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| Product Name: | Fmoc-L-Pro-D-Pro-OH | CAS No: | NA |
|---|---|---|---|
| M.W: | 434.5 | Appearance: | White Powder |
| HPLC: | 98% | Storage: | Room Temp |
| Highlight: | Fmoc-L-Pro-D-Pro-OH HPLC impurity,Fmoc-AA impurity research chemical,Fmoc amino acid with 98% purity |
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| Name | Fmoc-L-Pro-D-Pro-OH |
|---|---|
| CAS NO | NA |
| Molecular Weight | 434.5 |
| Appearance | White Powder |
| HPLC Purity | 98%+ |
| Synonyms | Fmoc-L-Pro-D-Pro-OH |
Used as a dipeptide building block in Fmoc-based solid-phase peptide synthesis
Enables direct incorporation of an L/D-configured Pro–Pro motif, minimizing racemization and coupling inefficiencies associated with stepwise amino acid assembly
Particularly useful for:
Proline-rich peptide sequences
Improving synthetic efficiency and sequence accuracy
Proline imposes strong conformational rigidity due to its cyclic pyrrolidine ring
The L-Pro–D-Pro motif is known to:
Promote specific turn geometries, often distinct from D-Pro–L-Pro
Modulate backbone dihedral angles and local folding patterns
Widely applied in peptide folding studies and conformation–function investigations
Employed in:
Cyclic peptide synthesis
Conformationally constrained peptidomimetics
Benefits include:
Improved proteolytic resistance
Enhanced structural definition and target selectivity
Proline-rich motifs frequently participate in protein–protein interaction interfaces
The L-Pro–D-Pro dipeptide can:
Mimic non-canonical turn structures
Serve as a scaffold element in the design of PPI modulators or inhibitory peptides
Used as a model unit to study:
The influence of proline stereochemistry on peptide folding
Structural differences between L/D vs D/L Pro-Pro motifs
Valuable in collagen-mimetic and proline-rich peptide research
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