• Title/Summary/Keyword: stilbene

Search Result 162, Processing Time 0.026 seconds

A New Stilbene Diglycoside from Rheum undulatum

  • Ko, Sung-Kwon
    • Archives of Pharmacal Research
    • /
    • v.23 no.2
    • /
    • pp.159-162
    • /
    • 2000
  • A new stilbene diglycoside, piceatannol-3, 4'-O-$\beta$-D-diglucopyranoside (I), together with desoxyrhaponticin (II), emodin-1-O-$\beta$-D-glucopyranoside (III), and physcion-8-O-b-D-gluco-pyranoside (IV), were isolated from the rhizomes of cultivated Korean rhubarb rhizomes(Rheum undulatum), Jong DaeWhang, and the structures of 1-IV were identified on the basis of chemical and spectral evidences.

  • PDF

Application of Reaction Path Smoluchowski Equation Formalism to the Photoisomerization of Trans-Stilbene

  • Kim, Dong-Sup;Lee, Sang-Youb
    • Bulletin of the Korean Chemical Society
    • /
    • v.12 no.6
    • /
    • pp.692-698
    • /
    • 1991
  • The reaction path Smoluchowski equation approach developed in a recent work to calculate the rate constant for a diffusive multidimensional barrier crossing process is extended to incorporate the configuration-dependent diffusion matrix. The resulting formalism is then applied to the investigation of stilbene photoisomerization dynamics. Adapting a model two-dimensional potential and a model diffusion matrix proposed by Agmon and Kosloff [J. Phys. Chem.,91 (1987) 1988], we derive an eigenvalue equlation for the relaxation rate constant of the stilbene photoisomerization. This eigenvalue equation is solved numerically by using the finite element method. The advantages and limitations of the present method are discussed.

Multidimensional Frictional Coupling Effect in the Photoisomerization of trans-Stilbene

  • Gwak, Gi Jeong;Lee, Sang Yeop;Sin, Guk Jo
    • Bulletin of the Korean Chemical Society
    • /
    • v.16 no.5
    • /
    • pp.427-432
    • /
    • 1995
  • A model based on two coupled generalized Langevin equations is proposed to investigate the trans-stilbene photoisomerization dynamics. In this model, a system which has two independent coordinates is considered and these two system coordinates are coupled to the same harmonic bath. The direct coupling between the system coordinates is assumed negligible and these two coordinates influence each other through the frictional coupling mediated by solvent molecules. From the Hamiltonian which is equivalent to the coupled generalized Langevin equations, we obtain the transition state theory rate constants of the stilbene photoisomerization. The rates obtained from this model are compared to experimental results in n-alkane solvents.

Inhibitory Effects of Stilbene Derivatives from Rheum undulatum on Cyclooxygenase Activity (종대황 스틸벤 유도체의 Cyclooxygenase 저해작용)

  • Lee, Chung-Ryul;Lee, Hak-Sung;Kim, Hyun;Baek, Koo-Hyun;Tokuoka, Kiyoshi;Chung, Sung-Hyun;Ko, Sung-Kwon
    • Korean Journal of Pharmacognosy
    • /
    • v.34 no.1 s.132
    • /
    • pp.25-27
    • /
    • 2003
  • In order to clarify the anti-thrombosis activity of rhubarb, we investigated the effect of stilbene derivatives from rhizomes of Rheum undulatun on cyclooxygenase activity. Stilbene derivatives (desoxyrhapontigenin, rhapontigenin, piceatannol) exhibited the inhibitory effects on COX-1, and desoxyrhapontigenin showed inhibitory effect on COX-2. These inhibitory effect may partially contributed to anti-thrombosis activity of rhubarb.

The Radical Scavenging Effects of Stilbene Glucosides from Polygonum multiflorum

  • Ryu, Geon-Seek;Ju, Jeung-Hoon;Park, Yong-Ju;Ryu, Shi-Yong;Choi, Byoung-Wook;Lee, Bong-Ho
    • Archives of Pharmacal Research
    • /
    • v.25 no.5
    • /
    • pp.636-639
    • /
    • 2002
  • The extract of the root of Polygonum multiflorum exhibited a significant antioxidant activity assessed by the DPPH radical scavenging activity in vitro. The bioassay-guided fractionation of the extract yielded a stilbene glucoside, (E)-2,3,5,4'-tetrahydroxystilbene-2-Ο-$\beta$-d-glucopyranoside (1) as an active constituent responsible for the antioxidant property. Compound 1 demonstrated a moderate DPPH radical scavenging activity ($IC_{50}$, 40 $\mu$M), while the corresponding deglucosylated stilbene 2 exhibited a much higher activity ($IC_{50}$, 0.38 $\mu$M).

Isolation and Identification of Stilbene glycosides from the Bark of Pinus koraiensis (잣나무 수피의 Stilbene glycosides의 분리 및 동정)

  • Song, Hong-Keun
    • Journal of the Korean Wood Science and Technology
    • /
    • v.29 no.4
    • /
    • pp.97-102
    • /
    • 2001
  • EtOAc extract from the bark of Pinus koraiensis Sieb. et Zucc was isolated by column chromatography which was packed with Sephadex LH-20 or TSK-gel HW-40F. Several stilbene glycosides were identified by $^1H{\cdot}^{13}C$-NMR, HMQC, HMBC and $FAB^+$ MS. Three stilbene glycosides, Z-pinostilbenoside, E-desoxyrhaponticin, and E-resveratroloside, were identified.

  • PDF

Comparative study of the pulse shape discrimination (PSD) performance of pixelated stilbene and plastic scintillator (EJ-276) arrays for a coded-aperture-based hand-held dual-particle imager

  • Jihwan Boo ;Manhee Jeong
    • Nuclear Engineering and Technology
    • /
    • v.55 no.5
    • /
    • pp.1677-1686
    • /
    • 2023
  • As the demand for the detection of special nuclear materials (SNMs) increases, the use of imaging instruments that can sensitively image both gamma-ray and neutron signatures has become necessary. This study compared the pulse shape discrimination (PSD) performance of gamma/neutron events when employing either a pixelated stilbene or a plastic (EJ-276) scintillator array coupled to a silicon photomultiplier (SiPM) array in a dual-particle imager. The stilbene array allowed a lower energy threshold above which neutron and gamma-ray events can be clearly distinguished. A greater number of events can, therefore, be used when forming both gamma-ray and neutron images, which shortens the time required to acquire the images by nearly seven times.

Growth Inhibition and G2/M Phase Cell Cycle Arrest by 3,4,5-Trimethoxy-4'-bromo-cis-stilbene in Human Colon Cancer Cells

  • Heo, Yeon-Hoi;Min, Hye-Young;Kim, Sang-Hee;Lee, Sang-Kook
    • Biomolecules & Therapeutics
    • /
    • v.15 no.2
    • /
    • pp.95-101
    • /
    • 2007
  • Resveratrol (3,5,4’-trihydroxy-trans-stilbene), a naturally occurring phytoallexin abundant in grapes and several plants, has been shown to be active in inhibiting proliferation and inducing apoptosis in several human cancer cell lines. On the line of the biological activity of resveratrol, a variety of resveratrol analogs were synthesized and evaluated for their growth inhibitory effects against several human cancer cell lines. In the present study, we found that one of the resveratrol analogs, 3,4,5-trimethoxy-4’-bromo-cis-stilbene, markedly suppressed human colon cancer cell proliferation (EC$_{50}$ = 0.01 ${\mu}$g/ml), and the inhibitory activity was superior to its corresponding trans-isomer (EC$_{50}$ = 1.6 ${\mu}$g/ml) and resveratrol (EC$_{50}$ = 18.7 ${\mu}$g/ml). Prompted by the strong growth inhibitory activity in cultured human colon cancer cells (Col2), we investigated its mechanism of action. 3,4,5-Trimethoxy-4’-bromo-cis-stilbene induced arrest of cell cycle progression at G2/M phase and increased at sub-G1 phase DNA contents of the cell cycle in a time- and dose-dependent manner. Colony formation was also inhibited in a dose-dependent manner, indicating the inhibitory activity of the compound on cell proliferation. Moreover, the morphological changes and condensation of the cellular DNA by the treatment of the compound were well correlated with the induction of apoptosis. These data suggest the potential of 3,4,5-trimethoxy-4’-bromo-cis-stilbene might serve as a cancer chemotherapeutic or chemopreventive agent by virtue of arresting the cell cycle and inducing apoptosis for the human colon cancer cells.