2014
DOI: 10.1016/j.phytol.2014.05.007
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Secundarellone A, B, and C from the leaves of Justicia secunda VAHL

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Cited by 10 publications
(11 citation statements)
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“…13,[16][17][18] Phytochemical screening of the plant has shown the presences of tannins, flavonoids, alkaloids, quinines and anthocyanins. 19 Luteolin, aurantamide acetate, auranamide, quindoline and pyrrolidone derivatives; secundarellone A, B and C have been isolated from J. secunda. [19][20][21] Notwithstanding the popular uses of J. secunda in folkloric medicine only few pharmacological studies have been done on the plant.…”
Section: Introductionmentioning
confidence: 99%
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“…13,[16][17][18] Phytochemical screening of the plant has shown the presences of tannins, flavonoids, alkaloids, quinines and anthocyanins. 19 Luteolin, aurantamide acetate, auranamide, quindoline and pyrrolidone derivatives; secundarellone A, B and C have been isolated from J. secunda. [19][20][21] Notwithstanding the popular uses of J. secunda in folkloric medicine only few pharmacological studies have been done on the plant.…”
Section: Introductionmentioning
confidence: 99%
“…19 Luteolin, aurantamide acetate, auranamide, quindoline and pyrrolidone derivatives; secundarellone A, B and C have been isolated from J. secunda. [19][20][21] Notwithstanding the popular uses of J. secunda in folkloric medicine only few pharmacological studies have been done on the plant. 22 This study investigated the antioxidant, anti-inflammatory, and antinociceptive effects of J. secunda leaf methanolic extract (J. secunda).…”
Section: Introductionmentioning
confidence: 99%
“…Compound 2 could be identified via HPLC and ESI‐MS n analyses as the diastereomeric mixture of the pyrrolidones secundarellone B and C (Fig. ), according to our previous studies for J. secunda (Theiler et al , ). HPLC comparison (including UV‐DAD and ELSD) of compound 2 and the previously isolated secundarellone B and C revealed the identical retention time (minute 9 corresponding to about 9.5% acetonitrile) on a LiChrospher® 100 RP‐18e column (250 mm × 4 mm, 5 μm) and identical UV spectra.…”
Section: Resultsmentioning
confidence: 95%
“…In the present article, we report on the HPTLC bioautography guided detection of the α-glucosidase inhibiting potential of J. secunda resulting in the isolation of two active diastereomeric mixtures from the methanol extract of the leaves. Compound 1 was new and structurally elucidated as 2-caffeoyloxy-4-hydroxy-glutaric acid, compound 2 was identified as the mixture of the diastereomers secundarellone B and C, published in our previous studies for J. secunda (Theiler et al, 2014).…”
Section: Introductionmentioning
confidence: 93%
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