Fmoc-β-(2-quinolyl)-Ala-OH
98%
- Product Code: 188264
CAS:
214852-56-9
| Molecular Weight: | 438.48 g./mol | Molecular Formula: | C₂₇H₂₂N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318745 | |
| Melting Point: | Boiling Point: | 685.5±55.0 °C(Predicted) | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Used in peptide synthesis as a protected amino acid building block, particularly in the development of bioactive peptides and pharmaceutical research. The Fmoc group allows for solid-phase synthesis through base-labile protection, enabling stepwise assembly of peptide chains. The quinoline moiety introduces structural rigidity and can enhance interactions with biological targets, making this compound valuable in the design of enzyme inhibitors or receptor ligands. Its aromatic side chain also aids in spectroscopic monitoring during synthesis due to UV absorbance. Commonly applied in medicinal chemistry for creating peptide-based drug candidates and studying structure-activity relationships.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | ฿3,380.00 |
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| 100mg | 10-20 days | ฿4,450.00 |
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| 250mg | 10-20 days | ฿9,080.00 |
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Fmoc-β-(2-quinolyl)-Ala-OH
Used in peptide synthesis as a protected amino acid building block, particularly in the development of bioactive peptides and pharmaceutical research. The Fmoc group allows for solid-phase synthesis through base-labile protection, enabling stepwise assembly of peptide chains. The quinoline moiety introduces structural rigidity and can enhance interactions with biological targets, making this compound valuable in the design of enzyme inhibitors or receptor ligands. Its aromatic side chain also aids in spectroscopic monitoring during synthesis due to UV absorbance. Commonly applied in medicinal chemistry for creating peptide-based drug candidates and studying structure-activity relationships.
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