アルカロイド アルカロイドの例

アルカロイド

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アルカロイドの例


  1. ^ Andreas Luch (2009). Molecular, clinical and environmental toxicology. Springer. p. 20. ISBN 3-7643-8335-6. https://books.google.co.jp/books?id=MtOiLVWBn8cC&pg=PA20&redir_esc=y&hl=ja 
  2. ^ a b IUPAC. Compendium of Chemical Terminology, 2nd ed. (The "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997) ISBN 0-9678550-9-8 doi:10.1351/goldbook
  3. ^ R. H. F. Manske. The Alkaloids. Chemistry and Physiology. Volume VIII. – New York: Academic Press, 1965, p. 673
  4. ^ Robert Alan Lewis. Lewis' dictionary of toxicology. CRC Press, 1998, p. 51 ISBN 1-56670-223-2
  5. ^ a b c d Chemical Encyclopedia: alkaloids
  6. ^ a b c Robert A. Meyers Encyclopedia of Physical Science and Technology – Alkaloids, 3rd edition. ISBN 0-12-227411-3
  7. ^ Leland J. Cseke Natural Products from Plants Second Edition. – CRC, 2006, p. 30 ISBN 0-8493-2976-0
  8. ^ A. William Johnson Invitation to Organic Chemistry, Jones and Bartlett, 1999, p. 433 ISBN 0-7637-0432-6
  9. ^ Raj K Bansal A Text Book of Organic Chemistry. 4th Edition, New Age International, 2004, p. 644 ISBN 81-224-1459-1
  10. ^ a b c d Aniszewski, p. 110
  11. ^ In the penultimate sentence of his article [W. Meissner (1819) "Über Pflanzenalkalien: II. Über ein neues Pflanzenalkali (Alkaloid)" (On plant alkalis: II. On a new plant alkali (alkaloid)), Journal für Chemie und Physik, vol. 25, pp. 377–381] Meissner wrote "Überhaupt scheint es mir auch angemessen, die bis jetzt bekannten Pflanzenstoffe nicht mit dem Namen Alkalien, sondern Alkaloide zu belegen, da sie doch in manchen Eigenschaften von den Alkalien sehr abweichen, sie würden daher in dem Abschnitt der Pflanzenchemie vor den Pflanzensäuren ihre Stelle finden." (In general, it seems appropriate to me to impose on the known plant substances not the name "alkalis" but "alkaloids", since they differ greatly in some properties from the alkalis; among the chapters of plant chemistry, they would therefore find their place before plant acids [since "Alkaloid" would precede "Säure" (acid)].)
  12. ^ Hesse, pp. 1–3
  13. ^ a b Hesse, p. 5
  14. ^ 接尾辞 "ine" はギリシャ語の女性父称を作る接尾辞であり、「〜の娘」を意味する。すなわち、アトロピンは「Atropa(ベラドンナ)の娘」を意味する。[1]
  15. ^ Hesse, p. 7
  16. ^ a b Aniszewski, p. 182
  17. ^ Hesse, p. 338
  18. ^ Hesse, p. 350
  19. ^ Hesse, pp. 313–316
  20. ^ a b TSB: Coniine
  21. ^ Hesse, p. 204
  22. ^ Begley, Natural Products in Plants
  23. ^ a b Hesse, p. 11
  24. ^ Orekhov, p. 6
  25. ^ Aniszewski, p. 109
  26. ^ a b Dewick, p. 307
  27. ^ Hesse, p. 12
  28. ^ a b Plemenkov, p. 223
  29. ^ Aniszewski, p. 108
  30. ^ a b c d Hesse, p. 84
  31. ^ a b c Dewick, p. 381
  32. ^ a b Hesse, p. 31
  33. ^ a b c d e f g h i Dimitris C. Gournelif, Gregory G. Laskarisb and Robert Verpoorte (1997). “Cyclopeptide alkaloids”. Nat. Prod. Rep. 14 (1): 75–82. doi:10.1039/NP9971400075. PMID 9121730. 
  34. ^ Aniszewski, p. 11
  35. ^ Plemenkov, p. 246
  36. ^ a b Aniszewski, p. 12
  37. ^ a b Dewick, p. 382
  38. ^ Hesse, pp. 44, 53
  39. ^ a b c Plemenkov, p. 224
  40. ^ a b c Aniszewski, p. 75
  41. ^ Orekhov, p. 33
  42. ^ a b c Chemical Encyclopedia: Tropan alkaloids
  43. ^ Hesse, p. 34
  44. ^ Aniszewski, p. 27
  45. ^ a b c d Chemical Encyclopedia: Pyrrolizidine alkaloids
  46. ^ Plemenkov, p. 229
  47. ^ Blankenship JD, Houseknecht JB, Pal S, Bush LP, Grossman RB, Schardl CL (2005). “Biosynthetic precursors of fungal pyrrolizidines, the loline alkaloids”. Chembiochem 6 (6): 1016–1022. doi:10.1002/cbic.200400327. PMID 15861432. 
  48. ^ Faulkner JR, Hussaini SR, Blankenship JD, Pal S, Branan BM, Grossman RB, Schardl CL (2006). “On the sequence of bond formation in loline alkaloid biosynthesis”. Chembiochem 7 (7): 1078–1088. doi:10.1002/cbic.200600066. PMID 16755627. 
  49. ^ Schardl CL, Grossman RB, Nagabhyru P, Faulkner JR, Mallik UP (2007). “Loline alkaloids: currencies of mutualism”. Phytochemistry 68 (7): 980–996. doi:10.1016/j.phytochem.2007.01.010. PMID 17346759. 
  50. ^ Plemenkov, p. 225
  51. ^ Aniszewski, p. 95
  52. ^ Orekhov, p. 80
  53. ^ a b c d e f Chemical Encyclopedia: Quinolizidine alkaloids
  54. ^ J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 1. – London: The Chemical Society, 1971, p. 93
  55. ^ Aniszewski, p. 98
  56. ^ J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 1. – London: The Chemical Society, 1971, p. 91
  57. ^ Joseph P. Michael (2002). “Indolizidine and quinolizidine alkaloids”. Nat. Prod. Rep 19: 458–475. doi:10.1039/b208137g. 
  58. ^ J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 1. – London: The Chemical Society, 1971, p. 92
  59. ^ Dewick, p. 310
  60. ^ Aniszewski, p. 96
  61. ^ Aniszewski, p. 97
  62. ^ a b c Plemenkov, p. 227
  63. ^ a b Chemical Encyclopedia: pyridine alkaloids
  64. ^ a b Aniszewski, p. 107
  65. ^ a b Aniszewski, p. 85
  66. ^ Plemenkov, p. 228
  67. ^ a b Hesse, p. 36
  68. ^ a b c d e f g h i j k l m n o p q r s t Chemical Encyclopedia: isoquinoline alkaloids
  69. ^ Aniszewski, pp. 77–78
  70. ^ a b c d Begley, Alkaloid Biosynthesis
  71. ^ a b J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 3. – London: The Chemical Society, 1973, p. 122
  72. ^ a b c Hesse, p. 54
  73. ^ a b Hesse, p. 37
  74. ^ Hesse, p. 38
  75. ^ a b c Hesse, p. 46
  76. ^ a b c Hesse, p. 50
  77. ^ a b c Kenneth W. Bentley (1997). “β-Phenylethylamines and the isoquinoline alkaloids”. Nat. Prod. Rep 14 (4): 387–411. doi:10.1039/NP9971400387. PMID 9281839. 
  78. ^ a b Hesse, p. 47
  79. ^ Hesse, p. 39
  80. ^ a b Hesse, p. 41
  81. ^ a b Hesse, p. 49
  82. ^ Hesse, p. 44
  83. ^ a b c J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 3. – London: The Chemical Society, 1973, p. 164
  84. ^ a b Hesse, p. 51
  85. ^ a b c Plemenkov, p. 236
  86. ^ J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 3. – London: The Chemical Society, 1973, p. 163
  87. ^ J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 3. – London: The Chemical Society, 1973, p. 168
  88. ^ Hesse, p. 52
  89. ^ Hesse, p. 53
  90. ^ a b c d e Plemenkov, p. 241
  91. ^ Arnold Brossi The Alkaloids: Chemistry and Pharmacology, Volume 35. – Academic Press, 1989, p. 261
  92. ^ Arnold Brossi The Alkaloids: Chemistry and Pharmacology, Volume 35. – Academic Press, 1989, pp. 260–263
  93. ^ a b Plemenkov, p. 242
  94. ^ Begley, Cofactor Biosynthesis
  95. ^ John R. Lewis (2000). “Amaryllidaceae, muscarine, imidazole, oxazole, thiazole and peptide alkaloids, and other miscellaneous alkaloids”. Nat. Prod. Rep 17 (1): 57–84. doi:10.1039/a809403i. PMID 10714899. http://www.rsc.org/publishing/journals/NP/article.asp?doi=a809403i. 
  96. ^ Chemical Encyclopedia: Quinazoline alkaloids
  97. ^ Aniszewski, p. 106
  98. ^ a b Aniszewski, p. 105
  99. ^ Richard B. Herbert; Herbert, Richard B.; Herbert, Richard B. (1999). “The biosynthesis of plant alkaloids and nitrogenous microbial metabolites”. Nat. Prod. Rep 16: 199–208. doi:10.1039/a705734b. http://www.rsc.org/publishing/journals/NP/article.asp?doi=a705734b. 
  100. ^ Plemenkov, pp. 231, 246
  101. ^ Hesse, p. 58
  102. ^ Plemenkov, p. 231
  103. ^ a b c d Chemical Encyclopedia: Quinoline alkaloids
  104. ^ a b Aniszewski, p. 114
  105. ^ Orekhov, p. 205
  106. ^ Hesse, p. 55
  107. ^ a b Plemenkov, p. 232
  108. ^ Orekhov, p. 212
  109. ^ Aniszewski, p. 118
  110. ^ a b Aniszewski, p. 112
  111. ^ a b c d e f Aniszewski, p. 113
  112. ^ Hesse, p. 15
  113. ^ J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 1. – London: The Chemical Society, 1971, p. 467
  114. ^ Dewick, p. 349-350
  115. ^ a b c Aniszewski, p. 119
  116. ^ Hesse, p. 29
  117. ^ Hesse, pp. 23–26
  118. ^ J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 1. – London: The Chemical Society, 1971, p. 169
  119. ^ J. E. Saxton The Alkaloids. A Specialist Periodical Report. Volume 5. – London: The Chemical Society, 1975, p. 210
  120. ^ Hesse, pp. 17–18
  121. ^ Dewick, p. 357
  122. ^ a b Aniszewski, p. 104
  123. ^ Hesse, p. 72
  124. ^ Hesse, p. 73
  125. ^ Dewick, p. 396
  126. ^ PlantCyc Pathway: ephedrine biosynthesis
  127. ^ Hesse, p. 76
  128. ^ a b Chemical Encyclopedia: colchicine alkaloids
  129. ^ Aniszewski, p. 77
  130. ^ a b Hesse, p. 81
  131. ^ Arnold Brossi The Alkaloids: Chemistry and Pharmacology, Volume 23. – Academic Press, 1984, p. 376
  132. ^ a b Hesse, p. 77
  133. ^ Arnold Brossi The Alkaloids: Chemistry and Pharmacology, Volume 23. – Academic Press, 1984, p. 268
  134. ^ Arnold Brossi The Alkaloids: Chemistry and Pharmacology, Volume 23. – Academic Press, 1984, p. 231
  135. ^ a b c d e f Hesse, p. 82
  136. ^ Spermine Biosynthesis
  137. ^ a b c d e f Plemenkov, p. 243
  138. ^ Chemical Encyclopedia: Terpenes
  139. ^ Begley, Natural Products: An Overview
  140. ^ Atta-ur-Rahman and M. Iqbal Choudhary (1997). “Diterpenoid and steroidal alkaloids”. Nat. Prod. Rep 14 (2): 191–203. doi:10.1039/np9971400191. PMID 9149410. http://www.rsc.org/publishing/journals/NP/article.asp?doi=NP9971400191. 
  141. ^ Hesse, p. 88
  142. ^ Dewick, p. 388
  143. ^ Plemenkov, p. 247
  144. ^ TSB: Nicotine
  145. ^ a b c Grinkevich, p. 131
  146. ^ a b G. A. Spiller Caffeine, CRC Press, 1997 ISBN 0-8493-2647-8
  147. ^ Fattorusso, p. 53
  148. ^ Thomas Acamovic, Colin S. Stewart, T. W. Pennycott (2004). Poisonous plants and related toxins, Volume 2001. CABI. p. 362. ISBN 0-85199-614-0. https://books.google.co.jp/books?id=nixyqfGIGHcC&pg=PA362&redir_esc=y&hl=ja 
  149. ^ Fattorusso, p. XVII
  150. ^ Aniszewski, p. 13
  151. ^ Orekhov, p. 11
  152. ^ Hesse, p.4
  153. ^ Grinkevich, pp. 122–123
  154. ^ Orekhov, p. 12
  155. ^ Aniszewski, pp. 110–111
  156. ^ a b c d Hesse, p. 116
  157. ^ a b Grinkevich, p. 132
  158. ^ Grinkevich, p. 5
  159. ^ Grinkevich, pp. 132–134
  160. ^ Grinkevich, pp. 134–136
  161. ^ a b c Plemenkov, p. 253
  162. ^ Plemenkov, p. 254
  163. ^ a b Dewick, p. 19
  164. ^ Plemenkov, p. 255
  165. ^ Dewick, p. 305
  166. ^ Hesse, pp. 91–105
  167. ^ Aniszewski, p. 142
  168. ^ Hesse, pp. 283–291
  169. ^ Aniszewski, pp. 142–143
  170. ^ Hesse, p. 303
  171. ^ Hesse, pp. 303–309
  172. ^ Hesse, p. 309
  173. ^ Dewick, p. 335
  174. ^ György Matolcsy, Miklós Nádasy, Viktor Andriska Pesticide chemistry, Elsevier, 2002, pp. 21–22 ISBN 0-444-98903-X
  175. ^ Veselovskaya, p. 75
  176. ^ Hesse, p. 79
  177. ^ Veselovskaya, p. 136
  178. ^ Geoffrey A. Cordell The Alkaloids: Chemistry and Biology. Volume 56, Elsevier, 2001, p. 8
  179. ^ Veselovskaya, p. 6
  180. ^ Veselovskaya, pp. 51–52






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