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doi: 10.1097/WOX.0b013e3182439613 40 BouayedJBohnT
doi: 10.1038/s41424-018-0058-8 146
administration of Selank, Noopept, and Semax resulted in 15, 63, and 95% increase in the number of glycine binding sites in BALB/c mice, respectively, while in C57Bl/6 mice all three peptides were not effective
It received the first approval as a drug for palliative care in late stage breast cancer in 1982
