Avitinib maleate (CAS: 1557268-88-8)
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SKU-Pack Size | Availability | Size | Price | |
EBC51029-1ML | In Stock | 1mL(10mM in DMSO) | €193.70 | |
EBC51029-5MG | In Stock | 5mg | €89.70 | |
EBC51029-10MG | In Stock | 10mg | €141.70 | |
EBC51029-50MG | In Stock | 50mg | €518.70 | |
EBC51029100MG | In Stock | 100mg | €791.70 |
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Product Information | |||||||||||||||||||||
Synonym(s) | AC0010MA£¬ AC-0010MA£¬ AC 0010MA£¬ AC0010£¬ AC-0010£¬ AC 0010 | ||||||||||||||||||||
Chemical Name | N-[3-[[2-[3-fluoro-4-(4-methylpiperazin-1-yl)anilino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxy]phenyl]prop-2-enamide | ||||||||||||||||||||
Application | Avitinib maleate is a pyrrolopyrimidine-based irreversible epidermal growth factor receptor (EGFR) inhibitor. | ||||||||||||||||||||
CAS Number | 1557268-88-8 | ||||||||||||||||||||
Purity | ¡Ý99.0% | ||||||||||||||||||||
Molecular Weight | 603.61 | ||||||||||||||||||||
Molecular Formula | C₃₀H₃₀FN₇O₆ | ||||||||||||||||||||
SMILES | CN1CCN(CC1)C2=C(C=C(C=C2)NC3=NC4=C(C=CN4)C(=N3)OC5=CC=CC(=C5)NC(=O)C=C)F.C(=C\C(=O)O)\C(=O)O | ||||||||||||||||||||
Target & IC50 | EGFR | ||||||||||||||||||||
Solubility | DMSO: 300 mg/mL (497.02 mM) | ||||||||||||||||||||
Preparing Stock Solutions |
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Shipping | Gel Pack | ||||||||||||||||||||
Storage | Store at -20¡ãC | ||||||||||||||||||||
Research Use | For Research Use Only. Not Intended for Diagnostic Or Therapeutic Use. |
Product Description | |
Avitinib, also known as AC0010 or AC0010MA, is an orally available, irreversible, epidermal growth factor receptor (EGFR) mutant-selective inhibitor, with potential antineoplastic activity. Upon oral administration, avitinib covalently binds to and inhibits the activity of mutant forms of EGFR, including the drug-resistant T790M EGFR mutant, which prevents signaling mediated by mutant forms of EGFR. This may both induce cell death and inhibit tumor growth in EGFR-mutated tumor cells. EGFR, a receptor tyrosine kinase that is mutated in a variety of cancers, plays a key role in tumor cell proliferation and tumor vascularization. As this agent is selective towards mutant forms of EGFR, its toxicity profile may be reduced when compared to non-selective EGFR inhibitors, which also inhibit wild-type EGFR. |
Specific Protocols | |