397884-07-0

Basic information

• Product Name: methyl (Z)-2-[6'-(6-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)-amino)-hexanamide)-β-D-galactopyranosyloxy]-3-p-hydroxyphenyl-acrylate
• CAS NO: 397884-07-0
• Molecular Weight: 631.596
• Mol File: 397884-07-0.mol

Chemical Properties

• CAS DataBase Reference: methyl (Z)-2-[6'-(6-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)-amino)-hexanamide)-β-D-galactopyranosyloxy]-3-p-hydroxyphenyl-acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (Z)-2-[6'-(6-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)-amino)-hexanamide)-β-D-galactopyranosyloxy]-3-p-hydroxyphenyl-acrylate(397884-07-0)
• EPA Substance Registry System: methyl (Z)-2-[6'-(6-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)-amino)-hexanamide)-β-D-galactopyranosyloxy]-3-p-hydroxyphenyl-acrylate(397884-07-0)

Safety Data

• Hazardous Substances Data: 397884-07-0(Hazardous Substances Data)

Upstream product

• 295797-74-9 methyl (Z)-2-(6'-azido-β-D-galactopyranosyloxy)-3-p-hydroxyphenylacrylate 
• 287934-39-8 (Z)-2-((2S,3R,4S,5R,6R)-6-Aminomethyl-3,4,5-trihydroxy-tetrahydro-pyran-2-yloxy)-3-(4-hydroxy-phenyl)-acrylic acid methyl ester 

Relevant articles and documents

Direct observation of the target cell for leaf-movement factor using novel fluorescence-labeled probe compounds: Fluorescence studies of nyctinasty in legumes. Part 1

We synthesized fluorescence-labeled probe compounds bearing AMCA (1), NBD (2), and dansyl (3) groups as the fluorescent functionality. In these probe compounds, NBD-type probe, 2, showed leaf-opening activity at 5×10-6 M. The bioactivity of 2 is one-fifth as strong as that of the natural product, potassium isolespedezate (6). We carried out the binding experiment using 1 in a plant body.

Fluorescence study on the nyctinasty of Cassia mimosoides L. using novel fluorescence-labeled probe compounds

We synthesized fluorescence-labeled probe compounds bearing 6-((7-amino-4-methylcoumarin-3-acetyl)amino)-hexanoyl (AMCA, 1), 6-N-(7-nitrobenz-2-oxa-1, 3-diazol-4-yl)-aminohexanoyl (NBD, 2), and 6-(4-((5-dimethylaminonaphthalene-1-sulfonyl)-amino))-hexanoyl (dansyl, 3) groups as the fluorescent functionality. In these probe compounds, NBD-type probe, 2, showed leaf-opening activity at 5×10-6 M. The bioactivity of 2 is one-fifth as strong as that of the natural product, potassium isolespedezate (6). We carried out the binding experiment using 1 in a plant body. Then, it was suggested that fluorescence-labeled probe compound directly bound to a motor cell in pulvina of Cassia mimosoides. And this binding was specific to C. mimosoides. Probe compounds cannot bind plant sections of other nyctinastic plants.