traditional medicine to treat eczema, wounds, ulcers, fistulae, cancer, and also as a diuretic and anthelminthic agent. In modern herbal medicine Scrophularia nodosa L. is used to treat eruptive skin diseases, eczemas, psoriasis, pruritus, ulcers and also as a purgative agent [1][2][3].The main active components from Scrophularia nodosa L. are iridoid glycosides (aucubine, catalpol, and harpagoside), flavonoids, phenolic acids, and cardio-active glycosides. Phenolic and polyphenolic compounds represent one of the most widespread groups of secondary plant metabolites. They are divided into several structural classes, as follows: phenol carboxylic acids and derivatives, flavonoids, tannins, coumarins, anthranoids, and lignans [4,5]. Some of the polyphenols show therapeutic properties such as antioxidant, antibacterial, antiviral, analgesic, antispasmodic, neuroprotective, cytostatic, and antiinflammatory activity [6][7][8][9][10][11].In Romanian flora there are only five species of Scrophularia genus from the 300 species of the genus growing all over the world. Scrophularia scopolii L. is an herb with red-brown flowers that grows in all regions of Romania. This herb is not recognized as a medicinal plant.The main objective of this work was the characterization and quantification of phenolic compounds in Scrophularia nodosa L. and Scrophularia scopolii L. as part of a phytochemical study of these species. In order to obtain more accurate data regarding the flavonol and flavone glycosides and aglycones content, the plant material was analyzed with and without acid hydrolysis. The separation of the isolated phenolic compounds was achieved by HPLC (Table 1), previously elaborated at our university [12,13]. In order to perform the qualitative and quantitative analysis, 18 polyphenolic standards were used, as follows: seven cinnamic acid derivatives (p-coumaric acid, caffeic acid, ferulic acid, sinapic acid, chlorogenic acid, caftaric acid, and gentisic acid), four quercetin glycosides (hyperoside, isoquercetin, quercitrin, and rutoside), five flavonol aglycones (quercetin, kaempferol, patuletin, myricetol, and fisetin) and two flavone aglycones (apigenin and luteolin). The polyphenols were identified by comparison with authentic standards and additionally by liquid chromatography-electrospray ionizationmass spectrometry (LC-ESI-MS or MS/MS), followed by their quantification based on a HPLC-UV analysis.The HPLC-UV and HPLC-MS (MS/MS) analysis of the plant materials revealed varying concentrations for some of the analyzed polyphenols, while a few of the chosen 18 polyphenol standards were absent in the different plant tissues ( Table 2).The pattern of phenol carboxylic acids showed the absence of gentisic acid and sinapic acid in all plant materials that were analyzed from both Scrophularia species. Also the tartaric ester of caftaric acid could not be detected in these samples. p-Coumaric acid appears to be the most abundant constituent in the leaves of Scrophularia nodosa L. and the herba of Scrophularia scopolii L., ma...