(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid
95%
- Product Code: 57127
CAS:
84030-19-3
| Molecular Weight: | 467.52 g./mol | Molecular Formula: | C₂₈H₂₅N₃O₄ |
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| EC Number: | MDL Number: | MFCD00038537 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, dry, sealed |
Product Description:
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide chain elongation. The benzyl-protected imidazole moiety allows for the incorporation of histidine-like structures into peptides, which is valuable for studying enzyme active sites, protein-protein interactions, and designing bioactive peptides. Its application is crucial in pharmaceutical research, where it aids in the development of peptide-based drugs, including antimicrobial agents, hormone analogs, and enzyme inhibitors. Additionally, it is used in biochemical studies to investigate the role of histidine residues in protein function and stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿900.00 |
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| 1.000 | 10-20 days | ฿2,340.00 |
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| 5.000 | 10-20 days | ฿8,190.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during peptide chain elongation. The benzyl-protected imidazole moiety allows for the incorporation of histidine-like structures into peptides, which is valuable for studying enzyme active sites, protein-protein interactions, and designing bioactive peptides. Its application is crucial in pharmaceutical research, where it aids in the development of peptide-based drugs, including antimicrobial agents, hormone analogs, and enzyme inhibitors. Additionally, it is used in biochemical studies to investigate the role of histidine residues in protein function and stability.
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