694527-95-2

Upstream product

• 308279-70-1 N-methyl-L-leucine-L-allo-isoleucine-O-benzyl-L-serine allyl ester 
• 90281-99-5 N-tert-butyloxycarbonyl-L-aminobutyrylglycine benzyl ester 
• 34306-42-8 Boc-Abu 
• 308279-65-4 (+)-(2R,3R)-3-hydroxy-2-methylnonanoic acid 
• 308279-71-2 (S)-3-Benzyloxy-2-((2S,3R)-2-{(S)-2-[((2R,3R)-3-hydroxy-2-methyl-nonanoyl)-methyl-amino]-4-methyl-pentanoylamino}-3-methyl-pentanoylamino)-propionic acid allyl ester 
• 656252-75-4 Boc-L-Abu-Gly-OH 

Downstream Products

• 742064-32-0 (S)-2-{(2S,3R)-2-[(S)-2-({(2R,3R)-3-[2-((S)-2-Amino-butyrylamino)-acetoxy]-2-methyl-nonanoyl}-methyl-amino)-4-methyl-pentanoylamino]-3-methyl-pentanoylamino}-3-benzyloxy-propionic acid 
• 694528-10-4 22-deoxy-24-O-benzyl-globomycin 

Relevant academic research and scientific papers

Structure-activity relationships of globomycin analogues as antibiotics

Globomycin (1a), a signal peptidase II inhibitor, and its derivatives show potent antibacterial activity against Gram-negative bacteria. The synthesis and antimicrobial activity of novel globomycin analogues are reported. The hydroxyl group in the L-Ser r

Synthesis and antimicrobial activity of novel globomycin analogues

Globomycin, a signal peptidase II inhibitor, and its derivatives show potent antibacterial activity against Gram-negative bacteria. The synthesis and antimicrobial activity of novel globomycin analogues are reported. One of the analogues showed a more pot