| Literature DB >> 26678273 |
Ui Joung Youn1, Joo Yun Lee2, Yun-Seo Kil1, Ah-Reum Han1, Chong Hak Chae2, Shi Yong Ryu2, Eun-Kyoung Seo3.
Abstract
Three new minor pyrrole alkaloids, 3-[2-formyl-5-(hydroxymethyl)-1H-pyrrol-1-yl]pentanedioic acid (1), (2R)-[2-formyl-5-(hydroxymethyl)-1H-pyrrol-1-yl]-1-methoxy-1-oxobutanoic acid (2), and methyl (2R)-[2-formyl-5-(methoxymethyl)-1H-pyrrol-1-yl]-4-methylpentanoate (3) were isolated from the fruits of Lycium chinense Miller (Solanaceae), along with the known compound, methyl (2R)-[2-formyl-5-(methoxymethyl)-1H-pyrrol-1-yl]-3-(phenyl)propanoate (4). The structures of 1-4 were elucidated by analysis of their 1D- and 2D-NMR and HRMS data. The absolute configurations of 2-4, possessing a stereogenic center in each structure, were determined by comparison of their experimental electronic circular dichroism (ECD) with those of calculated ECD values.Entities:
Keywords: Absolute configuration; ECD; Lycium chinense; Pyrrole alkaloid; Solanaceae
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Year: 2015 PMID: 26678273 DOI: 10.1007/s12272-015-0695-3
Source DB: PubMed Journal: Arch Pharm Res ISSN: 0253-6269 Impact factor: 4.946