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Erlotinib was first approved by the Food and Drug Administration on November 18, 2004, as a monotherapy for patients with locally advanced or metastatic non-small cell lung cancer (NSCLC)
Selank is a synthetic heptapeptide derived from tuftsin (Thr-Lys-Pro-Arg) with a stabilizing Gly-Pro C-terminal sequence
10.1038/s41467-021-26066-5 138 PhamM
Lyophilized for stability Research-grade compound Laboratory research only Independently verified by Freedom Diagnostics via HPLC and mass spec
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