10399-86-7

Upstream product

• 530-26-7 D-Mannose 
• 62-53-3 aniline 

Downstream Products

• 913057-30-4 N-(2,3,4,6-tetra-O-acetyl-α,β-D-mannopyranosyl)aniline 
• 1629138-92-6 1-(β-D-mannopyranosyl)-3,3-diphenylindolin-2-one 
• 1629138-93-7 1-(β-D-mannopyranosyl)-3,3-bis(4-methylphenyl)indolin-2-one 
• 1629138-94-8 1-(β-D-mannopyranosyl)-3,3-bis(4-methoxyphenyl)indolin-2-one 
• 1629138-95-9 1-(β-D-mannopyranosyl)-3,3-bis[4-(dimethylamino)phenyl]indolin-2-one 
• 1629138-80-2 1-(2,3,4,6-tetra-O-acetyl-β-D-mannopyranosyl)-3,3-diphenylindolin-2-one 
• 1629138-81-3 1-(2,3,4,6-tetra-O-acetyl-β-D-mannopyranosyl)-3,3-bis(4-methylphenyl)indolin-2-one 
• 1629138-82-4 1-(2,3,4,6-tetra-O-acetyl-β-D-mannopyranosyl)-3,3-bis(4-methoxyphenyl)indolin-2-one 
• 1629138-83-5 1-(2,3,4,6-tetra-O-acetyl-β-D-mannopyranosyl)-3,3-bis[4-(dimethylamino)phenyl]indolin-2-one 
• 1150659-78-1 ethyl [(5-hydrxymethylfuran-2-yl)(phenylamino)methyl]phenylphosphinate 
• 1150659-80-5 phenyl [(5-hydroxymethylfuran-2-yl)(phenylamino)methyl]phenylphosphinate 

Relevant academic research and scientific papers

Synthesis of thia-analogous indirubin n-glycosides and their influence onmelanoma cell growth and apoptosis

Stopping cancer in its tracks Thia-analogues of indirubin-N-glycosides, prepared by condensation of N-glycosylisatines with thiaindane-3-one and subsequent deprotection, were tested for their activity against malignant melanoma cells. These indirubin-N-gl

Synthesis and bioactivity of N-glycosylated 3-(2-oxo-2-arylethylidene)-indolin-2-ones

N-Glycosyl-3-alkylideneoxindoles, N-glycosylated 3-(2-oxo-2-arylethylidene)indolin-2-ones, were prepared by reaction of isatin-N-glycosides with substituted acetophenones. The biological activities of these new compounds revealed significant antitumor act

Synthesis and antiproliferative activity of N-glycosyl-3,3-diaryloxindoles

N-Glycosylated 3,3-diaryloxindoles were prepared by Lewis acid catalyzed reaction of acetylated N-glycosylisatins with various benzene derivatives and subsequent deprotection. Some of the products showed antiproliferative activity against malignant cutane

Synthesis of N,N′-diglycosylated isoindigos

The first N,N′-diglycosylated isoindigos were prepared by P(NEt 2)3-mediated dimerization of acetyl protected N-glycosyl-5-alkylisatins. Subsequent deacetylation yielded the corresponding deprotected N,N′-diglycosylated isoindigos. I

First synthesis of indirubin N-glycosides (red sugars)

The first indirubin N-glycosides were prepared by reaction of isatine N-glycosides with indoxyl acetate under basic conditions.