Fmoc-Tyr(tBu)-Thr(psiMe,Mepro)-OH

98%

  • Product Code: 96124
  CAS:    920519-31-9
Molecular Weight: 600.70 g./mol Molecular Formula: C₃₅H₄₀N₂O₇
EC Number: MDL Number: MFCD08064321
Melting Point: Boiling Point: 796.2±60.0 °C(Predicted)
Density: 1.217±0.06 g/cm3(Predicted) Storage Condition: 2-8°C, dry
Product Description: This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methodologies. The Fmoc group serves as a protecting group for the amine functionality, ensuring selective deprotection during the synthesis process. The tert-butyl (tBu) group protects the hydroxyl group of tyrosine, while the psiMe and Mepro modifications on threonine enhance stability and control stereochemistry during peptide chain assembly. This compound is valuable in the production of complex peptides and peptidomimetics, often employed in pharmaceutical research for developing therapeutic agents, enzyme inhibitors, or bioactive peptides. Its application is crucial in constructing peptides with specific structural and functional properties, aiding in drug discovery and biochemical studies.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿2,187.00
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Fmoc-Tyr(tBu)-Thr(psiMe,Mepro)-OH
This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methodologies. The Fmoc group serves as a protecting group for the amine functionality, ensuring selective deprotection during the synthesis process. The tert-butyl (tBu) group protects the hydroxyl group of tyrosine, while the psiMe and Mepro modifications on threonine enhance stability and control stereochemistry during peptide chain assembly. This compound is valuable in the production of complex peptides and peptidomimetics, often employed in pharmaceutical research for developing therapeutic agents, enzyme inhibitors, or bioactive peptides. Its application is crucial in constructing peptides with specific structural and functional properties, aiding in drug discovery and biochemical studies.
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