694528-13-7

Upstream product

• 694527-99-6 N-((2R,3R)-3-[Boc-L-allo-Thr(TBS)-GlyO]-2-methylnonanoyl)-N-Et-L-Leu-L-allo-Ile-L-Ser(Bn)-OAllyl 
• 742062-95-9 (S)-3-Benzyloxy-2-{(2S,3R)-2-[(S)-2-({(2R,3R)-3-[2-((2S,3S)-2-tert-butoxycarbonylamino-3-hydroxy-butyrylamino)-acetoxy]-2-methyl-nonanoyl}-ethyl-amino)-4-methyl-pentanoylamino]-3-methyl-pentanoylamino}-propionic acid 
• 694527-85-0 N-((2R,3R)-3-hydroxy-2-methylnonanoyl)-N-Et-L-Leu-L-allo-Ile-L-Ser(Bn)-OAllyl 
• 694527-73-6 (S)-3-Benzyloxy-2-{(2S,3R)-2-[(S)-2-(tert-butoxycarbonyl-ethyl-amino)-4-methyl-pentanoylamino]-3-methyl-pentanoylamino}-propionic acid allyl ester 
• 694527-74-7 (S)-3-Benzyloxy-2-[(2S,3R)-2-((S)-2-ethylamino-4-methyl-pentanoylamino)-3-methyl-pentanoylamino]-propionic acid allyl ester 
• 308279-67-6 (S)-3-Benzyloxy-2-((2S,3R)-2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-propionic acid allyl ester 
• 13139-16-7 Boc-L-aIle-OH 

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