首个被分离出的生物碱,吗啡 ,于1804年由罂粟 中提取[ 1] 。
生物鹼 (英語:alkaloid )是一種天然存在的含氮鹼性 化合物 。一些人工合成 但結構类似的化合物有時也被稱作生物鹼。除了碳 、氫 、氮 ,生物鹼也可以含有氧 、硫 、氯 、溴 、磷 等元素。[ 2] 生物鹼与其它含氮碱性化合物之间的分界并不明确,但氨基酸 、核苷酸 及胺 类物质通常不被称作生物碱。
生物鹼在人或動物体内产生藥理反應。雖然大部份的生物鹼對人體有毒,但有些也能入药,起鎮痛或麻醉 的作用,以嗎啡 及可待因 尤为重要。生物鹼大都是氨基酸 衍生物,嚐起來有苦澀味,是植物(如馬鈴薯 、蕃茄 、罂粟 )、動物(如貝类 )、细菌 和真菌 等多种生命体的次生代谢物 。通过对生物体的粗提取物进行酸碱萃取 纯化,可以获得大部份的生物鹼。
发现史
自古以来,人类就将含有生物碱的植物用于治疗和娱乐。
例如,早在公元前 2000 年左右,美索不达米亚 就已发现药用植物[ 3] 。[30] 荷马 (作家)的奥德赛 提到了埃及女王送给海伦的礼物,一种带来遗忘的药物。
据信,这份礼物是一种含有鸦片的药物[ 4] 。一本写于公元前一至三世纪的中国室内植物书籍提到了麻黄 和罂粟 的医疗用途[ 5] 。此外,古柯叶 自古以来就被南美 原住民使用。
德国化学家--弗里德里希·塞图纳第一次从鸦片中分离出吗啡。
含有有毒生物碱 (例如乌头碱 和管箭毒碱 )的植物提取物自古以来就被用于毒箭[ 3] 。
生物碱的研究始于 19 世纪。
1804年,德国化学家弗里德里希·瑟图纳 从鸦片中分离出一种“催眠原理”(拉丁语:principium somniferum),他将其称为“吗啡 ”,指的是希腊 梦神 墨菲斯 ; 在德语和其他一些中欧语言中,这仍然是该药物的名称。 “吗啡”一词在英语和法语中使用,由法国物理学家盖-吕萨克 提出。
法国研究人员皮埃尔-佩尔提埃 和约瑟夫·卡旺图 在生物碱发展的早期对化学做出了重大贡献,他们发现了奎宁 (1820年) 和士的宁 (1818年)。
大约在同一时期还发现了其他几种生物碱,包括黄嘌呤 (1817年)、阿托品 (1819年)、咖啡因(1820年)、可尼碱(1827年)、尼古丁(1828年)、秋水仙碱(1833年)、金雀花碱(1851年)和可卡因(1860年)。
20 世纪光谱 和色谱 方法的出现加速了生物碱化学的发展,到 2008 年已鉴定出超过 12,000 种生物碱[ 6] 。
1886 年,德国化学家阿尔伯特·拉登堡 首次完成了生物碱的合成。 他通过2-甲基吡啶 与乙醛 反应并用钠还原生成的2-丙烯基吡啶 来生产乌头碱 [ 7] 。
生物鹼的分類
与大多数其他天然化合物相比,生物碱的特征在于其丰富的结构多样性,没有统一分类。
類別
主要結構
主要合成路線
例子
與含氮雜環生物鹼(真正生物鹼)
吡咯烷 類衍生物[ 8]
鳥氨酸 或 精氨酸 → 腐胺 → N-甲基腐胺 → N-methyl-Δ1 -pyrroline [ 9]
Cuscohygrine , hygrine , hygroline, stachydrine[ 8] [ 10]
托烷 類衍生物[ 11]
阿托品 類 原子取代於位置 3, 6 或 7
鳥氨酸或精氨酸→腐胺→N-甲基腐胺→N-甲基-Δ1 -吡咯烷酮 [ 9]
Atropine , scopolamine , hyoscyamine [ 8] [ 11] [ 12]
可卡因 類 原子取代於位置 2, 3
Cocaine , ecgonine [ 11] [ 13]
吡咯里西啶 類衍生物[ 14]
非酯 類
鳥氨酸,精氨酸→腐→類精脒→惹卓裂鹼 [ 9]
Retronecine , heliotridine, laburnine [ 14] [ 15]
一元羧酸 的複合酯
Indicine, lindelophin, sarracine [ 14]
大環內二酯
Platyphylline , trichodesmine[ 14]
1-氨基吡咯烷類 (lolines )
L-脯氨酸+ L-高絲氨酸→N-(3-氨基-3-羧丙基)脯氨酸→降黑麥草堿 [ 16] [ 17]
Loline, N -formylloline, N -acetylloline[ 18]
哌啶 類衍生物[ 19]
賴氨酸 → 屍胺 → Δ1 -piperideine [ 20]
Sedamine , lobeline, anaferine, piperine [ 21] [ 22]
辛酸 → coniceine → 毒芹碱 [ 23]
Coniine , coniceine [ 23]
喹 類衍生物[ 24] [ 25]
羽扇豆碱 類
賴氨酸 → 屍胺 → Δ1 -piperideine [ 26]
Lupinine , nupharidin [ 24]
野靛碱 類
野靛碱 [ 24]
司巴丁 類
司巴丁 , lupanine , anahygrine [ 24]
苦參鹼 類
Matrine, oxymatrine, allomatridine[ 24] [ 27] [ 28]
苦豆鹼 類
Ormosanine, piptantine[ 24] [ 29]
吲哚聯啶 類衍生物[ 30]
賴氨酸 → δ-semialdehyde of Α-氨基己二酸 → pipecolic acid → 1 indolizidinone [ 31]
Swainsonine , castanospermine [ 32]
吡啶 類衍生物[ 33] [ 34]
吡啶簡單衍生物
烟酸 → dihydronicotinic acid → 1,2-dihydropyridine [ 35]
Trigonelline , ricinine, arecoline [ 33] [ 36]
多環芳烴 非冷凝 吡啶衍生物
Nicotine , nornicotine , anabasine , anatabine [ 33] [ 36]
多環芳烴冷凝吡啶衍生物
Actinidine , gentianine, pediculinine [ 37]
Sesquiterpene pyridine derivatives
烟酸 , 異亮氨酸 [ 38]
Evonine, hippocrateine, triptonine [ 34] [ 35]
異喹啉 類衍生物及相關生物鹼[ 39]
Simple derivatives of isoquinoline [ 40]
Tyrosine or 苯丙氨酸 → 多巴胺 or 酪胺 (for alkaloids Amarillis) [ 41] [ 42]
Salsoline, lophocerine [ 39] [ 40]
Derivatives of 1- and 3-isoquinolines [ 43]
N-methylcoridaldine, noroxyhydrastinine [ 43]
Derivatives of 1- and 4-phenyltetrahydroisoquinolines [ 40]
Cryptostilin [ 40] [ 44]
Derivatives of 5-naftil-isoquinoline [ 45]
Ancistrocladine [ 45]
Derivatives of 1- and 2-benzyl-izoquinolines [ 46]
Papaverine , laudanosine , sendaverine
Cularine group[ 47]
Cularine, yagonine [ 47]
Pavine s and isopavines [ 48]
Argemonine, amurensine [ 48]
Benzopyrrocolines [ 49]
Cryptaustoline [ 40]
Protoberberines [ 40]
Berberine , canadine , ophiocarpine, mecambridine, corydaline [ 50]
Phthalidisoquinolines [ 40]
Hydrastine , narcotine (Noscapine) [ 51]
Spirobenzylisoquinolines [ 40]
Fumaricine [ 48]
Ipecacuanha alkaloids[ 52]
Emetine, protoemetine, ipecoside [ 52]
Benzophenanthridines [ 40]
Sanguinarine, oxynitidine, corynoloxine [ 53]
Aporphine s [ 40]
Glaucine , coridine, liriodenine [ 54]
Proaporphines [ 40]
Pronuciferine, glaziovine [ 40] [ 49]
Homoaporphines [ 55]
Kreysiginine, multifloramine [ 55]
Homoproaporphines [ 55]
Bulbocodine [ 47]
嗎啡 s[ 56]
嗎啡 , 可待因 , 蒂巴因 , 青藤碱 [ 57] , 海洛因
Homomorphines [ 58]
Kreysiginine, androcymbine [ 56]
Tropoloisoquinolines [ 40]
Imerubrine [ 40]
Azofluoranthenes [ 40]
Rufescine, imeluteine [ 59]
Amaryllis alkaloids[ 60]
Lycorine , ambelline, tazettine, galantamine , montanine [ 61]
Erythrina alkaloids[ 44]
Erysodine, erythroidine [ 44]
Phenanthrene derivatives [ 40]
Atherosperminine [ 40] [ 50]
Protopine s [ 40]
Protopine , oxomuramine, corycavidine [ 53]
Aristolactam [ 40]
Doriflavin [ 40]
噁唑 類衍生物[[ 62]
Tyrosine → tyramine [ 63]
Annuloline, halfordinol, texaline, texamine[ 64]
異噁唑 類衍生物
Ibotenic acid → Muscimol
Ibotenic acid, Muscimol
噻唑 類衍生物[ 65]
1-Deoxy-D-xylulose 5-phosphate (DOXP), tyrosine , cysteine [ 66]
Nostocyclamide, thiostreptone [ 65] [ 67]
喹唑啉 類衍生物[ 68]
3,4-Dihydro-4-quinazolone derivatives
Anthranilic acid or phenylalanine or ornithine [ 69]
Febrifugine [ 70]
1,4-Dihydro-4-quinazolone derivatives
Glycorine, arborine, glycosminine[ 70]
Pyrrolidine and piperidine quinazoline derivatives
Vazicine (peganine) [ 62]
吖啶 類衍生物[ 62]
Anthranilic acid [ 71]
Rutacridone, acronicine [ 72] [ 73]
喹啉 類衍生物[ 74] [ 75]
Simple derivatives of quinoline derivatives of 2 – quinolones and 4-quinolone
Anthranilic acid → 3-carboxyquinoline [ 76]
Cusparine, echinopsine , evocarpine[ 75] [ 77] [ 78]
Tricyclic terpenoids
Flindersine[ 75] [ 79]
Furanoquinoline derivatives
Dictamnine , fagarine, skimmianine[ 75] [ 80] [ 81]
Quinine s
Tryptophan → tryptamine → strictosidine (with secologanin ) → korinanteal → cinhoninon [ 42] [ 76]
Quinine , quinidine , cinchonine , cinhonidine [ 79]
吲哚 類衍生物[ 57]
非異戊二烯 吲哚生物鹼
Simple indole derivatives [ 82]
Tryptophan → tryptamine or 5-hydroxitriptofan [ 83]
Serotonin , psilocybin , dimethyltryptamine (DMT), bufotenin [ 84] [ 85]
Simple derivatives of β-carboline [ 86]
Harman, harmine , harmaline , eleagnine [ 82]
Pyrroloindole alkaloids [ 87]
Physostigmine (eserine), etheramine, physovenine, eptastigmine[ 87]
半萜類 吲哚生物鹼'
Ergot alkaloids [ 57]
Tryptophan → chanoclavine → agroclavine → elimoclavine → paspalic acid → lysergic acid [ 87]
Ergotamine , ergobasine, ergosine[ 88]
單萜 吲哚生物鹼
Corynanthe type alkaloids[ 83]
Tryptophan → tryptamine → strictosidine (with secologanin ) [ 83]
Ajmalicine, sarpagine, vobasine, ajmaline , yohimbine , reserpine , mitragynine ,[ 89] [ 90] group strychnine and (Strychnine brucine , aquamicine, vomicine [ 91] )
Iboga -type alkaloids[ 83]
Ibogamine , ibogaine , voacangine [ 83]
Aspidosperma -type alkaloids[ 83]
Vincamine , vinca alkaloids , vincotine, aspidospermine[ 92] [ 93]
咪唑 類衍生物[ 62]
Directly from histidine [ 94]
Histamine , pilocarpine, pilosine, stevensine[ 62] [ 94]
嘌呤 類衍生物[ 95]
Xanthosine (formed in purine biosynthesis) → 7 methylxantosine → 7-methyl xanthine → theobromine → caffeine [ 42]
Caffeine , theobromine , theophylline , saxitoxin [ 96] [ 97]
側鏈上含氮原子的生物側鏈鹼
β-苯乙胺 類衍生物[ 49]
Tyrosine or phenylalanine → dioxyphenilalanine → dopamine → adrenaline and mescaline tyrosine → tyramine phenylalanine → 1-phenylpropane-1,2-dione → cathinone → ephedrine and pseudoephedrine [ 38] [ 98] [ 99]
Tyramine , ephedrine , pseudoephedrine , mescaline , cathinone , catecholamines (adrenaline , noradrenaline , dopamine )[ 38] [ 100]
秋水仙素 類衍生物 [ 101]
Tyrosine or phenylalanine → dopamine → autumnaline → colchicine [ 102]
Colchicine , colchamine[ 101]
毒蕈鹼 [ 103]
Glutamic acid → 3-ketoglutamic acid → muscarine (with pyruvic acid )[ 104]
Muscarine , allomuscarine, epimuscarine, epiallomuscarine[ 103]
芐胺 [ 105]
Phenylalanine with valine , leucine or isoleucine [ 106]
Capsaicin , dihydrocapsaicin , nordihydrocapsaicin, vanillylamine [ 105] [ 107]
多胺生物鹼
腐胺 衍生物[ 108]
ornithine → putrescine → spermidine → spermine [ 109]
Paucine [ 108]
亞精胺 衍生物[ 108]
Lunarine, codonocarpine[ 108]
精胺 衍生物[ 108]
Verbascenine, aphelandrine [ 108]
Peptide (cyclopeptide) alkaloids
Peptide alkaloids with a 13-membered cycle [ 110] [ 111]
Nummularine C type
From different amino acids [ 110]
Nummularine C, Nummularine S [ 110]
Ziziphine type
Ziziphine A, sativanine H [ 110]
Peptide alkaloids with a 14-membered cycle [ 110] [ 111]
Frangulanine type
Frangulanine, scutianine J [ 111]
Scutianine A type
Scutianine A [ 110]
Integerrine type
Integerrine, discarine D [ 111]
Amphibine F type
Amphibine F, spinanine A [ 110]
Amfibine B type
Amphibine B, lotusine C [ 110]
Peptide alkaloids with a 15-membered cycle [ 111]
Mucronine A type
Mucronine A [ 112] [ 111]
Pseudoalkaloids (terpenes and steroids )
Diterpenes [ 112]
Lycoctonine type
Mevalonic acid → izopentenilpyrophosfate → geranyl pyrophosphate [ 113] [ 114]
Aconitine , delphinine [ 112] [ 115]
Steroids [ 116]
Cholesterol , arginine [ 117]
Solasodine, solanidine , veralkamine, batrachotoxin [ 118]
参考文献
引用
^ Andreas Luch. Molecular, clinical and environmental toxicology . Springer. 2009: 20. ISBN 3-7643-8335-6 .
^ Chemical Encyclopedia: alkaloids (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ 3.0 3.1 Aniszewski, Tadeusz. Preface. Alkaloids . Elsevier. 2015: xvii–xviii.
^ Hesse, Stefan. Industrieroboterperipherie. Industrieroboterpraxis . Wiesbaden: Vieweg+Teubner Verlag. 1998: 327–338. ISBN 978-3-322-88982-9 .
^ Backmatter. Frankfurt – Hesse-Darmstadt . Walter de Gruyter – K. G. Saur. 2007-06-16: 291–304.
^ Begley, Tadhg P. Overview and Introduction. Comprehensive Natural Products II . Elsevier. 2010: 1–2.
^ Lieberstein, Samuel. Great Soviet Encyclopedia: A Translation of the Third Edition. Vol. 1 . Russian Review. 1975-04, 34 (2). ISSN 0036-0341 . doi:10.2307/127750 .
^ 8.0 8.1 8.2 Plemenkov , p. 224
^ 9.0 9.1 9.2 Aniszewski , p. 75
^ Orekhov , p. 33
^ 11.0 11.1 11.2 Chemical Encyclopedia: Tropan alkaloids (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ Hesse , p. 34
^ Aniszewski , p. 27
^ 14.0 14.1 14.2 14.3 Chemical Encyclopedia: Pyrrolizidine alkaloids (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ Plemenkov , p. 229
^ Blankenship JD, Houseknecht JB, Pal S, Bush LP, Grossman RB, Schardl CL. Biosynthetic precursors of fungal pyrrolizidines, the loline alkaloids. Chembiochem. 2005, 6 (6): 1016–1022. PMID 15861432 . doi:10.1002/cbic.200400327 .
^ Faulkner JR, Hussaini SR, Blankenship JD, Pal S, Branan BM, Grossman RB, Schardl CL. On the sequence of bond formation in loline alkaloid biosynthesis. Chembiochem. 2006, 7 (7): 1078–1088. PMID 16755627 . doi:10.1002/cbic.200600066 .
^ Schardl CL, Grossman RB, Nagabhyru P, Faulkner JR, Mallik UP. Loline alkaloids: currencies of mutualism. Phytochemistry . 2007, 68 (7): 980–996. PMID 17346759 . doi:10.1016/j.phytochem.2007.01.010 .
^ Plemenkov , p. 225
^ Aniszewski , p. 95
^ Hesse , p. 31
^ Orekhov , p. 80
^ 23.0 23.1 Dewick , p. 381
^ 24.0 24.1 24.2 24.3 24.4 24.5 Chemical Encyclopedia: Quinolizidine alkaloids (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ Saxton , Vol. 1, p. 93
^ Aniszewski , p. 98
^ Saxton , Vol. 1, p. 91
^ Joseph P. Michael. Indolizidine and quinolizidine alkaloids. Nat. Prod. Rep. 2002, 19 : 458–475. doi:10.1039/b208137g .
^ Saxton , Vol. 1, p. 92
^ Dewick , p. 310
^ Aniszewski , p. 96
^ Aniszewski , p. 97
^ 33.0 33.1 33.2 Plemenkov , p. 227
^ 34.0 34.1 Chemical Encyclopedia: pyridine alkaloids (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ 35.0 35.1 Aniszewski , p. 107
^ 36.0 36.1 Aniszewski , p. 85
^ Plemenkov , p. 228
^ 38.0 38.1 38.2 Aniszewski , p. 110
^ 39.0 39.1 Hesse , p. 36
^ 40.00 40.01 40.02 40.03 40.04 40.05 40.06 40.07 40.08 40.09 40.10 40.11 40.12 40.13 40.14 40.15 40.16 40.17 40.18 40.19 Chemical Encyclopedia: isoquinoline alkaloids (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ Aniszewski , pp. 77–78
^ 42.0 42.1 42.2 Begley , Alkaloid Biosynthesis
^ 43.0 43.1 Saxton , Vol. 3, p. 122
^ 44.0 44.1 44.2 Hesse , p. 54
^ 45.0 45.1 Hesse , p. 37
^ Hesse , p. 38
^ 47.0 47.1 47.2 Hesse , p. 46
^ 48.0 48.1 48.2 Hesse , p. 50
^ 49.0 49.1 49.2 Kenneth W. Bentley. β-Phenylethylamines and the isoquinoline alkaloids (PDF) . Nat. Prod. Rep. 1997, 14 (4): 387–411 [2016-04-23 ] . PMID 9281839 . doi:10.1039/NP9971400387 . (原始内容存档 (PDF) 于2014-04-13).
^ 50.0 50.1 Hesse , p. 47
^ Hesse , p. 39
^ 52.0 52.1 Hesse , p. 41
^ 53.0 53.1 Hesse , p. 49
^ Hesse , p. 44
^ 55.0 55.1 55.2 Saxton , Vol. 3, p. 164
^ 56.0 56.1 Hesse , p. 51
^ 57.0 57.1 57.2 Plemenkov , p. 236
^ Saxton , Vol. 3, p. 163
^ Saxton , Vol. 3, p. 168
^ Hesse , p. 52
^ Hesse , p. 53
^ 62.0 62.1 62.2 62.3 62.4 Plemenkov , p. 241
^ Brossi , Vol. 35, p. 261
^ Brossi , Vol. 35, pp. 260–263
^ 65.0 65.1 Plemenkov , p. 242
^ Begley , Cofactor Biosynthesis
^ John R. Lewis. Amaryllidaceae, muscarine, imidazole, oxazole, thiazole and peptide alkaloids, and other miscellaneous alkaloids. Nat. Prod. Rep. 2000, 17 (1): 57–84. PMID 10714899 . doi:10.1039/a809403i .
^ Chemical Encyclopedia: Quinazoline alkaloids (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ Aniszewski , p. 106
^ 70.0 70.1 Aniszewski , p. 105
^ Richard B. Herbert; Herbert, Richard B.; Herbert, Richard B. The biosynthesis of plant alkaloids and nitrogenous microbial metabolites. Nat. Prod. Rep. 1999, 16 : 199–208. doi:10.1039/a705734b .
^ Plemenkov , pp. 231, 246
^ Hesse , p. 58
^ Plemenkov , p. 231
^ 75.0 75.1 75.2 75.3 Chemical Encyclopedia: Quinoline alkaloids (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ 76.0 76.1 Aniszewski , p. 114
^ Orekhov , p. 205
^ Hesse , p. 55
^ 79.0 79.1 Plemenkov , p. 232
^ Orekhov , p. 212
^ Aniszewski , p. 118
^ 82.0 82.1 Aniszewski , p. 112
^ 83.0 83.1 83.2 83.3 83.4 83.5 Aniszewski , p. 113
^ Hesse , p. 15
^ Saxton , Vol. 1, p. 467
^ Dewick , pp. 349–350
^ 87.0 87.1 87.2 Aniszewski , p. 119
^ Hesse , p. 29
^ Hesse , pp. 23–26
^ Saxton , Vol. 1, p. 169
^ Saxton , Vol. 5, p. 210
^ Hesse , pp. 17–18
^ Dewick , p. 357
^ 94.0 94.1 Aniszewski , p. 104
^ Hesse , p. 72
^ Hesse , p. 73
^ Dewick , p. 396
^ Dewick , p. 382
^ PlantCyc Pathway: ephedrine biosynthesis 互联网档案馆 的存檔 ,存档日期2011-12-10.
^ Hesse , p. 76
^ 101.0 101.1 Chemical Encyclopedia: colchicine alkaloids (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ Aniszewski , p. 77
^ 103.0 103.1 Hesse , p. 81
^ Brossi , Vol. 23, p. 376
^ 105.0 105.1 Hesse , p. 77
^ Brossi , Vol. 23, p. 268
^ Brossi , Vol. 23, p. 231
^ 108.0 108.1 108.2 108.3 108.4 108.5 Hesse , p. 82
^ Spermine Biosynthesis . [2016-04-23 ] . (原始内容存档 于2016-12-04).
^ 110.0 110.1 110.2 110.3 110.4 110.5 110.6 110.7 Dimitris C. Gournelif; Gregory G. Laskarisb; Robert Verpoorte. Cyclopeptide alkaloids. Nat. Prod. Rep. 1997, 14 (1): 75–82. PMID 9121730 . doi:10.1039/NP9971400075 .
^ 111.0 111.1 111.2 111.3 111.4 111.5 Plemenkov , p. 243
^ 112.0 112.1 112.2 Hesse , p. 84
^ Chemical Encyclopedia: Terpenes (页面存档备份 ,存于互联网档案馆 ). xumuk.ru
^ Begley , Natural Products: An Overview
^ Atta-ur-Rahman and M. Iqbal Choudhary. Diterpenoid and steroidal alkaloids . Nat. Prod. Rep. 1997, 14 (2): 191–203. PMID 9149410 . doi:10.1039/np9971400191 .
^ Hesse , p. 88
^ Dewick , p. 388
^ Plemenkov , p. 247
来源
Aniszewski, Tadeusz. Alkaloids – secrets of life. Amsterdam: Elsevier . 2007. ISBN 978-0-444-52736-3 .
Begley, Tadhg P. Encyclopedia of Chemical Biology. Wiley. 2009. ISBN 978-0-471-75477-0 . doi:10.1002/cbic.200900262 .
Brossi, Arnold. The Alkaloids: Chemistry and Pharmacology . Academic Press. 1989.
Dewick, Paul M. Medicinal Natural Products. A Biosynthetic Approach 2nd. Wiley. 2002. ISBN 0-471-49640-5 .
Fattorusso, E.; Taglialatela-Scafati, O. Modern Alkaloids: Structure, Isolation, Synthesis and Biology . Wiley-VCH. 2008. ISBN 978-3-527-31521-5 .
Grinkevich, N. I.; Safronich, L. N. The chemical analysis of medicinal plants: Proc. allowance for pharmaceutical universities. M. 1983.
Hesse, Manfred. Alkaloids: Nature's Curse or Blessing? . Wiley-VCH. 2002. ISBN 978-3-906390-24-6 .
Knunyants, I. L. Chemical Encyclopedia . Soviet Encyclopedia. 1988 [2014-08-23 ] . (原始内容存档 于2021-03-07).
Orekhov, A. P. Chemistry alkaloids Acad. 2. M.: USSR. 1955.
Plemenkov, V. V. Introduction to the Chemistry of Natural Compounds. Kazan. 2001.
Saxton, J. E. The Alkaloids. A Specialist Periodical Report. London: The Chemical Society. 1971.
Veselovskaya, N. B.; Kovalenko, A. E. Drugs. Moscow: Triada-X. 2000.
Wink, M. Mode of action and toxicology of plant toxins and poisonous plants . Mitt. Julius Kühn-Inst. 2009, 421 : 93–112 [18 March 2014] . (原始内容存档 于2014-03-18).
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