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References

  • Hanka, L.J. J. Antibiot, 1978, 31, 1211 (isol)

    Google Scholar 

  • Martin, D.G. J. Antibiot, 1980, 33, 902 (struct)

    Google Scholar 

  • Chidester, C.G. J. Am. Chem. Soc, 1981, 103, 7629 (cryst struct)

    Google Scholar 

  • Martin, D.G. J. Antibiot, 1981, 34, 1119 (isol)

    Google Scholar 

  • Sundberg, R.I. J. Org . Chem, 1985, 50, 425 (bibi)

    Google Scholar 

  • Reynolds, V.L. J. Antibiot, 1986, 39, 319 (rev)

    Google Scholar 

  • Bolton, R.E. Tetrahedron Lett, 1987, 28, 3163 (synth, bibi)

    Google Scholar 

  • Watt, W. Acta Crystallogr, Sect. C, 1988, 44, 1675 (cryst struct)

    Google Scholar 

  • Eur. Pat.,60 235, (1982); CA,98, 53687 (synth)

    Google Scholar 

  • Koehler, C. Biochem. Pharmacol, 1985, 34, 2251 (pharmacol)

    Google Scholar 

  • De Paulis, T. J. Med. Chem, 1986, 29, 61 (synth, isomers, cmr)

    Google Scholar 

  • Ehrin, E. J. Labelled Compd. Radiopharm, 1987, 24, 931 (synth)

    Google Scholar 

  • Hoegberg, T. J. Pharm. Pharmacol, 1987, 39, 787 (cryst struct, pharmacol)

    Google Scholar 

  • Mrozik, H. Experientia, 1969, 25, 883 (synth, pharmacol)

    Google Scholar 

  • Brown, W.R. Toxicol. Appl. Pharmacol, 1972, 21, 532 (tox)

    Google Scholar 

  • Caillier, R.L. Rev. Med. Vet, 1973, 124, 789 (Ranizole)

    Google Scholar 

  • U.S.P,3 914 418, (1975); CA,84, 30707u (synth, pharmacol)

    Google Scholar 

  • Sindt, A.C. Aust. J. Chem, 1980, 33, 203 (cryst struct)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 13206.

    Google Scholar 

  • Ger. Pat.,3 317 000, (1984); CA,102, 113476 (synth)

    Google Scholar 

  • Bartoszyk, G.D. Curr. Probi. Epilepsy, 1986, 4, 309 (rev)

    Google Scholar 

  • Wakeling, A.E. J. Endocrinol, 1983, 99, 455 (pharmacol)

    Google Scholar 

  • Jones, C.D. J. Med. Chem, 1984, 27, 1057 (synth, pharmacol)

    Google Scholar 

  • Lindstrom, T.D. Xenobiotica, 1984, 14, 841 (metab)

    Google Scholar 

  • Wakeling, A.E. J. Steroid Biochem, 1984, 20, 111 (phar-macol)

    Google Scholar 

  • Darvas, F. Pharmacochem. Libr, 1985, 8, 199 (pharmacol)

    Google Scholar 

  • Banci, F. Arzneim.-Forsch, 1971, 21, 1665 (synth, pharmacol)

    Google Scholar 

  • Beyer, K.H. Dtsch. Apoth.-Ztg, 1983, 123, 1527 (metab)

    Google Scholar 

  • Marciniec, B., Pharmazie, 1985, 40, 110 (ms)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2660.

    Google Scholar 

  • Eur. Pat,79 022, (1983); CA,100, 52012 (synth)

    Google Scholar 

  • Metzger, H. Arzneim.-Forsch, 1984, 34, 1399 (synth, pharmacol, tox, ester)

    Google Scholar 

  • Becker, R.H.A. Am. J. Cardiol,1987, 59, 3D, 18D, 23D (revs, Ramipril)

    Google Scholar 

  • Paulus, E.F. Acta Crystallogr, Sect. C, 1987, 43, 941 (cryst struct)

    Google Scholar 

  • Eur. Pat,60 182, (1982); CA,98, 34508 (synth)

    Google Scholar 

  • Necciari, J. Int. J. Clin. Pharmacol. Res, 1985, 5, 457 (pharmacol)

    Google Scholar 

  • Lavezzo, A. J. Pharm. Pharmacol, 1986, 38, 853 (pharmacol)

    Google Scholar 

  • Wilson, J.A. Eur. J. Clin. Pharmacol, 1986, 30, 33 (pharmacol)

    Google Scholar 

  • Ger. Pat,2 734 070, (1978); CA,88, 190580b (synth, pharmacol)

    Google Scholar 

  • Brogden, R.N. Drugs, 1982, 24, 267 (rev, pharmacol)

    Google Scholar 

  • Kojic-Prodic, B. Acta Crystallogr, Sect. B, 1982, 38, 1837 (cryst struct)

    Google Scholar 

  • Riley, A.J. Eds., Curr. Clin. Practice Ser, No. 1: Ranitidine,Excerpta Medica, Amsterdam, 1982 (book)

    Google Scholar 

  • Daly, M.J. Prog. Med. Chem, 1983, 20, 337 (rev, pharmacol)

    Google Scholar 

  • Gaginella, T.S. Drug /ntell. Clin. Pharm, 1983, 17, 873 (rev, pharmacol)

    Google Scholar 

  • Cholerton, T.J. J. Chem. Soc, Perkin Trans. 2,1984, 1761 (uv, ir, pmr, struct)

    Google Scholar 

  • Hohnjec, M. Anal. Profiles Drug Subst, 1986, 15, 533 (rev, synth, anal, metab)

    Google Scholar 

  • Geraldes, C.F. Magn. Reson. Chem, 1987, 25, 203 (pmr, cmr)

    Google Scholar 

  • Kirch, W., Pharmacol. Ther, 1987, 33, 129 (rev)

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 2946.

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds.

    Google Scholar 

  • /1989, Pharmaceutical Press, London, 3777, 6162.

    Google Scholar 

  • Eur. Pat,126 449, (1984); CA,102, 166777 (synth, pharmacol)

    Google Scholar 

  • Delee, E. Chromatographia, 1987, 24, 357 (hplc, resoln)

    Google Scholar 

  • U.S.P,3 993 749, (1972); CA,86, 41806 (synth, ir, pmr)

    Google Scholar 

  • Vézina, C. J. Antibiot,1975, 28, 721; 1983, 36, 351 (iso!) Baker, H. J

    Google Scholar 

  • Antibiot,1978, 31, 539; 1979, 32, 630(pharmacol)

    Google Scholar 

  • Swindells, D.C.N. Can. J. Chem, 1978, 56, 2491 (cryst struct)

    Google Scholar 

  • Findlay, J.A. Can. J. Chem, 1982, 60, 2046 (uv, ir, pmr, cmr, ms, cd)

    Google Scholar 

  • Ger. Pat,1 926 075, (1969); CA,74, 42391m (synth, pharmacol)

    Google Scholar 

  • Eur. Pat,24 038, (1981); CA,95, 81034 (synth)

    Google Scholar 

  • Hock, F.J. Psychopharmacology (Berlin), 1985, 86, 114 (pharmacol)

    Google Scholar 

  • Creighton, A.M. Nature (London), 1969, 222, 384

    Google Scholar 

  • Ger. Pat,1 941 564, (1970); CA,72, 121579r (synth, pharmacol)

    Google Scholar 

  • Repta, A.J. J. Pharm. Sci, 1976, 65, 238.

    Google Scholar 

  • Hempel, A. J. Am. Chem. Soc, 1982, 104, 3453 (cryst struct, bibi)

    Google Scholar 

  • Herman, E.H. Adv. Pharmacol. Chemother, 1982, 19, 249 (rev, pharmacol)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 1861.

    Google Scholar 

  • From N. aerocolonigenes Active against gram-positive and -negative bacteria and tumours. Yellow solid.

    Google Scholar 

  • Nettleton, D.E. Tetrahedron Lett, 1985, 26, 4011 (isol, struct, props)

    Google Scholar 

  • Kaneko, T. Tetrahedron Lett,1985,26, 4015 (synth) U.S.P,4 524 154, (1985); CA,103, 159104 (deny)

    Google Scholar 

  • Bush, J.A. J. Antibiot, 1987, 40, 668 (manuf, props, bibi)

    Google Scholar 

  • Melloni, P. Eur. J. Med. Chem, 1984, 19, 235 (synth, pharmacol)

    Google Scholar 

  • Melloni, P. Tetrahedron,1985, 41, 1393 (synth, config) Ger. Pat,2 540 093, (1986); CA,105, 191 107 (synth, resoln, pharmacol)

    Google Scholar 

  • Ger. Pat 2 805 185, (1978); CA 90, 6664 (synth)

    Google Scholar 

  • Sekido, S. Cancer Treat. Rep, 1979, 63, 961 (pharmacol)

    Google Scholar 

  • B.P,202 5 406, (1980); CA,93, 1 1417Ig (synth)

    Google Scholar 

  • Bergey, J.L. Arzneim.-Forsch, 1983, 33, 1258 (pharmacol)

    Google Scholar 

  • Badia, A., Drugs Future, 1984, 9, 38 (rev)

    Google Scholar 

  • Anderson, J.L. Am. J. Cardiol, 1987, 60, 281 (pharmacol)

    Google Scholar 

  • Colatsky, T.J. J. Cardiovasc. Pharmacol, 1988, 11, 308 (pharmacol)

    Google Scholar 

  • U.S.P,4 208 327, (1980); CA,94, 30804 (synth, pharmacol)

    Google Scholar 

  • Florvall, L. J. Med. Chem, 1982, 25, 1280 (synth, tox, pharmacol)

    Google Scholar 

  • Oegren, S.O. Eur. J. Pharmacol, 1984, 102, 459 (pharmacol)

    Google Scholar 

  • Hoegberg, T. Mol. Pharmacol, 1986, 30, 345 (cryst struct, pharmacol)

    Google Scholar 

  • Stensland, B. Acta Crystallogr, Sect. C, 1987, 43, 2393 (cryst struct)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 497.

    Google Scholar 

  • Oya, M. Chem. Pharm. Bull,1982, 30, 440, 484, 2705 (synth, abs config, cryst struct, ms)

    Google Scholar 

  • Shimada, K. J. Pharm. Sci, 1984, 73, 119 (hplc)

    Google Scholar 

  • In, Y, J. Chem. Soc, Chem. Commun,1986, 473 (cryst struct, conformn)

    Google Scholar 

  • Yamauchi, H. Arzneim.-Forsch, 1987, 37, 157 (pharmacol)

    Google Scholar 

  • Eur. Pat,94 742, (1983); CA,100, 68166 (synth)

    Google Scholar 

  • Eur. Pat,239 321, (1987); CA,108, 75227 (synth, hydrate)

    Google Scholar 

  • Sanger, G.J., Br. J. Pharmacol, 1987, 91, 77 (pharmacol)

    Google Scholar 

  • Hawthorn, J, Q.J. Exp. Physiol,1988, 73, 7 (pharmacol)

    Google Scholar 

  • Morinaka, Y, Eur. J. Med. Chem.-Chim. Ther,1981, 16, 251 (synth, pharmacol)

    Google Scholar 

  • Nagase, M. CA,1986, 105, 108121, 108122, 108123 (tox)

    Google Scholar 

  • Takahashi, K. Oyo Yakuri, 1986, 32, 233 (pharmacol)

    Google Scholar 

  • Furumai, T. J. Antibiot, 1977, 30, 443 (isol, struct)

    Google Scholar 

  • Kinumaki, A. J. Antibiot, 1977, 30, 450 (struct)

    Google Scholar 

  • Yamaguchi, T. J. Antibiot, 1977, 30, 433 (props)

    Google Scholar 

  • Ganguly, A.K. J. Chem. Soc, Chem. Commun,1983, 1166 (synth)

    Google Scholar 

  • Fr. Pat,M5 969, (1970); CA,78, 72216h (synth, pharmacol)

    Google Scholar 

  • Klinger, K.H. Arzneim.-Forsch,1977, 27, 4, 14, 37, 45 (synth, pharmacol, tox)

    Google Scholar 

  • Niebch, G. Arzneim.-Forsch, 1978, 28, 765 (metab)

    Google Scholar 

  • Marmo, E., Clin. Ter. (Rome), 1981, 98, 481 (rev, pharmacol)

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 4921.

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2101.

    Google Scholar 

  • Kametani, T. J. Med. Chem, 1972, 15, 686 (synth, activity)

    Google Scholar 

  • Ger. Pat,2 221 123, (1973); CA,79, 5487e (synth)

    Google Scholar 

  • Kametani, T. J. Chem. Soc, Perkin Trans. 1, 1975, 10, 932 (synth, ms)

    Google Scholar 

  • Kato, H. Jpn. J. Pharmacol, 1977, 27, 87 (activity)

    Google Scholar 

  • Fujimoto, Y., CA, 1980, 93, 125349x (pharmacol)

    Google Scholar 

  • Matsuda, H., CA, 1981, 95, 215016g (pharmacol)

    Google Scholar 

  • Alkaloid from R. vomitoria, R. caffra, R. cumminsii, R. macrophylla, R. oreogiton, R. volkensii, R. mombasiana and many other R spp. (Apocynaceae).

    Google Scholar 

  • Furlenmeyer, A. Experientia, 1953, 9, 331 (uv, ir, ester)

    Google Scholar 

  • Klohs, M.W. J. Am. Chem. Soc, 1955, 77, 2241 (Rescinnamine)

    Google Scholar 

  • Kroneberg, G., Arzneirn.-Forsch, 1956, 6, 579 (Rescinnamine, pharmacol)

    Google Scholar 

  • Woodward, R.B. Tetrahedron,1958, 2, 1 (synth)

    Google Scholar 

  • Zoha, M.S. J. Pharm. Pharmacol,1958, 10, Suppl. 231T (Rescinnamine, pharmacol)

    Google Scholar 

  • Popelak, A. Naturwissenschaften, 1961, 48, 73. Rosen, W.E. J. Am. Chem. Soc, 1961, 83, 4816 (pmr, ester)

    Google Scholar 

  • Popelak, A., Arch. Pharm. (Weinheim, Ger.), 1963, 296, 261 (Rescidine)

    Google Scholar 

  • Chatterjee, A. Chem. Ind. (London),1969, 1388 (Veneserpine)

    Google Scholar 

  • Pantarotto, C. Adv. Mass Spectrom, 1977, 2, 351 (Rescinnamine, ms)

    Google Scholar 

  • Suzuki, Y., CA, 1982, 96, 115441 (pharmacol)

    Google Scholar 

  • Malik,A. J. Nat. Prod,1983, 46, 940 (isol)

    Google Scholar 

  • Lounasmaa, M. Heterocycles, 1985, 23, 371 (pmr)

    Google Scholar 

  • Siddiqui, S. J. Nat. Prod, 1987, 50, 238 (Rescinnamidine)

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 8064, 8065.

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 900, 905.

    Google Scholar 

  • Furlenmeyer, A. Experientia, 1953, 9, 331 (uv, ir)

    Google Scholar 

  • Klohs, M.W. J. Am. Chem. Soc, 1957, 79, 3763 (Pseudoreserpine)

    Google Scholar 

  • Ulshafer, P.R. C.R. Hebd. Seances Acad. Sci, 1957, 244, 2989 (oxide)

    Google Scholar 

  • Velluz, L. Bull. Soc. Chim. Fr, 1958, 145, 673 (synth)

    Google Scholar 

  • Woodward, R.B. Tetrahedron, 1958, 2, I (synth)

    Google Scholar 

  • B.P,894 866, (1961); CA,57, 9910e (Bietaserpine)

    Google Scholar 

  • Rosen, W.E. J. Am. Chem. Soc, 1961, 83, 4816 (pmr)

    Google Scholar 

  • Ban, Y. Tetrahedron, 1964, 20, 2877 (config)

    Google Scholar 

  • Berthaux, P. Arzneim.-Forsch,1964, 14,1040 (Bietaserpine)

    Google Scholar 

  • Schlittler, E., Alkaloids (N.Y.), 1965, 8, 287 (rev)

    Google Scholar 

  • Levin, R.H. J. Org . Chem, 1973, 38, 1983 (cmr)

    Google Scholar 

  • Becker, O. Org. Mass Spectrom, 1977, 12, 461 (ms)

    Google Scholar 

  • Mehri, M.H. Phytochemistry, 1978, 17, 1451 (oxide)

    Google Scholar 

  • Fanso-Free, S.N.Y. J. Am. Chem. Soc, 1979, 101, 1549 (N-15 nmr)

    Google Scholar 

  • Pearlman, B.A., J. Am. Chem. Soc, 1979, 101, 6404 (synth)

    Google Scholar 

  • Malik,A. Z. Naturforsch. B,1980, 35, 920 (Neonorreserpine)

    Google Scholar 

  • Wender, P.A. J. Am. Chem. Soc, 1980, 102, 6157 (.synth)

    Google Scholar 

  • Feng, X. Yaoxue Xuebao,1981, 16, 510; CA,97, 3593j (Diepipseudoreserpine)

    Google Scholar 

  • Juul, P., Handb. Exp. Pharmacol,1981, 54 (rev, pharmacol)

    Google Scholar 

  • Muhtadi, F.J., Anal. Profiles Drug Subst, 1984, 13, 737 (rev, ir, pmr, cmr, ms, anal)

    Google Scholar 

  • Lounasmaa, M. Heterocycles, 1985, 23, 371 (pmr)

    Google Scholar 

  • Szdntay, C. Alkaloids (IV.Y.), 1986, 27, 253 (pharmacol, bibi)

    Google Scholar 

  • Martin, S.F. J. Am. Chem. Soc, 1987, 109, 6124 (synth)

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms,6th

    Google Scholar 

  • Ed., Akademie-Verlag, Berlin, 1987, 7993 (synonyms)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 901, 12443.

    Google Scholar 

  • Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2362.

    Google Scholar 

  • Brockmann, H. Chem. Ber, 1969, 102, 1224 (struct, ir, uv, nmr)

    Google Scholar 

  • Eckhardt, K. Tetrahedron, 1970, 26, 5875 (struct, ir, uv, nmr)

    Google Scholar 

  • Kingston, J.F Can. J. Chem. 1977, 55, 785 (synth) Keay, B.A J. Am. Chem. Soc.1982, 104, 4725 (synth)

    Google Scholar 

  • Höfle, G. Justus Liebigs Ann. Chem,1983, 835 (isol, bio-synth cmr)

    Google Scholar 

  • Arora, S.K J. Antibiot.1985, 38, 113 (struct)

    Google Scholar 

  • Kelly, T.R J. Am. Chem. Soc. 1985, 107, 3879 (synth)

    Google Scholar 

  • Fr. Pat,1 503 260, (1967); CA,69, 106542t (synth) Elliot, M. Pestic. Sci,1971, 2, 243 (use)

    Google Scholar 

  • Ueda, K. J. Agric. Food Chem, 1974, 22, 212; 1975, 23, 106 (metab)

    Google Scholar 

  • Wickham, J.C Pestic. Sci. 1976, 7, 273 (use)

    Google Scholar 

  • Nakazawa, H. Agric. Biol. Chem,1980, 44, 1173 (cmr)

    Google Scholar 

  • Bisagni, E. J. Chem. Soc, Perkin Trans 1, 1979, 1706 (synth)

    Google Scholar 

  • Rivalle, C. J. Med. Chem,1980, 23, 1212; 1983, 26, 181 (synth, pharmacol)

    Google Scholar 

  • Dowling, J Vitam. Horm. (N.Y.)1960, 18, 515 (rev)

    Google Scholar 

  • Borua, A.B Tetrahedron Lett.1972, 1823 (synth)

    Google Scholar 

  • Stam, C.H Acta Crystallogr. Sect. B1972, 28, 2936 (cryst struct)

    Google Scholar 

  • Cainelli, G Gazz. Chim. Ital.1973, 103, 117 (i.som)

    Google Scholar 

  • Julia, M Bull. Chim. Soc. Fr.1973, 746 (synth)

    Google Scholar 

  • Englert, G He!v. Chim. Acta 197558, 2367 (cmr)

    Google Scholar 

  • Bard, D.R Br. J. Cancer 1977, 35, I IO (pharmacol tux)

    Google Scholar 

  • McCormick, A.M et a! Anal. Biochem.1978, 86, 25 (hplc)

    Google Scholar 

  • Bernard, M J. Org. Chem.1983, 48, 3164 (synth)

    Google Scholar 

  • De Paolis, A.N., J. Chromatogr, 1983, 258, 314 (tic)

    Google Scholar 

  • Perry, M.D. Clin. Pharm, 1983, 2, 12 (rev)

    Google Scholar 

  • Bestmann, H.J Justus Liebigs Ann. Chem.1984, 1740 (synth)

    Google Scholar 

  • Chytil, F., Pharmacol. Rev, 1984, 36, 93 (rev, pharmacol, props)

    Google Scholar 

  • Ward, A. Drugs, 1984, 28, 6 (rev, Isotretinoin)

    Google Scholar 

  • Madani, K.A., Nutr. Res, 1986, 6, 107 (rev)

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms,6th Ed., Akademie-Verlag, Berlin, 1987, 5902. Martindale, The Extra Pharmacopoeia,28th/29th Eds.

    Google Scholar 

  • /1989, Pharmaceutical Press, London, 1616, 1656. Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2364.

    Google Scholar 

  • Ger. Pat,3 132 915, (1983); CA,98, 198214 (synth)

    Google Scholar 

  • Gielsdorf, W. et a, J. Chromatogr, 1987, 419, 351 (chromatog)

    Google Scholar 

  • Potts, W.J., Life Sci, 1971, 10, 655 (pharmacol)

    Google Scholar 

  • Reinis, S., Bull. Psychon. Soc, 1973, 2, 385 (pharmacol)

    Google Scholar 

  • Ohnuki, T. Tetrahedron Lett, 1981, 22, 1267 (struct)

    Google Scholar 

  • Okami, Y. J. Antibiot, 1981, 34, 344 (iso!)

    Google Scholar 

  • Takashio, M. Agric. Biol. Chem, 1982, 46, 1457, 1987, 2449 (props)

    Google Scholar 

  • Kotaki, A. J. Vitaminol. (Kyoto), 1968, 14, 247 (synth, tetranicotinate)

    Google Scholar 

  • Beach, R. Tetrahedron Lett,1969, 3489 (synth)

    Google Scholar 

  • Kotaki, A. Bitamin, 1969, 39, 382 (metab, tetranicotinate)

    Google Scholar 

  • Paterson, T. et a, J. Chem. Soc, Chem. Commun,1969, 290 (biosynth)

    Google Scholar 

  • Tanaka, N. Bull. Chem. Soc. Jpn, 1969, 42, 1546 (cryst struct)

    Google Scholar 

  • Yagi, K. J. Vitaminol. (Kyoto), 1969, 15, 155 (metab, tetrabutyrate)

    Google Scholar 

  • Japan. Pat,70 07 749, (1970); CA,73, 15177u (synth, tetrabutyrate)

    Google Scholar 

  • McCormick, D.A., J. Heterocycl. Chem, 1974, 11, 969. Yoneda, F., J. Am. Chem. Soc, 1976, 98, 830 (synth)

    Google Scholar 

  • Holmgren, A., Experientia, 1980, 36, 149 (rev, FAD)

    Google Scholar 

  • Walt,D.R. J. Am. Chem. Soc,1980, 102, 7805 (synth, 5’-phosphate)

    Google Scholar 

  • Bacher, A. J. Am. Chem. Soc, 1982, 104, 3754 (biosynth)

    Google Scholar 

  • Brown, G.M. Adv. Enzymol. Relat. Areas Mol. Biol, 1982, 53, 345 (rev, biosynth)

    Google Scholar 

  • Keller, P.J. J. Am. Chem. Soc, 1983, 105, 2505 (biosynth, cmr, tetraacetate)

    Google Scholar 

  • Keller, P.J. Tetrahedron, 1983, 39, 3471 (biosynth)

    Google Scholar 

  • Shimizu, S. Appl. Biochem. Biotechnol, 1983, 8, 237 (synth, FAD)

    Google Scholar 

  • Ulrich, E.L. Tetrahedron Lett, 1983, 24, 473 (pmr)

    Google Scholar 

  • Yoneda, F., Kirk-Othmer Encycl. Chem. Technol, 3rd Ed,1983, 24, 108 (rev, synth)

    Google Scholar 

  • Cooperman, J.M. Food Sci. Technol, 1984, 13, 299 (rev, metab, props)

    Google Scholar 

  • Moonen, C.T. Biochemistry, 1984, 23, 4859 (pmr, conformn, tetraacetate, 5’-phosphate)

    Google Scholar 

  • Vervoort, J, Eur. J. Biochem,1985, 151, 49 (cmr, 3-Me, tetraacetate)

    Google Scholar 

  • Nielsen, P. Methods Enzymol, 1986, 122, 209 (synth, phosphates)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 7841, 7842, 7843, 7844, 7845.

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 4425, 4473, 7551, 7999.

    Google Scholar 

  • Srivastava, P. J. Med. Chem, 1983, 26, 445 (synth)

    Google Scholar 

  • Boritzki, T.J. Biochem. Pharmacol, 1985, 34, 1109 (pharmacol)

    Google Scholar 

  • Goldstein, B.M. J. Am. Chem. Soc, 1985, 107, 1394 (cryst struct)

    Google Scholar 

  • Hennen, W.J,J. Org . Chem,1985, 50, 1741 (synth, cmr)

    Google Scholar 

  • Cook, P.D. J. Heterocycl. Chem, 1986, 23, 155 (synth)

    Google Scholar 

  • Akita, E. J. Antibiot,1970, 23, 155, 173 (isol, struct)

    Google Scholar 

  • Ito, T. Antimicrob. Agents Chemother, 1970, 33; Agric. Biol. Chem, 1970, 34, 980 (synth, ir, pmr)

    Google Scholar 

  • Ikeda, D. Bull. Chem. Soc. Jpn, 1973, 46, 3210 (synth, derivs)

    Google Scholar 

  • Kojima, M. J. Antibiot, 1973, 26, 784 (biosynth, derivs)

    Google Scholar 

  • Fukami, H. Agric. Biol. Chem, 1977, 41, 1689 (synth)

    Google Scholar 

  • Suami, T. Carbohydr. Res, 1977, 56, 415 (synth)

    Google Scholar 

  • Kumar, V. J. Org . Chem, 1981, 46, 4298 (synth)

    Google Scholar 

  • Miyadoh, S. CA, 1982, 96, 50625 (iso!)

    Google Scholar 

  • Inouye, S. CA, 1982, 98, 83105 (rev, pharmacol)

    Google Scholar 

  • Yoshikawa, M. Chem. Len,1984, 2097 (synth)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 144.

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 4622.

    Google Scholar 

  • B.P,1 603 127, (1981); CA,96, 162439 (synth, props)

    Google Scholar 

  • Vigevani, A. J. Antibiot, 1985, 38, 1799 (metab)

    Google Scholar 

  • Heifets, L.B. Int. Congr. Ser.-Excerpta Med, 1986, 697, 180 (pharmacol)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 16512.

    Google Scholar 

  • Gadret, M. Acta Crystallogr, Sect. B, 1975, 31, 1454 (cryst struct)

    Google Scholar 

  • Gallo, E.G. Anal. Profiles Drug Subst, 1976, 5, 467 (rev, synth, anal)

    Google Scholar 

  • Girling, D.T. J. Antimicrob. Chemother, 1977, 3, 115 (tox, rev)

    Google Scholar 

  • Sensi, P., Chron. Drug Discovery, 1982, 1, 201 (rev)

    Google Scholar 

  • Sensi, P., Rev. Infect. Dis,1983, 5 (Suppl. 3),402 (rev)

    Google Scholar 

  • 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 

  • Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2369.

    Google Scholar 

  • Gallo, G.G. Farmaco, Ed. Prat, 1963, 18, 78 (isol)

    Google Scholar 

  • Oppolzer, W. Experientia, 1964, 20, 336 (struct)

    Google Scholar 

  • Brufani, M. Experientia, 1964, 20, 339 (cryst struct)

    Google Scholar 

  • Gurgo, C. Handb. Exp. Pharmacol, 1982, 61, 519 (rev)

    Google Scholar 

  • Seong, B.L. Chem. Lett,1982, 627 (biosynth)

    Google Scholar 

  • Arora, S.K. Mol. Pharmacol, 1983, 23, 133 (cryst struct)

    Google Scholar 

  • Sensi, P., Rev. Infect. Dis,1983, 5 (Suppl. 3),402 (bibi)

    Google Scholar 

  • Ghisalba, O. Drugs. Pharm. Sci, 1984, 22, 281 (rev)

    Google Scholar 

  • Lancini, G., Biotechnology, 1986, 4, 431 (rev)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia,28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 146.

    Google Scholar 

  • Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2369, 2370.

    Google Scholar 

  • Belg. Pat,632 770, (1964); CA,61, 4166 (iso!)

    Google Scholar 

  • Sensi, P. J. Med. Chem,1964, 7, 596 (Rifamide) Launchburg, A.P., Prog. Med. Chem,1970, 7, 1 (rev, Rifamide)

    Google Scholar 

  • Fr. Pat,2 043 847, (1971); CA,76, 44674 (isol)

    Google Scholar 

  • Oppolzer, W. HeIv. Chim. Acta, 1973, 56, 2287 (config)

    Google Scholar 

  • 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 

  • Ghisalba, O. J. Antibiot, 1980, 33, 847 (deriy) Brufani, M. Mol. Pharmacol, 1982, 21, 394 (struct)

    Google Scholar 

  • Ghisalba, O. J. Antibiot, 1982, 35, 74, 1361 (biosynth) Martindale, The Extra Pharmacopoeia, 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 145.

    Google Scholar 

  • Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2369.

    Google Scholar 

  • Brufani, M. J. Antibiot, 1984, 37, 1611 (synth, pmr, pharmacol)

    Google Scholar 

  • Marchi, E. J. Med. Chem, 1985, 28, 960 (synth, pharmacol)

    Google Scholar 

  • Venturini, A.P. Chemioterapia 1986, 5, 257, 263 (pharmacol, tox)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 503.

    Google Scholar 

  • Ger. Pat 3 009 034, (1981); CA 95, 203640 (synth)

    Google Scholar 

  • Hirai, K. J. Heterocycl. Chem, 1982, 19, 1363 (synth, props)

    Google Scholar 

  • Koike, M. Drug Metab. Dispos, 1987, 15, 426 (metab, props)

    Google Scholar 

  • Koike, M. Xenobiotica, 1988, 18, 257 (metab, props)

    Google Scholar 

  • Ger. Pat 2 362 754, (1974); CA 81, 105533 (synth, pharmacol)

    Google Scholar 

  • Laubie, M. J. Pharmacol, 1985, 16, 259 (pharmacol)

    Google Scholar 

  • Van Zwieten, P.A., Am. J. Cardiol 1988, 61, 6D (rev, pharma-col)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 3157.

    Google Scholar 

  • U.S.P 4 378 362, (1983); CA 99, 22316d (synth, pharmacol)

    Google Scholar 

  • Rosseels, G. Eur. J. Med. Chem.-Chim. Ther, 1983, 18, 339 (synth, pharmacol)

    Google Scholar 

  • Knoll, J. Arzneim.-Forsch 1971, 21, 719 (pharmacol)

    Google Scholar 

  • Meszaros, Z. Arzneim.-Forsch, 1972, 22, 815 (synth, pmr, ms)

    Google Scholar 

  • Simon, K. Acta Crystallogr., Sect. B, 1975, 31, 1695 (cryst struct)

    Google Scholar 

  • Szasz, Gy. J. Chromatogr, 1976, 117, 345 (tic)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 13214.

    Google Scholar 

  • Ferris, R.M. J. Pharm. Pharmacol, 1982, 34, 388 (pharmacol)

    Google Scholar 

  • U.S.P 4 400 383, (1983); CA 99, 158469 (synth)

    Google Scholar 

  • Harfenist, M. J. Org . Chem, 1985, 50, 1356 (isom, pmr, cmr)

    Google Scholar 

  • Ferris, R.M. Drug Dey. Res, 1986, 9, 171 (pharmacy!)

    Google Scholar 

  • Morales-Rios, M.S. Magn. Reson. Chem, 1987, 25, 377 (cmr)

    Google Scholar 

  • Fox, P.K. Arzneim.-Forsch, 1980, 30, 55 (pharmacol)

    Google Scholar 

  • Lewis, A.J. Agents Actions, 1980, 10, 258 (pharmacol)

    Google Scholar 

  • Cairns, J. J. Chem. Soc., Perkin Trans. 1 1981, 2306 (synth)

    Google Scholar 

  • Barnes, J.C. Acta Crystallogr., Sect. C, 1985, 41, 763 (cryst struct)

    Google Scholar 

  • Sankey, G.H. J. Heterocycl. Chem, 1972, 9, 1049 (synth)

    Google Scholar 

  • Pinder, R.M. Drugs, 1977, 14, 81 (rev)

    Google Scholar 

  • Aasen, A.J. Acta Chem. Scand., Ser. B, 1988, 42, 216 (abs config)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2102.

    Google Scholar 

  • Capek, A. Folia Microbiol 1972, 17 396; 1976, 21, 155 (pharmacol)

    Google Scholar 

  • Budesinsky, Z. Collect. Czech. Chem. Commun, 1975, 40, 1078 (synth)

    Google Scholar 

  • Pavlikova, L. Cesk. Farm, 1975, 24, 249 (metab)

    Google Scholar 

  • Imamura, H. CA 1986, 105, 222611 (pharmacol) Yamamoto, H. Oyo Yakuri 1987, 34, 453, 461 (pharmacol)

    Google Scholar 

  • Kastrons, V.V. Arzneim.-Forsch 1985, 35, 668, 672, 680, 808, 813, 907, 915 (synth, ir, pmr, ms, pharmacol, tox)

    Google Scholar 

  • Eur. Pat 66 475, (1982); CA 98, 160515y (synth, pharmacol)

    Google Scholar 

  • Shriver, D.A. et a!, Arzneim.-Forsch, 1985, 35, 839 (pharmacol)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 18675.

    Google Scholar 

  • deWald, H.A. J. Med. Chem, 1973, 16, 1346 (synth, pharmacol)

    Google Scholar 

  • Poschel, B.P.H. Psychopharmacologia, 1974, 35, 257 (pharmacol)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 7103.

    Google Scholar 

  • Eur. Pat 196 132, (1986); CA 106, 67292x (synth, pharmacol)

    Google Scholar 

  • Janssen, P.A.J. J. Pharmacol. Exp. Ther, 1988, 244, 685 (pharmacol)

    Google Scholar 

  • U.S.P 4 246 263, (1981); CA 95, I 32938h (synth, pharmacol)

    Google Scholar 

  • Panizzon, L., Hely. Chim. Acta, 1944, 27, 1748 (synth, ester)

    Google Scholar 

  • Reisch, J. J. Pharm. Pharmacol, 1968, 20, 81 (ms, ester)

    Google Scholar 

  • Shafi’ee, A. J. Med. Chem, 1969, 12, 266 (abs config)

    Google Scholar 

  • Marozzi, E. Farmaco, Ed. Prat, 1976, 31, 180 (glc, ester)

    Google Scholar 

  • Padmanabhan, G.R., Anal. Profiles Drug Subst, 1981, 10, 473 (rev, pharmacol, esters)

    Google Scholar 

  • Redalieu, E. Drug Metab. Dispos, 1982, 10, 708 (metab)

    Google Scholar 

  • Lim H.K. J. Chromatogr 1985, 328, 378 (resoln)

    Google Scholar 

  • Nakajima, K. Chem. Pharm. Bull, 1986, 34, 1701 (glc, ms, anal)

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 3234.

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 1433.

    Google Scholar 

  • Eur. Pat., 110 435 (1984); CA, 102, 6522t (synth, pharmacol)

    Google Scholar 

  • Goodwin, G.M Br. J. Pharmacol., 1985, 84, 743 (pharmacol)

    Google Scholar 

  • Kennis, L.E.J. Drug Del). Res 1986, 8, 133, 187 (rev, pharmacol)

    Google Scholar 

  • Sandrini, G. Eur. J. Pharmacol, 1986, 130, 311 (pharmacol)

    Google Scholar 

  • Vinick, F.J Annu. Rep. Med. Chem., 1986, 21 1 (rev)

    Google Scholar 

  • Larsson, M Methods Find. Exp. Clin. Pharmacol., 1987, 9, 349 (hplc, anal)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 18677.

    Google Scholar 

  • Belg. Pat., 660 244 (1965); CA, 63, 17965h (synth, uv)

    Google Scholar 

  • Van Dijk, J. Recl. Tray. Chim. Pays-Bas 1973, 92, 1281 (synth)

    Google Scholar 

  • Finkelstein, B.W., Drug Intel!. Clin. Pharm, 1981, 15, 425 (rev, pharmacol)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2103.

    Google Scholar 

  • Fr. Pat., M2114 (1963); CA, 60, 14598f (synth, pharmacol)

    Google Scholar 

  • Austrian Pat., 236 930 (1964); CA, 62, 2710a (synth)

    Google Scholar 

  • Sandberg J. Cancer Chemother. Rep., Part 1, 1969, 53, 367; 1971, 55, 233 (pharmacol)

    Google Scholar 

  • Hegedus, L. Eur. J. Cancer Clin. Oncol, 1984, 20, 933 (pharmacol)

    Google Scholar 

  • Kantor, S. Science (Washington), 1970, 168, 373 (pharmacol)

    Google Scholar 

  • U.S.P 3 941 825, (1976); CA 85, 540w (synth, pharmacol)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds.,1982/1989, Pharmaceutical Press, London, 13216.

    Google Scholar 

  • U.S.P., 4 592 866 (1986); CA, 106, 67360 (synth, pharmacol)

    Google Scholar 

  • U.S.P., 4 705 853 (1987); CA, 109, 231085s (synth)

    Google Scholar 

  • Bergman J. J. Pharmacol. Exp. Ther., 1988, 245, 471 (pharmacol)

    Google Scholar 

  • Van Bever, W.F.M. J. Med. Chem, 1973, 16, 394 (synth, pharmacol)

    Google Scholar 

  • Eur. Pat 15 171, (1980); CA 94, 103373u (synth, pharmacol)

    Google Scholar 

  • Langlois, M. J. Heterocycl. Chem, 1983, 20, 393 (synth)

    Google Scholar 

  • Belg. Pat., 670 495 (1966); CA, 65, 13615a (synth, pharmacol)

    Google Scholar 

  • Belg. Pat., 855 392 (1977); CA, 88, I90586h (synth, pharmacol)

    Google Scholar 

  • Beattie, D.E. J. Med. Chem, 1985, 28, 1617 (synth, pharmacol)

    Google Scholar 

  • B.P 961 313, (1964); CA 61, 6954 (synth)

    Google Scholar 

  • B.P., 1 895, (1965); CA 63, 16307 (synth, use)

    Google Scholar 

  • McMonigle, J.J. Arch. Int. Pharmacodyn. Ther 1969, 178, 53 (pharmacol)

    Google Scholar 

  • Lowe, M.C. Eur. J. Pharmacol, 1973, 21, 46 (pharmacol)

    Google Scholar 

  • Schwabe, U. Mol. Pharmacol, 1976, 12, 900 (pharmacol)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 13218.

    Google Scholar 

  • Gottstein, W.J. J. Am. Chem. Soc, 1959, 81, 1198 (synth)

    Google Scholar 

  • Ther, L. Arzneim.-Forsch, 1959, 9, 63 (pharmacol)

    Google Scholar 

  • Dimmling, T. Antibiotics Ann 1959–60, 350, 365 (pharmacol)

    Google Scholar 

  • Butterfield, A.G. Antimicrob. Agents Chemother, 1973,4, 11 (chromatg)

    Google Scholar 

  • Mazzola, E.P. J. Pharm. Sci, 1980, 69, 229 (cmr)

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th Ed., Akademie-Verlag, Berlin, 1987, 7548.

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 149, 150.

    Google Scholar 

  • Sax, N.I., Dangerous Properties of Industrial Materials, 6th Ed., Van Nostrand-Reinhold, 1984, 2344.

    Google Scholar 

  • West, R.A. J. Org . Chem, 1961, 26, 3809 (synth)

    Google Scholar 

  • Norton, S. J. Pharmacol. Exp. Ther, 1966, 154, 152 (pharmacol)

    Google Scholar 

  • Taylor, E.D. J. Am. Pharm. Assoc. Sci. Ed, 1960, 49, 317 (synth, props)

    Google Scholar 

  • Kuliev, A.M. Zh. Org . Khim, 1972, 8, 1301 (synth, ir, nmr)

    Google Scholar 

  • Ger. Pat 2 630 060, (1978); CA 88, 121184 (synth, pharmacol)

    Google Scholar 

  • Ger. Pat 3 437 694, (1986); CA 105, 72691 (pharmacol)

    Google Scholar 

  • Takashima, M. CA, 1976, 84, 16904 (synth, pharmacol) Buzzelli, G. Clin. Ter, 1979, 89, 251 (pharmacol)

    Google Scholar 

  • B.P., 1 203 958, (1970); CA, 74, 31756h (synth, pharmacol)

    Google Scholar 

  • Bogan, J.A. Drugs of Today, 1977, 13, 510 (reu)

    Google Scholar 

  • Winkelmann, E. Arzneim.-Forsch., 1978, 28, 739 (synth,pharmacol)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 13219.

    Google Scholar 

  • Gallagher, G. J. Med. Chem, 1985, 28, 1533 (synth)

    Google Scholar 

  • U.S.P 4 006 232, (1977); CA 87, 5968 (synth)

    Google Scholar 

  • Vidrio, H. Arzneim.-Forsch, 1980, 30, 12 (pharmacol)

    Google Scholar 

  • Lynch, J. Arzneim.-Forsch 1986, 36, 475 (pharmacol)

    Google Scholar 

  • U.S.P 4 695 576, (1987); CA 108, 75228 (synth, pharmacol)

    Google Scholar 

  • Sahlberg, C., J. Labelled Compd. Radiopharm, 1987, 24, 529 (synth)

    Google Scholar 

  • Belg. Pat 623 058, (1963); CA 60, 9291h (synth, pharmacol)

    Google Scholar 

  • Ellefson, C.R. J. Med. Chem, 1976, 19, 1161 (pharmacol)

    Google Scholar 

  • Edmonds, H.L. J. Pharmacol. Exp. Ther, 1979, 208, 236 (pharmacol)

    Google Scholar 

  • Eur. Pat 59 698, (1982); CA 98, 34513 (synth, pharmacol)

    Google Scholar 

  • Kalland, T. J. Immunol, 1985, 134, 3956 (pharmacol)

    Google Scholar 

  • Tarkowski, A. Immunology, 1986, 59, 589 (pharmacol)

    Google Scholar 

  • Reimann, H J. Chem. Soc., Chem. Commun., 1972, 1270 (isol, struct, spectra)

    Google Scholar 

  • Waitz, J.A. J. Antibiot, 1972, 25, 647 (isol)

    Google Scholar 

  • Ganguly, A.K. J. Antibiot, 1976, 29, 976 (biosynth)

    Google Scholar 

  • Hatano, K. J. Antibiot., 1976 29, 1163 (isol, props)

    Google Scholar 

  • Kishi, T. J. Antibiot., 1976 29, 1171 (struct)

    Google Scholar 

  • Kinumaki, A. J. Antibiot, 1977, 30, 450 (struct)

    Google Scholar 

  • Suzuki, M. Heterocycles, 1977, 8, 199 (ms)

    Google Scholar 

  • Ganguly, A.K. Tetrahedron Lett 1980, 4699 (cryst struct)

    Google Scholar 

  • Puar, M.S J. Antibiot., 1981, 34, 602; 1982, 35, 381 (cmr, conformn)

    Google Scholar 

  • Puar, M.S J. Antibiot., 1982, 35, 381 (cmr)

    Google Scholar 

  • Ganguly, A.K J. Chem. Soc., Chem. Commun., 1983, 1 166 (synth, deriu)

    Google Scholar 

  • Lin, C.C Antimicrob. Agents Chemother., 1986, 29, 753 (metab)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia, 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 151

    Google Scholar 

  • Sax, N.I Dangerous Properties of Industrial Materials, 6 thEd., Van Nostrand-Reinhold, 1984, 2371.

    Google Scholar 

  • Valcavi, U. Farmaco, Ed. Sci, 1975, 30, 527 (synth)

    Google Scholar 

  • Ger. Pat 2 535 343, (1976); CA 85, 32512(synth,pharmacol)

    Google Scholar 

  • Valcavi, U. Arzneim.-Forsch, 1982, 32, 657 (pharmacol)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 16980.

    Google Scholar 

  • Ger. Pat 2 943 776, (1981); CA 95, 151023 (synth)

    Google Scholar 

  • Krause, W. J. Pharm. Sci, 1984, 73, 563 (glc, ms)

    Google Scholar 

  • Schmidt, J.B. Endocrinol. Exp 1987, 21, 71 (pharmacol)

    Google Scholar 

  • Hoshina, K. Arzneim.-Forsch, 1985, 35, 493 (pharmacol)

    Google Scholar 

  • Takeshita, T. Chem. Pharm. Bull, 1985, 33, 5059; 1986, 34, 3900 (synth, cryst struct)

    Google Scholar 

  • Eur. Pat 24 510, (1981); CA 95, 80465 (synth)

    Google Scholar 

  • Tarutani, M. Arzneim-Forsch, 1985, 35, 703 (pharmacol, acetate)

    Google Scholar 

  • Bickel, M. Arzneim-Forsch, 1986, 36, 1358 (pharmacol)

    Google Scholar 

  • Honma, S. Drug Metab. Dispos, 1987, 15, 551 (metab, acetate)

    Google Scholar 

  • Iwamura, S. J. Chromatogr, 1987, 413, 370 (hplc)

    Google Scholar 

  • In, Y. Chem. Pharm. Bull 1988, 36, 2295 (cryst struct)

    Google Scholar 

  • Scholtholt, J. Drugs 1988, 35, 30, 41 (revs)

    Google Scholar 

  • Martindale, The Extra Pharmacopoeia 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 2430.

    Google Scholar 

  • Fellipone, F. Steroids, 1984, 43, 271 (synth, pharmacol)

    Google Scholar 

  • Berti, F. Arzneim.-Forsch 1986, 36, 1369, 1372 (pharmacol)

    Google Scholar 

  • Ger. Pat 3 419 935, (1985); CA 104, 74999v (use)

    Google Scholar 

  • Seyfried, C.A. Dopaminergic Syst. Their Regul., [Proc. Symp.] 1986, 375 (pharmacol)

    Google Scholar 

  • Fr. Pat 2 473 525, (1981); CA 96, 123219 (synth)

    Google Scholar 

  • Jones, R.N. Antimicrob. Agents Chemother, 1983, 24, 209 (props)

    Google Scholar 

  • Barlam, T. Antimicrob. Agents Chemother, 1984, 25, 529 (props)

    Google Scholar 

  • Chantot, J.-F. J. Antibiot, 1986, 39, 661 (props)

    Google Scholar 

  • Phillips, I. J. Antimicrob. Chemother 1987, 20, Suppl. B (book)

    Google Scholar 

  • Ger. Pat 2 423 491, (1975); CA 84, 59794 (synth)

    Google Scholar 

  • B.P 1 447 162, (1976); CA 86, 90091 (synth, pharmacol)

    Google Scholar 

  • Fr. Pat M1741, (1963); CA 59, 10002e (synth)

    Google Scholar 

  • Mishkinsky, J. Arch. Int. Pharmacodyn. Ther 1969, 179, 94 (pharmacol)

    Google Scholar 

  • White, F.B. Kirk-Othmer Encycl. Chem. Tech, 3rd Ed., Wiley-Interscience, 1978–1984, 20, 497.

    Google Scholar 

  • Ando, A. Int. J. Nucl. Med. Biol, 1984, 11, 195 (use)

    Google Scholar 

  • Sax, N.I. Dangerous Properties of Industrial Materials, 7th Ed., Van Nostrand-Reinhold, 1989, 2985.

    Google Scholar 

  • Cecchetti, V. J. Med. Chem, 1987, 30, 465 (synth, pharmacol)

    Google Scholar 

  • Asahina, Y. J. Chem. Soc 1927, 1708 (synth)

    Google Scholar 

  • Pachter, I.J. J. Am. Chem. Soc, 1960, 82, 5187 (isol)

    Google Scholar 

  • Yamazaki, M. Tetrahedron Lett 1966, 3221; 1967, 3317 (biosynth)

    Google Scholar 

  • de Barros Corrêa, D. Phytochemistry, 1975, 14, 2059 (isol)

    Google Scholar 

  • Kametani, T. Heterocycles 1976, 4, 23; 1487; J. Am

    Google Scholar 

  • Chem. Soc 1976, 98, 6186 (synth, uv, ir, pmr, ms)

    Google Scholar 

  • Tamâs, J. Acta Chim. Acad. Sci. Hung., 1976, 89, 85 (ms)

    Google Scholar 

  • Toth, G. Justus Liebigs Ann. Chem., 1977, 529 (cmr)

    Google Scholar 

  • Danieli, B. Heterocycles, 1978, 9, 803 (synth)

    Google Scholar 

  • Kametani, T. J. Am. Chem. Soc 1977, 99, 2306; Chem

    Google Scholar 

  • Pharm. Bull 1978, 26, 1922 (synth)

    Google Scholar 

  • Kökösi, J. Tetrahedron Lett 1981, 4861 (synth)

    Google Scholar 

  • Bergman, J J. Org . Chem 1985, 50, 1246 (synth)

    Google Scholar 

  • Kaneko, C. Heterocycles, 1985, 23, 1385 (synth)

    Google Scholar 

  • U.S.P 2 646 428, (1953); CA 48, 8269 (Ethoxazorutoside)

    Google Scholar 

  • Griffith, J.Q., Rutin and Related Flavonoids, 1955, Mack, Easton.

    Google Scholar 

  • Fr. Pat 1 434 376, (1966); CA 66, 29043 (Ethoxazorutoside)

    Google Scholar 

  • Hörhammer, L. Tetrahedron Lett 1966, 567 (synth)

    Google Scholar 

  • Swiss Pat 458 389, (1968); CA 70, 68714m (Monoxerutin)

    Google Scholar 

  • Schmid, R.D., Tetrahedron, 1972, 28, 3259 (ms)

    Google Scholar 

  • Wenkert, E. Phytochemistry, 1977, 16, 1811 (cmr)

    Google Scholar 

  • Khalifa, T.I. Anal. Profiles Drug Subst, 1983, 12, 623 (rev)

    Google Scholar 

  • Voelter, W. n-((3-Hydroxyethyl)rutoside: New

    Google Scholar 

  • Results, Springer-Verlag, Berlin, 1983 (book) Martindale, The Extra Pharmacopoeia, 28th/29th Eds., 1982/1989, Pharmaceutical Press, London, 15304.

    Google Scholar 

  • Negwer, M., Organic-Chemical Drugs and their Synonyms 6th Ed., Akademie-Verlag, Berlin, 1987, 7530 (synonyms)

    Google Scholar 

  • Chelardoni, M. Chim. Farm, 1970, 109, 245 (synth, pharmacol)

    Google Scholar 

  • Pisanti, N. Farmaco, Ed. Sci, 1972, 27, 919 (pharmacol)

    Google Scholar 

  • Wiesner, K Tetrahedron Lett., 1966, 221 (struct)

    Google Scholar 

  • Wiesner, K Adv. Org. Chem., 1972, 8, 295 (pmr, rev, struct)

    Google Scholar 

  • Bélanger, A Can. J. Chem., 1979, 57, 3348 (synth)

    Google Scholar 

  • Jones, L.R J. Biol. Chem, 1981, 256, 11809 (pharmacol)

    Google Scholar 

  • Waterhouse, A.L J. Chem. Soc., Chem. Commun., 1984, 1265 (Dehydroryanodine)

    Google Scholar 

  • Ruest, L. Can. J. Chem, 1985, 63, 2840 (derivs)

    Google Scholar 

  • Waterhouse, A.L. J. Chem. Soc., Perkin Trans.2 1985, 1011 (cmr, pmr)

    Google Scholar 

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J. Elks C. R. Ganellin

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© 1990 Springer Science+Business Media Dordrecht

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Elks, J., Ganellin, C.R. (1990). R. In: Elks, J., Ganellin, C.R. (eds) Dictionary of Drugs. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-2085-3_18

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  • DOI: https://doi.org/10.1007/978-1-4757-2085-3_18

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