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      권백(Selaginella tamariscina)의 항암 활성성분

      한글로보기

      https://www.riss.kr/link?id=T10663120

      • 저자
      • 발행사항

        광주 : 조선대학교 대학원, 2006

      • 학위논문사항

        학위논문(박사) -- 朝鮮大學校 大學院 , 藥學科 , 2006. 8

      • 발행연도

        2006

      • 작성언어

        한국어

      • 주제어
      • KDC

        518.31 판사항(4)

      • DDC

        615.321 판사항(21)

      • 발행국(도시)

        광주

      • 기타서명

        Antitumor constituents of selaginelola tamariscina spring

      • 형태사항

        vii, 54 p. : 삽화 ; 26 cm.

      • 일반주기명

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        지도교수: 문영희
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      다국어 초록 (Multilingual Abstract)

      Selaginella tamariscina Spring(Selaginellaceae) is a perennial plant and is distributed in Korea, China, and Japan. In traditional medicine, the whole plants are used as an antiinflammatory, antihemorrhage, anticancer, and astringent. Previous phytochemical studies on this species afforded biflavonoids, triterpenoids, and flavonoids. In an ongoing investigation into antitumor active compounds from natural products, the methylene chloride soluble fraction of methanol extract from Selaginella tamariscina Spring.(Selaginellaceae) showed significant antitumor activity on the human cancer cell lines. By means of the activity-oriented purification procedure, 4α, 5α-4,14-dimethylcholest-8-en-3-one(1) ergosta-4,6,8(14),22-tetraene-3-one(2), ergosterol endoperoxide(3) cholest-5-ene-3,7-diol(7β-hydroxycholesterol)(4), stigmasta-5-ene-3β-7β-diol(7β-hydroxysitosterol)(5), stigmasta-5-ene-3β-7α-diol(7α-hydroxysitosterol) (6) were isolated. Their structures were determined by chemical analysis, as well as, 1D- with 2D-NMR spectroscopy. All compounds were isolated from this plant for the first time. Cytotoxic activity of isolated compounds was evaluated by SRB method against five human cancer cell lines. Most of the isolated compounds showed potent antitumor activity except for compound 1. It is of interest to compare the antitumor activity of compound 5 with that of compound 6. Compounds 2-6 could be mainly responsible for the potent antitumor effect of an methylene chloride soluble fraction of S. tamariscina, and might be suitable for further development as a leading antitumor agent.
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      Selaginella tamariscina Spring(Selaginellaceae) is a perennial plant and is distributed in Korea, China, and Japan. In traditional medicine, the whole plants are used as an antiinflammatory, antihemorrhage, anticancer, and astringent. Previous phytoch...

      Selaginella tamariscina Spring(Selaginellaceae) is a perennial plant and is distributed in Korea, China, and Japan. In traditional medicine, the whole plants are used as an antiinflammatory, antihemorrhage, anticancer, and astringent. Previous phytochemical studies on this species afforded biflavonoids, triterpenoids, and flavonoids. In an ongoing investigation into antitumor active compounds from natural products, the methylene chloride soluble fraction of methanol extract from Selaginella tamariscina Spring.(Selaginellaceae) showed significant antitumor activity on the human cancer cell lines. By means of the activity-oriented purification procedure, 4α, 5α-4,14-dimethylcholest-8-en-3-one(1) ergosta-4,6,8(14),22-tetraene-3-one(2), ergosterol endoperoxide(3) cholest-5-ene-3,7-diol(7β-hydroxycholesterol)(4), stigmasta-5-ene-3β-7β-diol(7β-hydroxysitosterol)(5), stigmasta-5-ene-3β-7α-diol(7α-hydroxysitosterol) (6) were isolated. Their structures were determined by chemical analysis, as well as, 1D- with 2D-NMR spectroscopy. All compounds were isolated from this plant for the first time. Cytotoxic activity of isolated compounds was evaluated by SRB method against five human cancer cell lines. Most of the isolated compounds showed potent antitumor activity except for compound 1. It is of interest to compare the antitumor activity of compound 5 with that of compound 6. Compounds 2-6 could be mainly responsible for the potent antitumor effect of an methylene chloride soluble fraction of S. tamariscina, and might be suitable for further development as a leading antitumor agent.

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      목차 (Table of Contents)

      • Contents = Ⅰ
      • List of Schemes = Ⅲ
      • List of Tables = Ⅲ
      • List of Figures = Ⅳ
      • Abstract = Ⅴ
      • Contents = Ⅰ
      • List of Schemes = Ⅲ
      • List of Tables = Ⅲ
      • List of Figures = Ⅳ
      • Abstract = Ⅴ
      • Ⅰ. 緖論 = 1
      • Ⅱ. 實驗 = 7
      • 1. 實驗材料 = 7
      • 2. 試藥 및 器機 = 7
      • 2-1. 試藥 = 7
      • 2-2. 器機 = 8
      • 2-3. 細胞株 = 8
      • 3. 化合物의 分離 = 9
      • 3-1. 抽出 및 分劃 = 9
      • 3-2. CH2Cl2 分劃으로부터 compound의 分離 = 10
      • 3-2-1. Compound 1의 分離 = 12
      • 3-2-2. Compound 2의 分離 = 13
      • 3-2-3. Compound 3의 分離 = 14
      • 3-2-4. Compound 4, 5의 分離 = 15
      • 3-2-5. Compound 6의 分離 = 17
      • 4. 抗癌活性 = 18
      • Ⅲ. 結果 및 考察 = 20
      • 1. Compound 1의 構造 = 20
      • 2. Compound 2의 構造 = 20
      • 3. Compound 3의 構造 = 21
      • 4. Compound 4의 構造 = 22
      • 5. Compound 5의 構造 = 22
      • 6. Compound 6의 構造 = 23
      • 7. Compounds 1-6의 抗癌活性 = 25
      • Ⅳ. 結論 = 27
      • Ⅴ. 參考文獻 = 29
      • APPENDIX = 32
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