• Title/Summary/Keyword: University Archives

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Inhibitory Activity of Isorhamnetin from Persicaria thunbergii on Farnesyl Protein Transferase

  • Oh Hyun Mi;Kwon Byoung-Mog;Baek Nam-In;Kim Sung-Hoon;Chung In-Sik;Park Mi-Hyun;Park Hee Wook;Lee Jae Hyeok;Park Hye Won;Kim Eun Jeong;Kim Dae Keun
    • Archives of Pharmacal Research
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    • v.28 no.2
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    • pp.169-171
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    • 2005
  • The methanolic extract of the aerial parts of Persicaria thunbergii was found to show inhibitory activity on Farnesyl Protein Transferase (FPTase). Bioassay-guided fractionation of the methanolic extract resulted in the isolation of isorhamnetin, as an inhibitor on FPTase. This compound inhibited FPTase activity in a dose-dependent manner, and the $IC_{50}$ value of isorhamnetin was $37.5\;{\mu}M$.

Diastereoselective Synthesis of Polysubstituted Pyrrolidinone as a Key Intermediate for the Anticancer Agents by Palladium(II)­Catalyzed Carboxylation

  • Choi Dong-Rack;Lee Kee-Young;Chung Yun-Sung;Joo Jae-Eun;Kim Yong-Hyun;Oh Chang-Young;Lee Yiu-Suk;Ham Won-Hun
    • Archives of Pharmacal Research
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    • v.28 no.2
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    • pp.151-158
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    • 2005
  • Palladium(II)-catalyzed carboxylation of chiral olefins 6a-d has been examined under various conditions. In the weak basic condition ($K_{2}CO_3$), 7a-d were obtained in good yields. Alternatively, in the strong basic condition, pyrrolidinones 8a-d were obtained resulting in excellent yields and with high diastereoselectivity.

Inducible Nitric Oxide Synthase Inhibitor form Mela azedarach var. Japonica

  • Kwon, Hak-Cheol;Lee, Byeong-Gon;Kim, Seung-Hee;Jung, Chil-Mann;Hong, Sung-Youl;Han, Jeung-Whan;Lee, Hyang-Woo;Zee, Ok-Pyo;Lee, Kang-Ro
    • Archives of Pharmacal Research
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    • v.22 no.4
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    • pp.410-413
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    • 1999
  • In bioassay-guided search for inducible nitric oxide synthase (iNOS) inhibitory compounds from higher plants of South Korea, two $\beta$-carboline (2) have been isolated form the cortex of Melia azedarach var. japonica. The structures of these compounds were elucidated on the basis of spectroscopic data. Compounds 1 to 2 showed marked inhibitory activity of iNOS on LPS-and interferon-${\gamma}$-stimulated RAW 264.7 cells.

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Diastereoselective Synthesis of anti-1,2-Aminoalcohol by Palladium(II) Catalyzed Aza-Claisen Rearrangement

  • Yoon, Youn-Jung;Chan, Myung-Hee;Joo, Jae-Eun;Kim, Yong-Hyun;Oh, Chang-Young;Lee, Kee-Young;Lee, Yiu-Suk;Ham, Won-Hun
    • Archives of Pharmacal Research
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    • v.27 no.2
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    • pp.136-142
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    • 2004
  • In this study, a highly diastereoselective synthesis of anti-1 ,2-aminoalcohol was explored starting from L-amino acids as chiral sources. The higher yield and diastereoselectivity was shown when the aza-Claisen rearranqement was performed with allylic trichloroacetimidate 6a in the presence of palldium(II) catalyst.

Anti-allergic Components from the Peels of Citrus nushiu

  • Kim, Dae-Keun;Lee, Ki-Taek;Eun, Jae-Soon;Zee, Ok-Pyo;Lim, Jong-Pil;Eum, Sang-Sup;Kim, Sang-Hyun;Shin, Tae-Yong
    • Archives of Pharmacal Research
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    • v.22 no.6
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    • pp.642-645
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    • 1999
  • In a bioassay-guided search for anti-allergic compounds from higher plants of Korea, poly-methoxyflavones, 3',4',5,6,7,8-hexamethoxyflavone (I), 5-hydroxy-3',4',6,7,8-pentamethoxyflavone (II) and 3',4',5,7,8-pentamethoxyflavone (III) have been isolated from the immature peels of Citrus unshiu. Structures of these compounds were elucidated on the basis of spectroscopic techniques. Compounds I and II inhibited dose-dependent histamine release from the rat peritoneal mast cells activated by compound 48/80 or anti-DNP IgE.

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Antioxidative Constituents from Buddleia officinalis

  • Piao, Mei-Shan;Kim, Mi-Ran;Lee, Dong-Gun;Park, Yoonkyung;Hahm, Kyung-Soo;Moon, Young-Hee;Woo, Eun-Rhan
    • Archives of Pharmacal Research
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    • v.26 no.6
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    • pp.453-457
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    • 2003
  • Four flavonoids (1-4), a phenylethyl glycoside (5), and a phenylpropanoid glycoside (6) were isolated from the flowers of Buddleia officinalis (Loganiaceae). Their structures were determined by chemical and spectral analysis. Among the isolated compounds, luteolin (1) and acteoside (6) exhibited the most potent antioxidative activity on the NBT superoxide scavenging assay. In addition, compounds 1-6 revealed weak antifungal activity, and no hemolytic activity.

Anti-Tumor Activities of Decursinol Angelate and Decursin from Angelica gigas

  • Lee, Sang-Hyun;Lee, Yeon-Sil;Jang, Sang-Hoon;Shin, Kuk-Hyun;Kim, Bak-Kwang;Kang, Sam-Sik
    • Archives of Pharmacal Research
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    • v.26 no.9
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    • pp.727-730
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    • 2003
  • The in vivo anti-tumor activities of decursinol angelate (1) and decursin (2) isolated from the roots of Angelica gigas were investigated. These two compounds, when administered consecutively for 9 days at 50 and 100 mg/kg i.p. in mice, caused a significant increase in the life span and a significant decrease in the tumor weight and volume of mice inoculated with Sarcoma-180 tumor cells. These results suggest that decursinol angelate (1) and decursin (2) from A. gigas have anti-tumor activities.

Malignant melanoma on a thermal burn scar

  • Lee, Han Byul;Han, So Eun;Chang, Lan Sook;Lee, Soo Hyang
    • Archives of Craniofacial Surgery
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    • v.20 no.1
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    • pp.58-61
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    • 2019
  • Chronic burn scars often cause various skin malignancies at rates of up to 2%. These lesions are usually squamous cell carcinomas, but rarely, malignant melanoma is reported. We report a 67-year-old male with a malignant melanoma on a burn scar with regional metastasis. This patient presented an ulcerative lesion only in 2 weeks. After histopathological diagnosis, we performed only palliative surgery on patient's demand, and followed up the subsequent deterioration course. Our case reemphasizes the need for rapid diagnosis and treatment when suspect lesions are present on chronic burn scar. Also, physician should be in mind and inform the patient about malignant melanoma and its aggressive course.

Periantral fungal abscess after zygoma reduction: a case report

  • Keun Hyung Kim;Hoon Kim;Soo Yeon Lim;In Chang Koh
    • Archives of Craniofacial Surgery
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    • v.24 no.6
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    • pp.288-291
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    • 2023
  • This case report describes our treatment of a persistent periantral abscess in a 35-year-old woman. The abscess developed following a zygoma-reduction surgery, during which a preexisting fungal ball had not been addressed. Our comprehensive treatment approach included functional endoscopic sinus surgery, fungal ball removal, abscess drainage, and debridement. Two weeks postoperatively, the patient's symptoms had resolved. A 6-month postoperative follow-up revealed no signs of recurrence or complications, and the patient reported satisfactory functional and aesthetic results. This case underscores the importance of thorough preoperative evaluations and raises awareness about the potential risks of untreated asymptomatic pathologies, which can potentially progress and lead to further complications.

In Vitro Chemosensitivity Test of SK-302B on Human Colon Carcinoma Cell Lines

  • Kim, Soo-Kie;Ahn, Chan-Mug;Kim, Tae-Ue;Choi, Sun-Ju;Park, Yoon-Sun;Shin, Woon-Seob;Koh, Choon-Myung
    • Archives of Pharmacal Research
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    • v.19 no.4
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    • pp.261-263
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    • 1996
  • SK-302B, an antibiotic purified from soil Streptomyces sp. 302, was structurally identified as echinomycin (C/sub 50/H/sub 66/N/sub 11/S/sub 2/). In the present experiment, the possibility of SK-302B as an anticolon cancer agent was investigated by using chemosensitivity system (MTT assay, clonogenic assay). Treatment of SK-302B on various colon cancer cell lines resulted in a significant cytotoxicity and tumor colony formation inhibition. These studies showed that SK-302B had a potent inhibition on colon cancer cells.

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