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Osimertinib

Osimertinib
Osimertinib
Osimertinib
Catalog Description Size Price (USD) Qty
GBM-5036-10MGOsimertinib10mg$105.00
GBM-5036-50MGOsimertinib50mg$315.00
Mutant EGFR kinase inhibitor
Bioassays Specification
Bio-Activity Mutant EGFR kinase inhibitor
Chemical Name N-[2-[[2-(Dimethylamino)ethyl]methylamino]-4-methoxy-5-[[4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl]amino]phenyl]-2-propenamide
Function / Pharmacology A potent, selective, irreversible inhibitor of mutant EFGR tyrosine kinase1. Osimertinib inhibits phosphorylation of EGFR in T790M-mutant cell lines (IC50 <15 nM) but was less potent at inhibition of EGFR phosphorylation in wild-type cells (IC50s in the range of 480 to 1,865 nM). It produces sustained tumor regression in EGFR-mutant tumor xenograft and transgenic rodent models2. Tumor cells develop resistance to osimertinib but combination treatment with an IL-6 antibody reverses resistance to a certain extent3. In clinical use for treatment of non-small cell lung cancer4.
CAS# 1421373-65-0
MW 499.6
Molecular Formula C28H33N7O2
Solubility Soluble in DMSO (up to 40 mg/ml)
Supplied powder
Storage as supplied -20°C
Ship temp Ambient
References 1. MRV Finlay et al. J. Med. Chem. 2014 57:8249 2. DAE Cross et al. Cancer Discov. 2014 4:1046 3. J Tan et al. Eur, J. Pharm. Sci. 2024 199:106805 4. H Patel et al. Eur. J. Med. Chem. 2017 142:32
Antibody Specification
Alternate Names AZD-9291
Protein Specification
Purity >98%

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