The chemical substance known as N~5~-(diaminomethylidene)-L-ornithyl-L-prolyl-(4R)-4-hydroxy-L-prolylglycyl-L-phenylalanyl-L-seryl-L-phenylalanyl-N-{4-[(diaminomethylidene)amino]-1-(trifluoroacetyl)butyl}-L-phenylalaninamide, with the CAS number 117201-47-5, is a complex peptide derivative characterized by its intricate structure comprising multiple amino acid residues. This compound features a combination of L-ornithine, L-proline, L-phenylalanine, and L-serine, which contribute to its biological activity and potential therapeutic applications. The presence of diaminomethylidene groups suggests enhanced reactivity and potential interactions with biological targets. Additionally, the trifluoroacetyl group may influence the compound's solubility and stability. Such peptides are often investigated for their roles in biological processes, including signaling pathways and enzyme regulation. The specific stereochemistry, particularly the (4R) configuration, is crucial for the compound's biological function and interaction with receptors or enzymes. Overall, this substance represents a class of bioactive peptides that may have implications in medicinal chemistry and drug development.

N~5~-(diaminomethylidene)-L-ornithyl-L-prolyl-(4R)-4-hydroxy-L-prolylglycyl-L-phenylalanyl-L-seryl-L-phenylalanyl-N-{4-[(diaminomethylidene)amino]-1-(trifluoroacetyl)butyl}-L-phenylalaninamide

117201-47-5: The chemical substance known as N~5~-(diaminomethylidene)-L-ornithyl-L-prolyl-(4R)-4-hydroxy-L-prolylglycyl-L-phenylalanyl-L-seryl-L-phenylalanyl-N-{4-[(diaminomethylidene)amino]-1-(trifluoroacetyl)butyl}-L-phenylalaninamide, with the CAS number 117201-47-5, is a complex peptide derivative characterized by its intricate structure comprising multiple amino acid residues. This compound features a combination of L-ornithine, L-proline, L-phenylalanine, and L-serine, which contribute to its biological activity and potential therapeutic applications. The presence of diaminomethylidene groups suggests enhanced reactivity and potential interactions with biological targets. Additionally, the trifluoroacetyl group may influence the compound's solubility and stability. Such peptides are often investigated for their roles in biological processes, including signaling pathways and enzyme regulation. The specific stereochemistry, particularly the (4R) configuration, is crucial for the compound's biological function and interaction with receptors or enzymes. Overall, this substance represents a class of bioactive peptides that may have implications in medicinal chemistry and drug development.

CAS 117201-47-5

N~5~-(diaminomethylidene)-L-ornithyl-L-prolyl-(4R)-4-hydroxy-L-prolylglycyl-L-phenylalanyl-L-seryl-L-phenylalanyl-N-{4-[(diaminomethylidene)amino]-1-(trifluoroacetyl)butyl}-L-phenylalaninamide

B-3852

Ref: TM-T71334