Fmoc-Pro-Pro-Pro-Pro-Pro-OH, with the CAS number 454693-94-8, is a synthetic peptide that features a sequence of proline (Pro) residues capped with a fluorenylmethyloxycarbonyl (Fmoc) protecting group. The Fmoc group is commonly used in peptide synthesis to protect the amino group of the first amino acid, allowing for selective coupling reactions. The presence of multiple proline residues in the sequence can impart unique structural characteristics, such as increased rigidity and the potential to form specific secondary structures, like turns or loops, which are important in peptide and protein folding. Proline is known for its ability to disrupt alpha-helices and promote beta-turns due to its cyclic structure. The hydroxyl (OH) group at the end of the peptide indicates that it is in its free acid form, which can influence its solubility and reactivity. Overall, Fmoc-Pro-Pro-Pro-Pro-Pro-OH is significant in peptide synthesis and research, particularly in studies related to protein structure and function.

Fmoc-Pro-Pro-Pro-Pro-Pro-Oh

454693-94-8: Fmoc-Pro-Pro-Pro-Pro-Pro-OH, with the CAS number 454693-94-8, is a synthetic peptide that features a sequence of proline (Pro) residues capped with a fluorenylmethyloxycarbonyl (Fmoc) protecting group. The Fmoc group is commonly used in peptide synthesis to protect the amino group of the first amino acid, allowing for selective coupling reactions. The presence of multiple proline residues in the sequence can impart unique structural characteristics, such as increased rigidity and the potential to form specific secondary structures, like turns or loops, which are important in peptide and protein folding. Proline is known for its ability to disrupt alpha-helices and promote beta-turns due to its cyclic structure. The hydroxyl (OH) group at the end of the peptide indicates that it is in its free acid form, which can influence its solubility and reactivity. Overall, Fmoc-Pro-Pro-Pro-Pro-Pro-OH is significant in peptide synthesis and research, particularly in studies related to protein structure and function.

Fmoc-pentaproline, Fmoc-PPPPP, potential building block for polyproline-based chiral stationary phases.

Fmoc-Pro-Pro-Pro-Pro-Pro-OH

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CAS 454693-94-8

Fmoc-Pro-Pro-Pro-Pro-Pro-Oh

Fmoc-Pro-Pro-Pro-Pro-Pro-OH

Ref: 01-4041053

Fmoc-Pro-Pro-Pro-Pro-Pro-OH

Ref: 3D-FF111345