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6 protocols using kaempferol

1

Phytochemical Reference Standards

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Reference standards quercetin-3-O-rutinoside (rutin), (+)-catechin, luteolin, quercetin and apigenin, kaempferol, isorhamnetin and cyanidin-3-O-glucoside were obtained from Carl Roth GmbH (Karlsruhe, Germany). Primeverin and primula acid I were purchased from Phytolab GmbH (Vestenbergsgreuth, Germany).
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2

Comprehensive Flavonoid Compound Library

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The compounds kaempferol, acacetin, galangin, chrysin, homoeriodictyol were obtained from Carl Roth GmbH (Karlsruhe, Germany), apigenin, nargingenin, hispidulin, scutellarein, baicalein, quercetin, wogonin, and diosmetin from Sigma-Aldrich (Vienna, Austria), herbacetin, pinocembrin, luteolin, eriodictyol, norwogonin from Extrasynthése (Genay, France) and nepetin as well as oroxylin A from Phytolab (Vestenbergsgreuth, Germany). All stock solutions were prepared in dimethylsulfoxide (DMSO; 99.7% cell culture grade, Sigma-Aldrich (Vienna, Austria).
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3

HPLC-MS Analysis of Polyphenolic Compounds

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References used for the HPLC-MS analysis were purchased from Sigma Aldrich (St. Louis, MO, USA): Chlorogenic acid, p-coumaric acid, caffeic acid, rutin, apigenin, quercetin, isoquercitrin, quercitrin, hyperoside, kaempferol, myricetol, and fisetin, Roth (Karlsruhe, Germany): Ferulic acid, sinapic acid, gentisic acid, gallic acid, patuletin, luteolin or from Dalton (Toronto, ON, Canada): cichoric acid, caftaric acid. HPLC grade solvents, analytical grade acids used for mobile phases and Folin-Ciocâlteu reagent were purchased from Merck (Darmstadt, Germany), together with sodium carbonate, dipotassium hydrogen phosphate, potassium dihydrogen phosphate and aluminium chloride used for antioxidant assays. ABTS (2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt) ≥98% purity, potassium peroxodisulfate (≥99% purity), DPPH, and Trolox (6-hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid; ≥97% purity) also used in antioxidant tests were purchased from Sigma Aldrich (Schnelldorf, Germany). Gallic acid monohydrate (99.5%) was purchased from Serva, (Heidelberg, Germany).
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4

Analytical Characterization of Phenolic Compounds

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Acetonitrile and water (HPLC grade), acetic acid, hydrochloric acid, sodium hydroxide, and sodium carbonate were from Merck (Darmstadt, Germany). Chlorogenic acid, caffeic acid, quercetin, luteolin, apigenin, kaempferol, isorhamnetin, apigenin 7-glucoside p-coumaric acid, salicylic acid, rutin were obtained from Carl Roth (Karlsruhe, Germany).
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5

Phytochemical Profiling and Bioactivity Evaluation

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Flavonoid and isoflavonoid compounds, including rutin, quercitrin, quercetin 3-β-D-glucoside, quercetin, isorhamnetin, formononetin, genistein, naringenin, biochanin A, and vitexin, were purchased from Sigma–Aldrich (Schnelldorf, Germany), daidzein was obtained from Fluka (Buchs, Switzerland), luteolin and kaempferol were purchased from Carl Roth (Karlsruhe, Germany), 2,2-difenil-1-picrilhidrazil (DPPH), potassium ferricyanide, sodium carbonate (Na2CO3), dinitrosalicylic acid (DNS), α-amylase from hog pancreas, α-glucosidase from Saccharomyces cerevisiae, and 4-nitrophenyl α-d-glucopyranoside (NPG) were purchased from Sigma–Aldrich, and iron chloride was bought from Fluka. All other used reagents, methanol (Riedel-de Haen), and ethanol (Chemical Company) were of chromatographic or analytical purity; the ultra-pure water was obtained using the distillation apparatus from Evoqua Water Technologies (Pittsburgh, PA, USA).
The medicinal plants were collected from the Cluj county (Romania) natural site, and voucher specimens were stored in the Herbarium of Babes-Bolyai University from Cluj-Napoca (code: 868.786 for Solidago virgaurea L.; code: 622172 for Medicago sativa).
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6

Isolation and Characterization of Plant Flavonoids

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p-Coumaric acid was purchased from Sigma-Aldrich (Steinheim, Germany). Kaempferol was purchased from Carl Roth GmbH (Karlsruhe, Germany). Astragalin (Kaempferol 3-O-β-D-glucopyranoside) and tiliroside (Kaempferol 3-O-β-D-(6″-E-p-coumaroyl)-glucopyranoside) were isolated from flowers of Ficaria verna Huds. (Ranunculaceae) and leaves of Rubus caesius L. (Rosaceae), respectively. Their chemical structures were identified by using spectral (UV, NMR, MS) methods. All isolated compounds were >96% pure, as measured by HPLC [46 (link),47 ].
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