Stock | |
| 5 mg | $156 | In Stock | |
| 10 mg | $248 | In Stock | |
| 25 mg | $493 | In Stock | |
| 50 mg | $793 | In Stock | |
| 100 mg | $1,090 | In Stock | |
| 200 mg | $1,480 | In Stock |
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Purity:98.60%
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Product Introduction
Bioactivity
Chemical Properties
| Description | GX-674 is a highly potent and selective voltage-gated sodium channel 1.7 (Nav1.7) antagonist with an IC50 value of 0.1 nM measured at -40 mV for the study of inflammatory and neuropathic pain. |
| Targets&IC50 | Nav1.7:0.1 nM |
| In vitro | In HEK293 cells, the patch-clamp analysis was performed for human Nav channels. GX-674 shows a potent inhibition effect on Nav.1.7 (IC50= 0.1nM). GX-674 also displays substantial selectivity on different Nav subtypes. It shows much higher inhibitory effects on Nav 1.7 over other Nav isoforms, such as 100000 times more potent for Nav1.7 than for Nav 1.5. GX-74 is also reported to bind to a high-affinity, isoform-selective, and extracellularly accessible site on VSD4.[1] |
| Molecular Weight | 534.95 |
| Formula | C21H13ClF2N6O3S2 |
| Cas No. | 1432913-36-4 |
| Smiles | O(C1=C(C=C(Cl)C=C1)C=2C=C3C(=CC2)N=C(N)N3)C4=C(F)C=C(S(NC5=NC=NS5)(=O)=O)C(F)=C4 |
| Relative Density. | 1.678 g/cm3 (Predicted) |
Storage & Solubility Information
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO: Soluble |
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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.
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