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Gefitinib-based PROTAC 3, MedChemExpress
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Quantity:
5 mg
10 mg
Unit Size:
10mg
5mg
Description
Gefitinib-based PROTAC 3, conjugating an EGFR binding element to a von Hippel-Lindau ligand via a linker, induces EGFR degradation with DC50s of 11.7 nM and 22.3 nM in HCC827(exon 19 del) and H3255 (L858R mutantion) cells, respectively.
Specifications
Specifications
| Chemical Name or Material | Gefitinib-based PROTAC 3 |
| CAS | 2230821-27-7 |
| Color | White |
| Purity Grade Notes | Research |
| Molecular Formula | C47H57ClFN7O8S |
| Quantity | 5 mg |
| Solubility Information | DMSO : ≥ 60 mg/mL (64.20 mM) |
| SMILES | O=C([C@H]1N(C([C@@H](NC(CCOCCOCCCCCOC2=CC3=C(NC4=CC=C(F)C(Cl)=C4)N=CN=C3C=C2OC)=O)C(C)(C)C)=O)C[C@H](O)C1)NCC5=CC=C(C6=C(C)N=CS6)C=C5 |
| Molecular Weight (g/mol) | 934.51 |
| Formula Weight | 934.51 |
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Research purposes only
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