27136-83-0

Upstream product

• 73-34-7 L-rhamnose 
• 62-53-3 aniline 

Downstream Products

• 913057-17-7 Acetic acid (3R,4R,5S,6S)-4,5-diacetoxy-6-methyl-2-phenylamino-tetrahydro-pyran-3-yl ester 
• 1629138-75-5 1-(2,3,4-tri-O-acetyl-β-L-rhamnopyranosyl)-3,3-diphenylindolin-2-one 
• 1629138-87-9 3,3-diphenyl-1-(β-L-rhamnopyranosyl)indolin-2-one 
• 1629138-88-0 3,3-bis(4-methylphenyl)-1-(β-L-rhamnopyranosyl)indolin-2-one 
• 1629138-89-1 3,3-bis(4-methoxyphenyl)-1-(β-L-rhamnopyranosyl)indolin-2-one 
• 1629138-90-4 3,3-bis[4-(dimethylamino)phenyl]-1-(β-L-rhamnopyranosyl)indolin-2-one 
• 1629138-76-6 1-(2,3,4-tri-O-acetyl-β-L-rhamnopyranosyl)-3,3-bis(4-methylphenyl)indolin-2-one 
• 1629138-77-7 1-(2,3,4-tri-O-acetyl-β-L-rhamnopyranosyl)-3,3-bis(4-methoxyphenyl)indolin-2-one 
• 1629138-78-8 1-(2,3,4-tri-O-acetyl-β-L-rhamnopyranosyl)-3,3-bis[4-(dimethylamino)phenyl]indolin-2-one 

Relevant academic research and scientific papers

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

Synthesis and antiproliferative activity of selenoindirubins and selenoindirubin-N-glycosides

Selenoindirubins and selenoindirubin-N-glycosides were prepared by the reaction of isatins and isatin-N-glycosides with 3-acetoxy-benzo[b]selenophene, respectively. While selenoindirubin-N-glycosides have not been reported before, three non-glycosylated s

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

First synthesis of oxa-analogous isoindigo-N-glycosides

Lactone-analogues of isoindigo-N-glycosides were prepared by condensation of N-glycosylisatines with 2-coumaranone and subsequent deprotection.

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.