• 제목/요약/키워드: University Archives

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Triterpenoids from Acanthopanax koreanum Root and Their Inhibitory Activities on NFAT Transcription

  • Cai, Xing-Fu;Lee, Im-Seon;Shen, Guanghai;Dat, Nguyen-Tien;Lee, Jung-Joon;Kim, Young-Ho
    • Archives of Pharmacal Research
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    • 제27권8호
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    • pp.825-828
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    • 2004
  • Two triterpenoids (1,4) and two triterpenoid glycosides (2,3) were isolated from the root of Acanthopanax koreanum (Araliaceae). Their structures were identified as impressic acid (1), acankoreoside A (2), 3-epi-betulinic acid 28-O-[(${\alpha}-L-rhamnopyranosyl(1{\rightarrow}4)-{\beta}-D-glucopyrano-syl(1{\rightarrow}6)]-{\beta}-D-glucopyranosyl]$ ester (3), and ursolic acid (4) by physicochemical and spectro-scopic methods. Of these compounds, impressic acid (1) exhibited a potent inhibitory activity against NFAT transcription factor ($IC_{50}:{\;}12.65{\;}{\mu\textrm{m}}$).

Synthesis and Antifungal Activities of Some Aryl (3-Methyl-Benzofuran-2-yl) Ketoximes

  • Benkli, Kadriye;Gundogdu-Karaburun, Nalan;Karaburun, Ahmet-Cagrl;Ucucu, Umit;Demirayak, Seref;Kiraz, Nuri
    • Archives of Pharmacal Research
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    • 제26권3호
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    • pp.202-206
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    • 2003
  • In this study, some aryl (3-methyl-benzofuran-2-yl) ketoximes and their ethers and esters were synthesised. The structure elucidation of the compounds was performed by IR, $^1H-NMR$, MASS spectroscopy and elemental analyses. Antifungal activities of the compounds were examined and moderate activity was obtained.

Synthesis of 7-Hydroxy-4-Oxo-4H-Chromene- and 7-Hydroxychroman-2-Carboxylic Acid N-Alkyl Amides and Their Antioxidant Activities

  • Kwak, Jae-Hwan;Kang, Hae-Eun;Jung, Jae-Kyung;Kim, Hwa-Jung;Cho, Jung-Sook;Lee, Hee-Soon
    • Archives of Pharmacal Research
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    • 제29권9호
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    • pp.728-734
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    • 2006
  • A series of 7-hydroxy-4-oxo-4H-chromene- (3a - h) and 7-hydroxychroman-2-carboxylic acid N-alkyl amides (4a - g) were synthesized and their antioxidant activities were evaluated. While compounds 3a - h were less active, compounds 4a - g exhibited more potent inhibition of lipid peroxidation initiated by $Fe^{2+}$ and ascorbic acid in rat brain homogenates. Among them, 7-hydroxychroman-2-carboxylic acid N-alkylamides (4e - g) bearing nonyl, decyl, and undecyl side chain exhibited 3 times more potent inhibition than trolox (1).

Potentiation of Ceramide-Induced Apoptosis by $p27^{kip1}$ Overexpression

  • Kim Hae Jong;Ghil Kyung Chul;Kim Moo Sung;Yeo Seong Hyun;Chun Young Jin;Kim Mie Young
    • Archives of Pharmacal Research
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    • 제28권1호
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    • pp.87-92
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    • 2005
  • The cyclin-dependent kinase inhibitor$p27^{kip1}$(p27) has been implicated in the regulation of cell cycle and apoptosis. Recently, we have demonstrated that ceramide induces apoptotic cell death associated with increase in the level of p27 in HL-60 cells. In the present study, we showed that overexpression of p27 increases ceramide-induced apoptotic cell death in HL-60 cells. Furthermore, overexpression of p27 accelerated DNA fragmentation, PARP cleavage and cytochrome c release induced by ceramide. In addition, ceramide induced Sax expression independent of p27. These findings indicate that enhanced effect on apoptosis by p27 is associated with mitochondrial signaling which involves cytochrome c release.

Epithelioid sarcoma associated with neurofibromatosis type I

  • Hwang, Sung Oh;Lee, Soo Hyang;Lee, Han Byul
    • 대한두개안면성형외과학회지
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    • 제21권1호
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    • pp.41-44
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    • 2020
  • In general, patients with neurofibromatosis type I have a higher risk than those with other types of neurofibromatosis of developing soft-tissue sarcomas related to the nervous system. We here present a 42-year-old man with neurofibromatosis type I who developed a protruding mass over only 2 weeks. The histopathological diagnosis was epithelioid sarcoma. Epithelioid sarcomas are rare and, to the best of our knowledge, no epithelioid sarcomas have been reported in patients with neurofibromatosis type I. Radical excision of the primary lesion was performed and postoperative radiotherapy and chemotherapy administered, as is recommended for epithelioid sarcoma. Our case emphasizes that patients with neurofibromatosis type I may develop malignant tumors.

Treatment of multiple craniofacial osteomas by endoscopic approach

  • Yoo, Hyokyung;Doh, Gyeonghyeon;Kim, Baek Kyu
    • 대한두개안면성형외과학회지
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    • 제21권4호
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    • pp.261-263
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    • 2020
  • Osteomas are benign osteogenic neoplasms that usually occur as solitary craniofacial lesions. Multiple osteomas are rare, particularly those that do not occur as part of an associated syndrome. We report a case of a 72-year-old woman who presented with multiple bony protrusions over the forehead and scalp. She denied any diagnosis of syndromes that are known to be associated with osteomas. Surgical excision was performed by endoscopically resecting more than 30 osteomas of the frontal and bilateral parietal bones. Compared with conventional surgical excision through a direct incision, endoscopic-assisted surgery is a simple and effective method for the treatment of multiple craniofacial osteomas and is associated with excellent cosmetic outcomes and no neurovascular complications.

A Synthetic Study on Cyclic Phosphate Derivatives of Seconucleosides as Potential Antiviral Agents (I) -Synthesis of 3',5'-cyclic phosphates of 2'-substituted secouridines and secoribavirins-

  • Hong, Kyong-Aie;Yang, Jae-Wook;Chun, Soo-Joon;Ha, Eun-Young;Kim, Joong-Hyup;Chun, Moon-Woo;Chung, Won-Keun
    • Archives of Pharmacal Research
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    • 제14권1호
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    • pp.30-34
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    • 1991
  • The synthetic study of 3',5-cyclic phosphates of 2'-substituted 2',3'-secouridines and 2',3'-secoribavirins toward development of new antiviral agents is described. These cyclic phosphates were synthesized from their respective 4-nitrophenyl 3',5'-cyclic phosphate triesters. These triesters were prepared from the corresponding 2'-azido and 2'-bromo 2',3'-seconucleosides.

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Flavonoids from the Aerial Parts of Lonicera japonica

  • Son, Kun-Ho;Park, Jung-Ok;Chung, Kyu-Charn;Chang, Hyeun-Wook;Kim, Hyun-Pyo;Kim, Ju-Sun;Kang, Sam-Sik
    • Archives of Pharmacal Research
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    • 제15권4호
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    • pp.365-370
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    • 1992
  • Seven flavonoids were isolated from the aerial parts of Lonicera japonica. Their structures were characterized as hydnocarpin 1, quercetin 2, ochnaflavone 3, ochnaflavone 4'-O-methylether 4, astragalin 5, isoquercitrin 6, and rhoifolin 7 by chemical and spectroscopic evidences.

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Synthesis of Antineoplaston A10 Analogs as Potential Antitumor Agents

  • Choi, Bo-Gil;Kim, Ok-Young;Chung, Byung-Ho;Cho, Won-Jea;Cheon, Seung-Hoon;Choi, Sang-Un;Lee, Chong-Ock
    • Archives of Pharmacal Research
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    • 제21권2호
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    • pp.157-163
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    • 1998
  • Several aniline mustard analogues were obtained by introducing N,N-bis(2-chloroethyl)amino moiety to phenyl ring of A10 analogues in order to increase reactivity of A10 analogs and selectivity into DNA. The in vitro antitumor activity of synthesized compounds was evaluated using five different solid tumor cell lines by SRB method. Aniline mustard analogues exhibited more potent antitumor activity than A10 analogs. Especially, m-aniline mustard of benzoyl analogue displayed remarkable antitumor activity.

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