201296-82-4

Upstream product

• 56-87-1 L-lysine 
• 65055-19-8 2,3-bis(acetyloxy)benzoyl chloride 

Downstream Products

• 439152-22-4 1-benzyl N-[N^2',N^6'-bis(2,3-diacetoxybenzoyl)-L-lysyl]-L-glutamate 
• 452303-69-4 (S)-4-(Benzoyloxy-methyl-carbamoyl)-2-[(S)-2,6-bis-(2,3-diacetoxy-benzoylamino)-hexanoylamino]-butyric acid benzyl ester 
• 439152-24-6 N-[N^2',N^6'-bis(2,3-diacetoxybenzoyl)-L-lysyl]-L-glutamic acid 5-(N-benzyloxy-N-methyl)amide 
• 439152-29-1 N²-[4-(N-benzyloxy-N-cyclohexylcarbamoyl)-n-butanoyl]-N⁶-[N^2',N^6'-bis(2,3-diacetoxybenzoyl)-L-lysyl]-L-lysine 
• 439152-26-8 N-[N^2',N^6'-bis(2,3-diacetoxybenzoyl)-L-lysyl]-L-glutamic acid 5-(N-benzyloxy-N-cyclohexyl)amide 
• 439152-28-0 N-[4-(N-benzyloxy-N-methylcarbamoyl)-n-butanoyl]-N⁶-[N^2',N^6'-bis(2,3-diacetoxybenzoyl)-L-lysyl]-L-lysine 

Relevant academic research and scientific papers

New synthetic siderophores and their β-lactam conjugates based on diamino acids and dipeptides

Linking of siderophores to antibiotics improves the penetration and therefore increases the antibacterial activity of the antibiotics. We synthesized the acylated catecholates and hydroxamates as siderophore components for antibiotic conjugates to reduce