848757-31-3

Upstream product

• 168170-58-9 (3’R,5’R-dibenzoyloxy-6’S-methyl-(2H)-tetrahydropyran-2-yloxy)-1-(2,2,2-trichloroacetimide) 
• 129234-94-2 (S)-2-hydroxy-7-octene 
• 168393-80-4 (2S,3R,5R)-5-(benzoyloxy)-6-hydroxy-2-methyloxan-3-yl benzoate 
• 211695-55-5 (R)-(-)-7-octen-2-ol 

Downstream Products

• 1451476-68-8 (2S,3R,5R,6R)-2-methyl-6-(((R)-7-oxooctan-2-yl)oxy)tetrahydro-2H-pyran-3,5-diyl dibenzoate 
• 1352061-35-8 (E)-1-[(5R)-5-(3,6-dideoxy-α-L-arabino-hexopyranosyloxy)hexyl]-3-phenyl-2-propen-1-one 
• 1451475-99-2 (2R,3R,5R,6S)-2-(((R)-9-methoxy-9-oxonon-7-en-2-yl)oxy)-6-methyltetrahydro-2H-pyran-3,5-diyl dibenzoate 
• 1451476-11-1 (2R,3R,5R,6S)-2-(((R)-9-methoxy-9-oxononan-2-yl)oxy)-6-methyltetrahydro-2H-pyran-3,5-diyl dibenzoate 
• 1258282-26-6 (2R)-hept-7-ol-2-yl 2,4-di-O-benzyl-3,6-dideoxy-α-L-arabino-hexopyranoside 

Relevant academic research and scientific papers

Synthesis of daumone derivatives and their antiangiogenic activities on chorioallantoic membrane

Daumone, a dauer-inducing pheromone and a series of lipid derivatives were synthesized from daumone to investigate structure-activity trends. Lipid derivatives demonstrated potent in vivo antiangiogenic activity on the chorioallantoic membrane, which exce

Ascaroside activity in Caenorhabditis elegans is highly dependent on chemical structure

The nematode Caenorhabditis elegans secretes ascarosides, structurally diverse derivatives of the 3,6-dideoxysugar ascarylose, and uses them in chemical communication. At high population densities, specific ascarosides, which are together known as the dau

6R-(3,6-DIDEOXY-L-ARABINO-HEXOPYRANOSYLOXY)HEPTANOIC ACID, PREPARATION PROCESS FOR THE SAME AND DAUER EFFECT THEREOF

The present invention relates to a determination of a stereochemistry, a synthesis and dauer effect of 6R-(3,6-dideoxy-L-arabino-hexopyranosyloxy) heptanoic acid as a pheromone isolated from the Caenorhabditis elegance related to suppress of aging and