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JCN037 is potent, non-covalent and brain-penetrant inhibitor of EGFR(EGFR, p-wtEGFR and pEGFRvⅢ with IC50 of 2.49 nM, 3.95 nM, 4.48 nM , respectively).

| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $48 | In Stock | |
| 10 mg | $75 | In Stock | |
| 25 mg | $132 | In Stock | |
| 50 mg | $201 | In Stock | |
| 100 mg | $288 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $53 | In Stock |
| Description | JCN037 is potent, non-covalent and brain-penetrant inhibitor of EGFR(EGFR, p-wtEGFR and pEGFRvⅢ with IC50 of 2.49 nM, 3.95 nM, 4.48 nM , respectively). |
| Targets&IC50 | p-EGFR Ⅷ:4.48 nM , p-EGFR (WT):3.95 nM , EGFR:2.49 nM |
| In vivo | Relative to the conventional EGFR TKIs erlotinib and lapatinib, JCN037 displayed potent activity against EGFR amplified/mutant patient-derived cell cultures, significant BBB penetration (2:1 brain-to-plasma ratio), and superior efficacy in an EGFR-driven orthotopic glioblastoma xenograft model. |
| Molecular Weight | 376.18 |
| Formula | C16H11BrFN3O2 |
| Cas No. | 2305154-31-6 |
| Smiles | Fc1c(Br)cccc1Nc1ncnc2cc3OCCOc3cc12 |
| Relative Density. | 1.669 g/cm3 (Predicted) |
| Color | White |
| Appearance | Solid |
| 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: 10 mg/mL (26.58 mM), Sonication is recommended. | |||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||
DMSO
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