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Home  > N1-(D-phenylalanyl-D-phenylalanyl-D-leucyl-D-lysyl)-4-amino-4-piperidinecarboxylic acid acetate

BA36022

1024829-44-4 | N1-(D-phenylalanyl-D-phenylalanyl-D-leucyl-D-lysyl)-4-amino-4-piperidinecarboxylic acid acetate

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Description
Catalog Number: BA36022
Chemical Name: N1-(D-phenylalanyl-D-phenylalanyl-D-leucyl-D-lysyl)-4-amino-4-piperidinecarboxylic acid acetate
CAS Number: 1024829-44-4
Molecular Formula: C38H57N7O8
Molecular Weight: 739.9013
SMILES: CC(=O)O.NCCCC[C@H](C(=O)N1CCC(CC1)(N)C(=O)O)NC(=O)[C@H](NC(=O)[C@H](NC(=O)[C@@H](Cc1ccccc1)N)Cc1ccccc1)CC(C)C

 

Upstream Synthesis Route
  • N1-(D-phenylalanyl-D-phenylalanyl-D-leucyl-D-lysyl)-4-amino-4-piperidinecarboxylic acid acetate has found widespread application in chemical synthesis as a crucial building block in peptide synthesis. This compound serves as a key component for designing and constructing complex peptide structures due to its specific sequence of amino acids and unique piperidinecarboxylic acid moiety. Its controlled coupling and deprotection properties make it an essential tool in the creation of custom peptides with high purity and precision. Researchers and chemists utilize this compound to develop peptides for various applications in drug discovery, biochemical research, and therapeutic interventions. Its role in chemical synthesis showcases its importance as a foundational element in peptide chemistry and molecular design strategies.
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