Fig. 4: Phosphatase activity of [L2Zn3]6+. | Nature Communications

Fig. 4: Phosphatase activity of [L2Zn3]6+.

From: Self-assembly of an anion receptor with metal-dependent kinase inhibition and potent in vitro anti-cancer properties

Fig. 4

31P NMR spectra using different substrates including PhOPO32− (spectra ad), serine phosphate (spectra eh), threonine phosphate (spectra il) and tyrosine phosphate (spectra mp). Specific details for each 31P NMR spectra are as follows: Spectra a, e, i and m represent substrate alone (44 h incubated @ 37 °C); Spectra b, f, j and n represents [L2Zn3]6+ plus substrate (t = 0 min); Spectra c, g, k and o represents [L2Zn3]6+ plus substrate incubated @ 37 °C for 19 h; Spectra d, h, l and p represents [L2Zn3]6+ plus substrate incubated @ 37 °C for 44 h. The 31P NMR of [L2Zn3(PO4)]3+ gives a signal at 8.6 ppm. The doubling up of some of the 31P signals in [L2Zn3(PO4)]3+ (h, p and l) is attributed to formation of a mixture of diastereoisomers between the racemic cryptand and the resolved chiral amino acids which will form an ion-pair ([L2Zn3(PO4)](RCH(NH2)CO2)2+) and does not occur with the achiral phenyl phosphate. 31P NMR spectra of the phosphate esters are 1H-coupled (a, e, i and m) and the remainder are 1H-decoupled.

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