Imatinib Impurity E is the impurity of Imatinib. Imatinib is an orally bioavailable tyrosine kinases inhibitor that selectively inhibits BCR/ABL, v-Abl, PDGFR and c-kit kinase activity. Imatinib (STI571) works by binding close to the ATP binding site, locking it in a closed or self-inhibited conformation, therefore inhibiting the enzyme activity of the protein semicompetitively[1][2][3][4]. Imatinib also is an inhibitor of SARS-CoV and MERS-CoV[5].
Molecular Weight:
873.02
Purity:
96.05
CAS Number:
[1365802-18-1]
Formula:
C52H48N12O2
Target:
Drug Metabolite
Application Notes:
MCE Product type: Reference compound
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