872346-84-4

Upstream product

• 100-39-0 benzyl bromide 

Downstream Products

• 1354551-61-3 C₃₅H₄₇N₃O₆ 
• 1354551-62-4 C₃₅H₄₅N₃O₅ 
• 1354551-67-9 C₄₂H₅₃N₃O₈S 
• 1354551-68-0 C₃₅H₄₆N₆O₅ 
• 1354551-63-5 C₅₃H₇₄N₁₀O₈S 
• 1354551-64-6 (3S,4S)-3-(Boc-D-Chg-O)-4-methyloctanoic acid 
• 1354551-66-8 [(3S,4S)-3-(Boc-D-Chg-O)-4-methyloctanoyl]-L-Dph-D-Ser-OBn 
• 1354551-71-5 [(3S,4S)-3-(Boc-D-Chg-O)-4-methyloctanoyl]-L-Dph-D-Ser-OH 
• 1354551-70-4 benzyl (3S,4S)-3-(Boc-D-Chg-O)-4-methyloctanoate 
• 872346-89-9 benzyl (3S,4S)-3-[(2R,3S)-2-tert-butoxycarbonylamino-3-methylpentanoyloxy]-4-methyloctanoate 

Relevant academic research and scientific papers

Absolute stereochemistry of fungal beauveriolide III and ACAT inhibitory activity of four stereoisomers

(Chemical Equation Presented) Fungal beauveriolide III (BeauIII, 1b), a cyclodepsipeptide inhibiting acyl-CoA:cholesterol acyltransferase (ACAT) and showing antiatherogenic activity in mouse models, consists of L-Phe, L-Ala, D-allo-Ile, and 3-hydroxy-4-me