Ethers can again be classified into two varieties: if the alkyl or aryl groups are the same on both sides of the oxygen atom, 73724-45-5, formula is C18H17NO5, Name is Fmoc-Ser-OH. Then it is a simple or symmetrical ether, whereas if they are different, the ethers are called mixed or unsymmetrical ethers. Category: ethers-buliding-blocks.
Kruse, Thomas;Hansen, Jakob Lerche;Dahl, Kirsten;Schaffer, Lauge;Sensfuss, Ulrich;Poulsen, Christian;Schlein, Morten;Hansen, Ann Maria Kruse;Jeppesen, Claus Bekker;Dornonville de la Cour, Charlotta;Clausen, Trine Ryberg;Johansson, Eva;Fulle, Simone;Skyggebjerg, Rikke Bjerring;Raun, Kirsten research published ã?Development of Cagrilintide, a Long-Acting Amylin Analogueã? the research content is summarized as follows. A hallmark of the pancreatic hormone amylin is its high propensity toward the formation of amyloid fibrils, which makes it a challenging drug design effort. The amylin analog pramlintide is com. available for diabetes treatment as an adjunct to insulin therapy but requires three daily injections due to its short half-life. We report here the development of the stable, lipidated long-acting amylin analog cagrilintide (23) and some of the structure-activity efforts that led to the selection of this analog for clin. development with obesity as an indication. Cagrilintide is currently in clin. trial and has induced significant weight loss when dosed alone or in combination with the GLP-1 analog semaglutide.
Category: ethers-buliding-blocks, 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