2011
DOI: 10.3109/13880209.2011.575790
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Iridoid content and biological activities ofVeronica cuneifoliasubsp.cuneifoliaandV. cymbalaria

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Cited by 35 publications
(19 citation statements)
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“…The 1 H NMR spectrum of 1 (Table ) showed trans olefinic protons at δ H 6.31 (1H, d, J = 15.6 Hz) and δ H 7.60 (1H, d, J = 15.6 Hz), ABX‐type coupled aromatic protons at δ H 6.79 (1H, d, J = 7.8 Hz), δ H 6.97 (1H, dd, J = 1.8, 7.8 Hz), and δ H 7.07 (1H, d, J = 1.8 Hz), three hemiacetal protons at δ H 4.75 (1H, d, J = 7.8 Hz), δ H 4.80 (1H, dd, J = 2.4, 9.0 Hz), and δ H 5.18 (1H, d, J = 7.8 Hz), three methylene protons at δ H 3.88 (1H, m), δ H 3.52 (1H, m), δ H 1.57 (2H, m), and δ H 1.38 (2H, m), and one methyl proton at δ H 0.93 (3H, t, J = 7.2 Hz). They suggested the presence of a caffeoyl moiety, a hexose sugar residue, and a butoxy group in the structure. This was confirmed by the successively lose two units of 162 Da and one unit of 74 Da in HRESI‐MS n .…”
Section: Resultsmentioning
confidence: 99%
“…The 1 H NMR spectrum of 1 (Table ) showed trans olefinic protons at δ H 6.31 (1H, d, J = 15.6 Hz) and δ H 7.60 (1H, d, J = 15.6 Hz), ABX‐type coupled aromatic protons at δ H 6.79 (1H, d, J = 7.8 Hz), δ H 6.97 (1H, dd, J = 1.8, 7.8 Hz), and δ H 7.07 (1H, d, J = 1.8 Hz), three hemiacetal protons at δ H 4.75 (1H, d, J = 7.8 Hz), δ H 4.80 (1H, dd, J = 2.4, 9.0 Hz), and δ H 5.18 (1H, d, J = 7.8 Hz), three methylene protons at δ H 3.88 (1H, m), δ H 3.52 (1H, m), δ H 1.57 (2H, m), and δ H 1.38 (2H, m), and one methyl proton at δ H 0.93 (3H, t, J = 7.2 Hz). They suggested the presence of a caffeoyl moiety, a hexose sugar residue, and a butoxy group in the structure. This was confirmed by the successively lose two units of 162 Da and one unit of 74 Da in HRESI‐MS n .…”
Section: Resultsmentioning
confidence: 99%
“…Their structures were identified by comparison of their spectroscopic data (1D and 2D NMR, ESIMS and [α] D ) with those published in the literature (Harput et al, 2002b;Varel, 2004;Kupeli et al, 2005). Purities of the isolated iridoid glucosides were determined using the HPLC-DAD system (Saracoglu et al, 2011).…”
Section: Methodsmentioning
confidence: 99%
“…Mocan et al [12] found in veronica orchidea, officinallis, teucrium, antioxidants, phytochemical and antimicrobial. Dunkic et al [13] in veronica spicataconfirmed antioxidants plus antimicrobial while Exarchou [14] isolated compounds hispidulin also antiviral [15] an effective anti-cancer, anti-mutagenic and antitumor with new compounds [16][17][18][19] anti-ulcerogenic [20,21] anti-cholinesterase [22] antiinflammatory [18] anti-insecticidal [23] anti-hepatocarcinoma [24] antioxidants [25] angiogenic, neuroprotective potency [26] wound healing, cough, catarrh, and kidney medication [12] natural preservatives, dietary supplement, and hyperglycemia [27,28] was reported in this genus species, Javadsharif rad et al [29] found in veronica persicapoiracetylcholinesterase, scolicidal, tyrosinase, xanthine oxidase, lipoxygenase. Our current study is to focused only on antioxidant analysis by (1,1-diphenyl-2-picryl-hydrazyl) method and phytochemical confirmation also yield calculation for the first time in the genus veronica medicinal plant a specie veronica biloba.…”
Section: Introductionmentioning
confidence: 99%