2009
DOI: 10.1002/mrc.2546
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Structural determination of abutilins A and B, new flavonoids from Abutilon pakistanicum, by 1D and 2D NMR spectroscopy

Abstract: Two new flavonoids, abutilin A and B, were isolated from the chloroform soluble fraction of Abutilon pakistanicum and their structures assigned from (1)H and (13)C NMR spectra, DEPT and by 2D COSY, HMQC and HMBC experiments. Ferulic acid (3), (E)-cinnamic acid (4), 5-hydroxy-4',6,7,8-tetramethoxyflavone (5), kaempferol (6), luteolin (7) and luteolin 7-O-beta-D-glucopyranoside (8) have also been reported from this species.

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Cited by 10 publications
(6 citation statements)
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“…( m / z 503→461) and the hexose fragment ( m / z 461→299). The existence of several O -acetyl-hexosides of chrysoeriol, including 7- O -(6′′- O -acetyl)glucoside from Sideritis lanata L. (Lamiaceae) [47], 4′- O -(2′′- O -acetyl)glucoside (abutilin A) from Abutilon pakistanicum Jafri and Ali (Malvaceae) [48] and 4′- O -(6′′- O -acetyl) glucoside from Onobrychis viciifolia Scop. (Leguminosae) [43], is known.…”
Section: Resultsmentioning
confidence: 99%
“…( m / z 503→461) and the hexose fragment ( m / z 461→299). The existence of several O -acetyl-hexosides of chrysoeriol, including 7- O -(6′′- O -acetyl)glucoside from Sideritis lanata L. (Lamiaceae) [47], 4′- O -(2′′- O -acetyl)glucoside (abutilin A) from Abutilon pakistanicum Jafri and Ali (Malvaceae) [48] and 4′- O -(6′′- O -acetyl) glucoside from Onobrychis viciifolia Scop. (Leguminosae) [43], is known.…”
Section: Resultsmentioning
confidence: 99%
“…A. indicum Chrysoeriol-7-O-β-glupyranoside [19] Flowers A. indicum Apigenin-7-O-β-glupyranoside [20] Whole plant A. pannosum Apigenin-7-O-β-D(6''-p-coumaroyl) glucopyranoside [134] Whole plant A. pakistanicum 5,7,4'-Trihydroxy-3'-methoxy flavone-4'-O-β-D-(2"-O-acetyl) glucopyranoside [28] Whole plant A. pakistanicum Scutellarein-4'-O-α-L- […”
Section: Flowers Leavesmentioning
confidence: 99%
“…42 -7.38 (m, 3H), 6.51 (d, J = 15.9, 1H, H-α) and 13 2 Hz, H-2'), 6.9 (d, J = 8.3 Hz, H-5'), 6.8 (d, J = 2.2 Hz, H-8), 6.7 (s, H-3), 6.4 (d, J = 2.2 Hz, H-6) and signal appeared as doublet at d ppm 5.08 (d, J = 6.6 Hz, H-1'' of glucose) assignable for the anomeric proton of the sugar moiety and 13 C-NMR spectrum (DMSO-d 6 ). 13 3) [31].…”
Section: All Collected Fraction Was Investigated Individually By Tlc ...mentioning
confidence: 99%