R

  • J. Elks
  • C. R. Ganellin

Keywords

Antihypertensive Agent Industrial Material Roxatidine Acetate Glycyrrhetic Acid Antiulcer Agent 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Hanka, L.J. J. Antibiot, 1978, 31, 1211 (isol) Google Scholar
  2. Martin, D.G. J. Antibiot, 1980, 33, 902 (struct) Google Scholar
  3. Chidester, C.G. J. Am. Chem. Soc, 1981, 103, 7629 (cryst struct) Google Scholar
  4. Martin, D.G. J. Antibiot, 1981, 34, 1119 (isol) Google Scholar
  5. Sundberg, R.I. J. Org . Chem, 1985, 50, 425 (bibi) Google Scholar
  6. Reynolds, V.L. J. Antibiot, 1986, 39, 319 (rev) Google Scholar
  7. Bolton, R.E. Tetrahedron Lett, 1987, 28, 3163 (synth, bibi) Google Scholar
  8. Watt, W. Acta Crystallogr, Sect. C, 1988, 44, 1675 (cryst struct) Google Scholar
  9. Eur. Pat.,60 235, (1982); CA,98, 53687 (synth) Google Scholar
  10. Koehler, C. Biochem. Pharmacol, 1985, 34, 2251 (pharmacol) Google Scholar
  11. De Paulis, T. J. Med. Chem, 1986, 29, 61 (synth, isomers, cmr) Google Scholar
  12. Ehrin, E. J. Labelled Compd. Radiopharm, 1987, 24, 931 (synth) Google Scholar
  13. Hoegberg, T. J. Pharm. Pharmacol, 1987, 39, 787 (cryst struct, pharmacol) Google Scholar
  14. Mrozik, H. Experientia, 1969, 25, 883 (synth, pharmacol) Google Scholar
  15. Brown, W.R. Toxicol. Appl. Pharmacol, 1972, 21, 532 (tox) Google Scholar
  16. Caillier, R.L. Rev. Med. Vet, 1973, 124, 789 (Ranizole) Google Scholar
  17. U.S.P,3 914 418, (1975); CA,84, 30707u (synth, pharmacol) Google Scholar
  18. Sindt, A.C. Aust. J. Chem, 1980, 33, 203 (cryst struct) Google Scholar
  19. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 13206.Google Scholar
  20. Ger. Pat.,3 317 000, (1984); CA,102, 113476 (synth) Google Scholar
  21. Bartoszyk, G.D. Curr. Probi. Epilepsy, 1986, 4, 309 (rev) Google Scholar
  22. Wakeling, A.E. J. Endocrinol, 1983, 99, 455 (pharmacol) Google Scholar
  23. Jones, C.D. J. Med. Chem, 1984, 27, 1057 (synth, pharmacol) Google Scholar
  24. Lindstrom, T.D. Xenobiotica, 1984, 14, 841 (metab) Google Scholar
  25. Wakeling, A.E. J. Steroid Biochem, 1984, 20, 111 (phar-macol) Google Scholar
  26. Darvas, F. Pharmacochem. Libr, 1985, 8, 199 (pharmacol) Google Scholar
  27. Banci, F. Arzneim.-Forsch, 1971, 21, 1665 (synth, pharmacol) Google Scholar
  28. Beyer, K.H. Dtsch. Apoth.-Ztg, 1983, 123, 1527 (metab) Google Scholar
  29. Marciniec, B., Pharmazie, 1985, 40, 110 (ms) Google Scholar
  30. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2660.Google Scholar
  31. Eur. Pat,79 022, (1983); CA,100, 52012 (synth) Google Scholar
  32. Metzger, H. Arzneim.-Forsch, 1984, 34, 1399 (synth, pharmacol, tox, ester) Google Scholar
  33. Becker, R.H.A. Am. J. Cardiol,1987, 59, 3D, 18D, 23D (revs, Ramipril) Google Scholar
  34. Paulus, E.F. Acta Crystallogr, Sect. C, 1987, 43, 941 (cryst struct) Google Scholar
  35. Eur. Pat,60 182, (1982); CA,98, 34508 (synth) Google Scholar
  36. Necciari, J. Int. J. Clin. Pharmacol. Res, 1985, 5, 457 (pharmacol) Google Scholar
  37. Lavezzo, A. J. Pharm. Pharmacol, 1986, 38, 853 (pharmacol) Google Scholar
  38. Wilson, J.A. Eur. J. Clin. Pharmacol, 1986, 30, 33 (pharmacol) Google Scholar
  39. Ger. Pat,2 734 070, (1978); CA,88, 190580b (synth, pharmacol) Google Scholar
  40. Brogden, R.N. Drugs, 1982, 24, 267 (rev, pharmacol) Google Scholar
  41. Kojic-Prodic, B. Acta Crystallogr, Sect. B, 1982, 38, 1837 (cryst struct) Google Scholar
  42. Riley, A.J. Eds., Curr. Clin. Practice Ser, No. 1: Ranitidine,Excerpta Medica, Amsterdam, 1982 (book) Google Scholar
  43. Daly, M.J. Prog. Med. Chem, 1983, 20, 337 (rev, pharmacol) Google Scholar
  44. Gaginella, T.S. Drug /ntell. Clin. Pharm, 1983, 17, 873 (rev, pharmacol) Google Scholar
  45. Cholerton, T.J. J. Chem. Soc, Perkin Trans. 2,1984, 1761 (uv, ir, pmr, struct) Google Scholar
  46. Hohnjec, M. Anal. Profiles Drug Subst, 1986, 15, 533 (rev, synth, anal, metab) Google Scholar
  47. Geraldes, C.F. Magn. Reson. Chem, 1987, 25, 203 (pmr, cmr) Google Scholar
  48. Kirch, W., Pharmacol. Ther, 1987, 33, 129 (rev) Google Scholar
  49. Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 2946.Google Scholar
  50. Martindale, The Extra Pharmacopoeia,28th/29th Eds.Google Scholar
  51. /1989, Pharmaceutical Press, London, 3777, 6162.Google Scholar
  52. Eur. Pat,126 449, (1984); CA,102, 166777 (synth, pharmacol) Google Scholar
  53. Delee, E. Chromatographia, 1987, 24, 357 (hplc, resoln) Google Scholar
  54. U.S.P,3 993 749, (1972); CA,86, 41806 (synth, ir, pmr) Google Scholar
  55. Vézina, C. J. Antibiot,1975, 28, 721; 1983, 36, 351 (iso!) Baker, H. J Google Scholar
  56. Antibiot,1978, 31, 539; 1979, 32, 630(pharmacol) Google Scholar
  57. Swindells, D.C.N. Can. J. Chem, 1978, 56, 2491 (cryst struct) Google Scholar
  58. Findlay, J.A. Can. J. Chem, 1982, 60, 2046 (uv, ir, pmr, cmr, ms, cd) Google Scholar
  59. Ger. Pat,1 926 075, (1969); CA,74, 42391m (synth, pharmacol) Google Scholar
  60. Eur. Pat,24 038, (1981); CA,95, 81034 (synth) Google Scholar
  61. Hock, F.J. Psychopharmacology (Berlin), 1985, 86, 114 (pharmacol) Google Scholar
  62. Creighton, A.M. Nature (London), 1969, 222, 384Google Scholar
  63. Ger. Pat,1 941 564, (1970); CA,72, 121579r (synth, pharmacol) Google Scholar
  64. Repta, A.J. J. Pharm. Sci, 1976, 65, 238.Google Scholar
  65. Hempel, A. J. Am. Chem. Soc, 1982, 104, 3453 (cryst struct, bibi) Google Scholar
  66. Herman, E.H. Adv. Pharmacol. Chemother, 1982, 19, 249 (rev, pharmacol) Google Scholar
  67. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 1861.Google Scholar
  68. From N. aerocolonigenes Active against gram-positive and -negative bacteria and tumours. Yellow solid.Google Scholar
  69. Nettleton, D.E. Tetrahedron Lett, 1985, 26, 4011 (isol, struct, props) Google Scholar
  70. Kaneko, T. Tetrahedron Lett,1985,26, 4015 (synth) U.S.P,4 524 154, (1985); CA,103, 159104 (deny) Google Scholar
  71. Bush, J.A. J. Antibiot, 1987, 40, 668 (manuf, props, bibi) Google Scholar
  72. Melloni, P. Eur. J. Med. Chem, 1984, 19, 235 (synth, pharmacol) Google Scholar
  73. Melloni, P. Tetrahedron,1985, 41, 1393 (synth, config) Ger. Pat,2 540 093, (1986); CA,105, 191 107 (synth, resoln, pharmacol) Google Scholar
  74. Ger. Pat 2 805 185, (1978); CA 90, 6664 (synth) Google Scholar
  75. Sekido, S. Cancer Treat. Rep, 1979, 63, 961 (pharmacol) Google Scholar
  76. B.P,202 5 406, (1980); CA,93, 1 1417Ig (synth) Google Scholar
  77. Bergey, J.L. Arzneim.-Forsch, 1983, 33, 1258 (pharmacol) Google Scholar
  78. Badia, A., Drugs Future, 1984, 9, 38 (rev) Google Scholar
  79. Anderson, J.L. Am. J. Cardiol, 1987, 60, 281 (pharmacol) Google Scholar
  80. Colatsky, T.J. J. Cardiovasc. Pharmacol, 1988, 11, 308 (pharmacol) Google Scholar
  81. U.S.P,4 208 327, (1980); CA,94, 30804 (synth, pharmacol) Google Scholar
  82. Florvall, L. J. Med. Chem, 1982, 25, 1280 (synth, tox, pharmacol) Google Scholar
  83. Oegren, S.O. Eur. J. Pharmacol, 1984, 102, 459 (pharmacol) Google Scholar
  84. Hoegberg, T. Mol. Pharmacol, 1986, 30, 345 (cryst struct, pharmacol) Google Scholar
  85. Stensland, B. Acta Crystallogr, Sect. C, 1987, 43, 2393 (cryst struct) Google Scholar
  86. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 497.Google Scholar
  87. Oya, M. Chem. Pharm. Bull,1982, 30, 440, 484, 2705 (synth, abs config, cryst struct, ms) Google Scholar
  88. Shimada, K. J. Pharm. Sci, 1984, 73, 119 (hplc) Google Scholar
  89. In, Y, J. Chem. Soc, Chem. Commun,1986, 473 (cryst struct, conformn) Google Scholar
  90. Yamauchi, H. Arzneim.-Forsch, 1987, 37, 157 (pharmacol) Google Scholar
  91. Eur. Pat,94 742, (1983); CA,100, 68166 (synth) Google Scholar
  92. Eur. Pat,239 321, (1987); CA,108, 75227 (synth, hydrate) Google Scholar
  93. Sanger, G.J., Br. J. Pharmacol, 1987, 91, 77 (pharmacol) Google Scholar
  94. Hawthorn, J, Q.J. Exp. Physiol,1988, 73, 7 (pharmacol) Google Scholar
  95. Morinaka, Y, Eur. J. Med. Chem.-Chim. Ther,1981, 16, 251 (synth, pharmacol) Google Scholar
  96. Nagase, M. CA,1986, 105, 108121, 108122, 108123 (tox) Google Scholar
  97. Takahashi, K. Oyo Yakuri, 1986, 32, 233 (pharmacol) Google Scholar
  98. Furumai, T. J. Antibiot, 1977, 30, 443 (isol, struct) Google Scholar
  99. Kinumaki, A. J. Antibiot, 1977, 30, 450 (struct) Google Scholar
  100. Yamaguchi, T. J. Antibiot, 1977, 30, 433 (props) Google Scholar
  101. Ganguly, A.K. J. Chem. Soc, Chem. Commun,1983, 1166 (synth) Google Scholar
  102. Fr. Pat,M5 969, (1970); CA,78, 72216h (synth, pharmacol) Google Scholar
  103. Klinger, K.H. Arzneim.-Forsch,1977, 27, 4, 14, 37, 45 (synth, pharmacol, tox) Google Scholar
  104. Niebch, G. Arzneim.-Forsch, 1978, 28, 765 (metab) Google Scholar
  105. Marmo, E., Clin. Ter. (Rome), 1981, 98, 481 (rev, pharmacol) Google Scholar
  106. Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 4921.Google Scholar
  107. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2101.Google Scholar
  108. Kametani, T. J. Med. Chem, 1972, 15, 686 (synth, activity) Google Scholar
  109. Ger. Pat,2 221 123, (1973); CA,79, 5487e (synth) Google Scholar
  110. Kametani, T. J. Chem. Soc, Perkin Trans. 1, 1975, 10, 932 (synth, ms) Google Scholar
  111. Kato, H. Jpn. J. Pharmacol, 1977, 27, 87 (activity) Google Scholar
  112. Fujimoto, Y., CA, 1980, 93, 125349x (pharmacol) Google Scholar
  113. Matsuda, H., CA, 1981, 95, 215016g (pharmacol) Google Scholar
  114. Alkaloid from R. vomitoria, R. caffra, R. cumminsii, R. macrophylla, R. oreogiton, R. volkensii, R. mombasiana and many other R spp. (Apocynaceae).Google Scholar
  115. Furlenmeyer, A. Experientia, 1953, 9, 331 (uv, ir, ester) Google Scholar
  116. Klohs, M.W. J. Am. Chem. Soc, 1955, 77, 2241 (Rescinnamine) Google Scholar
  117. Kroneberg, G., Arzneirn.-Forsch, 1956, 6, 579 (Rescinnamine, pharmacol) Google Scholar
  118. Woodward, R.B. Tetrahedron,1958, 2, 1 (synth) Google Scholar
  119. Zoha, M.S. J. Pharm. Pharmacol,1958, 10, Suppl. 231T (Rescinnamine, pharmacol) Google Scholar
  120. Popelak, A. Naturwissenschaften, 1961, 48, 73. Rosen, W.E. J. Am. Chem. Soc, 1961, 83, 4816 (pmr, ester) Google Scholar
  121. Popelak, A., Arch. Pharm. (Weinheim, Ger.), 1963, 296, 261 (Rescidine) Google Scholar
  122. Chatterjee, A. Chem. Ind. (London),1969, 1388 (Veneserpine) Google Scholar
  123. Pantarotto, C. Adv. Mass Spectrom, 1977, 2, 351 (Rescinnamine, ms) Google Scholar
  124. Suzuki, Y., CA, 1982, 96, 115441 (pharmacol) Google Scholar
  125. Malik,A. J. Nat. Prod,1983, 46, 940 (isol) Google Scholar
  126. Lounasmaa, M. Heterocycles, 1985, 23, 371 (pmr) Google Scholar
  127. Siddiqui, S. J. Nat. Prod, 1987, 50, 238 (Rescinnamidine) Google Scholar
  128. Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 8064, 8065.Google Scholar
  129. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 900, 905.Google Scholar
  130. Furlenmeyer, A. Experientia, 1953, 9, 331 (uv, ir) Google Scholar
  131. Klohs, M.W. J. Am. Chem. Soc, 1957, 79, 3763 (Pseudoreserpine) Google Scholar
  132. Ulshafer, P.R. C.R. Hebd. Seances Acad. Sci, 1957, 244, 2989 (oxide) Google Scholar
  133. Velluz, L. Bull. Soc. Chim. Fr, 1958, 145, 673 (synth) Google Scholar
  134. Woodward, R.B. Tetrahedron, 1958, 2, I (synth) Google Scholar
  135. B.P,894 866, (1961); CA,57, 9910e (Bietaserpine) Google Scholar
  136. Rosen, W.E. J. Am. Chem. Soc, 1961, 83, 4816 (pmr) Google Scholar
  137. Ban, Y. Tetrahedron, 1964, 20, 2877 (config) Google Scholar
  138. Berthaux, P. Arzneim.-Forsch,1964, 14,1040 (Bietaserpine) Google Scholar
  139. Schlittler, E., Alkaloids (N.Y.), 1965, 8, 287 (rev) Google Scholar
  140. Levin, R.H. J. Org . Chem, 1973, 38, 1983 (cmr) Google Scholar
  141. Becker, O. Org. Mass Spectrom, 1977, 12, 461 (ms) Google Scholar
  142. Mehri, M.H. Phytochemistry, 1978, 17, 1451 (oxide) Google Scholar
  143. Fanso-Free, S.N.Y. J. Am. Chem. Soc, 1979, 101, 1549 (N-15 nmr) Google Scholar
  144. Pearlman, B.A., J. Am. Chem. Soc, 1979, 101, 6404 (synth) Google Scholar
  145. Malik,A. Z. Naturforsch. B,1980, 35, 920 (Neonorreserpine) Google Scholar
  146. Wender, P.A. J. Am. Chem. Soc, 1980, 102, 6157 (.synth) Google Scholar
  147. Feng, X. Yaoxue Xuebao,1981, 16, 510; CA,97, 3593j (Diepipseudoreserpine) Google Scholar
  148. Juul, P., Handb. Exp. Pharmacol,1981, 54 (rev, pharmacol) Google Scholar
  149. Muhtadi, F.J., Anal. Profiles Drug Subst, 1984, 13, 737 (rev, ir, pmr, cmr, ms, anal) Google Scholar
  150. Lounasmaa, M. Heterocycles, 1985, 23, 371 (pmr) Google Scholar
  151. Szdntay, C. Alkaloids (IV.Y.), 1986, 27, 253 (pharmacol, bibi) Google Scholar
  152. Martin, S.F. J. Am. Chem. Soc, 1987, 109, 6124 (synth) Google Scholar
  153. Negwer, M., Organic-Chemical Drugs and their Synonyms,6thGoogle Scholar
  154. Ed., Akademie-Verlag, Berlin, 1987, 7993 (synonyms) Google Scholar
  155. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 901, 12443.Google Scholar
  156. Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2362.Google Scholar
  157. Brockmann, H. Chem. Ber, 1969, 102, 1224 (struct, ir, uv, nmr) Google Scholar
  158. Eckhardt, K. Tetrahedron, 1970, 26, 5875 (struct, ir, uv, nmr) Google Scholar
  159. Kingston, J.F Can. J. Chem. 1977, 55, 785 (synth) Keay, B.A J. Am. Chem. Soc.1982, 104, 4725 (synth)Google Scholar
  160. Höfle, G. Justus Liebigs Ann. Chem,1983, 835 (isol, bio-synth cmr)Google Scholar
  161. Arora, S.K J. Antibiot.1985, 38, 113 (struct)Google Scholar
  162. Kelly, T.R J. Am. Chem. Soc. 1985, 107, 3879 (synth)Google Scholar
  163. Fr. Pat,1 503 260, (1967); CA,69, 106542t (synth) Elliot, M. Pestic. Sci,1971, 2, 243 (use) Google Scholar
  164. Ueda, K. J. Agric. Food Chem, 1974, 22, 212; 1975, 23, 106 (metab) Google Scholar
  165. Wickham, J.C Pestic. Sci. 1976, 7, 273 (use)Google Scholar
  166. Nakazawa, H. Agric. Biol. Chem,1980, 44, 1173 (cmr) Google Scholar
  167. Bisagni, E. J. Chem. Soc, Perkin Trans 1, 1979, 1706 (synth) Google Scholar
  168. Rivalle, C. J. Med. Chem,1980, 23, 1212; 1983, 26, 181 (synth, pharmacol) Google Scholar
  169. Dowling, J Vitam. Horm. (N.Y.)1960, 18, 515 (rev)Google Scholar
  170. Borua, A.B Tetrahedron Lett.1972, 1823 (synth)Google Scholar
  171. Stam, C.H Acta Crystallogr. Sect. B1972, 28, 2936 (cryst struct) Google Scholar
  172. Cainelli, G Gazz. Chim. Ital.1973, 103, 117 (i.som)Google Scholar
  173. Julia, M Bull. Chim. Soc. Fr.1973, 746 (synth)Google Scholar
  174. Englert, G He!v. Chim. Acta 197558, 2367 (cmr)Google Scholar
  175. Bard, D.R Br. J. Cancer 1977, 35, I IO (pharmacol tux)Google Scholar
  176. McCormick, A.M et a! Anal. Biochem.1978, 86, 25 (hplc)Google Scholar
  177. Bernard, M J. Org. Chem.1983, 48, 3164 (synth)Google Scholar
  178. De Paolis, A.N., J. Chromatogr, 1983, 258, 314 (tic) Google Scholar
  179. Perry, M.D. Clin. Pharm, 1983, 2, 12 (rev) Google Scholar
  180. Bestmann, H.J Justus Liebigs Ann. Chem.1984, 1740 (synth) Google Scholar
  181. Chytil, F., Pharmacol. Rev, 1984, 36, 93 (rev, pharmacol, props) Google Scholar
  182. Ward, A. Drugs, 1984, 28, 6 (rev, Isotretinoin) Google Scholar
  183. Madani, K.A., Nutr. Res, 1986, 6, 107 (rev) Google Scholar
  184. Negwer, M., Organic-Chemical Drugs and their Synonyms,6th Ed., Akademie-Verlag, Berlin, 1987, 5902. Martindale, The Extra Pharmacopoeia,28th/29th Eds.Google Scholar
  185. /1989, Pharmaceutical Press, London, 1616, 1656. Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2364.Google Scholar
  186. Ger. Pat,3 132 915, (1983); CA,98, 198214 (synth) Google Scholar
  187. Gielsdorf, W. et a, J. Chromatogr, 1987, 419, 351 (chromatog) Google Scholar
  188. Potts, W.J., Life Sci, 1971, 10, 655 (pharmacol) Google Scholar
  189. Reinis, S., Bull. Psychon. Soc, 1973, 2, 385 (pharmacol) Google Scholar
  190. Ohnuki, T. Tetrahedron Lett, 1981, 22, 1267 (struct) Google Scholar
  191. Okami, Y. J. Antibiot, 1981, 34, 344 (iso!) Google Scholar
  192. Takashio, M. Agric. Biol. Chem, 1982, 46, 1457, 1987, 2449 (props) Google Scholar
  193. Kotaki, A. J. Vitaminol. (Kyoto), 1968, 14, 247 (synth, tetranicotinate) Google Scholar
  194. Beach, R. Tetrahedron Lett,1969, 3489 (synth) Google Scholar
  195. Kotaki, A. Bitamin, 1969, 39, 382 (metab, tetranicotinate) Google Scholar
  196. Paterson, T. et a, J. Chem. Soc, Chem. Commun,1969, 290 (biosynth) Google Scholar
  197. Tanaka, N. Bull. Chem. Soc. Jpn, 1969, 42, 1546 (cryst struct) Google Scholar
  198. Yagi, K. J. Vitaminol. (Kyoto), 1969, 15, 155 (metab, tetrabutyrate) Google Scholar
  199. Japan. Pat,70 07 749, (1970); CA,73, 15177u (synth, tetrabutyrate) Google Scholar
  200. McCormick, D.A., J. Heterocycl. Chem, 1974, 11, 969. Yoneda, F., J. Am. Chem. Soc, 1976, 98, 830 (synth) Google Scholar
  201. Holmgren, A., Experientia, 1980, 36, 149 (rev, FAD) Google Scholar
  202. Walt,D.R. J. Am. Chem. Soc,1980, 102, 7805 (synth, 5’-phosphate) Google Scholar
  203. Bacher, A. J. Am. Chem. Soc, 1982, 104, 3754 (biosynth) Google Scholar
  204. Brown, G.M. Adv. Enzymol. Relat. Areas Mol. Biol, 1982, 53, 345 (rev, biosynth) Google Scholar
  205. Keller, P.J. J. Am. Chem. Soc, 1983, 105, 2505 (biosynth, cmr, tetraacetate) Google Scholar
  206. Keller, P.J. Tetrahedron, 1983, 39, 3471 (biosynth) Google Scholar
  207. Shimizu, S. Appl. Biochem. Biotechnol, 1983, 8, 237 (synth, FAD) Google Scholar
  208. Ulrich, E.L. Tetrahedron Lett, 1983, 24, 473 (pmr) Google Scholar
  209. Yoneda, F., Kirk-Othmer Encycl. Chem. Technol, 3rd Ed,1983, 24, 108 (rev, synth) Google Scholar
  210. Cooperman, J.M. Food Sci. Technol, 1984, 13, 299 (rev, metab, props) Google Scholar
  211. Moonen, C.T. Biochemistry, 1984, 23, 4859 (pmr, conformn, tetraacetate, 5’-phosphate) Google Scholar
  212. Vervoort, J, Eur. J. Biochem,1985, 151, 49 (cmr, 3-Me, tetraacetate) Google Scholar
  213. Nielsen, P. Methods Enzymol, 1986, 122, 209 (synth, phosphates) Google Scholar
  214. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 7841, 7842, 7843, 7844, 7845.Google Scholar
  215. Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 4425, 4473, 7551, 7999.Google Scholar
  216. Srivastava, P. J. Med. Chem, 1983, 26, 445 (synth) Google Scholar
  217. Boritzki, T.J. Biochem. Pharmacol, 1985, 34, 1109 (pharmacol) Google Scholar
  218. Goldstein, B.M. J. Am. Chem. Soc, 1985, 107, 1394 (cryst struct) Google Scholar
  219. Hennen, W.J,J. Org . Chem,1985, 50, 1741 (synth, cmr) Google Scholar
  220. Cook, P.D. J. Heterocycl. Chem, 1986, 23, 155 (synth) Google Scholar
  221. Akita, E. J. Antibiot,1970, 23, 155, 173 (isol, struct) Google Scholar
  222. Ito, T. Antimicrob. Agents Chemother, 1970, 33; Agric. Biol. Chem, 1970, 34, 980 (synth, ir, pmr) Google Scholar
  223. Ikeda, D. Bull. Chem. Soc. Jpn, 1973, 46, 3210 (synth, derivs) Google Scholar
  224. Kojima, M. J. Antibiot, 1973, 26, 784 (biosynth, derivs) Google Scholar
  225. Fukami, H. Agric. Biol. Chem, 1977, 41, 1689 (synth) Google Scholar
  226. Suami, T. Carbohydr. Res, 1977, 56, 415 (synth) Google Scholar
  227. Kumar, V. J. Org . Chem, 1981, 46, 4298 (synth) Google Scholar
  228. Miyadoh, S. CA, 1982, 96, 50625 (iso!) Google Scholar
  229. Inouye, S. CA, 1982, 98, 83105 (rev, pharmacol) Google Scholar
  230. Yoshikawa, M. Chem. Len,1984, 2097 (synth) Google Scholar
  231. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 144.Google Scholar
  232. Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 4622.Google Scholar
  233. B.P,1 603 127, (1981); CA,96, 162439 (synth, props) Google Scholar
  234. Vigevani, A. J. Antibiot, 1985, 38, 1799 (metab) Google Scholar
  235. Heifets, L.B. Int. Congr. Ser.-Excerpta Med, 1986, 697, 180 (pharmacol) Google Scholar
  236. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 16512.Google Scholar
  237. Gadret, M. Acta Crystallogr, Sect. B, 1975, 31, 1454 (cryst struct) Google Scholar
  238. Gallo, E.G. Anal. Profiles Drug Subst, 1976, 5, 467 (rev, synth, anal) Google Scholar
  239. Girling, D.T. J. Antimicrob. Chemother, 1977, 3, 115 (tox, rev) Google Scholar
  240. Sensi, P., Chron. Drug Discovery, 1982, 1, 201 (rev) Google Scholar
  241. Sensi, P., Rev. Infect. Dis,1983, 5 (Suppl. 3),402 (rev) Google Scholar
  242. Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 8227 (synonyms) Martindale, The Extra Pharmacopoeia, 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 7569.Google Scholar
  243. Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2369.Google Scholar
  244. Gallo, G.G. Farmaco, Ed. Prat, 1963, 18, 78 (isol) Google Scholar
  245. Oppolzer, W. Experientia, 1964, 20, 336 (struct) Google Scholar
  246. Brufani, M. Experientia, 1964, 20, 339 (cryst struct) Google Scholar
  247. Gurgo, C. Handb. Exp. Pharmacol, 1982, 61, 519 (rev) Google Scholar
  248. Seong, B.L. Chem. Lett,1982, 627 (biosynth) Google Scholar
  249. Arora, S.K. Mol. Pharmacol, 1983, 23, 133 (cryst struct) Google Scholar
  250. Sensi, P., Rev. Infect. Dis,1983, 5 (Suppl. 3),402 (bibi) Google Scholar
  251. Ghisalba, O. Drugs. Pharm. Sci, 1984, 22, 281 (rev) Google Scholar
  252. Lancini, G., Biotechnology, 1986, 4, 431 (rev) Google Scholar
  253. Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 146.Google Scholar
  254. Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2369, 2370.Google Scholar
  255. Belg. Pat,632 770, (1964); CA,61, 4166 (iso!) Google Scholar
  256. Sensi, P. J. Med. Chem,1964, 7, 596 (Rifamide) Launchburg, A.P., Prog. Med. Chem,1970, 7, 1 (rev, Rifamide) Google Scholar
  257. Fr. Pat,2 043 847, (1971); CA,76, 44674 (isol) Google Scholar
  258. Oppolzer, W. HeIv. Chim. Acta, 1973, 56, 2287 (config) Google Scholar
  259. Zerilli, L.F. Ann. Chim. (Rome),1974, 64, 199 (ms) Japan. Pats,79 110 392, 79 110 393, (1979); CA,92, 20566, 56812 (isol) Google Scholar
  260. Ghisalba, O. J. Antibiot, 1980, 33, 847 (deriy) Brufani, M. Mol. Pharmacol, 1982, 21, 394 (struct) Google Scholar
  261. Ghisalba, O. J. Antibiot, 1982, 35, 74, 1361 (biosynth) Martindale, The Extra Pharmacopoeia, 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 145.Google Scholar
  262. Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2369.Google Scholar
  263. Brufani, M. J. Antibiot, 1984, 37, 1611 (synth, pmr, pharmacol) Google Scholar
  264. Marchi, E. J. Med. Chem, 1985, 28, 960 (synth, pharmacol) Google Scholar
  265. Venturini, A.P. Chemioterapia 1986, 5, 257, 263 (pharmacol, tox) Google Scholar
  266. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 503.Google Scholar
  267. Ger. Pat 3 009 034, (1981); CA 95, 203640 (synth) Google Scholar
  268. Hirai, K. J. Heterocycl. Chem, 1982, 19, 1363 (synth, props) Google Scholar
  269. Koike, M. Drug Metab. Dispos, 1987, 15, 426 (metab, props) Google Scholar
  270. Koike, M. Xenobiotica, 1988, 18, 257 (metab, props) Google Scholar
  271. Ger. Pat 2 362 754, (1974); CA 81, 105533 (synth, pharmacol) Google Scholar
  272. Laubie, M. J. Pharmacol, 1985, 16, 259 (pharmacol) Google Scholar
  273. Van Zwieten, P.A., Am. J. Cardiol 1988, 61, 6D (rev, pharma-col) Google Scholar
  274. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 3157.Google Scholar
  275. U.S.P 4 378 362, (1983); CA 99, 22316d (synth, pharmacol) Google Scholar
  276. Rosseels, G. Eur. J. Med. Chem.-Chim. Ther, 1983, 18, 339 (synth, pharmacol) Google Scholar
  277. Knoll, J. Arzneim.-Forsch 1971, 21, 719 (pharmacol) Google Scholar
  278. Meszaros, Z. Arzneim.-Forsch, 1972, 22, 815 (synth, pmr, ms) Google Scholar
  279. Simon, K. Acta Crystallogr., Sect. B, 1975, 31, 1695 (cryst struct) Google Scholar
  280. Szasz, Gy. J. Chromatogr, 1976, 117, 345 (tic) Google Scholar
  281. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 13214.Google Scholar
  282. Ferris, R.M. J. Pharm. Pharmacol, 1982, 34, 388 (pharmacol) Google Scholar
  283. U.S.P 4 400 383, (1983); CA 99, 158469 (synth) Google Scholar
  284. Harfenist, M. J. Org . Chem, 1985, 50, 1356 (isom, pmr, cmr) Google Scholar
  285. Ferris, R.M. Drug Dey. Res, 1986, 9, 171 (pharmacy!) Google Scholar
  286. Morales-Rios, M.S. Magn. Reson. Chem, 1987, 25, 377 (cmr) Google Scholar
  287. Fox, P.K. Arzneim.-Forsch, 1980, 30, 55 (pharmacol) Google Scholar
  288. Lewis, A.J. Agents Actions, 1980, 10, 258 (pharmacol) Google Scholar
  289. Cairns, J. J. Chem. Soc., Perkin Trans. 1 1981, 2306 (synth) Google Scholar
  290. Barnes, J.C. Acta Crystallogr., Sect. C, 1985, 41, 763 (cryst struct) Google Scholar
  291. Sankey, G.H. J. Heterocycl. Chem, 1972, 9, 1049 (synth) Google Scholar
  292. Pinder, R.M. Drugs, 1977, 14, 81 (rev) Google Scholar
  293. Aasen, A.J. Acta Chem. Scand., Ser. B, 1988, 42, 216 (abs config) Google Scholar
  294. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2102.Google Scholar
  295. Capek, A. Folia Microbiol 1972, 17 396; 1976, 21, 155 (pharmacol) Google Scholar
  296. Budesinsky, Z. Collect. Czech. Chem. Commun, 1975, 40, 1078 (synth) Google Scholar
  297. Pavlikova, L. Cesk. Farm, 1975, 24, 249 (metab) Google Scholar
  298. Imamura, H. CA 1986, 105, 222611 (pharmacol) Yamamoto, H. Oyo Yakuri 1987, 34, 453, 461 (pharmacol) Google Scholar
  299. Kastrons, V.V. Arzneim.-Forsch 1985, 35, 668, 672, 680, 808, 813, 907, 915 (synth, ir, pmr, ms, pharmacol, tox) Google Scholar
  300. Eur. Pat 66 475, (1982); CA 98, 160515y (synth, pharmacol) Google Scholar
  301. Shriver, D.A. et a!, Arzneim.-Forsch, 1985, 35, 839 (pharmacol) Google Scholar
  302. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 18675.Google Scholar
  303. deWald, H.A. J. Med. Chem, 1973, 16, 1346 (synth, pharmacol) Google Scholar
  304. Poschel, B.P.H. Psychopharmacologia, 1974, 35, 257 (pharmacol) Google Scholar
  305. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 7103.Google Scholar
  306. Eur. Pat 196 132, (1986); CA 106, 67292x (synth, pharmacol) Google Scholar
  307. Janssen, P.A.J. J. Pharmacol. Exp. Ther, 1988, 244, 685 (pharmacol) Google Scholar
  308. U.S.P 4 246 263, (1981); CA 95, I 32938h (synth, pharmacol) Google Scholar
  309. Panizzon, L., Hely. Chim. Acta, 1944, 27, 1748 (synth, ester) Google Scholar
  310. Reisch, J. J. Pharm. Pharmacol, 1968, 20, 81 (ms, ester) Google Scholar
  311. Shafi’ee, A. J. Med. Chem, 1969, 12, 266 (abs config) Google Scholar
  312. Marozzi, E. Farmaco, Ed. Prat, 1976, 31, 180 (glc, ester) Google Scholar
  313. Padmanabhan, G.R., Anal. Profiles Drug Subst, 1981, 10, 473 (rev, pharmacol, esters) Google Scholar
  314. Redalieu, E. Drug Metab. Dispos, 1982, 10, 708 (metab) Google Scholar
  315. Lim H.K. J. Chromatogr 1985, 328, 378 (resoln) Google Scholar
  316. Nakajima, K. Chem. Pharm. Bull, 1986, 34, 1701 (glc, ms, anal) Google Scholar
  317. Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 3234.Google Scholar
  318. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 1433.Google Scholar
  319. Eur. Pat., 110 435 (1984); CA, 102, 6522t (synth, pharmacol)Google Scholar
  320. Goodwin, G.M Br. J. Pharmacol., 1985, 84, 743 (pharmacol)Google Scholar
  321. Kennis, L.E.J. Drug Del). Res 1986, 8, 133, 187 (rev, pharmacol) Google Scholar
  322. Sandrini, G. Eur. J. Pharmacol, 1986, 130, 311 (pharmacol) Google Scholar
  323. Vinick, F.J Annu. Rep. Med. Chem., 1986, 21 1 (rev)Google Scholar
  324. Larsson, M Methods Find. Exp. Clin. Pharmacol., 1987, 9, 349 (hplc, anal)Google Scholar
  325. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 18677.Google Scholar
  326. Belg. Pat., 660 244 (1965); CA, 63, 17965h (synth, uv)Google Scholar
  327. Van Dijk, J. Recl. Tray. Chim. Pays-Bas 1973, 92, 1281 (synth) Google Scholar
  328. Finkelstein, B.W., Drug Intel!. Clin. Pharm, 1981, 15, 425 (rev, pharmacol) Google Scholar
  329. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2103.Google Scholar
  330. Fr. Pat., M2114 (1963); CA, 60, 14598f (synth, pharmacol)Google Scholar
  331. Austrian Pat., 236 930 (1964); CA, 62, 2710a (synth)Google Scholar
  332. Sandberg J. Cancer Chemother. Rep., Part 1, 1969, 53, 367; 1971, 55, 233 (pharmacol)Google Scholar
  333. Hegedus, L. Eur. J. Cancer Clin. Oncol, 1984, 20, 933 (pharmacol) Google Scholar
  334. Kantor, S. Science (Washington), 1970, 168, 373 (pharmacol) Google Scholar
  335. U.S.P 3 941 825, (1976); CA 85, 540w (synth, pharmacol) Google Scholar
  336. Martindale, The Extra Pharmacopoeia 28th/29th Eds.,1982/1989, Pharmaceutical Press, London, 13216.Google Scholar
  337. U.S.P., 4 592 866 (1986); CA, 106, 67360 (synth, pharmacol)Google Scholar
  338. U.S.P., 4 705 853 (1987); CA, 109, 231085s (synth)Google Scholar
  339. Bergman J. J. Pharmacol. Exp. Ther., 1988, 245, 471 (pharmacol) Google Scholar
  340. Van Bever, W.F.M. J. Med. Chem, 1973, 16, 394 (synth, pharmacol) Google Scholar
  341. Eur. Pat 15 171, (1980); CA 94, 103373u (synth, pharmacol) Google Scholar
  342. Langlois, M. J. Heterocycl. Chem, 1983, 20, 393 (synth) Google Scholar
  343. Belg. Pat., 670 495 (1966); CA, 65, 13615a (synth, pharmacol)Google Scholar
  344. Belg. Pat., 855 392 (1977); CA, 88, I90586h (synth, pharmacol)Google Scholar
  345. Beattie, D.E. J. Med. Chem, 1985, 28, 1617 (synth, pharmacol) Google Scholar
  346. B.P 961 313, (1964); CA 61, 6954 (synth) Google Scholar
  347. B.P., 1 895, (1965); CA 63, 16307 (synth, use) Google Scholar
  348. McMonigle, J.J. Arch. Int. Pharmacodyn. Ther 1969, 178, 53 (pharmacol) Google Scholar
  349. Lowe, M.C. Eur. J. Pharmacol, 1973, 21, 46 (pharmacol) Google Scholar
  350. Schwabe, U. Mol. Pharmacol, 1976, 12, 900 (pharmacol) Google Scholar
  351. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 13218.Google Scholar
  352. Gottstein, W.J. J. Am. Chem. Soc, 1959, 81, 1198 (synth) Google Scholar
  353. Ther, L. Arzneim.-Forsch, 1959, 9, 63 (pharmacol) Google Scholar
  354. Dimmling, T. Antibiotics Ann 1959–60, 350, 365 (pharmacol) Google Scholar
  355. Butterfield, A.G. Antimicrob. Agents Chemother, 1973,4, 11 (chromatg) Google Scholar
  356. Mazzola, E.P. J. Pharm. Sci, 1980, 69, 229 (cmr) Google Scholar
  357. Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 7548.Google Scholar
  358. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 149, 150.Google Scholar
  359. Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2344.Google Scholar
  360. West, R.A. J. Org . Chem, 1961, 26, 3809 (synth) Google Scholar
  361. Norton, S. J. Pharmacol. Exp. Ther, 1966, 154, 152 (pharmacol) Google Scholar
  362. Taylor, E.D. J. Am. Pharm. Assoc. Sci. Ed, 1960, 49, 317 (synth, props) Google Scholar
  363. Kuliev, A.M. Zh. Org . Khim, 1972, 8, 1301 (synth, ir, nmr) Google Scholar
  364. Ger. Pat 2 630 060, (1978); CA 88, 121184 (synth, pharmacol) Google Scholar
  365. Ger. Pat 3 437 694, (1986); CA 105, 72691 (pharmacol) Google Scholar
  366. Takashima, M. CA, 1976, 84, 16904 (synth, pharmacol) Buzzelli, G. Clin. Ter, 1979, 89, 251 (pharmacol) Google Scholar
  367. B.P., 1 203 958, (1970); CA, 74, 31756h (synth, pharmacol)Google Scholar
  368. Bogan, J.A. Drugs of Today, 1977, 13, 510 (reu)Google Scholar
  369. Winkelmann, E. Arzneim.-Forsch., 1978, 28, 739 (synth,pharmacol)Google Scholar
  370. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 13219.Google Scholar
  371. Gallagher, G. J. Med. Chem, 1985, 28, 1533 (synth) Google Scholar
  372. U.S.P 4 006 232, (1977); CA 87, 5968 (synth) Google Scholar
  373. Vidrio, H. Arzneim.-Forsch, 1980, 30, 12 (pharmacol) Google Scholar
  374. Lynch, J. Arzneim.-Forsch 1986, 36, 475 (pharmacol) Google Scholar
  375. U.S.P 4 695 576, (1987); CA 108, 75228 (synth, pharmacol) Google Scholar
  376. Sahlberg, C., J. Labelled Compd. Radiopharm, 1987, 24, 529 (synth) Google Scholar
  377. Belg. Pat 623 058, (1963); CA 60, 9291h (synth, pharmacol) Google Scholar
  378. Ellefson, C.R. J. Med. Chem, 1976, 19, 1161 (pharmacol) Google Scholar
  379. Edmonds, H.L. J. Pharmacol. Exp. Ther, 1979, 208, 236 (pharmacol)Google Scholar
  380. Eur. Pat 59 698, (1982); CA 98, 34513 (synth, pharmacol) Google Scholar
  381. Kalland, T. J. Immunol, 1985, 134, 3956 (pharmacol) Google Scholar
  382. Tarkowski, A. Immunology, 1986, 59, 589 (pharmacol) Google Scholar
  383. Reimann, H J. Chem. Soc., Chem. Commun., 1972, 1270 (isol, struct, spectra)Google Scholar
  384. Waitz, J.A. J. Antibiot, 1972, 25, 647 (isol) Google Scholar
  385. Ganguly, A.K. J. Antibiot, 1976, 29, 976 (biosynth) Google Scholar
  386. Hatano, K. J. Antibiot., 1976 29, 1163 (isol, props) Google Scholar
  387. Kishi, T. J. Antibiot., 1976 29, 1171 (struct) Google Scholar
  388. Kinumaki, A. J. Antibiot, 1977, 30, 450 (struct) Google Scholar
  389. Suzuki, M. Heterocycles, 1977, 8, 199 (ms) Google Scholar
  390. Ganguly, A.K. Tetrahedron Lett 1980, 4699 (cryst struct)Google Scholar
  391. Puar, M.S J. Antibiot., 1981, 34, 602; 1982, 35, 381 (cmr, conformn)Google Scholar
  392. Puar, M.S J. Antibiot., 1982, 35, 381 (cmr)Google Scholar
  393. Ganguly, A.K J. Chem. Soc., Chem. Commun., 1983, 1 166 (synth, deriu)Google Scholar
  394. Lin, C.C Antimicrob. Agents Chemother., 1986, 29, 753 (metab)Google Scholar
  395. Martindale, The Extra Pharmacopoeia, 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 151 Google Scholar
  396. Sax, N.I Dangerous Properties of Industrial Materials, 6 thEd., Van Nostrand-Reinhold, 1984, 2371.Google Scholar
  397. Valcavi, U. Farmaco, Ed. Sci, 1975, 30, 527 (synth) Google Scholar
  398. Ger. Pat 2 535 343, (1976); CA 85, 32512(synth,pharmacol) Google Scholar
  399. Valcavi, U. Arzneim.-Forsch, 1982, 32, 657 (pharmacol) Google Scholar
  400. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 16980.Google Scholar
  401. Ger. Pat 2 943 776, (1981); CA 95, 151023 (synth) Google Scholar
  402. Krause, W. J. Pharm. Sci, 1984, 73, 563 (glc, ms) Google Scholar
  403. Schmidt, J.B. Endocrinol. Exp 1987, 21, 71 (pharmacol) Google Scholar
  404. Hoshina, K. Arzneim.-Forsch, 1985, 35, 493 (pharmacol) Google Scholar
  405. Takeshita, T. Chem. Pharm. Bull, 1985, 33, 5059; 1986, 34, 3900 (synth, cryst struct) Google Scholar
  406. Eur. Pat 24 510, (1981); CA 95, 80465 (synth) Google Scholar
  407. Tarutani, M. Arzneim-Forsch, 1985, 35, 703 (pharmacol, acetate) Google Scholar
  408. Bickel, M. Arzneim-Forsch, 1986, 36, 1358 (pharmacol) Google Scholar
  409. Honma, S. Drug Metab. Dispos, 1987, 15, 551 (metab, acetate) Google Scholar
  410. Iwamura, S. J. Chromatogr, 1987, 413, 370 (hplc) Google Scholar
  411. In, Y. Chem. Pharm. Bull 1988, 36, 2295 (cryst struct) Google Scholar
  412. Scholtholt, J. Drugs 1988, 35, 30, 41 (revs) Google Scholar
  413. Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2430.Google Scholar
  414. Fellipone, F. Steroids, 1984, 43, 271 (synth, pharmacol) Google Scholar
  415. Berti, F. Arzneim.-Forsch 1986, 36, 1369, 1372 (pharmacol) Google Scholar
  416. Ger. Pat 3 419 935, (1985); CA 104, 74999v (use) Google Scholar
  417. Seyfried, C.A. Dopaminergic Syst. Their Regul., [Proc. Symp.] 1986, 375 (pharmacol) Google Scholar
  418. Fr. Pat 2 473 525, (1981); CA 96, 123219 (synth) Google Scholar
  419. Jones, R.N. Antimicrob. Agents Chemother, 1983, 24, 209 (props) Google Scholar
  420. Barlam, T. Antimicrob. Agents Chemother, 1984, 25, 529 (props) Google Scholar
  421. Chantot, J.-F. J. Antibiot, 1986, 39, 661 (props) Google Scholar
  422. Phillips, I. J. Antimicrob. Chemother 1987, 20, Suppl. B (book) Google Scholar
  423. Ger. Pat 2 423 491, (1975); CA 84, 59794 (synth) Google Scholar
  424. B.P 1 447 162, (1976); CA 86, 90091 (synth, pharmacol) Google Scholar
  425. Fr. Pat M1741, (1963); CA 59, 10002e (synth) Google Scholar
  426. Mishkinsky, J. Arch. Int. Pharmacodyn. Ther 1969, 179, 94 (pharmacol) Google Scholar
  427. White, F.B. Kirk-Othmer Encycl. Chem. Tech, 3rd Ed., Wiley-Interscience, 1978–1984, 20, 497.Google Scholar
  428. Ando, A. Int. J. Nucl. Med. Biol, 1984, 11, 195 (use) Google Scholar
  429. Sax, N.I. Dangerous Properties of Industrial Materials, 7th Ed., Van Nostrand-Reinhold, 1989, 2985.Google Scholar
  430. Cecchetti, V. J. Med. Chem, 1987, 30, 465 (synth, pharmacol) Google Scholar
  431. Asahina, Y. J. Chem. Soc 1927, 1708 (synth) Google Scholar
  432. Pachter, I.J. J. Am. Chem. Soc, 1960, 82, 5187 (isol) Google Scholar
  433. Yamazaki, M. Tetrahedron Lett 1966, 3221; 1967, 3317 (biosynth) Google Scholar
  434. de Barros Corrêa, D. Phytochemistry, 1975, 14, 2059 (isol) Google Scholar
  435. Kametani, T. Heterocycles 1976, 4, 23; 1487; J. Am Google Scholar
  436. Chem. Soc 1976, 98, 6186 (synth, uv, ir, pmr, ms) Google Scholar
  437. Tamâs, J. Acta Chim. Acad. Sci. Hung., 1976, 89, 85 (ms) Google Scholar
  438. Toth, G. Justus Liebigs Ann. Chem., 1977, 529 (cmr) Google Scholar
  439. Danieli, B. Heterocycles, 1978, 9, 803 (synth) Google Scholar
  440. Kametani, T. J. Am. Chem. Soc 1977, 99, 2306; Chem Google Scholar
  441. Pharm. Bull 1978, 26, 1922 (synth) Google Scholar
  442. Kökösi, J. Tetrahedron Lett 1981, 4861 (synth) Google Scholar
  443. Bergman, J J. Org . Chem 1985, 50, 1246 (synth) Google Scholar
  444. Kaneko, C. Heterocycles, 1985, 23, 1385 (synth) Google Scholar
  445. U.S.P 2 646 428, (1953); CA 48, 8269 (Ethoxazorutoside) Google Scholar
  446. Griffith, J.Q., Rutin and Related Flavonoids, 1955, Mack, Easton.Google Scholar
  447. Fr. Pat 1 434 376, (1966); CA 66, 29043 (Ethoxazorutoside) Google Scholar
  448. Hörhammer, L. Tetrahedron Lett 1966, 567 (synth) Google Scholar
  449. Swiss Pat 458 389, (1968); CA 70, 68714m (Monoxerutin) Google Scholar
  450. Schmid, R.D., Tetrahedron, 1972, 28, 3259 (ms) Google Scholar
  451. Wenkert, E. Phytochemistry, 1977, 16, 1811 (cmr) Google Scholar
  452. Khalifa, T.I. Anal. Profiles Drug Subst, 1983, 12, 623 (rev) Google Scholar
  453. Voelter, W. n-((3-Hydroxyethyl)rutoside: NewGoogle Scholar
  454. Results, Springer-Verlag, Berlin, 1983 (book) Martindale, The Extra Pharmacopoeia, 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 15304.Google Scholar
  455. Negwer, M., Organic-Chemical Drugs and their Synonyms 6th Ed., Akademie-Verlag, Berlin, 1987, 7530 (synonyms) Google Scholar
  456. Chelardoni, M. Chim. Farm, 1970, 109, 245 (synth, pharmacol) Google Scholar
  457. Pisanti, N. Farmaco, Ed. Sci, 1972, 27, 919 (pharmacol) Google Scholar
  458. Wiesner, K Tetrahedron Lett., 1966, 221 (struct)Google Scholar
  459. Wiesner, K Adv. Org. Chem., 1972, 8, 295 (pmr, rev, struct)Google Scholar
  460. Bélanger, A Can. J. Chem., 1979, 57, 3348 (synth)Google Scholar
  461. Jones, L.R J. Biol. Chem, 1981, 256, 11809 (pharmacol)Google Scholar
  462. Waterhouse, A.L J. Chem. Soc., Chem. Commun., 1984, 1265 (Dehydroryanodine)Google Scholar
  463. Ruest, L. Can. J. Chem, 1985, 63, 2840 (derivs) Google Scholar
  464. Waterhouse, A.L. J. Chem. Soc., Perkin Trans.2 1985, 1011 (cmr, pmr) Google Scholar

Copyright information

© Springer Science+Business Media Dordrecht 1990

Authors and Affiliations

  • J. Elks
  • C. R. Ganellin

There are no affiliations available

Personalised recommendations