140629-84-1

Upstream product

• 237075-27-3 (5S,6R)-6-[(E)-4-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-but-1-enyl]-2,2-dimethyl-8-triethylsilanyloxy-1,3-dioxa-spiro[4.5]dec-7-ene 
• 237075-36-4 Benzoic acid (5S,6S,7S,8R)-6-[(E)-4-(tert-butyl-dimethyl-silanyloxy)-1-methyl-but-1-enyl]-7-methoxy-2,2-dimethyl-1,3-dioxa-spiro[4.5]dec-8-yl ester 
• 237075-29-5 (5S,6S,7S,8R)-6-[(E)-4-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-but-1-enyl]-7-methoxy-2,2-dimethyl-1,3-dioxa-spiro[4.5]decan-8-ol 
• 237075-28-4 (5S,6S,7S)-6-[(E)-4-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-but-1-enyl]-7-hydroxy-2,2-dimethyl-1,3-dioxa-spiro[4.5]decan-8-one 
• 237075-30-8 Benzoic acid (1R,2S,3S,4S)-4-hydroxy-4-hydroxymethyl-3-((E)-4-hydroxy-1-methyl-but-1-enyl)-2-methoxy-cyclohexyl ester 
• 237075-35-3 (5S,6S,7S)-6-[(E)-4-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-but-1-enyl]-7-methoxy-2,2-dimethyl-1,3-dioxa-spiro[4.5]decan-8-one 
• 237075-32-0 Benzoic acid (3R,4S,5S,6R)-4-[(2R,3R)-3-(2-hydroxy-ethyl)-2-methyl-oxiranyl]-5-methoxy-1-oxa-spiro[2.5]oct-6-yl ester 
• 237075-31-9 Benzoic acid (3R,4S,5S,6R)-4-((E)-4-hydroxy-1-methyl-but-1-enyl)-5-methoxy-1-oxa-spiro[2.5]oct-6-yl ester 
• 237075-23-9 2,2-dimethyl-4-(3-methylbut-3-enyl)[1,3]dioxolane 
• 237075-22-8 (S)-2,2-Dimethyl-1,3-dioxa-spiro[4.5]dec-6-en-8-one 
• 237075-24-0 2,2,7-trimethyl-1,3-dioxaspiro[4,4]non-6-ene 
• 16666-80-1 triphenylphosphonio-1-methylethanide 
• 98-88-4 benzoyl chloride 
• 35903-52-7 fumagillol 

Relevant academic research and scientific papers

Chemical modification of fumagillin. I. 6-O-Acyl, 6-O-sulfonyl, 6-O-alkyl, and 6-O-(N-substituted-carbamoyl)fumagillols

The hydroxy group of fumagillol (3), a degradation product of fumagillin (1), was acylated, sulfonylated, alkylated or carbamoylated, and the anti-angiogenic activity of the resulting products was examined. These compounds inhibited the angiogenesis induced by basic fibroblast growth factor in the rat corneal micropocket assay and the growth of vascular endothelial cells in vitro. Among them, compound 2 (AGM-1470) was found to show the most potent inhibitory effect on the growth of vascular endothelial cells and was selected from this series as a candidate for further development.