Category: 73724-45-5

Adams, Gregory L. team published research on Journal of Medicinal Chemistry in 2022 | 73724-45-5

Product Details of 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.

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. Product Details of C18H17NO5.

Adams, Gregory L.;Pall, Parul S.;Grauer, Steven M.;Zhou, Xiaoping;Ballard, Jeanine E.;Vavrek, Marissa;Kraus, Richard L.;Morissette, Pierre;Li, Nianyu;Colarusso, Stefania;Bianchi, Elisabetta;Palani, Anandan;Klein, Rebecca;John, Christopher T.;Wang, Deping;Tudor, Matthew;Nolting, Andrew F.;Biba, Mirlinda;Nowak, Timothy;Makarov, Alexey A.;Reibarkh, Mikhail;Buevich, Alexei V.;Zhong, Wendy;Regalado, Erik L.;Wang, Xiao;Gao, Qi;Shahripour, Aurash;Zhu, Yuping;de Simone, Daniele;Frattarelli, Tommaso;Pasquini, Nicolo’ Maria;Magotti, Paola;Iaccarino, Roberto;Li, Yuxing;Solly, Kelli;Lee, Keun-Joong;Wang, Weixun;Chen, Feifei;Zeng, Haoyu;Wang, Jixin;Regan, Hilary;Amin, Rupesh P.;Regan, Christopher P.;Burgey, Christopher S.;Henze, Darrell A.;Sun, Chengzao;Tellers, David M. research published 《 Development of ProTx-II analogs as highly selective peptide blockers of Nav1.7 for the treatment of pain》, the research content is summarized as follows. Inhibitor cystine knot peptides, derived from venom, have evolved to block ion channel function but are often toxic when dosed at pharmacol. relevant levels in vivo. The article describes the design of analogs of ProTx-II that safely display systemic in vivo blocking of Nav1.7, resulting in a latency of response to thermal stimuli in rodents. The new designs achieve a better in vivo profile by improving ion channel selectivity and limiting the ability of the peptides to cause mast cell degranulation. The design rationale, structural modeling, in vitro profiles, and rat tail flick outcomes are disclosed and discussed.

Product Details of 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