(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-methyl-3H-diazirin-3-yl)propanoic acid
98%
- Product Code: 232534
CAS:
1360651-24-6
| Molecular Weight: | 365.38 g./mol | Molecular Formula: | C₂H₁₉N₃O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31380715 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.41±0.1 g/cm3(Predicted) | Storage Condition: | -20°C, Inert Gas |
Product Description:
Used primarily as a photoactivatable amino acid analog in biochemical and proteomic research. Enables covalent crosslinking of interacting proteins upon UV irradiation due to the reactive diazirine group, which generates highly reactive carbenes. The Fmoc group allows for solid-phase peptide synthesis, making it suitable for incorporation into peptides. Commonly applied in photoaffinity labeling studies to identify and characterize transient or weak protein-ligand and protein-protein interactions. Its stereochemistry supports natural peptide backbone compatibility, enhancing its utility in studying biologically relevant systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿28,770.00 |
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| 0.250 | 10-20 days | ฿48,900.00 |
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| 1.000 | 10-20 days | ฿132,000.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-methyl-3H-diazirin-3-yl)propanoic acid
Used primarily as a photoactivatable amino acid analog in biochemical and proteomic research. Enables covalent crosslinking of interacting proteins upon UV irradiation due to the reactive diazirine group, which generates highly reactive carbenes. The Fmoc group allows for solid-phase peptide synthesis, making it suitable for incorporation into peptides. Commonly applied in photoaffinity labeling studies to identify and characterize transient or weak protein-ligand and protein-protein interactions. Its stereochemistry supports natural peptide backbone compatibility, enhancing its utility in studying biologically relevant systems.
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