| Identification | Back Directory | [Name]
AST2818 mesylate | [CAS]
2130958-55-1 | [Synonyms]
AST2818 mesylate
Alflutinib mesylate
Alflutinib methanesulfonate
Alflutinib (AST2818 mesylate)
Alflutinib mesylate (AST2818)
N-[2-[[2-(Dimethylamino)ethyl]methylamino]-5-[[4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl]amino]-6-(2,2,2-trifluoroethoxy)-3-pyridinyl]-2-propenamide compd. with methanesulfonate (1:1) | [Molecular Formula]
C29H35F3N8O5S | [MDL Number]
MFCD31746903 | [MOL File]
2130958-55-1.mol | [Molecular Weight]
664.71 |
| Chemical Properties | Back Directory | [storage temp. ]
Store at -20°C,unstable in solution, ready to use. | [solubility ]
Chloroform: 10 mg/ml; DMF: slightly soluble; DMSO: slightly soluble | [form ]
A crystalline solid | [color ]
Light yellow to yellow |
| Hazard Information | Back Directory | [Description]
Furmonertinib (formerly known as alflutinib) is another me-too third-generation EGFR TKI that has a pyridyl ring replacing the phenyl ring of osimertinib and a trifluoroethyl group replacing the methyl group (Fig. 4). This TKI, which was discovered and developed by Shanghai Allist Pharma, was approved in November 2019 by the NMPA of China for the second-line treatment of NSCLC with EGFR sensitive mutation and EGFR T790M drug-resistant mutation, and more recently as a first-line treatment for classical EGFR mutant NSCLC. In June 2022, furmonertinib was granted the Fast Track designation by the FDA in patients with advanced or metastatic NSCLC with activating EGFR or HER2 mutations, including exon 20 insertion mutations.
| [storage]
Store at -20°C,unstable in solution, ready to use. |
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