A novel O-heteroside, (3RS,4RS)-3,4-dihydroxy-4-(2-hydroxy-5-acetylphenyl)-2-[(beta-O-glucopyranosyl)methyl]-but-1-ene (1), named nauplathizine, and a previously known compound, acetophenone-4-O-glucoside (2), were isolated from the antibacterial acetone extract of the aerial parts of Nauplius aquaticus (L) (Asteraceae, Inulae). The structure of 1 was established via its acetylated derivative by means of spectroscopic and chemical data.
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http://dx.doi.org/10.1080/14786410412331302127 | DOI Listing |
Nat Prod Res
July 2005
Laboratoire de Chimie des Substances Naturelles et de Synthèse Organique, Faculté des Sciences de Monastir, 5000 Monastir, Tunisia.
A novel O-heteroside, (3RS,4RS)-3,4-dihydroxy-4-(2-hydroxy-5-acetylphenyl)-2-[(beta-O-glucopyranosyl)methyl]-but-1-ene (1), named nauplathizine, and a previously known compound, acetophenone-4-O-glucoside (2), were isolated from the antibacterial acetone extract of the aerial parts of Nauplius aquaticus (L) (Asteraceae, Inulae). The structure of 1 was established via its acetylated derivative by means of spectroscopic and chemical data.
View Article and Find Full Text PDFNat Prod Lett
March 2002
Laboratoire de Chimie des Substances Naturelles et de Synthèse Organique, Faculté des Sciences de Monastir, Tunisia.
The aerial part of Nauplius aquaticus afforded a new sesquiterpene lactone with a humulanolide skeleton, 6,7,9,10-tetrahydroasteriscunolide (1), in addition to the known asteriscunolides A (2) and D (3). Their structures were established principally by two-dimensional NMR spectroscopy.
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