Fmoc-HoCit-OH
97%
- Product Code: 51118
CAS:
201485-17-8
Molecular Weight: | 411.45 g./mol | Molecular Formula: | C₂₂H₂₅N₃O₅ |
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EC Number: | MDL Number: | MFCD00237387 | |
Melting Point: | Boiling Point: | 676°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
Fmoc-HoCit-OH is widely used in peptide synthesis as a building block for introducing hydroxycitrulline residues into peptides. It is particularly valuable in the study of post-translational modifications, especially in the context of citrullination, which plays a role in autoimmune diseases like rheumatoid arthritis. The Fmoc protecting group ensures selective deprotection during solid-phase peptide synthesis, allowing for the precise construction of complex peptide sequences. Additionally, it is employed in the development of peptide-based drugs and biomaterials, where the incorporation of hydroxycitrulline can influence peptide stability, solubility, and biological activity. Its application extends to research in protein-protein interactions and the design of enzyme inhibitors.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿810.00 |
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1.000 | 10-20 days | ฿2,052.00 |
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5.000 | 10-20 days | ฿7,353.00 |
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10.000 | 10-20 days | ฿11,943.00 |
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Fmoc-HoCit-OH
Fmoc-HoCit-OH is widely used in peptide synthesis as a building block for introducing hydroxycitrulline residues into peptides. It is particularly valuable in the study of post-translational modifications, especially in the context of citrullination, which plays a role in autoimmune diseases like rheumatoid arthritis. The Fmoc protecting group ensures selective deprotection during solid-phase peptide synthesis, allowing for the precise construction of complex peptide sequences. Additionally, it is employed in the development of peptide-based drugs and biomaterials, where the incorporation of hydroxycitrulline can influence peptide stability, solubility, and biological activity. Its application extends to research in protein-protein interactions and the design of enzyme inhibitors.
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