Unknown

Dataset Information

0

Combined MS/MS-NMR Annotation Guided Discovery of Iris lactea var. chinensis Seed as a Source of Viral Neuraminidase Inhibitory Polyphenols.


ABSTRACT: In this study, the chemical diversity of polyphenols in Iris lactea var. chinensis seeds was identified by combined MS/MS-NMR analysis. Based on the annotated chemical profile, the isolation of stilbene oligomers was conducted, and consequently, stilbene oligomers (1-10) were characterized. Of these, compounds 1 and 2 are previously undescribed stilbene dimer glycoside (1) and tetramer glycoside (2), respectively. Besides, to evaluate this plant seed as a rich source of stilbene oligomers, we quantified three stilbene oligomers of I. lactea var. chinensis seeds. The contents of three major stilbene oligomers-trans-ε-viniferin (3), vitisin A (6), and vitisin B (9)-in I. lactea var. chinensis seeds were quantified as 2.32 (3), 4.95 (6), and 1.64 (9) mg/g dry weight (DW). All the isolated compounds were tested for their inhibitory activities against influenza neuraminidase. Compound 10 was found to be active with the half maximal inhibitory concentration (IC50) values at 4.76 μM. Taken together, it is concluded that I. lactea var. chinensis seed is a valuable source of stilbene oligomers with a human health benefit.

SUBMITTER: Kim HW 

PROVIDER: S-EPMC7435927 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Combined MS/MS-NMR Annotation Guided Discovery of <i>Iris lactea</i> var. <i>chinensis</i> Seed as a Source of Viral Neuraminidase Inhibitory Polyphenols.

Kim Hyun Woo HW   Kim Soo Sung SS   Kang Kyo Bin KB   Ryu Byeol B   Park Eunjin E   Huh Jungmoo J   Jeon Won Kyung WK   Chae Hee-Sung HS   Oh Won Keun WK   Kim Jinwoong J   Sung Sang Hyun SH   Chin Young-Won YW  

Molecules (Basel, Switzerland) 20200726 15


In this study, the chemical diversity of polyphenols in <i>Iris lactea</i> var<i>. chinensis</i> seeds was identified by combined MS/MS-NMR analysis. Based on the annotated chemical profile, the isolation of stilbene oligomers was conducted, and consequently, stilbene oligomers (<b>1</b>-<b>10</b>) were characterized. Of these, compounds <b>1</b> and <b>2</b> are previously undescribed stilbene dimer glycoside (<b>1</b>) and tetramer glycoside (<b>2</b>), respectively. Besides, to evaluate this  ...[more]

Similar Datasets

| PRJNA697945 | ENA
| S-EPMC8081313 | biostudies-literature
| PRJNA345119 | ENA
| S-EPMC8002972 | biostudies-literature
| S-EPMC8069374 | biostudies-literature
| S-EPMC9667474 | biostudies-literature
| S-EPMC9827652 | biostudies-literature
| S-EPMC4058273 | biostudies-literature
| S-EPMC9959467 | biostudies-literature
| PRJNA714717 | ENA