Fmoc-D-Tyr(3-I)-OH
95%
- Product Code: 37423
CAS:
244028-70-4
| Molecular Weight: | 529.3238 g./mol | Molecular Formula: | C₂₄H₂₀INO₅ |
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| EC Number: | MDL Number: | MFCD03840398 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
Fmoc-D-Tyr(3-I)-OH is primarily used in peptide synthesis as a building block for creating custom peptides. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise construction of peptide chains. The iodine substitution on the tyrosine residue enhances the peptide's stability and can be utilized in further chemical modifications, such as radioiodination for imaging or therapeutic purposes. This compound is particularly valuable in research involving peptide-based drug development, where specific modifications are required to achieve desired biological activity or targeting properties. Its application extends to studying protein-protein interactions, enzyme activity, and receptor binding, making it a versatile tool in biochemistry and pharmaceutical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,600.00 |
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Fmoc-D-Tyr(3-I)-OH
Fmoc-D-Tyr(3-I)-OH is primarily used in peptide synthesis as a building block for creating custom peptides. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise construction of peptide chains. The iodine substitution on the tyrosine residue enhances the peptide's stability and can be utilized in further chemical modifications, such as radioiodination for imaging or therapeutic purposes. This compound is particularly valuable in research involving peptide-based drug development, where specific modifications are required to achieve desired biological activity or targeting properties. Its application extends to studying protein-protein interactions, enzyme activity, and receptor binding, making it a versatile tool in biochemistry and pharmaceutical research.
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