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Stilbenes and Oligostilbenes from Leaf and Stem of Vitis amurensis and Their Cytotoxic Activity
Do Thi Ha,Quan Cheng Chen,Tran Manh Hung,Tran Minh Ngoc,Phuong Thien Thuong,김홍진,성연희,민병선,배기환,윤의중 대한약학회 2009 Archives of Pharmacal Research Vol.32 No.2
Chromatographic separation of the EtOAc fraction from the leaf and stem of Vitis amurensis led to the isolation of six oligostilbenoids (i.e., r-2-viniferin (1), trans-amurensin B (2), trans-ε -viniferin (3), gnetinH (4), amurensin G (5), (+)-ampelopsin A (8)) and four stilbenoids (i.e., trans-resveratrol (6), (+)- ampelopsin F (7), piceatannol (9), and trans-piceid (10)). The structures have been identified on the basis of spectroscopic evidence and physicochemical properties. The isolates were investigated for cytotoxic activity against three cancer cell lines in vitro using the MTT assay method. Amurensin G (5) and trans-resveratrol (6) showed significant cytotoxic activity against L1210, K562 and HTC116 cancer cell lines with IC50 values ranging from 15.7 ± 2.1 to 30.9 ± 1.8 μM. (+)-Ampelopsin A (8) and trans-piceid (10) exhibited considerable cytotoxic activity against L1210 (IC50 values of 30.6 ± 4.1 and 28.7 ± 2.81μM, respectively) and K562 (IC50 values of 38.6 ± 0.82 and 24.6 ± 0.76 μM, respectively). Gnetin H (4)showed only weak cytotoxic activity against L1210 with an IC50 value of 40.1 ± 4.23 μM. On the other hand, r-2-viniverin (1), trans-amurensin B (2), trans-ε -viniferin (3), (+)-ampelopsin F (7), and piceatannol(9) exhibited no activity on three cancer cell lines.
Minh Thien Tran,틴휭,Soumayya Chakir,Dong-Hun Lee,Young-Bok Kim 대한기계학회 2022 JOURNAL OF MECHANICAL SCIENCE AND TECHNOLOGY Vol.36 No.4
In this paper, a robust adaptive pole-placement control (RAPPC) scheme is proposed for application to a single ducted-fan unmanned aerial vehicle (DUAV). By using the proposed control system, the yaw angle of the single DUAV system is required to track the desired trajectory with the tracking error staying within a compact set despite the presence of bounded disturbances and uncertainties. The pole-placement control (PPC) is designed based on a simple linear model of the system, and the adaptation law is incorporated to compensate for the perturbations in the real DUAV system. Moreover, the sigma-modification law guarantees the boundedness of the states in the presence of disturbances, and the stability of the whole system is proven in the sense of Lyapunov. Comparative simulations of the proposed RAPPC controller, RAPPC without the sigma-modification law, and a PID controller are conducted to investigate performance characteristics. Experimental studies with the proposed controller and a PID controller are carried out to enhance the practical feasibility of the RAPPC control system.
Lipoxygenase Inhibitory Constituents from Rhubarb
Tran Minh Ngoc,Pham Thi Hong Minh,Tran Manh Hung,IkSoo Lee,민병선,Phuong Thien Thuong,배기환 대한약학회 2008 Archives of Pharmacal Research Vol.31 No.5
Phytochemical study on the ethanol extract of rhubarb led to the isolation of fifteen compounds, including five anthraquinones: chrysophanol (1), physcion (2), emodin (7), chrysophanol- 8-O-β-D-glucopyranoside (9) and emodin-8-O-β-D-glucopyranoside (15), and ten stilbenes: desoxyrhaponticin (3), rhaponticin (4), resveratrol (5), desoxyrhapotigenin (6), rhapontigenin (8), piceatannol-3'-O-β-D-glucopyranoside (10), piceid (11), ε -viniferin (12), ampelopsin B (13) and isorhaponticin (14). Their structures were identified by comparing the physicochemical data with those of published papers. Among the isolated compounds, stilbene derivatives (3-6, 8 and 10-14) showed remarkable inhibitory effect on lipoxygenase with IC50 values ranging from 6.7 to 74.1 μM. The inhibition kinetics analyzed by Lineweaver-Burk plots found that they were competitive inhibitors with the linoleic acid at the active site of lipoxygenase. In addition, stilbenes exhibited significantly free radical scavenging activity against ABTS•+ with trolox equivalent activity capacity (TEAC) values ranging from 1.16 to 4.64. Whereas, anthraquinone derivatives (1-2, 7, 9 and 15) neither inhibited lipoxygenase nor scavenged free radical ABTS•+. These results indicated that stilbene derivatives were considerate to be mainly lipoxygenase inhibitor and free radical scavenger constituents of rhubarb.
NGOC, Tran Minh,HUNG, Tran Manh,THUONG, Phuong Thien,KIM, Jin-Cheon,CHOI, Jae Sue,BAE, KiHwan,HATTORI, Masao,CHOI, Chung-Sig,LEE, Joon Seok,MIN, Byung-Sun Japan Society for Bioscience, Biotechnology, and A 2008 Bioscience, Biotechnology, and Biochemistry Vol.72 No.8
<P>Two phenolics, 1,2,6-trigalloylglucose (<B>1</B>) and 1,2,3,6-tetragalloylglucose (<B>2</B>), isolated from the stem-bark of <I>Juglans mandshurica</I> were evaluated for their antioxidative activities. The results showed that compounds <B>1</B> and <B>2</B> exhibited strong scavenging activities against 1,1′-diphenyl-1-picrylhydrazyl (DPPH), 2,2′-azino-bis-(3-ethylbenzenthiazoline-6-sulphonic) acid (ABTS<SUP>•+</SUP>), and superoxide radicals (O<SUB>2</SUB><SUP>•−</SUP>), and also had a significant inhibitory effect on lipid peroxidation and low-density lipoprotein (LDL) oxidation. The strong superoxide radical scavenging of <B>1</B> and <B>2</B> resulted from the potential competitive inhibition with xanthine at the active site of xanthine oxidase (OX). In addition, compounds <B>1</B> and <B>2</B> displayed significant lipoxygenase inhibitory activity, the mode of inhibition also being identified as competitive. In comparison, the antioxidative activities of compounds <B>1</B> and <B>2</B>, together with gallic acid, indicated that the number of galloyl moieties could play an important role in the antioxidative activity.</P>
Lipoxygenase Inhibitory Constituents from Rhubarb
Ngoc, Tran Minh,Minh, Pham Thi Hong,Hung, Tran Manh,Thuong, Phuong Thien,Lee, Ik-Soo,Min, Byung-Sun,Bae, Ki-Hwan 대한약학회 2008 Archives of Pharmacal Research Vol.31 No.5
Phytochemical study on the ethanol extract of rhubarb led to the isolation of fifteen compounds, including five anthraquinones: chrysophanol (1), physcion (2), emodin (7), chrysophanol-8-O-$\beta$-D-glucopyranoside (9) and emodin-8-O-$\beta$-D-glucopyranoside (15), and ten stilbenes: desoxyrhaponticin (3), rhaponticin (4), resveratrol (5), desoxyrhapotigenin (6), rhapontigenin (8), piceatannol-3'-O-$\beta$-D-glucopyranoside (10), piceid (11), $\varepsilon$-viniferin (12), ampelopsin B (13) and isorhaponticin (14). Their structures were identified by comparing the physicochemical data with those of published papers. Among the isolated compounds, stilbene derivatives (3-6, 8 and 10-14) showed remarkable inhibitory effect on lipoxygenase with $IC_{50}$ values ranging from 6.7 to $74.1\;{\mu}M$. The inhibition kinetics analyzed by Lineweaver-Burk plots found that they were competitive inhibitors with the linoleic acid at the active site of lipoxygenase. In addition, stilbenes exhibited significantly free radical scavenging activity against $ABTS^{\bullet+}$ with trolox equivalent activity capacity (TEAC) values ranging from 1.16 to 4.64. Whereas, anthraquinone derivatives (1-2, 7, 9 and 15) neither inhibited lipoxygenase nor scavenged free radical $ABTS^{\bullet+}$. These results indicated that stilbene derivatives were considerate to be mainly lipoxygenase inhibitor and free radical scavenger constituents of rhubarb.
Lan Ngoc Vuong,Tu Hoang Kim Trinh,Tuan Diep Tran,Duy Le Pham,Vinh Nhu Nguyen,Quan Tran Thien Vu,Toan Duong Pham,Phong Hoai Nguyen,Minh Kieu Le,Diem Dinh Kieu Truong,Vu Anh Hoang,Nghia Huynh,Dat Quoc N 연세대학교의과대학 2024 Yonsei medical journal Vol.65 No.9
Purpose: Although some immune protection from close contact with individuals who have coronavirus disease 2019 (COVID-19) has been documented, there is limited data on the seroprevalence of antibodies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals who were in lockdown with confirmed COVID-19 cases. This study investigated immunogenicity against SARS-CoV-2 in household members and people who lived near home-quarantined patients with COVID-19. Materials and Methods: This cross-sectional study was conducted during the community-based care that took place during lockdowns in District 10, Ho Chi Minh City, Vietnam from July to September 2021. SARS-CoV-2 antibody levels were determined in index cases of COVID-19, household contacts, and a no-contact group from the same area. Results: A total of 770 participants were included (355 index cases, 103 household contacts, and 312 no contacts). All index cases were unvaccinated, but >90% of individuals in the household and no-contact groups had received ≥1 vaccine dose. SARS-CoV-2 neutralizing antibodies (Nabs) were present in >77% of unvaccinated index cases versus 64%/65.4% in the household/no-contact groups (p=0.001). Antibody concentrations in unvaccinated index cases were significantly higher than those in household contacts and no contacts, with no difference between the latter groups. In all cases, antibody levels declined markedly ≥6 weeks after infection, and failed to persist beyond this time in the household and no-contact groups. Conclusion: Community-based care may have helped to create community immunogenicity, but Nabs did not persist, highlighting a need for vaccination for all individuals before, or from 6 weeks after, infection with SARS-CoV-2.