2020
DOI: 10.1155/2020/6965306
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Antibacterial, Anticandidal, Phytochemical, and Biological Evaluations of Pellitory Plant

Abstract: Pellitory plant (Parietaria judaica (PJ)) is one of the most widely used Arabian traditional medicinal plants due to its ability to cure several infectious diseases and other illnesses. The current study is aimed at assessing the phytoconstituents, antilipase, antiamylase, antimicrobial, and cytotoxic characters of the Pellitory plant (Parietaria judaica (PJ)). Phytochemical screening and procyanidin detection were conducted according to the standard phytochemical procedures. Porcine pancreatic lipase and α-am… Show more

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Cited by 11 publications
(2 citation statements)
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“…Within the realm of plant phytochemicals, phenolic compounds hold diverse physiological functions, encompassing free radical scavenging, antibacterial, anticancer, and antioxidant activities ( Mueen et al., 2010 ; Barad et al., 2014 ; Acidri et al., 2020 ; Qadi et al., 2020 ; Stuper-Szablewska et al., 2022 ; Bini et al., 2023 ). Flavonoids, featuring flavones as their fundamental structure, are present in flowers, stems, and fruits of plants and are recognized for their antioxidant, anticancer, and anti-inflammatory properties ( Grassi et al., 2010 ; Yonekura-Sakakibara et al., 2019 ; Wen et al., 2020 ).…”
Section: Resultsmentioning
confidence: 99%
“…Within the realm of plant phytochemicals, phenolic compounds hold diverse physiological functions, encompassing free radical scavenging, antibacterial, anticancer, and antioxidant activities ( Mueen et al., 2010 ; Barad et al., 2014 ; Acidri et al., 2020 ; Qadi et al., 2020 ; Stuper-Szablewska et al., 2022 ; Bini et al., 2023 ). Flavonoids, featuring flavones as their fundamental structure, are present in flowers, stems, and fruits of plants and are recognized for their antioxidant, anticancer, and anti-inflammatory properties ( Grassi et al., 2010 ; Yonekura-Sakakibara et al., 2019 ; Wen et al., 2020 ).…”
Section: Resultsmentioning
confidence: 99%
“…Fractions of 20 µL containing the enzyme solution were added to 180 µL substrate solution (1% soluble starch in 50 mM Tris-HCl, pH 7.5), and the mixture was then incubated at 50 • C for 10 min. The reaction was stopped by the addition of dinitrosalicylic acid (DNS) solution and boiled for 5 min [27]. After cooling, ddH 2 O was added up to 2.5 mL, and amylase activity was determined using a spectrophotometer at OD 540 .…”
Section: Amylase Assaymentioning
confidence: 99%