1995
DOI: 10.1016/0031-9422(95)00206-m
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Revised structure for hortensin, a flavonoid from Millingtonia hortensis

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Cited by 74 publications
(44 citation statements)
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“…(Gu et al, 2001), Salvia officinalis (Kavvadias et al, 2003) and Artemisia species (Tan et al, 1999). The spectral data of 1 were in accordance with published results (Hase et al, 1995).…”
Section: Resultssupporting
confidence: 77%
See 1 more Smart Citation
“…(Gu et al, 2001), Salvia officinalis (Kavvadias et al, 2003) and Artemisia species (Tan et al, 1999). The spectral data of 1 were in accordance with published results (Hase et al, 1995).…”
Section: Resultssupporting
confidence: 77%
“…The spectroscopic data identified 1 as the known 4',5,7-trihydroxy-6-methoxyflavone which is trivially referred to as hispidulin and has been previously isolated from a variety of plant species including Millingtonia hortensis L. (Chulasiri et al, 1992 andHase et al, 1995), Salvia plebeia R. Br. (Gu et al, 2001), Salvia officinalis (Kavvadias et al, 2003) and Artemisia species (Tan et al, 1999).…”
Section: Resultsmentioning
confidence: 99%
“…HPLC to afford 27 compounds. Twenty two were identified as known compounds; plucheoside B (1), alangionoside C (2) (Otsuka et al, 1995), premnaionoside (4) (Sudo et al, 2000), (2R)-2-O-b-d-glucopyranosyl-2H-1,4-benzoxazin-3(4H)-one (HBOA-Glc, 8) (Tietze et al, 1991), (2R)-2-O-b-d-glucopyranosyl-4-hydroxy-2H-1,4-benzoxazin-3(4H)-one (DIBOA-Glc, 9) (Hartenstein and Sicker, 1994) (Ono et al, 1999) (Okamura et al, 1981), adenosine (13) (Otsuka et al, 1989), verbascoside (14), isoverbascoside (15), leucosceptoside A (16) (Miyase et al, 1982), martynoside (17) (Sasaki et al, 1978), b-hydroxyacteoside (18) (Kitakawa et al, 1984), vecenin-2 (19), schaftoside (20) (Markham and Chari, 1982) (Hase et al, 1995) (Achenbach et al, 1992) (Ida et al, 1994), magnolenin C (26) (Rao and Wu, 1978), and ( (Kinjo et al, 1991) by comparison of physical data with literature values and from spectroscopic evidence.…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, the proton signals of the methoxyl groups at δ H 3.65 and 3.75 showed long-range correlation with C-6″ (δ C 169.79) and C-6 (δ C 132.97) indicated the location of the methoxyl groups at position-6″ of the glucuronic acid and C-6 of aglycone, respectively. Based on these data and comparison with literature data, 17 1 was determined to be hispidulin-7-O-glucuronide methyl ester. Furthermore, it revealed an anomeric proton signal appeared at δ H 5.07 (1H, d, J=7.2 Hz) indicated the presence of β-D-glucopyranosyl moiety.…”
Section: Resultsmentioning
confidence: 86%