Antimicrobial activity and active compounds of a Rhus verniciflua Stokes extract

2018 ◽  
Vol 73 (11-12) ◽  
pp. 457-463
Author(s):  
Jinfeng Yang ◽  
Yong Soo Kwon ◽  
Myong Jo Kim

Abstract The Rhus verniciflua Stokes (RVS) extract is used as a traditional herbal medicine in Southeast Asian countries such as Korea and China. In the present study, one phenolic acid and six flavonoids were isolated from an 80% ethanol RVS extract to examine their antimicrobial activities. These compounds were identified as 3′,4′,7-trihydroxyflavone (1), methyl gallate (2), gallic acid (3), fusti (4), fisetin (5), butin (6), and sulfuretin (7) by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and nuclear magnetic resonance spectroscopy. The antimicrobial activities of compounds 5 and 6 (at a dose of 16 μg/mL each) were superior to that of the control, cycloheximide (at a dose of 25 μg/mL), against Hypocrea nigricans; additionally, the activities of compounds 1 and 2 (at a dose of 8 μg/mL each) were superior to the control against Penicillium oxalicum. Also, chemical compounds 1 and 5 (at a dose of 16 μg/mL each) had higher activities than the control (25 μg/mL) against Trichoderma virens. Chemical compound 1 (at a dose of 8 μg/mL) had a similar activity to that of the control against Bacillus subtilis. The obtained results suggest that the RVS extract could be a promising food and nutraceutical source because of the antimicrobial properties of its phenolic compounds.

e-Polymers ◽  
2015 ◽  
Vol 15 (4) ◽  
pp. 227-235 ◽  
Author(s):  
Tobias Rudolph ◽  
Sarah Crotty ◽  
Ulrich S. Schubert ◽  
Felix H. Schacher

AbstractWe demonstrate the synthesis of star-shaped poly(2-ethyl-2-oxazoline) featuring a porphyrin core starting from alkyne-functionalized porphyrin ([TPP-TB]4) and azide-functionalized poly(2-ethyl-2-oxazoline) (PEtOx-N3) via copper-catalyzed azide-alkyne cycloaddition (CuAAC). The porphyrin core was further utilized for the complexation of either copper or iron within the central cavity. The obtained materials were investigated using a combination of nuclear magnetic resonance spectroscopy, fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, size-exclusion chromatography, and matrix assisted laser desorption/ionization time-of-flight mass spectrometry. In the case of copper, the inclusion of the metal ion was achieved in a one-pot reaction during the CuAAC reaction for attaching the PEtOx-N3 arms.


2006 ◽  
Vol 4 (4) ◽  
pp. 723-731
Author(s):  
Chengbin Liu ◽  
Yanhong Tang ◽  
Shuming Nie

AbstractTwo pentacene derivatives 1 and 2 were synthesized from the Diels-Alder reactions of furan derivatives with 1,4-benzoquinone. They were characterized by the methods of 1H — nuclear magnetic resonance spectroscopy (1H-NMR), matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF MS), ultraviolet and visible spectrophotometry (UV-VIS), photoluminescence (PL) spectrometry and cyclic voltammetry (CV). The energy gaps of 1 and 2, taken directly from spectroscopic measurements, are broad as 2.72 and 2.46 eV, leading to blue and greenish blue photoluminescence, respectively. The LUMO and HOMO energy levels are −2.77 and −5.49 eV for 1, and −2.91 and −5.37 eV for 2, respectively. The low energy levels make both 1 and 2 good air-stabilities and promising n-type semiconductor candidates for use in organic electronics.


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