跳到主要內容

臺灣博碩士論文加值系統

(216.73.216.66) 您好!臺灣時間:2026/08/14 07:57
字體大小: 字級放大   字級縮小   預設字形  
回查詢結果 :::

詳目顯示

我願授權國圖
: 
twitterline
研究生:鄭依萍
研究生(外文):I Ping Cheng
論文名稱:海南島產五蕊寄生及廣寄生之成分研究
論文名稱(外文):The chemical constituents of Dendrophthoe pentandra (L.) Miq. and Taxillus chinensis (DC.) Danser from Hainan Island
指導教授:呂彥禮
指導教授(外文):Y. L.Leu
學位類別:碩士
校院名稱:長庚大學
系所名稱:天然藥物研究所
學門:醫藥衛生學門
學類:藥學學類
論文種類:學術論文
論文出版年:2006
畢業學年度:94
語文別:中文
論文頁數:95
中文關鍵詞:五蕊寄生廣寄生化合物成分光譜鈍果海南島
外文關鍵詞:Dendrophthoe pentandra (L.) Miq.Taxillus chinensis (DC.) DanserHainan Island
相關次數:
  • 被引用被引用:4
  • 點閱點閱:262
  • 評分評分:
  • 下載下載:0
  • 收藏至我的研究室書目清單書目收藏:0
五蕊寄生(Dendrophthoe pentandra (L.) Miq.)及廣寄生(Taxillus chinensis (DC.) Danser)皆為桑寄生科(Loranthaceae)植物,分屬於五蕊寄生屬及鈍果寄生屬。
從新鮮五蕊寄生(367.75 g)總共分得15個化合物,其中11個化合物經光譜分析及文獻比對後,確認其結構為2,3-diaminopropionic acid (1)、gallic acid (3)、methyl gallate (4)、methylparaben (5)、phlorin (6)、(+)-catechin (10)、2-(3',4'-dihydroxyphenyl)-chroman-5,7-diol (11)、β-sitosterol (15)、β-sitosteryl-O-glucoside (16)、friedelin (18)與lupeol (20),以上之化合物皆為本屬首次分離得到之化合物。
從新鮮廣寄生(336.28 g)總共分離得到24個化合物,其中16個經光譜分析及文獻比對後,確認其結構分別為2,4-dimethoxy-
benzaldehyde (2)、gallic acid (3)、methyl gallate (4)、methylparaben(5)、phlorin (6)、syringaldehyde (7)、methyl-21-hydroxy-(21R)-pheophorbide-a (8)、methyl pheophorbide-a (9)、(+)-catechin (10)、2-(3',4'-dihydroxy-phenyl)-chroman-5,7-diol (11)、kaempferol-3-O-α-L-rhamnoside (12)、quercetin-3-O-α-L-rhamnoside (13)、quercetin-3-O-β-D-glucoside(14)、β-amyrin acetate (17)、friedelin (18) 與 lupenyl acetate (19)。
Dendrophthoe pentandra (L.) Miq. and Taxillus chinensis (DC.)Danser are species of Loranthaceae.
Fifteen compounds were isolated from the fresh Dendrophthoepentandra (L.) Miq., and eleven compounds were determined by spectralanalysis. They included 2,3-diamino-propionic acid (1), gallic acid (3),methyl gallate (4), methylparaben (5), phlorin (6), (+)-catechin (10),2-(3',4'-dihydroxyphenyl)-chroman-5,7-diol (11), β-sitosterol (15),β-sitosteryl-O-glucoside (16), friedelin (18) and lupeol (20).
Twenty-four compounds were isolated from the fresh Taxilluschinensis (DC.) Danser, and sixteen compounds were determined byspectral analysis. They included 2,4-dimethoxy-benzaldehyde (2), gallicacid (3), methyl gallate (4), methylparaben (5), phlorin (6),syringaldehyde(7), methyl-21-hydroxy-(21R)-pheophorbide-a (8), methylpheophorbide-a (9), (+)-catechin (10), 2-(3',4'-dihydrophenyl)-chroman-5,7-diol (11), kaempferol-3-O-α-L-rhamnoside (12), quercetin-3-O-α-L-rhamnoside (13), quercetin-3-O-β-D-glucoside (14), β-amyrin acetate(17), friedelin (18) and lupenyl acetate (19).
指導教授推薦書
口試委員審定書
授權書............................................................iii
謝誌..............................................................iv
中文摘要...........................................................v
英文摘要...........................................................vi
目錄..............................................................vii

第一章 緒論......................................................1
第一節 前言...................................................1
第二節 五蕊寄生之植物分佈及其形態................................3
第三節 廣寄生之植物分佈及其形態..................................5

第二章 文獻回顧...................................................7
第一節 化學成分回顧.............................................7
第二節 藥理研究回顧.............................................18

第三章 抽取與分離..................................................21
第一節 五蕊寄生之抽取與分離......................................21
第二節 廣寄生之抽取與分離........................................24
第三節 純化所得之化合物..........................................26

第四章 化合物之構造研究..............................................32
第一節 2,4-Dimethoxy-benzaldehyde(2)之結構研究.................32
第二節 Phlorin(6)之結構研究....................................36
第三節 2-(3',4'-Dihydroxyphenyl)-chroman-5,7-diol(11)之結構研
究......................................................38
第四節 Friedelin(18)之結構研究.................................43
第五節 其他化合物................................................47

第五章 生物活性試驗.................................................48
第一節 DPPH自由基的清除作用......................................49
第二節 超氧自由基 (O2.-) 釋放之測定...............................51
第三節 Elastase 釋放之測定.......................................53

第六章 結論.........................................................55
第七章 實驗部分.....................................................56
第一節 本實驗所用之儀器與藥品.....................................56
第二節 五蕊寄生之分離與純化.......................................58
第三節 廣寄生之分離與純化.........................................59
第四節 生物活性試驗..............................................61
光譜數據............................................................63
參考文獻............................................................81
〔1〕中國科學院昆明植物研究所長春中醫學院,中國本草圖錄,卷八,台灣商務印書館股
份有限公司,台北,p.25,1990.
〔2〕中國科學院中國植物志編輯委員會,中國植物志,第二十四卷,科學出版社,北京,
p.86-158,1988.
〔3〕童承福,「臺灣市售中藥誤用品種及寄生類藥材藥理活性之研究」,中國醫藥學院,
博士論文,p.158-161,1999.
〔4〕中國藥材公司,中國中藥資源志要,科學出版社,北京,p.211,1994.
〔5〕國家中醫藥管理局,中華本草,卷二,上海科學技術出版社,上海, p.2•598,
1999.
〔6〕中國科學院昆明植物研究所長春中醫學院,中國本草圖錄,卷九,台灣商務印書館股
份有限公司,台北,p.46,1990.
〔7〕G. Sadik, R. Islam, M. M. Rahman, ”Antimicrobial and
cytotoxic constituents of Loranthus globosus”, Fitoterapia ,
74, 308-311, 2003.
〔8〕李良瓊,李美蓉,朱愛江,「銹毛桑寄生化學成分的研究」,中國中藥雜誌,21,
34-35,1996.
〔9〕K. Ohashi, H. Winarno, M. Mukai, ” Indonesian medicinal plants
XXV. Cancer cell invasion inhibitory effects of chemical
constituents in the parasitic plant Scurrula atropurpurea
(Loranthaceae)”, Chemical & Pharmaceutical Bulletin, 51 , 343-
345, 2003.
〔10〕T. Konishi, T. Nishio, S. Kiyosawa, ”The constituents and
analysis of Taxillus kaempferi and the host, Pinus
thunbergii”, Natural Medicines, 50, 28-33, 1996.
〔11〕T. Fukunaga, K. Nishiya, I. Kajikawa, K. Takeya, and H.
Itokawa, ”Studies on the constituents of Japanese mistletoes
from different host tree, and their antimicrobial and
hypotensive properties”, Chemical & Pharmaceutical Bulletin,
37, 1543-1546, 1989.
〔12〕李良瓊,李美蓉,楊智彪,胡曉斌,「毛葉寄生化學成分的研究」,中草藥,26,
118-121,1995.
〔13〕J. H. Lin, Y. T. Lin, ”Flavonoids from the leaves of
Loranthus kaoi (Chao) Kiu”, Journal of Food and Drug
Analysis, 7, 185-190, 1999.
〔14〕C. C. Shen, Y. S. Chang, L. K. Ho, ” Nuclear magnetic
resonance studies of 5,7-dihydroxyflavonoids”,Phytochemistry,
34, 843-845, 1993.
〔15〕L. L. Yang, K. Y. Yen, Y. Kiso, H. Hikino, ”Antihepatotoxic
actions of formosan plant drugs”, Journal ofEthnopharmacolgy,
19, 103-110, 1987.
〔16〕H. Shibuya, K. Ohashi, I. kitagawa, ”Search for
pharmacochemical leads from tropical rainforest plants”, Pure
and Applied Chemistry, 71, 1109-1113, 1999.
〔17〕伍朝,張觀德,「馬桑寄生及馬桑子中內酯成分分析方法的研究」,藥學學報,
19,56-62,1984.
〔18〕A. Richter, ”Viscumitol, a dimethyl-ether of muco-inositol
from Viscum album”, Phytochemistry, 31, 3925-3927, 1992.
〔19〕T. Ishizu, H. Winarno, E. Tsujino, T. Morita, H.
Shibuya, ”Stereochemical structure of perseitol‧K+
complex isolated from the leaves of Scurrula fusca”,
Chemical & Pharmaceutical Bulletin, 50, 489-492, 2002.
〔20〕謝文全,陳忠川,邱年永,張永勳,歐潤芝,台灣常用藥
用植物圖鑑第一冊,行政院衛生署中醫藥委員會,台北,p.165,2002.
〔21〕陳政鴻,「台灣產大葉桑寄生正丁醇層萃取物對於自發性高血壓和正常血壓大白鼠
造成降血壓作用之研究」, 陽明醫學 院,碩士論文,p.29,1992.
〔22〕K. Ohashi, H. Winarno, ”Preparation and cancer cell invasion
inhibitory effects of C16-alkynic fatty acids”, Chemical &
Pharmaceutical Bulletin, 51, 463-466, 2003.
〔23〕R. Murwani, ”Indonesian tea mistletoe (Scurrula oortiana) stem
extract increases tumour cell sensitivity to tumour necrosis
factor alpha”, Phytotherapy Research, 17, 407-409, 2003.
〔24〕F. Lohezic-Le Devehat, A. Bakhtiar, ”Antiviral and cytotoxic
activities of some Indonesian plants”, Fitoterapia, 73, 400-
405, 2002.
〔25〕D. K. Obatomi, E. O. Bikomo, ”Anti-diabetic properties of
the African mistletoe in streptozotocin-induced diabetic rats”,
Journal of Ethnopharmacology, 43, 13-17, 1994.
〔26〕C. J. Pouchert, J. Behnke, The Aldrich Library of 13C and 1H
NMR Spectra, Aldrich Chemical Company, Inc., New York, 2, 954
c, 1983.
〔27〕C. J. Pouchert, J. Behnke, ”The Aldrich library of 13C and 1H
FTNMR spectra”, Aldrich Chemical Company, New York, edit.1,
Vol.1, p.298-300, 1993.
〔28〕G. Hussein, N. Nakamura, M. R. Meselhy, M. Hattori, “Phenolics
from Maytenus senegalensis”, Phytochemistry, 50, 689-694, 1999.
〔29〕K. Yoshikawa, S. Sugawara, S. Arihara, “Phenylpropanoids and
other secondary metabolites from fresh fruits of Picrasma
quassioides”, Phytochemistry, 40, 253-256, 1995.
〔30〕S. Roemmelt, N. Zimmermann, W. Rademacher, D.
Treutter, “Formation of novel flavonoids in apple (Malus ×
domestica) treated wiyh the 2-oxoglutarate-dependent
dioxygenase inhibitor prohexadione-Ca”, Phytochemistry, 64,
709-716, 2003.
〔31〕E. Garo, M. maillard, S. Antus, S. Mavi, K. Hostettmann, “Five
flavans from Mariscus psilostachys”, Phytochemistry, 43, 1265-
1269, 1996.
〔32〕T. Akihisa, K. Yamamoto, T. Tamura, Y. Kimura, T. Iida, T.
Nambara, F. C. Chang, ”Triterpenoid ketones from Lingnania
chungii mcclure : aborinone, freedelin and glutinone”, Chemical
& Pharmaceutical Bulletin, 40 , 789-791, 1992.
〔33〕J. Klass, W. F. Tinto, “Friedelane triterpenoids from
Peritassa compta : complete 1H and 13C assignments by 2d nmr
spectroscopy”, Journal of Natural Products, 55, 1626-1630, 1992.
〔34〕C. S. Evans, P. J. Burns, M. D. Dutton, S. Brown, “2-Amino-4N-
ureidopropionic acid (albizzine) and its oxalyl derivative in
hyphae of Coniophora puteana”, Phytochemistry, 29, 2159-2160,
1990.
〔35〕G. Roncari, Z. K. Borowska, L. C. Craig, “On th chemical
nature of the antibiotic edeine”, Biochemistry, 5, 2153-2159,
1966.
〔36〕張鳳珠,「石苓舅與臭辣樹葉部之成份研究」,國立成功大學,碩士論文,p.56-
57,1992.
〔37〕K. Takeya, H. Itokawa, “Isoflavonoids and the other
consituents in callus tissues of Pueraria lobata”, Chemical &
Pharmaceutical Bulletin, 30, 1496-1499, 1982.
〔38〕Y. L. Leu, L. S. Shi, A. G. Damu, “Chemical constituents of
Taraxacum formosanum”, Chemical & Pharmaceutical Bulletin, 51,
599-601, 2003.
〔39〕張鳳珠,「石苓舅與臭辣樹葉部之成份研究」,國立成功大學,碩士論文,p.15-
16,1992.
〔40〕Y. Nakatani, G.. Ourisson, J. P. Beck, ”Chemistry and
biochemistry of Chinese drugs Ⅶ. Cytostatic pheophytins from
Silkworm extreta and derived photocytotoxic pheophorbides ”,
Chemical & Pharmaceutical Bulletin, 29, 2261-2269, 1981.
〔41〕呂孝仁,「黃蝴蝶莢果之鞣質及相關連化合物之研究」,台北醫學大學,碩士論
文,p.71-73,2003.
〔42〕T. Fukunaga, K. Nishiya, ”Chemical studies on the constituents
of Hyphear tanakae Hosokawa from different host tress ”,
Chemical & Pharmaceutical Bulletin, 36, 1180-1184, 1988.
〔43〕Y. Hua, H. Q. Wang, ”Chemical components of Anaphalis sinica
Hance ”, Journal of Chinese Chemical Society, 51, 409-415, 2004.
〔44〕S. C. Cao, X. H. Wu, K. Y. Sim, B. K. Tan, J. T. Perreira, S.
H. Goh, “Styryl-lactones derivatives from Goniothalamuns
borneensis”, Tetrahedron, 54, 2143-2148, 1998.
〔45〕S. K. Talapatra, D. Basu, P. Chattopadhyay, B.
Talapatra, “Aristolactams of Goniothalamuns sesquipedalis”,
Phytochemistry, 27, 903-906, 1988.
〔46〕T. Fujita, M. Nakayama, “Monoterpene glucosides and other
constituents from Perilla frutescens”, Phytochemistry, 34,
1545-1548, 1993.
〔47〕T. S. Wu, F. C. Chang, P. L.Wu, C. S. Kuoh, I. S.
Chen, “Constituents of Tetradium glabrifolium”, Journal of the
Chinese Chemical Society, 42, 929-934, 1995.
〔48〕M. L. Flagg, S. Valcic, G. Montenegro, M. Gomez, B. N.
Timmermann, “Pentacyclic trierpenes from Chuquiraga ulicina”,
Phytochemistry, 52, 1345-1350, 1999.
〔49〕R. A. Appleton, C.R. Enzell,” Triterpenoids and aromatic
components of deertongue leaf ”, Phytochemistry, 10 , 447-
449 , 1971.
〔50〕G. H. Aynilian, N. R. Farnsworth, G. J. Persinos, “Isolation of
lupeol from Crataeva benthamii”, Phytochemistry, 11 , 2885-
2886 , 1972.
〔51〕P. F. Li, M. Harsdorf, ”Differential effect of hydrogen
peroxide and superoxide anion on apoptosis and proliferation of
vascular smooth muscle cell ”, Circulation, 96, 3602-3609, 1997.
〔52〕C. Dahlgren, A. Karlsson, ”Respiratory burst in human
neutrophils ”, Journal of Immunological Methods, 232, 3-14,
1999.
QRCODE
 
 
 
 
 
                                                                                                                                                                                                                                                                                                                                                                                                               
第一頁 上一頁 下一頁 最後一頁 top