The chemical substance with the name "L-Prolinamide, N-acetyl-L-phenylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanylglycyl-L-leucyl-2-methylalanyl-2-methylalanyl-(4R)-4-hydroxy-L-prolyl-L-glutaminyl-2-methylalanyl-(4R)-4-hydroxy-L-prolyl-2-methylalanyl-N-[(1S)-1-(hydroxymet" and CAS number 280774-64-3 is a complex peptide derivative. It features multiple amino acid residues, including proline, phenylalanine, leucine, and glutamine, which contribute to its structural and functional properties. The presence of N-acetyl and hydroxyl groups suggests potential roles in biological activity, possibly influencing solubility and reactivity. The compound's intricate structure may indicate its involvement in specific biochemical pathways or interactions, making it of interest in pharmaceutical and biochemical research. However, due to its complexity, detailed studies would be necessary to fully elucidate its properties, including stability, reactivity, and potential applications in drug development or therapeutic contexts.

L-Prolinamide,N-acetyl-L-phenylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanylglycyl-L-leucyl-2-methylalanyl-2-methylalanyl-(4R)-4-hydroxy-L-prolyl-L-glutaminyl-2-methylalanyl-(4R)-4-hydroxy-L-prolyl-2-methylalanyl-N-[(1S)-1-(hydroxymet

280774-64-3: The chemical substance with the name "L-Prolinamide, N-acetyl-L-phenylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanylglycyl-L-leucyl-2-methylalanyl-2-methylalanyl-(4R)-4-hydroxy-L-prolyl-L-glutaminyl-2-methylalanyl-(4R)-4-hydroxy-L-prolyl-2-methylalanyl-N-[(1S)-1-(hydroxymet" and CAS number 280774-64-3 is a complex peptide derivative. It features multiple amino acid residues, including proline, phenylalanine, leucine, and glutamine, which contribute to its structural and functional properties. The presence of N-acetyl and hydroxyl groups suggests potential roles in biological activity, possibly influencing solubility and reactivity. The compound's intricate structure may indicate its involvement in specific biochemical pathways or interactions, making it of interest in pharmaceutical and biochemical research. However, due to its complexity, detailed studies would be necessary to fully elucidate its properties, including stability, reactivity, and potential applications in drug development or therapeutic contexts.

<p>Cephaibol D is identified in the Acremonium tubaKii DSM 12774 strain and exhibits mild antibacterial activity.</p>

CAS 280774-64-3

L-Prolinamide,N-acetyl-L-phenylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanylglycyl-L-leucyl-2-methylalanyl-2-methylalanyl-(4R)-4-hydroxy-L-prolyl-L-glutaminyl-2-methylalanyl-(4R)-4-hydroxy-L-prolyl-2-methylalanyl-N-[(1S)-1-(hydroxymet

Cephaibol D

Ref: TM-TN10115