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Download COA here: Semax COA.pdf
Please note if you have a different Batch ID please contact us for the latest COA.
Semax
The mechanism of action of Semax is unknown.[2][3] It might interact with certain melanocortin receptors or inhibit enkephalinase enzymes.[2][3] Chemically, Semax is a peptide and a synthetic analogue of a fragment of adrenocorticotropic hormone (ACTH).[4][5]
Though the exact mechanism of action of Semax is unclear, there is evidence that it may act through melanocortin receptors. Specifically, there is a report of Semax competitively antagonizing the action of the melanocortin receptor full agonist α-melanocyte-stimulating hormone (α-MSH) at the MC4 and MC5 receptors in both in vitro and in vivo experimental conditions, indicating that it may act as an antagonist or partial agonist of these receptors.[2] Semax did not antagonize α-MSH at the MC3receptor, though this receptor could still be a target of the drug.[2] As for the MC1 and MC2 receptors, they were not assayed.[2]In addition to actions at receptors, Semax, as well as a related peptide drug, Selank, have been found to inhibit enzymesinvolved in the degradation of enkephalins and other endogenous regulatory peptides (IC50 = 10 μM), though the clinical significance of this property is uncertain.[3]
As of November 2023, there are no published clinical trials involving Semax outside of Russia and post-Soviet states.[7]
References
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Voronina TA (2023). “Cognitive Impairment and Nootropic Drugs: Mechanism of Action and Spectrum of Effects”. Neurochemical Journal. 17 (2): 180–188. doi:10.1134/S1819712423020198. ISSN 1819-7124.
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Bertolini A (March 2012). “Drug-induced activation of the nervous control of inflammation: a novel possibility for the treatment of hypoxic damage”. European Journal of Pharmacology. 679 (1–3): 1–8. doi:10.1016/j.ejphar.2012.01.004. PMID 22293371.
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Kost NV, Sokolov OI, Gabaeva MV, Grivennikov IA, Andreeva LA, Miasoedov NF, et al. (2001). “Semax and selank inhibit the enkephalin-degrading enzymes from human serum”. Bioorganicheskaia Khimiia (in Russian). 27 (3): 180–183. doi:10.1023/A:1011373002885. PMID 11443939. S2CID 26029820.
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Deigin VI, Poluektova EA, Beniashvili AG, Kozin SA, Poluektov YM (March 2022). “Development of Peptide Biopharmaceuticals in Russia”. Pharmaceutics. 14 (4): 716. doi:10.3390/pharmaceutics14040716. PMC 9030433. PMID 35456550.
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Potaman VN, Alfeeva LY, Kamensky AA, Levitzkaya NG, Nezavibatko VN (April 1991). “N-terminal degradation of ACTH(4-10) and its synthetic analog semax by the rat blood enzymes”. Biochemical and Biophysical Research Communications. 176 (2): 741–746. doi:10.1016/S0006-291X(05)80247-5. PMID 1851003.
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“Home”. AdisInsight. Retrieved 3 September 2024.
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“Semax – Search Results – PubMed”. PubMed. Retrieved 2023-11-12.
Keywords: Semax.
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