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研究生:宋秉欣
研究生(外文):Ping-Hsin Sung
論文名稱:細本山葡萄(VitisthunbergiiSIEB.&ZUCC.)根部化學成分之研究
論文名稱(外文):Studies on the Chemical Constituents of the Root of Vitis thunbergii SIEB. & ZUCC.
指導教授:張永勳張永勳引用關係
學位類別:碩士
校院名稱:中國醫藥大學
系所名稱:藥物化學研究所碩士班
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:105
中文關鍵詞:細本山葡萄山葡萄
外文關鍵詞:Vitis thunbergii SIEB. & ZUCC.Vitis thunbergii
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細本山葡萄Vitis thunbergii SIEB. & ZUCC.為葡萄科(Vitaceae)植物,又名小本山葡萄、小葉山葡萄、山葡萄等別名,其根莖具有清熱、利尿、袪濕、解毒、消腫止血、生肌之效。主治風濕關節痛、風濕痺痛、腳氣腫、肝炎黃疸、痢疾、淋病、小便不利、腫毒、跌打損傷,為台灣固有之民間用藥。
本研究自細本山葡萄根部之甲醇粗抽物分離出的成分有lupeol(H-1)、ß-sitosterol(H-2)、l-dotriacontanol(H-3)、friedelin (C-1)、betulin(C-2)、 vanillic acid(EA-1)、caffeic acid(EA-2)等成分。由於過去對於細本山葡萄研究甚少,因此希望藉由細本山葡萄植物的化學成分研究,來確定其成分種類,進而了解細本山葡萄在醫療上的功效。而本研究實驗所分離出成分之藥理活性,則有待進一步之探討與確認。
Vitis thunbergii SIEB. & ZUCC. is a native plant of Taiwan belonging to the Vitaceae family. It is a common folk medicine being used for rheumatism, hepatitis, jaundice, dysentery and blennorrhagia etc..
From its methanolic extracts, seven compounds were isolated: lupeol(H-1), ß-sitosterol(H-2), l-dotriacontanol(H-3), friedelin(C-1), betulin(C-2), vanillic acid(EA-1) and caffeic acid(EA-2). Their structures were determined by spectroscopic methods.
In the past, few reseaches were done on Vitis thunbergii SIEB. & ZUCC. Througt the chemical studies of the ingredients, the medical use of this plant can be understood. However, the pharmacological activities of the compounds isolated needs further investigation.
目 錄
目 錄 I
表目錄 II
圖目錄 IV
中文摘要 VII
英文摘要 VIII
第一章 緒言 1
第二章 總論 3
第一節 細本山葡萄之本草學考察 3
第二節 細本山葡萄之藥用植物學考察 8
第三節 細本山葡萄之Napralert文獻考察 17
第四節 葡萄屬植物之Napralert文獻考察 19
第五節 山葡萄植物之Napralert文獻考察 20
第三章 實驗部分 26
第一節 實驗試劑與儀器 26
第二節 實驗藥材來源及其抽提與分離 30
第四章 結 果 33
第五章 討 論 40
第六章 結 論 59
參考文獻…… 61
圖譜.........71



表目錄
Table 2-1:細本山葡萄植物形態特徵表 13
Table 2-2:Ethnomedical information on Vitis thunbergii 18
Table 2-3:Biological activities for extracts of Vitis thunbergii 20
Table 2-4:Presence of compounds in Vitis flexuosa 21
Table 2-5:Ethnomedical information on Ampelopsis brevipedunculata 22
Table 2-6:Biological activities for extracts of Ampelopsis brevipedunculata 23
Table2-7:Presence of compounds in Ampelopsis brevipedunculata 25
Table 5-1:化合物H-1碳譜數據與文獻lupeol碳譜數據比對表 48
Table 5-2:化合物H-2碳譜數據與文獻ß-sitosterol碳譜數據比對表 51
Table 5-4:化合物C-1碳譜數據與文獻friedelin碳譜數據比對表 57
Table 5-5:化合物C-2碳譜數據與文獻betulin碳譜數據比對表 61


圖目錄
Fig. 2-1:歷代本草所繪蘡薁(細本山葡萄)圖 6
Fig. 2-2:蘡薁(細本山葡萄)之本草系統圖 8
Fig. 2-3:細本山葡萄(Vitis thunbergii SIEB. & ZUCC.)植物圖 13
Fig. 2-4:細本山葡萄(Vitis thunbergii SIEB. & ZUCC.)植物型態特徵圖 14
Fig. 3-1:細本山葡萄根之抽提流程圖 38
Chart 1:The IR (KBr) spectrum of lupeo(H-1)…………………………….71
Chart 2:The MS (EI) spectrum of lupeol (H-1)……………………………..71
Chart 3:The 1H-NMR(CDCl3) spectrum of lupeol (H-1)………………...72
Chart 4:The 1H-NMR(CDCl3) spectrum of lupeol (H-1)…………...…73
Chart 5:The 13C-NMR (CDCl3) spectrum of lupeol (H-1)……………….73
Chart 6:The 13C-NMR (CDCl3) spectrum of lupeol (H-1)………………...74
Chart 7:The DEPT (π/4, 2π/4,3π/4) spectrum of lupeol (H-1)…………. 75
Chart 8:The IR (KBr) spectrum of ß-sitosterol (H-2)…………………….76
Chart 9:The MS (EI) spectrum of ß-sitosterol (H-2)………………………76
Chart 10:The 1H-NMR (CDCl3) spectrum of ß-sitosterol (H-2)…………77
Chart 11:The 1H-NMR (CDCl3) spectrum of ß-sitosterol (H-2)………...78
Chart 12:The 13C-NMR (CDCl3) spectrum of ß-sitosterol (H-2)………..78
Chart 13:The 13C-NMR (CDCl3) spectrum of ß-sitosterol (H-2)………..79
Chart 14:The DEPT (π/4, 2π/4,3π/4) spectrum of ß-sitosterol (H-2)……80
Chart 15:The IR (KBr) spectrum of l-dotriacontanol (H-3)………………81
Chart 16:The MS (EI) spectrum of l-dotriacontanol (H-3)……………….81
Chart 17:The 1H-NMR (CDCl3) spectrum of l-dotriacontanol (H-3)…..82
Chart 18:The 1H-NMR (CDCl3) spectrum of l-dotriacontanol (H-3)…..83
Chart 19:The 13C-NMR (CDCl3) spectrum of l-dotriacontanol (H-3)…..83
Chart 20:The 13C-NMR (CDCl3) spectrum of l-dotriacontanol (H-3)….84
Chart 21:The DEPT (π/4, 2π/4,3π/4) spectrum of l-dotriacontanol (H-3)….85
Chart 22:The IR (KBr) spectrum of friedelin (C-1)………………………..86
Chart 23:The MS (EI) spectrum of friedelin (C-1)………………………..86
Chart 24:The 1H-NMR(CDCl3) spectrum of friedelin (C-1)…………..….87
Chart 25:The 1H-NMR(CDCl3) spectrum of friedelin (C-1)…………….88
Chart 26:The 13C-NMR (CDCl3) spectrum of friedelin (C-1)………89
Chart 27:The 13C-NMR (CDCl3) spectrum of friedelin (C-1)……….90
Chart 28:The DEPT (π/4, 2π/4,3π/4) spectrum of friedelin (C-1)………90
Chart 29:The DEPT (π/4, 2π/4,3π/4) spectrum of friedelin (C-1)………91
Chart 30:The IR (KBr) spectrum of betulin (C-2)…………………………91
Chart 31:The 1H-NMR(CDCl3) spectrum of betulin (C-2)………………92
Chart 32:The 1H-NMR(CDCl3) spectrum of betulin (C-2)……………….93
Chart 33:The 1H-NMR(CDCl3) spectrum of betulin (C-2)……………….94
Chart 34:The The 13C-NMR (CDCl3) spectrum of betulin (C-2)……….94
Chart 35:The The 13C-NMR (CDCl3) spectrum of betulin (C-2)……….95
Chart 36:The DEPT (π/4, 2π/4,3π/4) spectrum of betulin (C-2)…………96
Chart 37:The IR (KBr) spectrum of vanillic acid (EA-1)……………...97
Chart 38:The MS (EI) spectrum of vanillic acid (EA-1)………………….97
Chart 39:The 1H-NMR (DMSO) spectrum of vanillic acid (EA-1)…….98
Chart 40:The 1H-NMR (DMSO) spectrum of vanillic acid (EA-1)….....99
Chart 41:The 13C-NMR (DMSO) spectrum of vanillic acid (EA-1)…...99
Chart 42:The 13C-NMR (DMSO) spectrum of vanillic acid (EA-1)….100
Chart 43:The DEPT (π/4, 2π/4,3π/4) spectrum of vanillic acid (EA-1).100
Chart 44:The IR (KBr) spectrum of caffeic acid(EA-2)…………………101
Chart 45:The MS (EI) spectrum of caffeic acid(EA-2)………………….101
Chart 46:The 1H-NMR (DMSO) spectrum of caffeic acid(EA-2)……..102
Chart 47:The 1H-NMR (DMSO) spectrum of caffeic acid(EA-2)……..103
Chart 48:The 13C-NMR (DMSO) spectrum of caffeic acid(EA-2)…….104
Chart 49:The DEPT (π/4, 2π/4,3π/4) spectrum of caffeic acid(EA-2)…105
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