859147-54-9

Basic information

• Product Name: N-1-[(1R,4S)-4-{(monomethoxytrityl)oxymethyl}cyclopent-2-en-1-yl]-2',3'-O-isopropylideneadenosine
• Synonyms: N-1-[(1R,4S)-4-{(monomethoxytrityl)oxymethyl}cyclopent-2-en-1-yl]-2',3'-O-isopropylideneadenosine
• CAS NO: 859147-54-9
• Molecular Weight: 675.784
• Mol File: 859147-54-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-1-[(1R,4S)-4-{(monomethoxytrityl)oxymethyl}cyclopent-2-en-1-yl]-2',3'-O-isopropylideneadenosine(CAS DataBase Reference)
• NIST Chemistry Reference: N-1-[(1R,4S)-4-{(monomethoxytrityl)oxymethyl}cyclopent-2-en-1-yl]-2',3'-O-isopropylideneadenosine(859147-54-9)
• EPA Substance Registry System: N-1-[(1R,4S)-4-{(monomethoxytrityl)oxymethyl}cyclopent-2-en-1-yl]-2',3'-O-isopropylideneadenosine(859147-54-9)

Safety Data

• Hazardous Substances Data: 859147-54-9(Hazardous Substances Data)

Upstream product

• 151792-53-9 tert-butyl (1R,4S)-(-)-3-oxo-2-azabicyclo[2.2.1]hept-5-ene-2-carboxylate 
• 168960-18-7 (1R,4S)-N-(tert-Butyloxycarbonyl)-1-amino-4-(hydroxymethyl)-2-cyclopentene 
• 79200-56-9 (-)-2-azabicyclo[2.2.1]hept-5-en-3-one 
• 368870-20-6 5-[(methoxymethylene)amino]-1-[5-O-(tert-butyldimethylsilyl)-2,3-O-(isopropylidene)-β-D-ribofuranosyl]imidazole-4-nitrile 
• 136522-35-5 (1R,4S)-1-amino-4-hydroxymethyl-2-cyclopentene 
• 859147-52-7 N-1-[(1R,4S)-4-{(monomethoxytrityl)oxymethyl}cyclopent-2-en-1-yl]-5',O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine 
• 859147-50-5 N-1-{(1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl}-5'-O-tert-butyldimethylsilyl-2',3'-O-isopropylideneadenosine 

Downstream Products

• 859147-58-3 N-1-{(1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl}-5,-O-{bis(phenylthio)phosphoryl}-2',3'-O-isopropylideneadenosine 
• 859147-56-1 N-1-[(1R,4S)-4-{(monomethoxytrityl)oxymethyl}cyclopent-2-en-1-yl]-5'-O-{bis(phenylthio)phosphoryl}-2',3'-O-isopropylideneadenosine 

Relevant articles and documents

Synthesis of stable and cell-type selective analogues of cyclic ADP-ribose, a Ca2+-mobilizing second messenger. Structure-activity relationship of the N1-ribose moiety

We previously developed cyclic ADP-carbocyclic ribose (cADPcR, 2) as a stable mimic of cyclic ADP-ribose (cADPR, 1), a Ca2+-mobilizing second messenger. A series of the N1-ribose modified cADPcR analogues, designed as novel stable mimics of cAD