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| Product Name: | Fmoc-D-Pro-L-Pro-OH | CAS No: | NA |
|---|---|---|---|
| M.W: | 434.5 | Appearance: | White Powder |
| HPLC: | 98% | Storage: | Room Temp |
| Highlight: | Fmoc-D-Pro-L-Pro-OH HPLC impurity,Fmoc amino acid research reagent,Fmoc-AA impurity 98% purity |
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| Name | Fmoc-D-Pro-L-Pro-OH |
|---|---|
| CAS NO | NA |
| Molecular Weight | 434.5 |
| Appearance | White Powder |
| HPLC Purity | 98%+ |
| Synonyms | Fmoc-D-Pro-L-Pro-OH |
Used as a dipeptide building block in Fmoc-based solid-phase peptide synthesis
Enables the direct incorporation of a D/L-configured Pro–Pro motif, reducing racemization risk and coupling inefficiencies associated with stepwise amino acid addition
Commonly applied to:
Construction of proline-rich peptides
Improvement of synthetic efficiency and sequence fidelity
Proline exhibits strong conformational constraints due to its cyclic structure
The D-Pro–L-Pro motif is widely employed to:
Induce β-turn or β-hairpin structures
Stabilize defined secondary structures
Plays a critical role in structural biology and structure–activity relationship (SAR) studies
Commonly used in:
Cyclic peptide synthesis
Conformational locking of peptide-based drug candidates
Contributes to:
Enhanced metabolic stability
Improved binding selectivity toward biological targets
Proline-rich motifs are frequently found at protein–protein interaction interfaces
The D-Pro–L-Pro unit can:
Mimic native turn structures
Serve as a structural element in the design of PPI-inhibitory peptides or peptidomimetics
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