N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-phenyl-L-serine features an O-phenyl ether that modifies polarity and steric influence. The structure supports investigation of aromatic substitutions on peptide folding and hydrogen bonding. Researchers use it to tune linker flexibility and side-chain interactions. Its Fmoc protection allows seamless peptide integration.
CAT No: R2116
CAS No:1401662-77-8
Synonyms/Alias:N-Fmoc-O-phenyl-L-serine;1401662-77-8;N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-phenyl-L-serine;Fmoc-L-Ser(O-phenyl)-OH;(2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-phenoxypropanoic acid;MFCD32263663;CS-0120521;F81089;(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenoxypropanoic acid;
2. Adipose tissue is a key organ for the beneficial effects of GLP-2 metabolic function
3. Autoinhibition and phosphorylation-induced activation of phospholipase C-γ isozymes
4. Adipose tissue is a key organ for the beneficial effects of GLP-2 metabolic function
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