268565-29-3

Upstream product

• 268565-26-0 N-tert-butoxycarbonyl-γ-methylleucyl-((R)-3-undecyl-β-alanine) methyl ester 
• 268565-21-5 (R)-3-((R)-1-Phenyl-ethylamino)-tetradecanoic acid methyl ester 
• 268565-23-7 (R)-3-undecyl-β-alanine methyl ester 
• 112695-98-4 N-(tert-butoxycarbonyl)-L-tert-leucine 
• 22104-73-0 tetradec-2-enoic acid methyl ester 
• 112-54-9 Dodecanal 
• 32769-95-2 Boc-Gly-L-Lys(Z) 

Relevant academic research and scientific papers

Synthesis and antifungal activity of rhodopeptin analogues. 1. Modification of the east and south amino acid moieties

(equation presented) East Amino Acid n=8, 10 South Amino Acid Synthetic Rhodopeptin Analogs Structure - activity relationships of the east and south amino acid modified analogues of rhodopeptins, novel antifungal cyclic tetrapeptides isolated from Rhodococcus species Mer-N1033, have been investigated. It was observed that a basic amino acid moiety (lysine or ornithine) as the east amino acid and a hydrophobic and bulky neutral amino acid (i.e., γ-methylleucine) as the south amino acid were indispensable structure motifs for antifungal activity of rhodopeptin analogues.