| Literature DB >> 27083799 |
Ziling Zhang1, Fansheng Kong2, Hui Ni3, Zhixian Mo4, Jian-Bo Wan5, Dehong Hua2, Chunyan Yan6.
Abstract
To explore the chemicals responsible for the health benefits of guava, water-soluble polysaccharides were extracted including GP90 and P90. They exhibited excellent α-glucosidase inhibition activity with an EC50 of 2.27μg/mL and 0.18mg/mL. This suggests that their activities were 1379- and 17-fold higher than the positive control. The DPPH scavenging activities of GP90 was even higher than Vc at some concentrations. Upon further isolation, a novel polysaccharide termed GB90-1B was obtained. Monosaccharide analysis, methylation analysis, and NMR were used to analyze the structural characterization of GB90-1B. Structural analysis revealed that its backbone consisted of (1→5)-linked-α-l-arabinose, (1→2,3,5)-linked-α-l-arabinose and (1→3)-linked-α-l-arabinose. Branch linkages included (1→6)-linked-α-d-glucose, (1→)-linked-α-d-glucose and (1→)-linked-α-l-arabinose. The structure of the repeating unit of GP90-1B was predicted.Entities:
Keywords: 1,1-diphenyl-2-picrylhydrazyl (PubChem CID:2735032); 1-phenyl-3-methyl-5-pyrazolone (PubChem CID:70335); 4-nitrophenyl-α-d-glucopyranoside (PubChem CID: 259380); Butanol (PubChem CID: 263); Chloroform (PubChem CID: 6212); DPPH scavenging activity; Dimethyl sulfoxide (PubChem CID: 679); Ethanol (PubChem CID: 702); Guava; Polysaccharides; Psidium guajava Linn.; Sodium chloride (PubChem CID: 5234); Sodium hydroxide (PubChem CID:14798); Structure; Trifluoroacetic acid (PubChem CID: 6422); α-Glucosidase inhibition activity
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Year: 2016 PMID: 27083799 DOI: 10.1016/j.carbpol.2016.02.030
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381