1986
DOI: 10.1039/p19860000033
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Erythrina studies. Part 2. Structures of three novel prenylated antibacterial flavanones, sigmoidins A–C, from Erythrina sigmoidea Hua

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Cited by 52 publications
(34 citation statements)
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“…Compounds 4 to 15 (Figure ) were known compounds and identified as α,α′‐dihydro‐3,5,4′‐trihydroxy‐4,3′‐diisopentenylstilbene ( 4 ) (Biondi et al., ), α,α′‐dihydro‐3,5,3′,4′‐tetrahydroxy‐2,5′‐diisopentenylstilbene ( 5 ) (Ye et al., ), 6‐prenyleriodictyol ( 6 ) (Bohlmannet al., ), 5′‐prenyleriodictyol ( 7 ) (Jia, Ma, & Wang, ), 6‐prenylquercetin‐ 3‐Me ether ( 8 ) (Harborne, Greenham, Williams, Eagles, & Markham, ), 5′‐prenylquercetin ( 9 ) (Jia et al., ), 6‐prenylquercetin ( 10 ) (Jia et al., ), 6‐prenylnaringenin ( 11 ) (Komatsu, Yokoe, & Shirataki, ), 3′‐prenylnaringenin ( 12 ) (Nkengfack, Sanson, Tempesta, & Fomum, ), sigmoidin C ( 13 ) (Fomum et al., ), 8‐[(E)‐3‐hydroxymethyl‐2‐butenyl]‐eriodictyol ( 14 ) (Hayashi et al., ), and quercetin‐3‐Me ether ( 15 ) (Guinot et al., ) by comparison of their spectral data with those reported…”
Section: Resultsmentioning
confidence: 99%
“…Compounds 4 to 15 (Figure ) were known compounds and identified as α,α′‐dihydro‐3,5,4′‐trihydroxy‐4,3′‐diisopentenylstilbene ( 4 ) (Biondi et al., ), α,α′‐dihydro‐3,5,3′,4′‐tetrahydroxy‐2,5′‐diisopentenylstilbene ( 5 ) (Ye et al., ), 6‐prenyleriodictyol ( 6 ) (Bohlmannet al., ), 5′‐prenyleriodictyol ( 7 ) (Jia, Ma, & Wang, ), 6‐prenylquercetin‐ 3‐Me ether ( 8 ) (Harborne, Greenham, Williams, Eagles, & Markham, ), 5′‐prenylquercetin ( 9 ) (Jia et al., ), 6‐prenylquercetin ( 10 ) (Jia et al., ), 6‐prenylnaringenin ( 11 ) (Komatsu, Yokoe, & Shirataki, ), 3′‐prenylnaringenin ( 12 ) (Nkengfack, Sanson, Tempesta, & Fomum, ), sigmoidin C ( 13 ) (Fomum et al., ), 8‐[(E)‐3‐hydroxymethyl‐2‐butenyl]‐eriodictyol ( 14 ) (Hayashi et al., ), and quercetin‐3‐Me ether ( 15 ) (Guinot et al., ) by comparison of their spectral data with those reported…”
Section: Resultsmentioning
confidence: 99%
“…As a continuation of a study on the neutral components of the genus Erythrim (1)(2)(3)(4)(5)(6)(7)(8), we now report the isolation and structural elucidation of the novel lupin;f0lia. The spectral data for 1 compares very favorably with that of amoradin, amoradicin, and amoradinin, three prenylated flavanones from A m e b a fruitzcosa ( I I) of similar structure.…”
Section: Tanee Fomum*j Foyere Ayafor Andjean Wandjimentioning
confidence: 97%
“…Les activites les plus frequemment repertoriees concernent des proprietes protectrices contre des attaques d'insectes (Lincoln, 1980 ;Lincoln et Walla, 1986 ;Roussis et at., 1987), fongiques (Maillard et al, 1989 ;Tahara et al, 1984Tahara et al, , 1994 ou microbiennes (Fukui et al, 1988 ;Fomum et at., 1986 ). Ces proprietes sont Ia traduction d'une certaine toxicite de ces composes.…”
Section: -Variation Structurale Et Repartition Botanique Des Flayonounclassified