Ethers do have nonbonding electron pairs on their oxygen atoms, 73724-45-5, formula is C18H17NO5, Name is Fmoc-Ser-OH. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds. Formula: C18H17NO5.
Pacifico, Salvatore;Albanese, Valentina;Illuminati, Davide;Marzola, Erika;Fabbri, Martina;Ferrari, Federica;Holanda, Victor A. D.;Sturaro, Chiara;Malfacini, Davide;Ruzza, Chiara;Trapella, Claudio;Preti, Delia;Lo Cascio, Ettore;Arcovito, Alessandro;Della Longa, Stefano;Marangoni, Martina;Fattori, Davide;Nassini, Romina;Calo, Girolamo;Guerrini, Remo research published 《 Novel mixed NOP/opioid receptor peptide agonists》, the research content is summarized as follows. The nociceptin/orphanin FQ (N/OFQ)/N/OFQ receptor (NOP) system controls different biol. functions including pain and cough reflex. Mixed NOP/opioid receptor agonists elicit similar effects to strong opioids but with reduced side effects. In this work, 31 peptides with the general sequence [Tyr/Dmt1,Xaa5]N/OFQ(1-13)-NH2 were synthesized and pharmacol. characterized for their action at human recombinant NOP/opioid receptors. The best results in terms of NOP vs. mu opioid receptor potency were obtained by substituting both Tyr1 and Thr5 at the N-terminal portion of N/OFQ(1-13)-NH2 with the noncanonical amino acid Dmt. [Dmt1,5]N/OFQ(1-13)-NH2 has been identified as the most potent dual NOP/mu receptor peptide agonist so far described. Exptl. data have been complemented by in silico studies to shed light on the mol. mechanisms by which the peptide binds the active form of the mu receptor. Finally, the compound exerted antitussive effects in an in vivo model of cough.
Formula: C18H17NO5, Fmoc-Ser-OH, also known as Fmoc-Ser-OH, is a useful research compound. Its molecular formula is C18H17NO5 and its molecular weight is 327.3 g/mol. The purity is usually 95%.
Fmoc-L-Ser-OH is a synthetic peptide that belongs to the group of glycopeptides. It is used as a model for such compounds and has been shown to have antimicrobial activity in vitro against gram-positive bacteria, especially Staphylococcus epidermidis. This compound was synthesized from 3-mercaptopropionic acid and chloride in the presence of hydroxyl groups and epidermal growth factor. The synthetic pathway can be divided into three steps: (1) condensation of 3-mercaptopropionic acid with hydrochloric acid to yield 3-mercaptoacrylic acid; (2) esterification of 3-mercaptoacrylic acid with glycine to form Fmoc-L-Ser; and (3) deprotection of Fmoc protecting group., 73724-45-5.
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem