The Plant Cell Culture Library

Eucalyptus saligna
Cell Line ID ES-08848
Media Type M72
Lowest Tolerable USDA Zone 8a
Drought Tolerance Averag
Availability Medium
Order Myrtales
Family Myrtaceae
Genus Eucalyptus
Antiviral Genus Level ➡ 18 citations
Antibacterial Genus Level ➡ 283 citations
Antifungal Genus Level ➡ 54 citations
Insecticidal Species Level
Anticancer Genus Level ➡ 1 citations
Culture Initiation Site Taastrup
Plant Habit Tree Evergreen
Plant Habitat Warm Temp/SubTrop
Culture Start Material Seed
Native Range Australia
Plant Supplier Comm/J.L. Hudson
Antiviral Citations
  1. Schmidt, O.T. et al., Justus Liebigs Ann. Chem., 1951, 571, 232- 237 (isol)
  2. Reddy, K.K. et al., Aust. J. Chem., 1964, 17, 238- 245 (isol, bibl)
  3. Matsuda, H. et al., Chem. Pharm. Bull., 1966, 14, 877- 883 (isol, uv) [https://doi.org/10.1248/cpb.14.877]
  4. Jochims, J.C. et al., Justus Liebigs Ann. Chem., 1968, 717, 169- 183 (pmr)
  5. Seikel, M. et al., Phytochemistry, 1970, 9, 1115- 1128 (pmr, struct) [https://doi.org/10.1016/S0031-9422(00)85235-8]
  6. Haddock, E.A. et al., J. Chem. Soc., Perkin Trans. 1, 1982, 2535- 2545 (pmr, cmr)
  7. Okuda, T. et al., Tetrahedron Lett., 1982, 23, 3937- 3940 (uv, cd) [https://doi.org/10.1016/S0040-4039(00)87748-5]
  8. Nawwar, M.A.M. et al., Phytochemistry, 1994, 36, 793- 798 (isol, pmr, cmr) [https://doi.org/10.1016/S0031-9422(00)89820-9]
  9. Berry, D.E. et al., J. Org. Chem., 1995, 57, 420- 422 (isol, activity) [https://doi.org/10.1021/jo00028a002]
  10. Lim, Y.A. et al., Phytother. Res., 1997, 11, 22- 27 (activity)
  11. Liu, K.C.S.C. et al., Planta Med., 1999, 65, 43- 46 (isol, activity) [https://doi.org/10.1055/s-1999-13960]
  12. Latté, K.P. et al., Phytochemistry, 2000, 54, 701- 708 (Isocorilagin) [https://doi.org/10.1016/S0031-9422(00)00176-X]
  13. Adesina, S.K. et al., Phytother. Res., 2000, 14, 371- 374 (isol, activity)
  14. Latté, K.P. et al., Z. Naturforsch., C, 2000, 55, 467- 472 (activity) [https://doi.org/10.1515/znc-2000-5-625]
  15. Rangkadilok, N. et al., J. Agric. Food Chem., 2005, 53, 1387- 1392 (Euphoria longana constit) [https://doi.org/10.1021/jf0403484]
  16. Liu, X. et al., Food Chem., 2008, 109, 909- 915 (Isocorilagin, activity)
  17. Yamada, H. et al., J. Am. Chem. Soc., 2008, 130, 7566- 7567 (synth) [https://doi.org/10.1021/ja803111z]
  18. Sprenger, R.F. et al., Org. Biomol. Chem., 2016, 14, 3369- 3375 (Isocorilagin, conformn,struct)
[top⬆]
Antibacterial Citations
  1. Japan. Pat., 1991, 03 101 687 (EU 89NF)
  2. Barton, D.H.R. et al., Q. Rev., Chem. Soc., 1957, 11, 189 (rev) [https://doi.org/10.1039/qr9571100189]
  3. Corey, E.J. et al., JACS, 1964, 86, 485 (synth, bibl) [https://doi.org/10.1021/ja01057a040]
  4. Hill, H.C. et al., JCS(C), 1968, 93 (ms)
  5. Gollnick, K. et al., Tet. Lett., 1968, 689 (synth) [https://doi.org/10.1016/S0040-4039(00)75613-9]
  6. Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhäuser Verlag, 1972, no. 1929 (occur)
  7. Croteau, R. et al., Phytochemistry, 1972, 11, 1055 (biosynth) [https://doi.org/10.1016/S0031-9422(00)88453-8]
  8. Warnhoff, E.W. et al., Can. J. Chem., 1973, 51, 3955 (purifn) [https://doi.org/10.1139/v73-589]
  9. Opdyke, D.L.J., Food Cosmet. Toxicol., 1973, 11, 1059 (rev, tox) [https://doi.org/10.1016/0015-6264(73)90250-2]
  10. Morris, W.W., J. Assoc. Off. Anal. Chem., 1973, 56, 1037 (ir)
  11. Robertson, J., Int. Rev. Sci.: Phys. Chem., Ser. Two, 1975, 11, 57 (rev)
  12. Kumar, A. et al., Synthesis, 1976, 461 (synth) [https://doi.org/10.1055/s-1976-24082]
  13. Peyron, L., Riv. Ital. Essenze, Profumi, Piante Off., Aromi, Saponi, Cosmet., Aerosol, 1977,59, 603 (rev)
  14. Mauer, B. et al., Helv. Chim. Acta, 1983, 66, 2223 (epoxide)
  15. McMurry, J.E., Tet. Lett., 1983, 24, 1885 (synth) [https://doi.org/10.1016/S0040-4039(00)81797-9]
  16. Ohtsuka, Y. et al., JOC, 1984, 49, 2326 (synth) [https://doi.org/10.1021/jo00187a006]
  17. Berry, K.M. et al., Phytochemistry, 1985, 24, 2893 (2-Epicaryophyllene) [https://doi.org/10.1016/0031-9422(85)80022-4]
  18. Hinkley, S.F.R. et al., Phytochemistry, 1994, 35, 1489 (2-Epicaryophyllene, abs config) [https://doi.org/10.1016/S0031-9422(00)86882-X]
  19. Suginome, H. et al., JCS Perkin 1, 1995, 69 (synth)
  20. Fricke, C. et al., Phytochemistry, 1995, 39, 1119 ((+)-β-Caryophyllene) [https://doi.org/10.1016/0031-9422(95)00184-9]
  21. Encyclopedia of Food and Color Additives, (ed. Burdock, G.A.), CRC Press, 1997, 527- 528 (β-Caryophyllene, occur)
  22. Collado, I.G. et al., Nat. Prod. Rep., 1998, 15, 187- 204 (rev)
  23. Hampel, D. et al., Phytochemistry, 2005, 66, 305- 311 (biosynth) [https://doi.org/10.1016/j.phytochem.2004.12.010]
  24. Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, CCN000
  25. Satwalekar, S.S. et al., J. Indian Inst. Sci., 1957, 39, 195- 212
  26. Linstedt, G. et al., Acta Chem. Scand., 1950, 4, 1042- 1046 (Pinostrobin, Pinocembrin,struct, S-form) [https://doi.org/10.3891/acta.chem.scand.04-1042]
  27. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 1- 12 (Pinus constits) [https://doi.org/10.3891/acta.chem.scand.05-0001]
  28. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 121- 128 (Pinus constits, chromatogr) [https://doi.org/10.3891/acta.chem.scand.05-0121]
  29. Hasegawa, M. et al., JACS, 1957, 79, 450- 452 (Verecundin) [https://doi.org/10.1021/ja01559a059]
  30. Hasegawa, M. et al., JACS, 1957, 79, 1738- 1740 (Verecundin) [https://doi.org/10.1021/ja01564a056]
  31. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (Pinocembrin, abs config)
  32. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (Alpinetin, pmr) [https://doi.org/10.1071/CH9640428]
  33. Mongkolsuk, S. et al., JCS, 1964, 4654- 4655 ((±)-Pinostrobin, (±)-Alpinetin)
  34. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms)
  35. Aurnhammer, G. et al., Chem. Ber., 1970, 103, 3667- 3673 (Isosarotanoside, Sarotanoside)
  36. Asakawa, Y. et al., Bull. Chem. Soc. Jpn., 1971, 44, 2761- 2766 (Pinocembrin, Alpinetin,Alnus sieboldiana constit) [https://doi.org/10.1246/bcsj.44.2761]
  37. Bick, I.R.C. et al., Aust. J. Chem., 1972, 25, 449- 451 (Eucalyptus sieberi constits) [https://doi.org/10.1071/CH9720449]
  38. The Flavonoids, (eds. Harborne, J.B. et al), Chapman and Hall, 1975, 563 (occur)
  39. Miyakado, M. et al., Phytochemistry, 1976, 15, 846- 847 (Pinocembrin, activity) [https://doi.org/10.1016/S0031-9422(00)94481-9]
  40. Wagner, H. et al., Tet. Lett., 1976, 17, 1799- 1802 (cmr) [https://doi.org/10.1016/S0040-4039(00)93787-0]
  41. Pomilio, A.B. et al., Phytochemistry, 1979, 18, 1410- 1411 (Sarotanoside) [https://doi.org/10.1016/0031-9422(79)83040-X]
  42. Tanaka, N. et al., Chem. Pharm. Bull., 1980, 28, 2843- 2845 (Pinocembroside) [https://doi.org/10.1248/cpb.28.2843]
  43. González, M.D. et al., Phytochemistry, 1981, 20, 1174- 1175 (7-(2'''-acetylneohesperidoside)) [https://doi.org/10.1016/0031-9422(81)83063-4]
  44. Ripperberger, H., Phytochemistry, 1981, 20, 1757- 1758 (4'''-Acetylsarotanoside) [https://doi.org/10.1016/S0031-9422(00)98578-9]
  45. Jaipetch, T. et al., Aust. J. Chem., 1982, 35, 351- 361 ((±)-Pinocembrin, (±)-Pinostrobin,Boesenbergia pandurata constit) [https://doi.org/10.1071/CH9820351]
  46. González, M.D. et al., Phytochemistry, 1982, 21, 757- 759 (7-(6''-acetylneohesperidoside),7-(3'''-acetylneohesperidoside)) [https://doi.org/10.1016/0031-9422(82)83182-8]
  47. The Flavonoids: Advances in Research, (eds. Harborne, J.B. et al), Chapman and Hall, 1982, 360 (occur)
  48. Bohlmann, F. et al., Phytochemistry, 1984, 23, 1338- 1339 (7-O-Prenylpinocembrin) [https://doi.org/10.1016/S0031-9422(00)80458-6]
  49. Norbedo, C. et al., Phytochemistry, 1984, 23, 2698- 2700 (7-O-2,3-epoxy-3-methylbutyl) [https://doi.org/10.1016/S0031-9422(00)84139-4]
  50. Bohlmann, F. et al., Planta Med., 1984, 50, 271- 272 (5-Methoxy-7-prenyloxyflavanone) [https://doi.org/10.1055/s-2007-969699]
  51. Talapatra, B. et al., Indian J. Chem., Sect. B, 1985, 24, 561 (Pinocembrin, synth)
  52. Kaouadji, M. et al., J. Nat. Prod., 1986, 49, 153- 155 (7-O-Prenylpinocembrin) [https://doi.org/10.1021/np50043a023]
  53. Jakupovic, J. et al., Phytochemistry, 1987, 26, 803- 807 (hydroxyethylphenyl ether) [https://doi.org/10.1016/S0031-9422(00)84791-3]
  54. Fukui, H. et al., Chem. Pharm. Bull., 1988, 36, 4174- 4176 (Pinocembrin, activity) [https://doi.org/10.1248/cpb.36.4174]
  55. Kapetanidis, J. et al., Pharm. Acta Helv., 1988, 63, 206- 208 (7-rutinoside)
  56. Tomimori, T. et al., Shoyakugaku Zasshi, 1988, 42, 98- 101 (7-glucuronide)
  57. The Flavonoids: Advances in Research Since 1980, (ed. Harborne, J.B.), Chapman and Hall, 1988, 358 (occur)
  58. González, A.G. et al., Phytochemistry, 1989, 28, 2871- 2872 (Salvia texana constit) [https://doi.org/10.1016/S0031-9422(00)98114-7]
  59. Shoja, M., Z. Kristallogr., Kristallgeom., Kristallphys., Kristallchem., 1989, 189, 89- 93 (cryst struct, Pinostrobin)
  60. Krause, M. et al., J. Chromatogr., A, 1990, 502, 287- 296 (chiral hplc, Pinocembrin) [https://doi.org/10.1016/S0021-9673(01)89593-5]
  61. Jung, J.H. et al., Phytochemistry, 1990, 29, 1271- 1275 (cmr) [https://doi.org/10.1016/0031-9422(90)85441-H]
  62. Geibel, M. et al., Phytochemistry, 1991, 30, 1519- 1521 (Prunus cerasus constit) [https://doi.org/10.1016/0031-9422(91)84200-C]
  63. Randriaminahy, M. et al., Z. Naturforsch., C, 1992, 47, 10- 16 (neryl ether)
  64. Yuniong, X. et al., Phytochemistry, 1993, 33, 510- 511 (Onychin) [https://doi.org/10.1016/0031-9422(93)85552-3]
  65. Bilia, A.R. et al., Phytochemistry, 1993, 33, 1449- 1452 (7-Me ether 5-glucoside) [https://doi.org/10.1016/0031-9422(93)85108-4]
  66. Hoeneison, M. et al., Phytochemistry, 1993, 34, 1653 (7-benzoyl) [https://doi.org/10.1016/S0031-9422(00)90867-7]
  67. Fukui, H. et al., Phytochemistry, 1993, 34, 1653 (Pinocembrin, activity)
  68. Houghton, P.J. et al., Pharm. Pharmacol. Lett., 1997, 7, 96- 98 (Pinocembrin, activity)
  69. Huang, Y.-L. et al., J. Nat. Prod., 1998, 61, 523- 524 (HHDP derivs) [https://doi.org/10.1021/np970428k]
  70. Meekes, M. et al., Phytomedicine, 1998, 5, 459- 463 (Pinostrobin, activity) [https://doi.org/10.1016/S0944-7113(98)80042-1]
  71. Tip-Pyang, S. et al., ACGC Chem. Res. Commun., 2000, 10, 21- 26 (Pinocembrin,Pinostrobin, Alpinetin, activity)
  72. Le Bail, J.-C. et al., Cancer Lett., 2000, 156, 37- 44 (Pinostrobin, activity) [https://doi.org/10.1016/S0304-3835(00)00435-3]
  73. Yuldashev, M.P., Chem. Nat. Compd. (Engl. Transl.), 2001, 37, 224- 225 (Pinocembroside) [https://doi.org/10.1023/A:1012505721054]
  74. Hodgetts, K.J. et al., Tet. Lett., 2001, 42, 3763- 3766 (Pinostrobin, synth) [https://doi.org/10.1016/S0040-4039(01)00567-6]
  75. Lin, J.-H. et al., J. Nat. Prod., 2002, 65, 638- 640 (7-apiosylapiosylglucoside) [https://doi.org/10.1021/np010548z]
  76. Gu, J.-Q. et al., J. Nat. Prod., 2002, 65, 1616- 1620 (±-7-Me ether)
  77. Hegde, V.R. et al., Bioorg. Med. Chem. Lett., 2003, 13, 2925- 2928 (Sch 644343) [https://doi.org/10.1016/S0960-894X(03)00584-5]
  78. Leu, Y.-L. et al., Chem. Pharm. Bull., 2004, 52, 858- 860 (Viscum articulatum glycosides) [https://doi.org/10.1248/cpb.52.858]
  79. He, W. et al., Bioorg. Med. Chem., 2005, 13, 1837- 1845 (Alpinetin, activity) [https://doi.org/10.1016/j.bmc.2004.11.038]
  80. Caccamese, S. et al., J. Chromatogr., A, 2005, 1076, 155- 162 (chiral hplc-cd, Pinocembrin) [https://doi.org/10.1016/j.chroma.2005.04.024]
  81. Urgaonkar, S. et al., Org. Lett., 2005, 7, 5609- 5612 ((±)-Pinocembrin, synth) [https://doi.org/10.1021/ol052269z]
  82. Ma, X.-M. et al., Chem. Biodiversity, 2007, 4, 2172- 2181 (isol, pmr, cmr)
  83. Matus-Cádiz, M.A. et al., J. Agric. Food Chem., 2008, 56, 1644- 1653 (7-rhamnoside, occur) [https://doi.org/10.1021/jf072970c]
  84. Yuan, Y. et al., J. Asian Nat. Prod. Res., 2008, 10, 999- 1002 (Pinocembrin, resoln)
  85. Drewes, S.E. et al., Phytochemistry, 2008, 69, 1745- 1749 (Dibenzylpinocembrin, activity) [https://doi.org/10.1016/j.phytochem.2008.02.022]
  86. Jeong, K.-W. et al., J. Nat. Prod., 2009, 72, 719- 724 (Pinocembrin, activity) [https://doi.org/10.1021/np800698d]
  87. Lotti, C. et al., J. Agric. Food Chem., 2010, 58, 2209- 2213 (Mexican propolis constit) [https://doi.org/10.1021/jf100070w]
  88. Chou, T.-S. et al., J. Nat. Prod., 2010, 73, 1470- 1475 (S-form, Pinostrobin, activity) [https://doi.org/10.1021/np100014j]
  89. Pick, A. et al., Bioorg. Med. Chem., 2011, 19, 2090- 2102 (Leptospermum scoparium constit,activity) [https://doi.org/10.1016/j.bmc.2010.12.043]
  90. Xu, X. et al., J. Agric. Food Chem., 2011, 59, 1205- 1209 (7-neohesperidoside, 7-rutinoside,Litchioside D) [https://doi.org/10.1021/jf104387y]
  91. Allard, P.-M. et al., J. Nat. Prod., 2011, 74, 2446- 2453 (Cryptocarya chartacea constits) [https://doi.org/10.1021/np200715v]
  92. Korenaga, T. et al., Org. Lett., 2011, 13, 2022- 2025 ((-)-Pinostrobin, synth, bibl) [https://doi.org/10.1021/ol2004148]
  93. Katerere, D.R. et al., Fitoterapia, 2012, 83, 932- 940 (Alpinetin, Pinocembrin) [https://doi.org/10.1016/j.fitote.2012.04.011]
  94. Ullah, Z. et al., Nat. Prod. Commun., 2012, 7, 1011- 1014 (Pistacide A)
  95. Ukida, K. et al., Chem. Pharm. Bull., 2013, 61, 1136- 1142 (Schoepfiajasmin G) [https://doi.org/10.1248/cpb.c13-00466]
  96. Wang, M. et al., Nat. Prod. Res., 2014, 28, 70- 73 (S-form, 5-Me ether 7-glucoside)
  97. Vuppalapati, S.V.N. et al., Synthesis, 2014, 46, 465- 474 ((±)-di-Me ether)
  98. Noble, H.M. et al., Planta Med., 1990, 56, 647 (GR 95647X) [https://doi.org/10.1055/s-2006-961297]
  99. Sidana, J. et al., Fitoterapia, 2010, 81, 878- 883 (Loxophlebal A) [https://doi.org/10.1016/j.fitote.2010.05.016]
  100. Yamakoshi, Y. et al., Biosci., Biotechnol., Biochem., 1992, 56, 1570 (isol, uv, ir, pmr, cmr,ms) [https://doi.org/10.1271/bbb.56.1570]
  101. Schiemenz, G.P. et al., Annalen, 1976, 1514- 1519 (Homobaeckeol, synth)
  102. Bolte, M.L. et al., Agric. Biol. Chem., 1984, 48, 373- 376; 1985, 49, 761 - 768 (Pulverulentone B)
  103. Ireland, B.D. et al., J. Essent. Oil Res., 2004, 16, 89- 94 (Homoisobaeckeol, O-Methylhomobaeckeol)
  104. Shiu, W.K.P. et al., Phytochemistry, 2006, 67, 2568- 2572 (6'-Me ether) [https://doi.org/10.1016/j.phytochem.2006.09.037]
  105. Wang, W. et al., J. Nat. Prod., 2010, 73, 1815- 1820 (Aspidinol D) [https://doi.org/10.1021/np1004483]
  106. Malterud, K.E. et al., Phytochemistry, 1977, 16, 1805- 1809 (Myrigalone E, synth) [https://doi.org/10.1016/0031-9422(71)85094-X]
  107. Misirlioglu, H. et al., Phytochemistry, 1978, 17, 2015- 2019 (synth, pmr) [https://doi.org/10.1016/S0031-9422(00)88754-3]
  108. Schiemenz, G.P. et al., Annalen, 1982, 1509- 1513 (synth, deriv)
  109. Malterud, K.E., Acta Pharm. Nord., 1992, 4, 65- 68 (Myrigalones G,H)
  110. Gafner, S. et al., Planta Med., 1996, 62, 67- 69 (Myrica serrata constits) [https://doi.org/10.1055/s-2006-957804]
  111. Japan. Pat., 1999, 11 80 012 (Myrigalone G, activity)
  112. Mustafa, K.A. et al., Tetrahedron, 2003, 59, 6113- 6120 (Leptospermum recurvum constits,synth, pmr, cmr) [https://doi.org/10.1016/S0040-4020(03)00940-2]
  113. Kuo, Y.-C. et al., Planta Med., 2004, 70, 1237- 1239 (Myrigalone H) [https://doi.org/10.1055/s-2004-835859]
  114. Shen, C.-C. et al., Nat. Prod. Res., 2007, 21, 377- 380 (2'-Me ether)
  115. Carroll, A.R. et al., J. Nat. Prod., 2008, 71, 881- 883 (Corymbia peltata constit) [https://doi.org/10.1021/np0706567]
  116. Manaharan, T. et al., Food Chem., 2012, 132, 1802- 1807 (Myrigalone G, activity) [https://doi.org/10.1016/j.foodchem.2011.11.147]
  117. Bolley, P.A., Annalen, 1841, 37, 101- 111 (Quercitrin, isol)
  118. Perkin, A.G., JCS, 1909, 95, 2181- 2193 (Isoquercitrin, isol)
  119. Sando, C.E., J. Biol. Chem., 1937, 117, 45- 57 (Hyperin, isol)
  120. Schindler, O., Helv. Chim. Acta, 1945, 28, 1157- 1159 (Meratin)
  121. Ice, C.H., JACS, 1952, 74, 4606 (Isoquercitrin, synth) [https://doi.org/10.1021/ja01138a048]
  122. Hänsel, R. et al., Arch. Pharm. (Weinheim, Ger.), 1954, 287, 117- 126 (Hyperin, occur)
  123. Hörhammer, L. et al., Arch. Pharm. (Weinheim, Ger.), 1955, 288, 419- 425 (Polystachoside)
  124. Nakaoki, T. et al., Yakugaku Zasshi, 1956, 76, 323- 324 (Reynoutrin, struct) [https://doi.org/10.1248/yakushi1947.76.3_323]
  125. El Khadem, H. et al., JCS, 1958, 3320- 3323 (Avicularin, Guaijaverin, activity)
  126. Ohta, T. et al., Yakugaku Zasshi, 1959, 79, 986 (Fenicularin) [https://doi.org/10.1248/yakushi1947.79.7_986]
  127. Nakaoki, T. et al., Yakugaku Zasshi, 1961, 81, 1158- 1159 (Nelumboside, struct) [https://doi.org/10.1248/yakushi1947.81.8_1158]
  128. Kovalev, I.P. et al., J. Gen. Chem. USSR (Engl. Transl.), 1963, 33, 1626- 1630 (ir)
  129. Pearl, I.A. et al., JOC, 1963, 28, 1442 (Miquelianin, struct) [https://doi.org/10.1021/jo01040a542]
  130. Bienenfeld, W. et al., Arch. Pharm. (Weinheim, Ger.), 1966, 299, 598- 602 (Drosera rotundifolia digalactoside)
  131. Litvinenko, V.I., CA, 1966, 66, 73264 (Glyphoside)
  132. Bagrii, A.K. et al., Chem. Nat. Compd. (Engl. Transl.), 1966, 2, 65- 66 (Rumarin)
  133. Hörhammer, L. et al., Tet. Lett., 1966, 7, 567- 571 (Quercitrin, synth) [https://doi.org/10.1016/S0040-4039(01)99666-2]
  134. Makhsudova, B. et al., Chem. Nat. Compd. (Engl. Transl.), 1967, 3, 8- 10 (Hybridin) [https://doi.org/10.1007/BF01171712]
  135. Hoerhammer, L. et al., Chem. Ber., 1968, 101, 450- 453 (Hyperin, Quercitrin, synth, struct)
  136. Wagner, H. et al., Chem. Ber., 1968, 101, 1186- 1189 (3-sophoroside, synth)
  137. Wagner, H. et al., Chem. Ber., 1968, 101, 3419- 3422 (gentiobioside, synth)
  138. Birkofer, L. et al., Annalen, 1969, 725, 196- 202 (Neopetunoside)
  139. Lebreton, P. et al., C. R. Seances Acad. Sci., Ser. D, 1969, 268, 1661- 1663 (Peltatoside)
  140. Farkas, L. et al., Chem. Ber., 1969, 102, 2583- 2587 (Isoquercitrin, synth)
  141. Maksyukhina, N.P. et al., Chem. Nat. Compd. (Engl. Transl.), 1969, 5, 597 (Zhealin)
  142. Wagner, H. et al., Chem. Ber., 1970, 103, 3674- 3677 (Miquelianin)
  143. Umarov, A. et al., Chem. Nat. Compd. (Engl. Transl.), 1971, 7, 499- 500 (rhamnofuranoside) [https://doi.org/10.1007/BF00564754]
  144. Komissarenko, N.F. et al., Chem. Nat. Compd. (Engl. Transl.), 1971, 7, 501 (Epirutin) [https://doi.org/10.1007/BF00564755]
  145. Glyzin, V.I. et al., Chem. Nat. Compd. (Engl. Transl.), 1971, 7, 640- 641 (Isohyperoside-Betula) [https://doi.org/10.1007/BF00568429]
  146. Khandsuren, S. et al., Chem. Nat. Compd. (Engl. Transl.), 1971, 7, 646 (Neoisorutin) [https://doi.org/10.1007/BF00568433]
  147. Williams, C.A. et al., Phytochemistry, 1971, 10, 1059- 1063 (3-neohesperidoside) [https://doi.org/10.1016/S0031-9422(00)89939-2]
  148. Gaind, K.N. et al., Planta Med., 1971, 20, 368- 373 (diarabinoside) [https://doi.org/10.1055/s-0028-1099718]
  149. Zakharov, A.M. et al., Chem. Nat. Compd. (Engl. Transl.), 1972, 8, 278- 281 (Primflaside)
  150. Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhäuser Verlag, 1972, no. 1531, no. 1525, no. 1527 (Hyperin, occur)
  151. Bykov, V.I. et al., Chem. Nat. Compd. (Engl. Transl.), 1973, 9, 526 (Bioquercetin)
  152. Farkas, L. et al., Chem. Ber., 1974, 107, 1518- 1525 (synth, diglucosides)
  153. Nahrstedt, A. et al., Tet. Lett., 1974, 15, 559- 562 (2''-O-Galloylhyperin) [https://doi.org/10.1016/S0040-4039(01)82270-X]
  154. Takemoto, T. et al., Yakugaku Zasshi, 1974, 94, 1597- 1602 (Boehmerin) [https://doi.org/10.1248/yakushi1947.94.12_1597]
  155. Buttery, B.R. et al., Can. J. Bot., 1975, 53, 219- 224 (Glycine max glucosides) [https://doi.org/10.1139/b75-026]
  156. Collins, F.W. et al., Phytochemistry, 1975, 14, 1099- 1102 (Tellimoside) [https://doi.org/10.1016/0031-9422(75)85195-8]
  157. Harborne, J.B. et al., Phytochemistry, 1975, 14, 1331- 1337 (glucuronide 7-sulfate) [https://doi.org/10.1016/S0031-9422(00)98620-5]
  158. Pohl, R. et al., Planta Med., 1975, 27, 301- 303 (galloylgalactosides) [https://doi.org/10.1055/s-0028-1097806]
  159. Candy, H.A. et al., Tet. Lett., 1975, 16, 1211- 1214 (Helichrysoside) [https://doi.org/10.1016/S0040-4039(00)72097-1]
  160. Wilkins, C.K. et al., Can. J. Bot., 1976, 54, 2133- 2140 (xylosylglucoside, dixyloside) [https://doi.org/10.1139/b76-230]
  161. El Ansari, M.A. et al., Phytochemistry, 1976, 15, 231- 232 (isoferuloylglucuronide) [https://doi.org/10.1016/S0031-9422(00)89100-1]
  162. Takagi, S. et al., Yakugaku Zasshi, 1976, 96, 284- 288 (3-glucosylglucosylrhamnoside) [https://doi.org/10.1248/yakushi1947.96.3_284]
  163. Wilkins, C.K. et al., Phytochemistry, 1977, 16, 144- 145 (sulforhamnoside) [https://doi.org/10.1016/0031-9422(77)83041-0]
  164. Rappaportt, I. et al., Phytochemistry, 1977, 16, 1115- 1116 (2-apiosyl-6-rhamnosylglucoside) [https://doi.org/10.1016/S0031-9422(00)86765-5]
  165. Dayal, R. et al., Planta Med., 1977, 31, 245- 248 (4-galactosylgalactoside) [https://doi.org/10.1055/s-0028-1097522]
  166. Ohmoto, T. et al., Yakugaku Zasshi, 1977, 97, 176- 180 (Alnus sieboldiana constit) [https://doi.org/10.1248/yakushi1947.97.2_176]
  167. Liu, Y.-L. et al., CA, 1978, 88, 85995 (Isohyperoside-Rhododendron)
  168. Tanaka, N. et al., Chem. Pharm. Bull., 1978, 26, 3580- 3582 (Acetylquercitrins) [https://doi.org/10.1248/cpb.26.3580]
  169. Dubey, P. et al., Phytochemistry, 1978, 17, 2138 (4-glucosylmannoside) [https://doi.org/10.1016/S0031-9422(00)89302-4]
  170. Markham, K.R. et al., Tetrahedron, 1978, 34, 1389- 1397 (cmr) [https://doi.org/10.1016/0040-4020(78)88336-7]
  171. Ivanova, S.Z., CA, 1979, 91, 2494 (Quercetin coumaroyl glucoside)
  172. Hiller, K. et al., Pharmazie, 1979, 34, 192- 193 (Rumarin)
  173. Bohm, B.A. et al., Phytochemistry, 1979, 18, 1079- 1080 (xylosylglucoside) [https://doi.org/10.1016/S0031-9422(00)91492-4]
  174. Markham, K.R. et al., Biochem. Syst. Ecol., 1980, 8, 11- 15 (galacturonide) [https://doi.org/10.1016/0305-1978(80)90019-8]
  175. Tsiklauri, G.C. et al., CA, 1980, 92, 18809 (6''-xylofuranosyl)
  176. Ivanova, S.Z. et al., Chem. Nat. Compd. (Engl. Transl.), 1980, 20, 547- 553 (di-4-hydroxycinnamoylglucoside)
  177. Zapesochnaya, G.G. et al., Dokl. Bolg. Akad. Nauk, 1980, 33, 933- 936 (Ledum palustre constits)
  178. Sakushima, A. et al., Phytochemistry, 1980, 19, 712- 713 (Manghaslin) [https://doi.org/10.1016/0031-9422(80)87052-X]
  179. Gehring, E. et al., Z. Naturforsch., C, 1980, 35, 380- 383 (4-hydroxycinnamoylglucoside)
  180. Isobe, T. et al., Bull. Chem. Soc. Jpn., 1981, 54, 3239 (2-galloylrhamnoside) [https://doi.org/10.1246/bcsj.54.3239]
  181. Abil'kaeva, S.A. et al., Chem. Nat. Compd. (Engl. Transl.), 1981, 17, 590 (rhamnofuranoside)
  182. Soltis, D.E. et al., J. Nat. Prod., 1981, 44, 50- 52 (3-galactosylglucuronoside) [https://doi.org/10.1021/np50013a009]
  183. Guinaudeau, H. et al., Phytochemistry, 1981, 20, 1113- 1116 (Faratroside) [https://doi.org/10.1016/0031-9422(81)83037-3]
  184. Ishikura, N., Agric. Biol. Chem., 1982, 46, 1705- 1706 (sambubioside)
  185. Imperato, F., Chem. Ind. (London), 1982, 604 (Malonylhyperin)
  186. Itokawa, H. et al., Chem. Lett., 1982, 49- 52 (ms) [https://doi.org/10.1246/cl.1982.49]
  187. Fujita, M. et al., Chem. Pharm. Bull., 1982, 30, 1151- 1156 (Hyperin, cmr) [https://doi.org/10.1248/cpb.30.1151]
  188. Kuroyanagi, M. et al., Chem. Pharm. Bull., 1982, 30, 1602- 1608 (2-galloylglucoside) [https://doi.org/10.1248/cpb.30.1602]
  189. Larsen, L.M. et al., Phytochemistry, 1982, 21, 1029- 1033 (2-xylosylgalactoside) [https://doi.org/10.1016/S0031-9422(00)82410-3]
  190. Saleh, N.A.M. et al., Phytochemistry, 1982, 21, 1995- 2000 (gentiotrioside) [https://doi.org/10.1016/0031-9422(82)83030-6]
  191. Shigematsu, N. et al., Phytochemistry, 1982, 21, 2156- 2158 (6''-Caffeoylhyperin) [https://doi.org/10.1016/0031-9422(82)83079-3]
  192. Riess-Maurer, I. et al., Tetrahedron, 1982, 38, 1269- 1278 (Quercetin 3-rhamnoside) [https://doi.org/10.1016/0040-4020(82)85113-2]
  193. Imperato, F., Chem. Ind. (London), 1983, 390- 391 (3-sulfoglucoside)
  194. Warnock, M.J. et al., Phytochemistry, 1983, 22, 1834- 1835 (Delphinium carolinianum benzoylglycosides) [https://doi.org/10.1016/S0031-9422(00)80287-3]
  195. Geiger, H. et al., Z. Naturforsch., C, 1983, 38, 490- 491 (2-rhamnosylarabinopyranoside)
  196. McDougal, K.M. et al., Am. J. Bot., 1984, 71, 301- 308 (arabinosylxyloside, occur) [https://doi.org/10.2307/2443490]
  197. Servettaz, O. et al., J. Nat. Prod., 1984, 47, 809- 814 (β-L-arabinopyranoside) [https://doi.org/10.1021/np50035a009]
  198. Hiller, K. et al., Pharmazie, 1984, 39, 51- 53 (6-glucosylgalactoside)
  199. Marston, A. et al., Phytochemistry, 1984, 23, 1824- 1825 (3-arabinoside) [https://doi.org/10.1016/S0031-9422(00)83511-6]
  200. Nawwar, M.A.M. et al., Phytochemistry, 1984, 23, 2347- 2349 (glucuronide Me, Et esters) [https://doi.org/10.1016/S0031-9422(00)80549-X]
  201. Strack, D. et al., Phytochemistry, 1984, 23, 2970- 2971 (2-glucosylgalactoside) [https://doi.org/10.1016/0031-9422(84)83059-9]
  202. Murakami, T. et al., Yakugaku Zasshi, 1984, 104, 142- 146 (Nikkoshidin) [https://doi.org/10.1248/yakushi1947.104.2_142]
  203. De Koster, C.G. et al., Biomed. Mass Spectrom., 1985, 12, 596- 601 (ms)
  204. Imperato, F., Chem. Ind. (London), 1985, 799 (4-glucosyl-?-galactosylrhamnoside)
  205. Chaturvedi, S.K. et al., J. Indian Chem. Soc., 1985, 62, 76- 77 (4-galactosylrhamnoside)
  206. Geslin, M. et al., J. Nat. Prod., 1985, 48, 111- 113 (6-malonylglucoside) [https://doi.org/10.1021/np50037a020]
  207. Reynaud, J. et al., Pharmazie, 1985, 40, 132- 133 (6-acetylglucoside, struct)
  208. Waage, S.K. et al., Phytochemistry, 1985, 24, 243- 245 (6-galactosylglucoside) [https://doi.org/10.1016/S0031-9422(00)83528-1]
  209. Hamburger, M. et al., Phytochemistry, 1985, 24, 2689- 2692 (Securidaca diversifolia apiosylglycosides) [https://doi.org/10.1016/S0031-9422(00)80695-0]
  210. Piegay, I. et al., Pharmazie, 1986, 41, 524- 525 (Senecio aureus constits)
  211. Brasseur, T. et al., Phytochemistry, 1986, 25, 563- 564 (robinobioside) [https://doi.org/10.1016/S0031-9422(00)85534-X]
  212. Wald, B. et al., Phytochemistry, 1986, 25, 2904- 2905 (6''-(3-Hydroxy-3-methylglutaroyl)hyperin) [https://doi.org/10.1016/S0031-9422(00)83768-1]
  213. Saxena, V.K. et al., Fitoterapia, 1987, 58, 283 (2-coumaroylglucoside)
  214. Nasr, C. et al., Phytochemistry, 1987, 26, 2869- 2870 (6-coumaroyl-2-glucosylrhamnoside) [https://doi.org/10.1016/S0031-9422(00)83613-4]
  215. Pachaly, P. et al., Planta Med., 1987, 53, 442- 444 (Polifolioside, Avicularin) [https://doi.org/10.1055/s-2006-962769]
  216. Stobiecki, M. et al., Biomed. Environ. Mass Spectrom., 1988, 15, 589- 594 (Erodium manescavii constit)
  217. Brasseur, T. et al., Phytochemistry, 1988, 27, 1487- 1490 (Variabilosides E,F) [https://doi.org/10.1016/0031-9422(88)80221-8]
  218. Yasukawa, K. et al., Phytochemistry, 1988, 27, 3017- 3018 (2-rhamnosylgalactoside, struct) [https://doi.org/10.1016/0031-9422(88)80719-2]
  219. Seabra, R.M. et al., Phytochemistry, 1988, 27, 3019- 3020 (glucuronide 3'-sulfate) [https://doi.org/10.1016/0031-9422(88)80720-9]
  220. Lachman, J.P. et al., CA, 1989, 111, 171121 (Sambucus racemosa 4-rhamnosylglucoside)
  221. Saito, K. et al., J. Nat. Prod., 1989, 52, 121- 1226 (Avicularin, activity)
  222. Nawwar, M.A.M. et al., Phytochemistry, 1989, 28, 1755- 1757 (2-rhamnosyl-6-glucosylgalactoside) [https://doi.org/10.1016/S0031-9422(00)97839-7]
  223. Yasukawa, K. et al., Phytochemistry, 1989, 28, 2215- 2216 (2,6-dirhamnosylgalactoside,struct) [https://doi.org/10.1016/S0031-9422(00)97951-2]
  224. Franke, A. et al., Phytochemistry, 1989, 28, 3566- 3568 (Libocedrus bidwillii acylrhamnosides) [https://doi.org/10.1016/0031-9422(89)80399-1]
  225. Kadota, S. et al., Chem. Pharm. Bull., 1990, 38, 2687- 2697 (galloylgalactosides) [https://doi.org/10.1248/cpb.38.2687]
  226. Saito, N. et al., Heterocycles, 1990, 30, 759- 764 (2-glucosyl-6-glucosylglucoside)
  227. Webby, R.F. et al., Phytochemistry, 1990, 29, 289- 292 (4-rhamnosyl-6-rhamnosylgalactoside) [https://doi.org/10.1016/0031-9422(90)89052-B]
  228. Iwagawa, T. et al., Phytochemistry, 1990, 29, 1013- 1014 (2-galloylarabinoside) [https://doi.org/10.1016/0031-9422(90)80075-R]
  229. Yasukawa, K. et al., Phytochemistry, 1990, 29, 1707- 1708 (2,6-dirhamnosylgalactoside) [https://doi.org/10.1016/0031-9422(90)80155-A]
  230. Iwashina, T. et al., Phytochemistry, 1990, 29, 3639- 3641 (Nikkoshidin) [https://doi.org/10.1016/0031-9422(90)85291-M]
  231. Soicke, H. et al., Planta Med., 1990, 56, 410- 412 (2-xylosylrhamnoside) [https://doi.org/10.1055/s-2006-960996]
  232. Razanamahefa, B. et al., Planta Med., 1990, 56, 583 (2-glucosylxyloside) [https://doi.org/10.1055/s-2006-961188]
  233. Shi, J. et al., Gaodeng Xuexiao Huaxue Xuebao, 1991, 12, 906- 909 (6-crotonylglucoside)
  234. Finger, A. et al., J. Sci. Food Agric., 1991, 55, 313- 321 (3-glucosyl-6-rhamnosylglucoside)
  235. Finger, A. et al., Phytochemistry, 1991, 30, 2057- 2060 (3-glucosyl-6-rhamnosylglucoside) [https://doi.org/10.1016/0031-9422(91)85066-9]
  236. Webby, R.F., Phytochemistry, 1991, 30, 2443- 2444 (2-xylosyl-6-rhamnosylglucoside) [https://doi.org/10.1016/0031-9422(91)83680-J]
  237. Seto, T. et al., Chem. Pharm. Bull., 1992, 40, 2080- 2082 (Multinoside A) [https://doi.org/10.1248/cpb.40.2080]
  238. Uniyal, S.K. et al., Int. J. Pharmacogn., 1992, 30, 209- 212 (4-glucosyl-4-xylosylrhamnoside)
  239. Markham, K.R. et al., Phytochemistry, 1992, 31, 549- 554 (2-xylosylglucoside) [https://doi.org/10.1016/0031-9422(92)90036-P]
  240. Hasler, A. et al., Phytochemistry, 1992, 31, 1391- 1394 (Ginkgo biloba constits) [https://doi.org/10.1016/0031-9422(92)80298-S]
  241. Tomas-Lorente, F. et al., Phytochemistry, 1992, 31, 2027- 2029 (6-xylosylglucoside) [https://doi.org/10.1016/0031-9422(92)80355-I]
  242. D'Agostino, M. et al., Phytochemistry, 1992, 31, 4387- 4388 (Diacetylhyperin,Triacetylhyperin) [https://doi.org/10.1016/0031-9422(92)80489-2]
  243. Sanz, M.-J. et al., J. Nat. Prod., 1993, 56, 1995- 1998 (2-caffeoylglucuronide) [https://doi.org/10.1021/np50101a022]
  244. Simon, A. et al., Phytochemistry, 1993, 32, 1045- 1049; 33, 1237 - 1240 (Guaijaverin,triacetylarabinosylglucosides) [https://doi.org/10.1016/0031-9422(93)85253-N]
  245. Liu, Y.-L. et al., Phytochemistry, 1993, 33, 1549- 1551 (2-apiosyl-6-rhamnosylglucoside) [https://doi.org/10.1016/0031-9422(93)85134-D]
  246. Sticher, O., Planta Med., 1993, 59, 2- 11 (Ginkgo biloba constits) [https://doi.org/10.1055/s-2006-959593]
  247. The Flavonoids: Advances in Research Since 1986, (ed. Harborne, J.B.), Chapman & Hall, 1993
  248. Matlawska, I. et al., Acta Pol. Pharm., 1994, 51, 263- 265 (2-arabinosylglucoside, 2-galactosylglucoside)
  249. Simon, A. et al., Phytochemistry, 1994, 36, 1043- 1045 (triacetylarabinosylgalactoside) [https://doi.org/10.1016/S0031-9422(00)90488-6]
  250. Senatore, F. et al., Biochem. Syst. Ecol., 1995, 23, 573- 574 (3',4'-Diacetylisoquercetin) [https://doi.org/10.1016/0305-1978(95)00039-W]
  251. Rastrelli, L. et al., J. Agric. Food Chem., 1995, 43, 2020- 2024 (2-apiosyl-6-rhamnosylgalactoside) [https://doi.org/10.1021/jf00056a012]
  252. Chulia, A.J. et al., J. Nat. Prod., 1995, 58, 560- 563 (6''-Hydroxybenzoylhyperin) [https://doi.org/10.1021/np50118a012]
  253. Hasan, A. et al., Phytochemistry, 1995, 39, 1211- 1213 (4-glucosylgalactoside) [https://doi.org/10.1016/0031-9422(95)00071-E]
  254. Ferreres, F. et al., Phytochemistry, 1995, 39, 1443- 1446 (Pisum sativum sophorotriosides) [https://doi.org/10.1016/0031-9422(95)00137-V]
  255. Abe, F. et al., Phytochemistry, 1995, 40, 577- 581 (Thevetia peruviana constits) [https://doi.org/10.1016/0031-9422(95)00316-Y]
  256. Imperato, F., Phytochemistry, 1995, 40, 1801- 1802 (laminaribioside) [https://doi.org/10.1016/0031-9422(95)00593-V]
  257. Amakura, Y. et al., Can. J. Chem., 1997, 75, 727- 733 (Quercetin digalloylglucoside) [https://doi.org/10.1139/v97-088]
  258. Li, T.M. et al., Chin. Chem. Lett., 1997, 8, 43- 46 (Artabotryside A)
  259. Olea, R.S.G. et al., J. Braz. Chem. Soc., 1997, 8, 257- 259 (6-rhamnosyl-2-p-coumaroylglucoside)
  260. Flamini, G. et al., J. Nat. Prod., 1997, 60, 449- 452 (Madreselvin B) [https://doi.org/10.1021/np9605551]
  261. Arot, L.O.M. et al., Nat. Prod. Sci., 1997, 3, 8- 10 (3-rhamnosylgalactoside)
  262. Arot, L.O.M. et al., Phytochemistry, 1997, 44, 1397- 1398 (2-galactosylrhamnoside) [https://doi.org/10.1016/S0031-9422(96)00706-6]
  263. Li, T.-M. et al., Phytochemistry, 1997, 45, 831- 833 (Arapetaloside A)
  264. Merfort, I. et al., Phytochemistry, 1997, 46, 359- 363 (Nigella 2-glucosyl-2-galactosylglucosides) [https://doi.org/10.1016/S0031-9422(97)00296-3]
  265. Zhong, X.-N. et al., Phytochemistry, 1997, 46, 943- 946 (Quercitrin, cmr) [https://doi.org/10.1016/S0031-9422(97)00366-X]
  266. Wang, T. et al., Zhiwu Xuebao, 1997, 39, 82- 84 (Craibiodendronin A)
  267. Kim, H.J. et al., J. Nat. Prod., 1998, 61, 145- 148 (galloylhyperins) [https://doi.org/10.1021/np970171q]
  268. Op de Beck, P. et al., Phytochemistry, 1998, 47, 1171- 1173 (rhamnoside 3'-sulfate, struct) [https://doi.org/10.1016/S0031-9422(98)80097-6]
  269. El-Mousallamy, A.M.D., Phytochemistry, 1998, 48, 759- 761 (6-rhamnosyl-6-glucosylgalactoside) [https://doi.org/10.1016/S0031-9422(97)01117-5]
  270. Bloor, S.J. et al., Phytochemistry, 1998, 49, 1427- 1430 (Petunia Mitchell derivs) [https://doi.org/10.1016/S0031-9422(98)00081-8]
  271. El-Sayed, N.H. et al., Rev. Latinoam. Quim., 1998, 26, 30- 35 (2-glucuronosylglucoside Et ester)
  272. Aqil, M. et al., Global J. Pure Appl. Sci., 1999, 5, 371- 373 (Euphorbianin)
  273. Vilegas, W. et al., J. Agric. Food Chem., 1999, 47, 403- 406 (Maytenus aquifolium tetraglycoside) [https://doi.org/10.1021/jf980114i]
  274. Beck, M.-A. et al., Phytochemistry, 1999, 50, 329- 332 (4-rhamnosyl-6-rhamnosylglucoside) [https://doi.org/10.1016/S0031-9422(98)00503-2]
  275. Fossen, T. et al., Phytochemistry, 1999, 51, 1133- 1137 (2''-Acetylquercitrin) [https://doi.org/10.1016/S0031-9422(99)00049-7]
  276. Huebner, G. et al., Planta Med., 1999, 65, 636- 642 (Aesculus hippocastanum constits) [https://doi.org/10.1055/s-1999-14038]
  277. Felser, C. et al., Planta Med., 1999, 65, 668- 670 (2-rhamnosylglucuronide) [https://doi.org/10.1055/s-2006-960845]
  278. Aimova, M.Z. et al., CA, 2000, 133, 56002j (Pakhirizin)
  279. Zhou, Z. et al., CA, 2000, 133, 161773j (Saluenin)
  280. Kang, S.S. et al., Chem. Pharm. Bull., 2000, 48, 1242- 1245 (Amurenosides A,B) [https://doi.org/10.1248/cpb.48.1242]
  281. Sharaf, M. et al., Fitoterapia, 2000, 71, 46- 49 (3-rhamnosylglucosylglucoside) [https://doi.org/10.1016/S0367-326X(99)00116-1]
  282. Datta, B.K. et al., Fitoterapia, 2000, 71, 459- 460 (6''-Caffeoylhyperin) [https://doi.org/10.1016/S0367-326X(99)00172-0]
  283. Flamini, G. et al., J. Nat. Prod., 2000, 63, 662- 663 (Horridin) [https://doi.org/10.1021/np990627z]
[top⬆]
Antifungal Citations
  1. Bowyer, R.C. et al., Chem. Ind. (London), 1963, 1245- 1246 (Eucalyptus spathulata constit,struct)
  2. Asakawa, Y. et al., Phytochemistry, 1980, 19, 2141- 2145 (Plagiochila yokogurensis constit,struct) [https://doi.org/10.1016/S0031-9422(00)82211-6]
  3. Surburg, H. et al., Chem. Ber., 1981, 114, 118- 131 (ent-Spathulenol, synth)
  4. Hubert, T.D. et al., Phytochemistry, 1985, 24, 1197- 1198 (insect repellant activity) [https://doi.org/10.1016/S0031-9422(00)81099-7]
  5. Van Lier, F.P. et al., Tet. Lett., 1985, 26, 2109- 2110 (synth) [https://doi.org/10.1016/S0040-4039(00)94792-0]
  6. Richardson, D.P. et al., J. Chem. Ecol., 1989, 15, 731- 747 (Dipterocarpus kerri constit) [https://doi.org/10.1007/BF01014715]
  7. Ulubelen, A. et al., Phytochemistry, 1994, 36, 971- 974 (Salvia sclarea consitit) [https://doi.org/10.1016/S0031-9422(00)90474-6]
  8. Tringali, C. et al., Phytochemistry, 1995, 40, 827- 831 (Epispathulenol) [https://doi.org/10.1016/0031-9422(95)00357-D]
  9. Toyota, M. et al., Phytochemistry, 1996, 41, 1347- 1350 (Dicranolejeunea yoshingana constit) [https://doi.org/10.1016/0031-9422(95)00798-9]
  10. Goud, V.T. et al., Biochem. Syst. Ecol., 2002, 30, 493- 495 (Sinularia kavarattiensis constit) [https://doi.org/10.1016/S0305-1978(01)00094-1]
  11. Vassallo, A. et al., Nat. Prod. Commun., 2008, 3, 1967- 1970 (Salvia palaestina constits)
  12. Tran, D.N. et al., Chem. - Eur. J., 2014, 20, 10654- 10660 (synth)
  13. Schmidt, O.T. et al., Annalen, 1951, 571, 232- 237 (isol)
  14. Reddy, K.K. et al., Aust. J. Chem., 1964, 17, 238- 245 (isol, bibl)
  15. Matsuda, H. et al., Chem. Pharm. Bull., 1966, 14, 877- 883 (isol, uv) [https://doi.org/10.1248/cpb.14.877]
  16. Jochims, J.C. et al., Annalen, 1968, 717, 169- 183 (pmr)
  17. Seikel, M. et al., Phytochemistry, 1970, 9, 1115- 1128 (pmr, struct) [https://doi.org/10.1016/S0031-9422(00)85235-8 145565]
  18. Haddock, E.A. et al., JCS Perkin 1, 1982, 2535- 2545 (pmr, cmr)
  19. Okuda, T. et al., Tet. Lett., 1982, 23, 3937- 3940 (uv, cd) [https://doi.org/10.1016/S0040-4039(00)87748-5]
  20. Nawwar, M.A.M. et al., Phytochemistry, 1994, 36, 793- 798 (isol, pmr, cmr) [https://doi.org/10.1016/S0031-9422(00)89820-9]
  21. Berry, D.E. et al., JOC, 1995, 57, 420- 422 (isol, activity) [https://doi.org/10.1021/jo00028a002]
  22. Lim, Y.A. et al., Phytother. Res., 1997, 11, 22- 27 (activity)
  23. Liu, K.C.S.C. et al., Planta Med., 1999, 65, 43- 46 (isol, activity) [https://doi.org/10.1055/s-1999-13960]
  24. Latté, K.P. et al., Phytochemistry, 2000, 54, 701- 708 (Isocorilagin) [https://doi.org/10.1016/S0031-9422(00)00176-X]
  25. Adesina, S.K. et al., Phytother. Res., 2000, 14, 371- 374 (isol, activity)
  26. Latté, K.P. et al., Z. Naturforsch., C, 2000, 55, 467- 472 (activity) [https://doi.org/10.1515/znc-2000-7-809]
  27. Rangkadilok, N. et al., J. Agric. Food Chem., 2005, 53, 1387- 1392 (Euphoria longana constit) [https://doi.org/10.1021/jf0403484]
  28. Yamada, H. et al., JACS, 2008, 130, 7566- 7567 (synth) [https://doi.org/10.1021/ja803111z]
  29. Zemplen, G. et al., Ber., 1942, 75, 1432- 1438 (Sakuranin, Sakuranetin, synth)
  30. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (R-Sakuranetin, abs config)
  31. Gupta, S.R. et al., Phytochemistry, 1972, 11, 2634- 2636 (Sakuranin) [https://doi.org/10.1016/S0031-9422(00)88569-6]
  32. Birch, A.J. et al., Aust. J. Chem., 1974, 27, 331- 344 (Sakuranetin) [https://doi.org/10.1071/CH9740331]
  33. Bohlmann, F. et al., Chem. Ber., 1976, 109, 3366- 3370 (Sakuranetin)
  34. Srivastava, S.K., Can. J. Chem., 1983, 61, 1827- 1830 (4'-rhamnoside) [https://doi.org/10.1139/v83-312]
  35. Baudouin, G. et al., J. Nat. Prod., 1983, 46, 681- 687 (Sakuranetin, synth) [https://doi.org/10.1021/np50029a016]
  36. Shoja, M., Acta Cryst. C, 1990, 46, 1969- 1971 (Sakuranetin, cryst struct) [https://doi.org/10.1107/S0108270190002979]
  37. Messana, I. et al., Phytochemistry, 1990, 29, 329- 332 (Hyptis salzmanii constit) [https://doi.org/10.1016/0031-9422(90)89065-H]
  38. Kodama, O. et al., Phytochemistry, 1992, 31, 3807- 3809 (Sakuranetin, rice phytoalexin) [https://doi.org/10.1016/S0031-9422(00)97532-0]
  39. Ahsan, M. et al., Phytochemistry, 1994, 37, 259- 266 (4'-prenyl ether) [https://doi.org/10.1016/0031-9422(94)85037-2]
  40. Vasconcelos, J.M.J. et al., Phytochemistry, 1998, 49, 1421- 1424 (Sakuranetin) [https://doi.org/10.1016/S0031-9422(98)00180-0]
  41. Azhar-ul-Haq, et al.Pol. J. Chem., 2004, 78, 1851- 1856 (Vitexoside)
  42. Hung, T.M. et al., Chem. Pharm. Bull., 2011, 59, 129- 131 (Chromolaena odorata constit) [https://doi.org/10.1248/cpb.59.129]
  43. Lotti, C. et al., J. Agric. Food Chem., 2012, 60, 10540- 10542 (Sakuranetin, multidrug resistance inhibitor) [https://doi.org/10.1021/jf302578r]
  44. Grecco, S.D.S. et al., Molecules, 2014, 19, 7528- 7542 (Sakuranetin, cryst struct, activity)
  45. Crow, W.D. et al., Tet. Lett., 1977, 18, 1073- 1074 (Eucalyptus grandis constit, struct) [https://doi.org/10.1016/S0040-4039(01)92832-1]
  46. Yuste, F. et al., Tet. Lett., 1978, 19, 4869- 4870 (synth) [https://doi.org/10.1016/S0040-4039(01)85756-7]
  47. Bolte, M.L. et al., Agric. Biol. Chem., 1984, 48, 373- 376 (Eucalyptus pulverulenta constit)
  48. Bolte, M.L. et al., Agric. Biol. Chem., 1985, 49, 761- 768 (synth, sar)
  49. Yoshida, S. et al., Phytochemistry, 1988, 27, 1943- 1946 (Eucalyptus grandis constit) [https://doi.org/10.1016/0031-9422(88)80072-4]
  50. Nakayama, R., Agric. Biol. Chem., 1990, 54, 231- 232 (Eucalyptus perriniana constit, activity)
  51. Singh, I.P. et al., Biosci., Biotechnol., Biochem., 1996, 60, 1522- 1523 (activity) [https://doi.org/10.1271/bbb.60.1522]
  52. Bharate, S.B. et al., Aust. J. Chem., 2005, 58, 551- 555 (synth) [https://doi.org/10.1071/CH05061]
  53. Bharate, S,B, et al., Bioorg. Med. Chem., 2006, 14, 1750- 1760 (synth, activity) [https://doi.org/10.1016/j.bmc.2005.10.027]
  54. Bharate, S.B. et al., Bioorg. Med. Chem., 2007, 15, 87- 96 (activity) [https://doi.org/10.1016/j.bmc.2006.10.006]
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Anticancer Citations
  1. Wang, J. et al., Tet. Lett., 2012, 53, 2654- 2658 (Eucalyptal E, abs config) [https://doi.org/10.1016/j.tetlet.2012.03.073]
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