(2R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(((benzyloxy)(hydroxy)phosphoryl)oxy)phenyl)propanoic acid

95%

  • Product Code: 229307
  CAS:    1926163-10-1
Molecular Weight: 573.53 g./mol Molecular Formula: C₃₁H₂₈NO₈P
EC Number: MDL Number: MFCD06657919
Melting Point: Boiling Point:
Density: 1.378±0.06 g/cm3(Predicted) Storage Condition: 2-8°C, sealed, dry
Product Description: Widely used in solid-phase peptide synthesis, this compound serves as a protected amino acid derivative for incorporating phosphotyrosine mimics into peptides. Its main application lies in the preparation of biologically active peptides that require phosphorylated tyrosine residues for function, such as substrates or inhibitors of protein tyrosine kinases and phosphatases. The phospho group is protected with a benzyloxy group, allowing for selective deprotection under mild conditions, while the Fmoc group enables orthogonal protection strategies in stepwise peptide assembly. It is especially valuable in research related to signal transduction pathways, drug discovery, and the study of post-translational modifications in proteins.
Sizes / Availability / Pricing:
Size Availability Price Quantity
0.100 10-20 days ฿8,250.00
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0.250 10-20 days ฿14,000.00
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1.000 10-20 days ฿37,790.00
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(2R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(((benzyloxy)(hydroxy)phosphoryl)oxy)phenyl)propanoic acid
Widely used in solid-phase peptide synthesis, this compound serves as a protected amino acid derivative for incorporating phosphotyrosine mimics into peptides. Its main application lies in the preparation of biologically active peptides that require phosphorylated tyrosine residues for function, such as substrates or inhibitors of protein tyrosine kinases and phosphatases. The phospho group is protected with a benzyloxy group, allowing for selective deprotection under mild conditions, while the Fmoc group enables orthogonal protection strategies in stepwise peptide assembly. It is especially valuable in research related to signal transduction pathways, drug discovery, and the study of post-translational modifications in proteins.
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