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A mixture-design method was used as a multivariate data analysis tool to investigate properties of gallate glasses in the GaO3/2 GeO2 NaO1/2 system.
The bulky hydrophobic portions of gallate derivatives were considered to interact with tyrosinase's hydrophobic protein bulk surrounding the binuclear copper active site and thus gallate derivatives exerted the anti-tyrosinase effect (Tanford [1980]).
The difference spectrum between inked and ink-free areas of unaged specimens (curve D1 in Fig. 8a) reveals the presence of ink along with its possible interactions with peaks at 1606 cm−1 (assigned to the aromatic absorbance of gallate and contributions from water [24]) and 1436 cm−1 (assigned to the symmetric stretch of iron (III)—gallate coordination complex [29, 32, 34]).
Ngo et al. [ 109] evaluated the antioxidant effect of gallate chitooligosaccharides in mouse macrophage RAW264.7 cells.
Differently, the content of gallate monomers and oligomers did not seem to be correlated to antifungal activity (r = − 0.4334, P = 0.1065).
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The reason for the formation of gallates and transport systems into cell vacuoles specifically accumulating these compounds remains unknown, as well as the processes for polymerisation of flavan 3-ol units.
The main GTP components were 99.25% pure, with 46.5% of epigallocatechin-3-gallate (EGCG), 21.25% of epigallocatechin (ECG), 10% of epicatechin (EC), 7.5% of epicatechin-3-gallate (EGC), 9.5% of gallocatechin gallate (GCG), and 4.5% of catechin.
Each GTP capsule contained 250 mg GTP ingredient [46.5% of epigallocatechin-3-gallate (EGCG), 21.25% of epigallocatechin (ECG), 10% of epicatechin (EC), 7.5% of epicatechin-3-gallate (EGC), 9.5% of gallocatechin gallate (GCG), and 4.5% of catechin] and the purity was higher than 98.5%.
Adachi, S. et al. The inhibitory effect of -epigallocatechin gallate on activation of the epidermal growth factor receptor is associated with altered lipid order in HT29 colon cancer cells.
Validation of the presence of ethyl gallate in A. nilotica (L).
He, Z. et al. Fyn is a novel target of -epigallocatechin gallate in the inhibition of JB6 cell cell transformation.
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