The Plant Cell Culture Library

Prunus dulcis

Cell Line ID: PD-14116-R1
Media Type: B122
Availability: Medium
Order: Rosales
Family: Rosaceae
Genus: Prunus
Antiviral:
Genus Level ➡ 29 citations
Antibacterial:
Genus Level ➡ 282 citations
Anticancer:
Genus Level ➡ 271 citations
Culture Start Material: Seed
Antiviral Citations:
  1. Corse, J. et al., Nature (London), 1953, 172, 771- 772 (Prunus persica constit)
  2. Scarpati, M.L. et al., Tet. Lett., 1963, 4, 1147- 1150 (struct) [https://doi.org/10.1016/S0040-4039(01)90792-0]
  3. Ruveda, E.A. et al., Chem. Ind. (London), 1964, 239- 240 (lactone, synth)
  4. Waiss, A.C. et al., Chem. Ind. (London), 1964, 1984- 1985 (pmr)
  5. Haslam, E. et al., JCS, 1964, 2137- 2146 (synth)
  6. Weinges, K. et al., Annalen, 1966, 691, 181- 185 (Z-form)
  7. Machida, K. et al., Phytochemistry, 1992, 31, 3654- 3656 (Me ester) [https://doi.org/10.1016/0031-9422(92)83751-J]
  8. Stevenson, P.C. et al., J. Chem. Ecol., 1993, 19, 2917- 2933 (activity) [https://doi.org/10.1007/BF00980592]
  9. Ida, Y. et al., Phytochemistry, 1994, 35, 209- 215 (5-Feruloylquinic acid) [https://doi.org/10.1016/S0031-9422(00)90536-3]
  10. Fuchs, C. et al., J. Mass Spectrom., 1996, 31, 602- 608 (hplc, ms)
  11. Gentry, E.J. et al., J. Nat. Prod., 1998, 61, 1187- 1193 (Hycandinic acid ester 2) [https://doi.org/10.1021/np9701889]
  12. Pauli, G.F. et al., Magn. Reson. Chem., 1999, 37, 827- 836 (pmr, cmr)
  13. Kwon, H.C. et al., Chem. Pharm. Bull., 2000, 48, 1796- 1798 (Aster scaber constit, activity) [https://doi.org/10.1248/cpb.48.1796]
  14. Nakatani, N. et al., J. Agric. Food Chem., 2000, 48, 5512- 5516 (Prunus domestica constit) [https://doi.org/10.1021/jf000422s]
  15. Wang, S.J. et al., Chin. Chem. Lett., 2001, 12, 509- 510 (Neochlorogenic γ-lactone)
  16. Sefkow, M. et al., Eur. J. Org. Chem., 2001, 2735- 2742 (synth)
  17. Zhang, W.-D. et al., Yaoxue Xuebao, 2001, 36, 360- 363 (butyl ester)
  18. Silva, B.M. et al., J. Agric. Food Chem., 2004, 52, 4705- 4712 (coffee constit) [https://doi.org/10.1021/jf040057v]
  19. Zhu, X.-D. et al., Helv. Chim. Acta, 2005, 88, 339- 342 (Me ester)
  20. Farah, A. et al., J. Agric. Food Chem., 2005, 53, 1505- 1513 (lactone, 3'-Me ether lactone,isol) [https://doi.org/10.1021/jf048701t]
  21. Kondo, T. et al., Tet. Lett., 2005, 46, 6645- 6649 (Hydrangea supramolecular pigment) [https://doi.org/10.1016/j.tetlet.2005.07.146]
  22. Toyama-Kato, Y. et al., Heterocycles, 2007, 72, 239- 254 (Hydrangea supramolecular pigment)
  23. Ogawa, Y. et al., Chem. Nat. Compd. (Engl. Transl.), 2013, 49, 991- 995 (Hemerocallis fulva salts)
  24. Liu, J. et al., Chem. Pharm. Bull., 2013, 61, 655- 661 (Hydrangea macrophylla constit,activity) [https://doi.org/10.1248/cpb.c13-00160]
  25. Jaiswal, R. et al., Phytochemistry, 2014, 108, 252- 263 (Z-form, Lonicera henryi constit,activity) [https://doi.org/10.1016/j.phytochem.2014.08.023]
  26. Yu, Y. et al., Acta Pharm. Sin. B, 2015, 5, 210- 214 (Lonicera 4''-glucoside) [https://doi.org/10.1016/j.apsb.2015.01.012]
  27. Chuda, Y. et al., J. Agric. Food Chem., 1999, 47, 828- 831 (Mumefural) [https://doi.org/10.1021/jf980960t]
  28. Sriwilaijaroen, N. et al., Food Chem., 2011, 127, 1- 9 (activity) [https://doi.org/10.1016/j.foodchem.2010.12.031]
  29. Sugimura, H. et al., Tetrahedron, 2016, 72, 7638- 7641 (synth) [https://doi.org/10.1016/j.tet.2016.10.026]
[top⬆]
Antibacterial Citations:
  1. 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]
  2. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 1- 12 (Pinus constits) [https://doi.org/10.3891/acta.chem.scand.05-0001]
  3. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 121- 128 (Pinus constits, chromatogr) [https://doi.org/10.3891/acta.chem.scand.05-0121]
  4. Hasegawa, M. et al., JACS, 1957, 79, 450- 452 (Verecundin) [https://doi.org/10.1021/ja01559a059]
  5. Hasegawa, M. et al., JACS, 1957, 79, 1738- 1740 (Verecundin) [https://doi.org/10.1021/ja01564a056]
  6. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (Pinocembrin, abs config)
  7. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (Alpinetin, pmr) [https://doi.org/10.1071/CH9640428]
  8. Mongkolsuk, S. et al., JCS, 1964, 4654- 4655 ((±)-Pinostrobin, (±)-Alpinetin)
  9. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms)
  10. Aurnhammer, G. et al., Chem. Ber., 1970, 103, 3667- 3673 (Isosarotanoside, Sarotanoside)
  11. 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]
  12. Bick, I.R.C. et al., Aust. J. Chem., 1972, 25, 449- 451 (Eucalyptus sieberi constits) [https://doi.org/10.1071/CH9720449]
  13. The Flavonoids, (eds. Harborne, J.B. et al), Chapman and Hall, 1975, 563 (occur)
  14. Miyakado, M. et al., Phytochemistry, 1976, 15, 846- 847 (Pinocembrin, activity) [https://doi.org/10.1016/S0031-9422(00)94481-9]
  15. Wagner, H. et al., Tet. Lett., 1976, 17, 1799- 1802 (cmr) [https://doi.org/10.1016/S0040-4039(00)93787-0]
  16. Pomilio, A.B. et al., Phytochemistry, 1979, 18, 1410- 1411 (Sarotanoside) [https://doi.org/10.1016/0031-9422(79)83040-X]
  17. Tanaka, N. et al., Chem. Pharm. Bull., 1980, 28, 2843- 2845 (Pinocembroside) [https://doi.org/10.1248/cpb.28.2843]
  18. González, M.D. et al., Phytochemistry, 1981, 20, 1174- 1175 (7-(2'''-acetylneohesperidoside)) [https://doi.org/10.1016/0031-9422(81)83063-4]
  19. Ripperberger, H., Phytochemistry, 1981, 20, 1757- 1758 (4'''-Acetylsarotanoside) [https://doi.org/10.1016/S0031-9422(00)98578-9]
  20. Jaipetch, T. et al., Aust. J. Chem., 1982, 35, 351- 361 ((±)-Pinocembrin, (±)-Pinostrobin,Boesenbergia pandurata constit) [https://doi.org/10.1071/CH9820351]
  21. 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]
  22. The Flavonoids: Advances in Research, (eds. Harborne, J.B. et al), Chapman and Hall, 1982, 360 (occur)
  23. Bohlmann, F. et al., Phytochemistry, 1984, 23, 1338- 1339 (7-O-Prenylpinocembrin) [https://doi.org/10.1016/S0031-9422(00)80458-6]
  24. 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]
  25. Bohlmann, F. et al., Planta Med., 1984, 50, 271- 272 (5-Methoxy-7-prenyloxyflavanone) [https://doi.org/10.1055/s-2007-969699]
  26. Talapatra, B. et al., Indian J. Chem., Sect. B, 1985, 24, 561 (Pinocembrin, synth)
  27. Kaouadji, M. et al., J. Nat. Prod., 1986, 49, 153- 155 (7-O-Prenylpinocembrin) [https://doi.org/10.1021/np50043a023]
  28. Jakupovic, J. et al., Phytochemistry, 1987, 26, 803- 807 (hydroxyethylphenyl ether) [https://doi.org/10.1016/S0031-9422(00)84791-3]
  29. Fukui, H. et al., Chem. Pharm. Bull., 1988, 36, 4174- 4176 (Pinocembrin, activity) [https://doi.org/10.1248/cpb.36.4174]
  30. Kapetanidis, J. et al., Pharm. Acta Helv., 1988, 63, 206- 208 (7-rutinoside)
  31. Tomimori, T. et al., Shoyakugaku Zasshi, 1988, 42, 98- 101 (7-glucuronide)
  32. The Flavonoids: Advances in Research Since 1980, (ed. Harborne, J.B.), Chapman and Hall, 1988, 358 (occur)
  33. González, A.G. et al., Phytochemistry, 1989, 28, 2871- 2872 (Salvia texana constit) [https://doi.org/10.1016/S0031-9422(00)98114-7]
  34. Shoja, M., Z. Kristallogr., Kristallgeom., Kristallphys., Kristallchem., 1989, 189, 89- 93 (cryst struct, Pinostrobin)
  35. Krause, M. et al., J. Chromatogr., A, 1990, 502, 287- 296 (chiral hplc, Pinocembrin) [https://doi.org/10.1016/S0021-9673(01)89593-5]
  36. Jung, J.H. et al., Phytochemistry, 1990, 29, 1271- 1275 (cmr) [https://doi.org/10.1016/0031-9422(90)85441-H]
  37. Geibel, M. et al., Phytochemistry, 1991, 30, 1519- 1521 (Prunus cerasus constit) [https://doi.org/10.1016/0031-9422(91)84200-C]
  38. Randriaminahy, M. et al., Z. Naturforsch., C, 1992, 47, 10- 16 (neryl ether)
  39. Yuniong, X. et al., Phytochemistry, 1993, 33, 510- 511 (Onychin) [https://doi.org/10.1016/0031-9422(93)85552-3]
  40. 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]
  41. Hoeneison, M. et al., Phytochemistry, 1993, 34, 1653 (7-benzoyl) [https://doi.org/10.1016/S0031-9422(00)90867-7]
  42. Fukui, H. et al., Phytochemistry, 1993, 34, 1653 (Pinocembrin, activity)
  43. Houghton, P.J. et al., Pharm. Pharmacol. Lett., 1997, 7, 96- 98 (Pinocembrin, activity)
  44. Huang, Y.-L. et al., J. Nat. Prod., 1998, 61, 523- 524 (HHDP derivs) [https://doi.org/10.1021/np970428k]
  45. Meekes, M. et al., Phytomedicine, 1998, 5, 459- 463 (Pinostrobin, activity) [https://doi.org/10.1016/S0944-7113(98)80042-1]
  46. Tip-Pyang, S. et al., ACGC Chem. Res. Commun., 2000, 10, 21- 26 (Pinocembrin,Pinostrobin, Alpinetin, activity)
  47. Le Bail, J.-C. et al., Cancer Lett., 2000, 156, 37- 44 (Pinostrobin, activity) [https://doi.org/10.1016/S0304-3835(00)00435-3]
  48. Yuldashev, M.P., Chem. Nat. Compd. (Engl. Transl.), 2001, 37, 224- 225 (Pinocembroside) [https://doi.org/10.1023/A:1012505721054]
  49. Hodgetts, K.J. et al., Tet. Lett., 2001, 42, 3763- 3766 (Pinostrobin, synth) [https://doi.org/10.1016/S0040-4039(01)00567-6]
  50. Lin, J.-H. et al., J. Nat. Prod., 2002, 65, 638- 640 (7-apiosylapiosylglucoside) [https://doi.org/10.1021/np010548z]
  51. Gu, J.-Q. et al., J. Nat. Prod., 2002, 65, 1616- 1620 (±-7-Me ether)
  52. 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]
  53. Leu, Y.-L. et al., Chem. Pharm. Bull., 2004, 52, 858- 860 (Viscum articulatum glycosides) [https://doi.org/10.1248/cpb.52.858]
  54. He, W. et al., Bioorg. Med. Chem., 2005, 13, 1837- 1845 (Alpinetin, activity) [https://doi.org/10.1016/j.bmc.2004.11.038]
  55. 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]
  56. Urgaonkar, S. et al., Org. Lett., 2005, 7, 5609- 5612 ((±)-Pinocembrin, synth) [https://doi.org/10.1021/ol052269z]
  57. Ma, X.-M. et al., Chem. Biodiversity, 2007, 4, 2172- 2181 (isol, pmr, cmr)
  58. Matus-Cádiz, M.A. et al., J. Agric. Food Chem., 2008, 56, 1644- 1653 (7-rhamnoside, occur) [https://doi.org/10.1021/jf072970c]
  59. Yuan, Y. et al., J. Asian Nat. Prod. Res., 2008, 10, 999- 1002 (Pinocembrin, resoln)
  60. Drewes, S.E. et al., Phytochemistry, 2008, 69, 1745- 1749 (Dibenzylpinocembrin, activity) [https://doi.org/10.1016/j.phytochem.2008.02.022]
  61. Jeong, K.-W. et al., J. Nat. Prod., 2009, 72, 719- 724 (Pinocembrin, activity) [https://doi.org/10.1021/np800698d]
  62. Lotti, C. et al., J. Agric. Food Chem., 2010, 58, 2209- 2213 (Mexican propolis constit) [https://doi.org/10.1021/jf100070w]
  63. Chou, T.-S. et al., J. Nat. Prod., 2010, 73, 1470- 1475 (S-form, Pinostrobin, activity) [https://doi.org/10.1021/np100014j]
  64. 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]
  65. Xu, X. et al., J. Agric. Food Chem., 2011, 59, 1205- 1209 (7-neohesperidoside, 7-rutinoside,Litchioside D) [https://doi.org/10.1021/jf104387y]
  66. Allard, P.-M. et al., J. Nat. Prod., 2011, 74, 2446- 2453 (Cryptocarya chartacea constits) [https://doi.org/10.1021/np200715v]
  67. Korenaga, T. et al., Org. Lett., 2011, 13, 2022- 2025 ((-)-Pinostrobin, synth, bibl) [https://doi.org/10.1021/ol2004148]
  68. Katerere, D.R. et al., Fitoterapia, 2012, 83, 932- 940 (Alpinetin, Pinocembrin) [https://doi.org/10.1016/j.fitote.2012.04.011]
  69. Ullah, Z. et al., Nat. Prod. Commun., 2012, 7, 1011- 1014 (Pistacide A)
  70. Ukida, K. et al., Chem. Pharm. Bull., 2013, 61, 1136- 1142 (Schoepfiajasmin G) [https://doi.org/10.1248/cpb.c13-00466]
  71. Wang, M. et al., Nat. Prod. Res., 2014, 28, 70- 73 (S-form, 5-Me ether 7-glucoside)
  72. Vuppalapati, S.V.N. et al., Synthesis, 2014, 46, 465- 474 ((±)-di-Me ether)
  73. Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 95C (ir)
  74. Aldrich Library of 13C and 1H FT-NMR Spectra, 1992, 2, 918C (nmr)
  75. Nadkarni, D.R. et al., JCS, 1938, 1320- 1322 (synth)
  76. Marsh, C.A., Biochem. J., 1955, 59, 58- 62 (7-glucuronopyranoside) [https://doi.org/10.1042/bj0590058]
  77. Katyal, M. et al., Proc. - Indian Acad. Sci., Sect. A, 1962, 56, 125 (detn, Th)
  78. Dev, B. et al., Fresenius' Z. Anal. Chem., 1963, 196, 178- 182 (7-Me ether, synth) [https://doi.org/10.1007/BF00636887]
  79. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms, Tectochrysin)
  80. Katyal, M. et al., Talanta, 1968, 15, 95- 106 (detn, U) [https://doi.org/10.1016/0039-9140(68)80012-8]
  81. Bowie, J.H. et al., JCS(B), 1969, 89- 93 (ms)
  82. Asakawa, Y., Bull. Chem. Soc. Jpn., 1971, 44, 2761- 2766 (Alnus sieboldiana constit) [https://doi.org/10.1246/bcsj.44.2761]
  83. Wagner, H. et al., Chem. Ber., 1972, 105, 257- 261 (7-glucuronoside, 7-rutinoside)
  84. Subramanian, S.S. et al., J. Indian Chem. Soc., 1972, 49, 1061- 1064 (7-rutinoside)
  85. Nevskaya, E.M. et al., Zh. Anal. Khim., 1972, 27, 1699- 1714 (reactions)
  86. Kingston, D.G.I. et al., Tetrahedron, 1973, 29, 4083- 4086 (ms) [https://doi.org/10.1016/0040-4020(73)80241-8]
  87. Thompson, M. et al., Anal. Chim. Acta, 1976, 85, 375- 381 (detn, Cu) [https://doi.org/10.1016/S0003-2670(01)84703-6]
  88. Gaydon, E.M. et al., Bull. Soc. Chim. Fr., Part II, 1978, 43- 47 (synth, uv, cmr)
  89. Garg, S.P. et al., Indian J. Chem., Sect. B, 1979, 17, 416- 417 (7-galactoside)
  90. Jain, P.K. et al., Synthesis, 1982, 221- 223 (synth, 5,7-Dimethoxyflavone) [https://doi.org/10.1055/s-1982-29755]
  91. Jaipetch, T. et al., Phytochemistry, 1983, 22, 625- 626 (Boesenbergia pandurata constit) [https://doi.org/10.1016/0031-9422(83)83075-1]
  92. De Rosa, S. et al., Phytochemistry, 1983, 22, 2323- 2324 (7-gentiobioside) [https://doi.org/10.1016/S0031-9422(00)80175-2]
  93. Agrawal, P.K. et al., Tet. Lett., 1983, 177- 180 (cmr) [https://doi.org/10.1016/S0040-4039(00)81359-3]
  94. Chauhan, J.S. et al., Phytochemistry, 1984, 23, 2404- 2405 (5-xyloside) [https://doi.org/10.1016/S0031-9422(00)80572-5]
  95. Saxena, S. et al., Synthesis, 1985, 697- 698 (synth) [https://doi.org/10.1055/s-1985-31319]
  96. Le Floc'h, Y. et al., Tet. Lett., 1986, 27, 5503- 5504 (synth) [https://doi.org/10.1016/S0040-4039(00)85249-1]
  97. Arriaga-Giner, F.J. et al., Z. Naturforsch., C, 1986, 41, 946- 948 (benzoate)
  98. Nikaido, T. et al., Chem. Pharm. Bull., 1988, 36, 654- 661 (7-glucuronoside, activity) [https://doi.org/10.1248/cpb.36.654]
  99. Yung-Qi, W. et al., Chem. Pharm. Bull., 1988, 36, 3206- 3209 (Citrus funadoko constit) [https://doi.org/10.1248/cpb.36.3206]
  100. The Flavonoids: Advances in Research Since 1980, (ed. Harborne, J.B.), Chapman and Hall, 1988
  101. Chantrapromma, K. et al., Aust. J. Chem., 1989, 42, 2289- 2293 (Uvaria rufas constit, cryst struct, Tectochrysin) [https://doi.org/10.1071/CH9892289]
  102. Jung, J.H. et al., Phytochemistry, 1990, 29, 1271- 1275 (pmr, cmr) [https://doi.org/10.1016/0031-9422(90)85441-H]
  103. Geibel, M. et al., Phytochemistry, 1990, 29, 1351- 1353 (Tectochrysin 5-glucoside) [https://doi.org/10.1016/0031-9422(90)85467-T]
  104. Liu, Q. et al., Phytochemistry, 1993, 34, 167- 170 (Aequinoctin)
  105. Shen, C.-C. et al., Phytochemistry, 1993, 34, 843- 845 (pmr, cmr) [https://doi.org/10.1016/0031-9422(93)85370-7]
  106. Mayer, R., Planta Med., 1993, 59, 269- 271 (5,7-Dimethoxyflavone) [https://doi.org/10.1055/s-2006-959667]
  107. Litkei, G. et al., Annalen, 1995, 1711- 1715 (synth, pmr)
  108. Hounghton, P.J. et al., Pharm. Pharmacol. Lett., 1997, 7, 96- 98 (activity)
  109. Rashad, M.A. et al., Phytomedicine, 1998, 5, 375- 381 (activity)
  110. Lee, J.-M. et al., Synthesis, 2001, 2247- 2254 (synth, pmr, cmr) [https://doi.org/10.1055/s-2001-18436]
  111. Montoro, P. et al., J. Agric. Food Chem., 2002, 49, 5156- 5160 (7-4-rhamnosylglucoside) [https://doi.org/10.1021/jf010318q]
  112. Pistelli, L. et al., Fitoterapia, 2003, 74, 417- 419 (Progenin, Calycotome villosa constit) [https://doi.org/10.1016/S0367-326X(03)00061-3]
  113. El Antri, A. et al., Molecules, 2004, 9, 568- 573 (7-6-acetylglucoside)
  114. Ahmed-Belkacem, A. et al., Cancer Res., 2005, 65, 4852- 4860 (Tectochrysin, pharmacol) [https://doi.org/10.1158/0008-5472.CAN-04-1817]
  115. Leu, S.J. et al., Biol. Pharm. Bull., 2006, 29, 740- 745 (Toringin, activity) [https://doi.org/10.1248/bpb.29.740]
  116. Park, Y. et al., Magn. Reson. Chem., 2007, 45, 674- 679, 1072 - 1075 (pmr, cmr)
  117. Berthier, A. et al., Planta Med., 2007, 73, 1447- 1451 (Progenin, activity) [https://doi.org/10.1055/s-2007-990248]
  118. Nallasivam, A. et al., Acta Cryst. E, 2008, 64, o2490- o2491 (dibenzyl ether, synth, cryst struct)
  119. Kraus, G.A. et al., Synthesis, 2008, 2427- 2431 (synth, pmr, cmr) [https://doi.org/10.1055/s-2008-1078597]
  120. Tashmatov, Z.O. et al., Chem. Nat. Compd. (Engl. Transl.), 2011, 47, 547- 549 (Schachristanoside)
  121. Uddin, N. et al., Phytochem. Lett., 2011, 4, 454- 458 (Lawsochrysinin) [https://doi.org/10.1016/j.phytol.2011.05.007]
  122. Chaipech, S. et al., Chem. Pharm. Bull., 2012, 60, 62- 69 (Kaempferia parviflora constit) [https://doi.org/10.1248/cpb.60.62]
  123. Senejoux, F. et al., Fitoterapia, 2012, 83, 377- 382 (Chrysin, Ziziphora clinopodioides constit,activity) [https://doi.org/10.1016/j.fitote.2011.11.023]
  124. Sermboonpaisarn, T. et al., Fitoterapia, 2012, 83, 780- 784 (Ficus foveolata constit, activity) [https://doi.org/10.1016/j.fitote.2012.03.009]
  125. Zhong, L. et al., Nat. Prod. Res., 2012, 26, 307- 313 (Chrysin, Populus nigra constits,activity)
  126. Ukida, K. et al., Chem. Pharm. Bull., 2013, 61, 1136- 1142 (Schoepfiajasmin H) [https://doi.org/10.1248/cpb.c13-00466]
  127. Dubrovskiy, A.V. et al., Tetrahedron, 2013, 69, 2789- 2798 (5,7-Dimethoxyflavone, synth) [https://doi.org/10.1016/j.tet.2013.01.078]
  128. Kim, K. et al., Org. Lett., 2015, 17, 2550- 2553 (synth, pmr, cmr) [https://doi.org/10.1021/acs.orglett.5b01138]
  129. Mani, R. et al., Phytochemistry, 2018, 145, 187- 196 (Chrysin, rev) [https://doi.org/10.1016/j.phytochem.2017.09.016]
  130. Cooper, R. et al., JACS, 1980, 102, 7953- 7955 (Myricoside) [https://doi.org/10.1021/ja00547a032]
  131. Kudo, K. et al., Planta Med., 1980, 40, 250- 261 (1-glucoside) [https://doi.org/10.1055/s-2008-1074966]
  132. Nishibe, S. et al., Chem. Pharm. Bull., 1982, 30, 1048- 1050 (Forsythiaside) [https://doi.org/10.1248/cpb.30.1048]
  133. Nonaka, G. et al., Chem. Pharm. Bull., 1982, 30, 2061- 2067 (6-galloylglucoside) [https://doi.org/10.1248/cpb.30.2061]
  134. Miyase, T. et al., Chem. Pharm. Bull., 1982, 30, 2732- 2737 (Acteoside, Leucosceptosides) [https://doi.org/10.1248/cpb.30.2732]
  135. Endo, K. et al., Heterocycles, 1982, 19, 261- 264 (Forsythoside B)
  136. Andary, C. et al., Phytochemistry, 1982, 21, 1123- 1127; 1985, 24, 362 - 364 (Acteoside,Poliumoside, Verbascoside) [https://doi.org/10.1016/S0031-9422(00)82429-2]
  137. Schilling, G. et al., Z. Naturforsch., B, 1982, 37, 1633- 1635 (Isoacteoside)
  138. Becker, H. et al., Z. Naturforsch., C, 1982, 37, 351- 353 (Echinacoside)
  139. Nakanishi, K. et al., CA, 1983, 98, 122834u, 194947f (Myricoside)
  140. Endo, K. et al., Can. J. Chem., 1984, 62, 2011- 2014 (Forsythoside E) [https://doi.org/10.1139/v84-343]
  141. Kobayashi, H. et al., Chem. Pharm. Bull., 1984, 32, 3880- 3885, 3009 - 3014 (Echinacoside,2-Acetylacteoside, Osmanthuside B) [https://doi.org/10.1248/cpb.32.3880]
  142. Andary, C. et al., J. Nat. Prod., 1985, 48, 778- 783 (Pheliposide) [https://doi.org/10.1021/np50041a010]
  143. Nicoletti, M. et al., Gazz. Chim. Ital., 1986, 116, 431- 433 (Calceolariosides A,B)
  144. Lahloub, M.F. et al., Planta Med., 1986, 52, 352- 355 (Ehrenoside) [https://doi.org/10.1055/s-2007-969182]
  145. Karasawa, H. et al., Yakugaku Zasshi, 1986, 106, 562- 566, 721 - 724 (Verbasoside,Cistanoside H) [https://doi.org/10.1248/yakushi1947.106.7_562]
  146. Andary, C. et al., Z. Naturforsch., C, 1986, 41, 18- 21 (Stachyoside)
  147. Kobayashi, H. et al., Chem. Pharm. Bull., 1987, 35, 3309- 3314 (Tubulosides) [https://doi.org/10.1248/cpb.35.3309]
  148. Konishi, T. et al., Chem. Pharm. Bull., 1987, 35, 4155- 4161 (Rossicaside A) [https://doi.org/10.1248/cpb.35.4155]
  149. Calis, I. et al., Phytochemistry, 1987, 26, 2057- 2061; 1988, 27, 1465 - 1468; 1989, 28, 1787 (Angorosides)
  150. Shimomura, H. et al., Phytochemistry, 1987, 26, 2363- 2366; 1988, 27, 4019 (Grayanoside B) [https://doi.org/10.1016/S0031-9422(00)84720-2]
  151. Matsumoto, M. et al., Phytochemistry, 1987, 26, 3225- 3227 (Purpureasides) [https://doi.org/10.1016/S0031-9422(00)82474-7]
  152. Kikuchi, M. et al., Yakugaku Zasshi, 1987, 107, 350- 354; 108, 647 - 652 (Isosyringalide,Neosyringalide) [https://doi.org/10.1248/yakushi1947.107.5_350]
  153. Hasegawa, T. et al., Chem. Pharm. Bull., 1988, 36, 1245- 1248 (Magnolosides) [https://doi.org/10.1248/cpb.36.1245]
  154. Basaran, A.A. et al., Helv. Chim. Acta, 1988, 71, 1483- 1490; 1989, 72, 631§ (Lavandulifolioside A)
  155. Takeda, Y., J. Nat. Prod., 1988, 51, 180- 183 (Phtheirospermoside) [https://doi.org/10.1021/np50055a033]
  156. Nicoletti, M. et al., Phytochemistry, 1988, 27, 639- 641 (Calceolarioside C) [https://doi.org/10.1016/0031-9422(88)83164-9]
  157. Gross, G.A. et al., Phytochemistry, 1988, 27, 1459- 1463 (Teucrioside) [https://doi.org/10.1016/0031-9422(88)80215-2]
  158. Cheminat, A. et al., Phytochemistry, 1988, 27, 2787- 2794 (6''-Caffeoylechinacoside,Echinacoside) [https://doi.org/10.1016/0031-9422(88)80664-2]
  159. Ravn, H. et al., Phytochemistry, 1988, 27, 3433- 3437; 1990, 29, 3627 - 3631 (Plantamajoside) [https://doi.org/10.1016/0031-9422(88)80744-1]
  160. Badouin, G. et al., Planta Med., 1988, 54, 321- 323 (Lugrandoside) [https://doi.org/10.1055/s-2006-962445]
  161. Andary, C. et al., Phytochemistry, 1989, 28, 288- 290 (Crassifolioside) [https://doi.org/10.1016/0031-9422(89)85064-2]
  162. Sasaki, H. et al., Phytochemistry, 1989, 28, 875- 879 (Jionosides) [https://doi.org/10.1016/0031-9422(89)80134-7]
  163. Sasaki, H. et al., Planta Med., 1989, 55, 458- 462 (Jionosides) [https://doi.org/10.1055/s-2006-962064]
  164. Kikuchi, M. et al., CA, 1990, 112, 52193 (Syringalide C)
  165. Yoshizawa, F. et al., Chem. Pharm. Bull., 1990, 38, 1927- 1930 (Tubuloside E) [https://doi.org/10.1248/cpb.38.1927]
  166. Sugiyama, M. et al., Chem. Pharm. Bull., 1990, 38, 2953- 2955 (Osmanthuside E) [https://doi.org/10.1248/cpb.38.2953]
  167. Endo, K. et al., Heterocycles, 1990, 30, 291- 294 (Forsythosides) [https://doi.org/10.3987/COM-89-S36]
  168. Calis, I. et al., Phytochemistry, 1990, 29, 1253- 1257; 1992, 31, 357 - 359 (Phlinosides,Leonosides) [https://doi.org/10.1016/0031-9422(90)85436-J]
  169. Nishimura, H. et al., Phytochemistry, 1990, 29, 3303- 3306; 1991, 30, 965 - 969 (Verbasoside) [https://doi.org/10.1016/0031-9422(90)80204-T]
  170. Yamahara, J. et al., Yakugaku Zasshi, 1990, 110, 652- 657, 932 - 935 (Stachysosides A-C,struct, activity) [https://doi.org/10.1248/yakushi1947.110.12_932]
  171. Oganesyan, G.B. et al., Chem. Nat. Compd. (Engl. Transl.), 1991, 27, 556- 559 (Teupolioside) [https://doi.org/10.1007/BF00630353]
  172. Kasai, R. et al., Chem. Pharm. Bull., 1991, 39, 927- 929 (Isoacteoside, Calceolarioside E,Isonuomioside A) [https://doi.org/10.1248/cpb.39.927]
  173. Kikuchi, Y. et al., Chem. Pharm. Bull., 1991, 39, 1047- 1050 (Scutellaria prostrata constits) [https://doi.org/10.1248/cpb.39.1047]
  174. Boros, C.A., J. Nat. Prod., 1991, 54, 506- 513 (2-Acetylrossicaside A) [https://doi.org/10.1021/np50074a024]
  175. Nishimura, H. et al., Phytochemistry, 1991, 30, 965- 969 (Stachysosides A-C) [https://doi.org/10.1016/0031-9422(91)85288-B]
  176. Liu, Z. et al., Phytochemistry, 1991, 30, 1341- 1344 (Pedicularioside A)
  177. Miyase, T. et al., Phytochemistry, 1991, 30, 2015- 2018 (Plantainosides) [https://doi.org/10.1016/0031-9422(91)85059-9]
  178. Calis, I. et al., Phytochemistry, 1991, 30, 3073- 3075 (Phlinosides) [https://doi.org/10.1016/S0031-9422(00)98255-4]
  179. Lahloub, M.F. et al., Planta Med., 1991, 57, 481- 485 (2'-Acetylpoliumoside) [https://doi.org/10.1055/s-2006-960177]
  180. Jia, Z.-J. et al., Gaodeng Xuexiao Huaxue Xuebao, 1992, 13, 481- 482 (Pedicularioside G)
  181. Calis, I. et al., Phytochemistry, 1992, 31, 3624- 3626 (Alyssonoside) [https://doi.org/10.1016/0031-9422(92)83740-P]
  182. He, Z. et al., CA, 1993, 118, 209388 (Ligupurpuroside A)
  183. Sasahara, M. et al., CA, 1993, 118, 219591g (Isoplantamajoside)
  184. Yamamoto, A. et al., Phytochemistry, 1993, 32, 421- 425 (Buddleja davidii constits) [https://doi.org/10.1016/S0031-9422(00)95007-6]
  185. Ofterdinger-Daegel, S. et al., Phytochemistry, 1993, 33, 1211- 1213 (Penprosides) [https://doi.org/10.1016/0031-9422(93)85051-R]
  186. Damtoft, S. et al., Phytochemistry, 1993, 34, 239- 243 (Paucifloside) [https://doi.org/10.1016/S0031-9422(00)90811-2]
  187. Zhong-Jian, J. et al., Phytochemistry, 1993, 34, 1188- 1190 (Pedicularioside M) [https://doi.org/10.1016/S0031-9422(00)90744-1]
  188. Rothenburger, J. et al., Annalen, 1994, 1113- 1115 (Forsythoside F)
  189. Jia, Z.J. et al., Indian J. Chem., Sect. B, 1994, 33, 460- 464 (cis-Leucosceptoside, cis-Martynoside)
  190. Jimenez, C. et al., Nat. Prod. Rep., 1994, 591- 606 (rev)
  191. He, Z.-D. et al., Phytochemistry, 1994, 36, 709- 716 (Lipedosides)
  192. Damtoft, S. et al., Phytochemistry, 1994, 37, 441- 443 (Chiritosides) [https://doi.org/10.1016/0031-9422(94)85075-5]
  193. Aoshima, H. et al., Phytochemistry, 1994, 37, 547- 550 (Isopersicoside) [https://doi.org/10.1016/0031-9422(94)85097-6]
  194. Mahato, S.B. et al., Tetrahedron, 1994, 50, 9439- 9446 (Lantanaside) [https://doi.org/10.1016/S0040-4020(01)85518-6]
  195. Saracoglu, I. et al., Biol. Pharm. Bull., 1995, 18, 1396- 1400 (Teucrioside) [https://doi.org/10.1248/bpb.18.1396]
  196. Wada, H. et al., Chem. Pharm. Bull., 1995, 43, 461- 465 (4-caffeoylalloside) [https://doi.org/10.1248/cpb.43.461]
  197. Brieger, D. et al., Pharmazie, 1995, 50, 707- 708 (Maxoside)
  198. Budzianowski, J. et al., Phytochemistry, 1995, 38, 997- 1001 (Lamalboside) [https://doi.org/10.1016/0031-9422(94)00727-B]
  199. Ismail, L.D. et al., Phytochemistry, 1995, 39, 1391- 1393 (Acetylmethylverbascosides) [https://doi.org/10.1016/0031-9422(95)00172-4]
  200. Ma, W. et al., Yunnan Zhiwu Yanjiu, 1995, 17, 96- 102 (Hemiphroside B)
  201. Canigueral, S. et al., J. Nat. Prod., 1996, 59, 419- 422 (Myconoside) [https://doi.org/10.1021/np960204m]
  202. Liu, Y. et al., Phytochemistry, 1996, 42, 1203; 1998, 48, 339 - 343 (Paucifloside, Lysionotoside) [https://doi.org/10.1016/0031-9422(96)00066-0]
  203. Miyase, T. et al., Phytochemistry, 1996, 43, 475- 479 (Betonyosides) [https://doi.org/10.1016/0031-9422(96)00322-6]
  204. Jensen, S.R. et al., Phytochemistry, 1996, 43, 777- 783 (Sanangoside, Conandroside) [https://doi.org/10.1016/0031-9422(96)00186-0]
  205. Toyota, M. et al., Phytochemistry, 1996, 43, 1087- 1088 (1-alloside) [https://doi.org/10.1016/S0031-9422(96)00504-3]
  206. Saracoglu, I. et al., Fitoterapia, 1997, 68, 434- 438 (Angoroside A, activity)
  207. Wong, C.Z. et al., Indian J. Chem., Sect. B, 1997, 36, 150- 153 (cis-Isoverbascoside)
  208. Mathuram, V. et al., J. Indian Chem. Soc., 1997, 74, 653- 655 (Nyctoside A)
  209. Gafner, S. et al., Phytochemistry, 1997, 44, 687- 690 (Newbouldioside) [https://doi.org/10.1016/S0031-9422(96)00611-5]
  210. Seidel, V. et al., Phytochemistry, 1997, 44, 691- 693 (Ballotetroside) [https://doi.org/10.1016/S0031-9422(96)00578-X]
  211. Kernan, M.R. et al., J. Nat. Prod., 1998, 61, 564- 570 (Luteosides) [https://doi.org/10.1021/np9703914]
  212. Benkrief, R. et al., Phytochemistry, 1998, 47, 825- 832 (Acteoside, Acteoside 6-cinnamate) [https://doi.org/10.1016/S0031-9422(97)00994-1]
  213. Franzyk, H. et al., Phytochemistry, 1998, 47, 1161- 1162 (Plantalloside) [https://doi.org/10.1016/S0031-9422(98)80092-7]
  214. Greca, M.D. et al., Phytochemistry, 1998, 49, 1299- 1304 (glucoside) [https://doi.org/10.1016/S0031-9422(98)00092-2]
  215. Su, B.N. et al., Planta Med., 1998, 64, 720- 723 (Artselaeroside B)
  216. Ozipek, M. et al., Chem. Pharm. Bull., 1999, 47, 561- 562 (Fuhsioside) [https://doi.org/10.1248/cpb.47.561]
  217. Park, H.-J. et al., Chem. Pharm. Bull., 1999, 47, 1029- 1031 (1-glucoside) [https://doi.org/10.1248/cpb.47.1029]
  218. Calis, I. et al., Chem. Pharm. Bull., 1999, 47, 1305- 1307 (Ferruginosides) [https://doi.org/10.1248/cpb.47.1305]
  219. Skrzypek, Z. et al., J. Nat. Prod., 1999, 62, 127- 129 (cis-Leucosceptoside) [https://doi.org/10.1021/np970465b]
  220. Kalpoutzakis, E. et al., J. Nat. Prod., 1999, 62, 342- 344 (Angorosides) [https://doi.org/10.1021/np980351f]
  221. Miyase, T. et al., J. Nat. Prod., 1999, 62, 1079- 1084 (Scrophulosides) [https://doi.org/10.1021/np9805746]
  222. Calis, I. et al., J. Nat. Prod., 1999, 62, 1165- 1168 (Trichosanthosides) [https://doi.org/10.1021/np9900526]
  223. Kawada, T. et al., JOC, 1999, 64, 9268- 9271 (Acteoside, synth) [https://doi.org/10.1021/jo9906983]
  224. Pradhan, K.J. et al., Lebensm.-Wiss. Technol., 1999, 32, 121- 123 (glucopyranoside,activity) [https://doi.org/10.1006/fstl.1998.0508]
  225. Iossifova, T. et al., Phytochemistry, 1999, 50, 297- 301 (Isolugrandoside) [https://doi.org/10.1016/S0031-9422(98)00538-X]
  226. Kisiel, W. et al., Phytochemistry, 1999, 51, 1083- 1085 (Isobetonyoside F) [https://doi.org/10.1016/S0031-9422(99)00167-3]
  227. Elgindi, M.R. et al., Asian J. Chem., 2000, 12, 127- 130 (Verbascum sinaiticum glycosides)
  228. Zaghloul, M.G. et al., CA, 2000, 133, 347105y (Crassoside)
  229. Gao, J. et al., Chem. Pharm. Bull., 2000, 48, 1075- 1078 (Incanoside C) [https://doi.org/10.1248/cpb.48.1075]
  230. Galindez, J. de S. et al., Magn. Reson. Chem., 2000, 38, 688- 391 (Angoroside D)
  231. Heilmann, J. et al., Planta Med., 2000, 66, 746- 748 (Lugrandoside, Calceolarioside A,activity) [https://doi.org/10.1055/s-2000-9566]
  232. Kyriakopoulou, I. et al., J. Nat. Prod., 2001, 64, 1095- 1097 (Samioside) [https://doi.org/10.1021/np010128+]
  233. Kanchanapoom, T. et al., Phytochemistry, 2001, 57, 1245- 1248 (2''-Apiosylverbascoside) [https://doi.org/10.1016/S0031-9422(01)00212-6]
  234. Saracoglu, I. et al., Chem. Pharm. Bull., 2002, 50, 665- 668 (Verpectosides, Ehrenoside) [https://doi.org/10.1248/cpb.50.665]
  235. Harput, U.S. et al., Chem. Pharm. Bull., 2002, 50, 869- 871 (Persicoside) [https://doi.org/10.1248/cpb.50.869]
  236. Chakravarty, A.K. et al., Chem. Pharm. Bull., 2002, 50, 1616- 1618 (Monnierasides) [https://doi.org/10.1248/cpb.50.1616]
  237. Hou, C.-C. et al., J. Nat. Prod., 2002, 65, 1759- 1763 (Bacopaside B) [https://doi.org/10.1021/np020238w]
  238. Sahpaz, S. et al., Nat. Prod. Lett., 2002, 16, 195- 199 (Marruboside) [https://doi.org/10.1080/10575630290013576]
  239. Kanchanapoom, T. et al., Phytochemistry, 2002, 59, 557- 563, 565 - 570 (Markhamiosides, Acetylacteosides) [https://doi.org/10.1016/S0031-9422(01)00466-6]
  240. Arnold, U.W. et al., Z. Naturforsch., C, 2002, 57, 969- 975 (2'-Acetylpurpureaside A, 2',6''-Diacetylpurpureaside A) [https://doi.org/10.1515/znc-2002-11-1202]
  241. Munkombwe, N.M., Phytochemistry, 2003, 62, 1231- 1234 (6-Acetylacteoside, 2,6-Diacetylacteoside) [https://doi.org/10.1016/S0031-9422(02)00700-8]
  242. Bedir, E. et al., Phytochemistry, 2003, 63, 977- 983 (Teucriosides) [https://doi.org/10.1016/S0031-9422(03)00378-9]
  243. Rønsted, N. et al., Phytochemistry, 2003, 64, 529- 533 (Aragoside) [https://doi.org/10.1016/S0031-9422(03)00157-2]
  244. Karioti, A. et al., Phytochemistry, 2003, 64, 655- 660 (Velutinosides) [https://doi.org/10.1016/S0031-9422(03)00242-5]
  245. Abougazar, H. et al., Planta Med., 2003, 69, 814- 819 (Wiedemanniosides)
  246. Zheng, X.-K. et al., Yaoxue Xuebao, 2003, 38, 116- 119, 268 - 271 (Corallodiscus flabellata glycosides)
  247. Saracoglu, I. et al., Z. Naturforsch., C, 2003, 58, 820- 825 (Integrifolioside A) [https://doi.org/10.1515/znc-2003-11-1213]
  248. Wang, H. et al., Chem. Pharm. Bull., 2004, 52, 615- 617 (Scroside D) [https://doi.org/10.1248/cpb.52.615]
  249. Tanaka, T. et al., Chem. Pharm. Bull., 2004, 52, 1242- 1245 (Cusianosides A,B) [https://doi.org/10.1248/cpb.52.1242]
  250. Huang, S.-X. et al., Helv. Chim. Acta, 2004, 87, 598- 604 (Scrosides, Hemiphroside B)
  251. Kirmizibekmez, H. et al., Helv. Chim. Acta, 2004, 87, 1172- 1179 (Globusintenoside)
  252. Ho, J.-C. et al., J. Chin. Chem. Soc. (Taipei), 2004, 51, 1073- 1076 (2,3'-Diacetylacteoside)
  253. Calis, I. et al., Phytochemistry, 2004, 65, 2619- 2625 (Lunariifolioside) [https://doi.org/10.1016/j.phytochem.2004.04.038]
  254. Lin, L.-C. et al., Planta Med., 2004, 70, 50- 53 (Caerulescenoside)
  255. Zhou, L. et al., Yunnan Zhiwu Yanjiu, 2004, 26, 349- 354 (Brandisia hancei galactoside)
  256. Es-Safi, N.E. et al., J. Nat. Prod., 2005, 68, 1293- 1296 (Neosyringalide) [https://doi.org/10.1021/np0501233]
  257. Calis, I. et al., Nat. Prod. Res., 2005, 19, 493- 501 (Oppositifloroside, Myricoside)
  258. Chang, J. et al., Phytochemistry, 2005, 66, 2752- 2758 (Cuneataside C) [https://doi.org/10.1016/j.phytochem.2005.09.018]
  259. Koo, K.A. et al., Planta Med., 2005, 71, 778- 780 (cis-Tubuloside E)
  260. Lu, J.-H. et al., Z. Naturforsch., B, 2005, 60, 211- 214 (Buddleoside A)
  261. Yoshikawa, M. et al., Bioorg. Med. Chem., 2006, 14, 7468- 7475 (Kankanoside F) [https://doi.org/10.1016/j.bmc.2006.07.018]
  262. Ito, N. et al., Chem. Pharm. Bull., 2006, 54, 1705- 1708 (Lamiusides A-C) [https://doi.org/10.1248/cpb.54.1705]
  263. Tu, P.-F. et al., Helv. Chim. Acta, 2006, 89, 927- 935 (Cistantubulosides B1,B2)
  264. Ahmad, V.U. et al., J. Asian Nat. Prod. Res., 2006, 8, 105- 111 (Parviflorosides A,B)
  265. Sinaphet, B. et al., J. Nat. Med. (Tokyo), 2006, 60, 251- 254 (Dolichandroside)
  266. Jo, Y. et al., J. Nat. Prod., 2006, 69, 1399- 1403 (Ternstrosides A-D) [https://doi.org/10.1021/np060096w]
  267. Taskova, R.M. et al., Phytochemistry, 2006, 67, 286- 301 (Hebeoside) [https://doi.org/10.1016/j.phytochem.2005.11.011]
  268. Gormann, R. et al., Phytochemistry, 2006, 67, 805- 811 (Newbouldiosides A-C) [https://doi.org/10.1016/j.phytochem.2006.01.016]
  269. Marzouk, M. et al., Z. Naturforsch., C, 2006, 61, 783- 791 (Tecoma stans diglycoside)
  270. Pedersen, P. et al., Biochem. Syst. Ecol., 2007, 35, 777- 784 (Cuproside) [https://doi.org/10.1016/j.bse.2007.06.011]
  271. Lei, L. et al., Helv. Chim. Acta, 2007, 90, 79- 85 (Salsaside F)
  272. Qu, J.-B. et al., Helv. Chim. Acta, 2007, 90, 2109- 2115 (Marchantia polymorpha constits)
  273. Yamasaki, T. et al., J. Nat. Med. (Tokyo), 2007, 61, 318- 322 (2-O-Acetylforsythoside B)
  274. Lin, S. et al., J. Nat. Prod., 2007, 70, 817- 823 (6-apiosylglucoside) [https://doi.org/10.1021/np0700467]
  275. Mostafa, M. et al., Nat. Prod. Res., 2007, 21, 354- 361 (3'''-O-Methylpoliumoside)
  276. Kostadinova, E.P. et al., Phytochemistry, 2007, 68, 1321- 1326 (Turrilliosides A,B) [https://doi.org/10.1016/j.phytochem.2007.02.014]
  277. Kirmizibekmez, H. et al., Helv. Chim. Acta, 2008, 91, 1525- 1532 (Galypumosides A,B,C)
  278. Huong, N.T.H. et al., J. Asian Nat. Prod. Res., 2008, 10, 1035- 1038 (6-Menthiafoloylacteoside)
  279. Li, S.-M. et al., Phytochemistry, 2008, 69, 2200- 2204 (Aeschynanthosides A,B,D)
  280. El-Desouky, S.K. et al., Z. Naturforsch., B, 2008, 63, 90- 94 (Forsythia koreana constit)
  281. Jensen, S.R. et al., Biochem. Syst. Ecol., 2009, 37, 421- 425 (Amherstianosides A,B) [https://doi.org/10.1016/j.bse.2009.04.013]
  282. Maggi, A. et al., Biochem. Syst. Ecol., 2009, 37, 731- 736 (Parahebeoside) [https://doi.org/10.1016/j.bse.2009.11.001]
[top⬆]
Anticancer Citations:
  1. Fukuyama, Y. et al., Phytochemistry, 1983, 22, 549- 552 (Hydropiperoside) [https://doi.org/10.1016/0031-9422(83)83043-X]
  2. Hamburger, M. et al., Phytochemistry, 1985, 24, 1793- 1797 (Polygala chamaebuxus constits) [https://doi.org/10.1016/S0031-9422(00)82553-4]
  3. King, R.R. et al., Chem. Comm., 1986, 1078- 1079 (6-octanoyl 3,4-bis-2-methylpropanoyl) [https://doi.org/10.1039/c39860001078]
  4. Nakano, K. et al., Chem. Pharm. Bull., 1986, 34, 5005- 5010 (Heloniosides A-D)
  5. Shimomura, H. et al., Phytochemistry, 1986, 25, 2897- 2899 (diferuloyl) [https://doi.org/10.1016/S0031-9422(00)83765-6]
  6. King, R.R. et al., Carbohydr. Res., 1987, 166, 113- 121 (Solanum berthaultii esters) [https://doi.org/10.1016/0008-6215(87)80048-4]
  7. King, R.R. et al., Carbohydr. Res., 1988, 173, 235- 241 (Solanum neocardenasii esters) [https://doi.org/10.1016/S0008-6215(00)90819-X]
  8. Garegg, P.J. et al., Carbohydr. Res., 1988, 181, 89- 96 (2,3,4-tris-3-methylpentanoyl) [https://doi.org/10.1016/0008-6215(88)84025-4]
  9. Shimomura, H. et al., Chem. Pharm. Bull., 1988, 36, 2430- 2446 (3'-feruloyl, 6-4-glucosylferuloyl) [https://doi.org/10.1248/cpb.36.2430]
  10. Kashiwada, Y. et al., Phytochemistry, 1988, 27, 1469- 1472 (gallates) [https://doi.org/10.1016/0031-9422(88)80217-6]
  11. James, C.E. et al., Prog. Chem. Org. Nat. Prod., 1989, 55, 117- 184 (rev)
  12. King, R.R. et al., Phytochemistry, 1990, 29, 2115- 2118 (Lycopersicon hirsutum esters) [https://doi.org/10.1016/0031-9422(90)83017-U]
  13. Sashida, Y. et al., Chem. Pharm. Bull., 1991, 39, 2362- 2368 (Lilium mackliniae esters) [https://doi.org/10.1248/cpb.39.2362]
  14. Ikeya, Y. et al., Chem. Pharm. Bull., 1991, 39, 2600- 2605 (Tenuifolisides A,B,C) [https://doi.org/10.1248/cpb.39.2600]
  15. De Tommasi, N. et al., J. Nat. Prod., 1993, 56, 134- 137 (Securidaca longipedunculata constits) [https://doi.org/10.1021/np50091a020]
  16. Lou, H. et al., J. Nat. Prod., 1993, 56, 1437- 1443 (Neohancoside D) [https://doi.org/10.1021/np50099a001]
  17. Bashir, A. et al., Phytochemistry, 1993, 32, 741- 745 (Polygala virgata constits) [https://doi.org/10.1016/S0031-9422(00)95164-1]
  18. Lou, H. et al., Phytochemistry, 1993, 32, 1283- 1286 (6-Sinapoylsucrose) [https://doi.org/10.1016/S0031-9422(00)95106-9]
  19. Bashir, A. et al., Phytochemistry, 1993, 32, 1633 (Polygala virgata constits, erratum) [https://doi.org/10.1016/S0031-9422(00)95164-1]
  20. Yamamoto, K. et al., Shoyakugaku Zasshi, 1993, 47, 12- 16 (tetrakis(3-methylbutanoyl),pentakis(3-methylbutanoyl))
  21. Miyase, T. et al., CA, 1994, 120, 240064p (Polygala tenuifolia esters)
  22. Saitoh, H. et al., Chem. Pharm. Bull., 1994, 42, 1879- 1885 (Reinoses A-F) [https://doi.org/10.1248/cpb.42.1879]
  23. Ikeya, Y. et al., Chem. Pharm. Bull., 1994, 42, 2305- 2308 (Tenuifoliside E) [https://doi.org/10.1248/cpb.42.2305]
  24. Zimmermann, M.L. et al., J. Nat. Prod., 1994, 57, 236- 242 (Vanicosides A,B) [https://doi.org/10.1021/np50104a007]
  25. Abdallah, O.M. et al., Phytochemistry, 1994, 37, 1689- 1692 (Prunus ssiori ester) [https://doi.org/10.1016/S0031-9422(00)89593-X]
  26. Harrison, L.J. et al., Phytochemistry, 1995, 38, 1497- 1500 (Bhesa paniculata ester) [https://doi.org/10.1016/0031-9422(94)00314-J]
  27. Lin, W.H. et al., Yaoxue Xuebao, 1995, 30, 752- 756 (Sibiriosides A,B)
  28. Qian-Cutrone, J. et al., J. Nat. Prod., 1996, 59, 196- 199 (Niruriside) [https://doi.org/10.1021/np9600560]
  29. Shirota, O. et al., J. Nat. Prod., 1996, 59, 242- 245 (Sparganium stoloniferum constits) [https://doi.org/10.1021/np960160h]
  30. Shirota, O. et al., Phytochemistry, 1997, 44, 695- 698 (Sparganium stoloniferum constits) [https://doi.org/10.1016/S0031-9422(96)00558-4]
  31. Zhang, D. et al., Phytochemistry, 1997, 45, 733- 741 (Fallaxoses A-E, Reinose D) [https://doi.org/10.1016/S0031-9422(97)00065-4]
  32. Brown, L.L. et al., J. Nat. Prod., 1998, 61, 762- 766 (Vanicosides C-F) [https://doi.org/10.1021/np970581e]
  33. Zhang, D. et al., Phytochemistry, 1998, 47, 45- 52 (Glomeratoses A-D) [https://doi.org/10.1016/S0031-9422(97)00490-1]
  34. Sang, S. et al., Phytochemistry, 1998, 48, 569- 571 (Segetoside A) [https://doi.org/10.1016/S0031-9422(97)00896-0]
  35. Wang, M. et al., J. Nat. Prod., 1999, 62, 454- 456 (6-Caffeoylsucrose) [https://doi.org/10.1021/np980436g]
  36. Miyase, T. et al., J. Nat. Prod., 1999, 62, 993- 996 (Sibiricoses A1-A6) [https://doi.org/10.1021/np990084t]
  37. Moser, D. et al., Pestic. Sci., 1999, 55, 336- 339 (Petunia hybrida esters)
  38. Murakami, N. et al., Bioorg. Med. Chem. Lett., 2000, 10, 2629- 2632 (Atractysucroses) [https://doi.org/10.1016/S0960-894X(00)00536-9]
  39. Tanaka, T. et al., Chem. Pharm. Bull., 2000, 48, 201- 207 (1'-Benzoylsucrose) [https://doi.org/10.1248/cpb.48.201]
  40. Kobayashi, W. et al., J. Nat. Prod., 2000, 63, 1066- 1069 (Arillatose B) [https://doi.org/10.1021/np0000567]
  41. Sun, X. et al., J. Nat. Prod., 2000, 63, 1094- 1097 (Polygonum perfoliatum constits) [https://doi.org/10.1021/np000055e]
  42. Chen, T. et al., Phytochemistry, 2000, 53, 1051- 1055 (Smiglasides A-E) [https://doi.org/10.1016/S0031-9422(99)00522-1]
  43. Wu, Z. et al., Yunnan Zhiwu Yanjiu, 2000, 22, 482- 494 (Arillanins A,B,C)
  44. Chen, C.-C. et al., J. Nat. Prod., 2001, 64, 990- 992 (6-Feruloyl-3'-sinapoylsucrose) [https://doi.org/10.1021/np000582y]
  45. Takasaki, M. et al., J. Nat. Prod., 2001, 64, 1305- 1308 (Lapathosides A-D) [https://doi.org/10.1021/np010222q]
  46. Takara, K. et al., Biosci., Biotechnol., Biochem., 2002, 66, 29- 35 (6-Syringoylsucrose, 6-Vanilloylsucrose)
  47. Li, S.Y. et al., J. Nat. Prod., 2002, 65, 262- 266 (Smilax bracteata glycosides) [https://doi.org/10.1021/np010338m]
  48. Yoshikawa, M. et al., J. Nat. Prod., 2002, 65, 1151- 1155 (Prunoses I,II) [https://doi.org/10.1021/np020058m]
  49. Weckerle, B. et al., Phytochemistry, 2002, 60, 409- 414 (3-methylbutanoyl ester) [https://doi.org/10.1016/S0031-9422(02)00042-0]
  50. Matsuda, H. et al., Chem. Pharm. Bull., 2003, 51, 440- 443 (Prunose III) [https://doi.org/10.1248/cpb.51.440]
  51. Wang, N. et al., Phytochemistry, 2003, 62, 741- 746 (6'-Coumaroylsucrose, 6,6'-Dicoumaroylsucrose) [https://doi.org/10.1016/S0031-9422(02)00454-5]
  52. Singh, A.P. et al., Phytochemistry, 2003, 63, 485- 489 (Petunia nyctaginiflora constits) [https://doi.org/10.1016/S0031-9422(03)00162-6]
  53. Tchinda, A.T. et al., Phytochemistry, 2003, 63, 841- 846 (pentakis-3-methylbutanoyl) [https://doi.org/10.1016/S0031-9422(03)00326-1]
  54. Cheng, Y.-B. et al., Acta Bot. Sin., 2004, 46, 618- 620 (Smiglaside F)
  55. Cervellati, R. et al., Chem. Biodiversity, 2004, 1, 415- 425 (Alpestriose A)
  56. Tian, S. et al., J. Agric. Food Chem., 2004, 52, 4808- 4813 (6-Feruloylsucrose, 6-Sinapoylsucrose) [https://doi.org/10.1021/jf049446f]
  57. Begum, A.S. et al., J. Indian Chem. Soc., 2004, 81, 495- 500 (Petunia nyctaginiflora esters)
  58. Yun, Y.S. et al., Phytochemistry, 2004, 65, 2167- 2171 (Canna edulis constits) [https://doi.org/10.1016/j.phytochem.2004.06.003]
  59. Begum, A.S. et al., Indian J. Chem., Sect. B, 2005, 44, 648- 650 (Petunia nyctaginiflora esters)
  60. Georgopoulou, C. et al., J. Asian Nat. Prod. Res., 2005, 7, 799- 803 (Acretoside)
  61. Ovenden, S.P.B. et al., J. Nat. Prod., 2005, 68, 282- 284 (Physaloside A) [https://doi.org/10.1021/np049746r]
  62. Li, J. et al., J. Nat. Prod., 2005, 68, 739- 744 (Tricornoses A,B) [https://doi.org/10.1021/np050023x]
  63. Itoh, A. et al., J. Nat. Prod., 2005, 68, 848- 852 (6-3,4,5-Trimethoxybenzoylglomeratose A) [https://doi.org/10.1021/np058007n]
  64. Kuo, Y.-H. et al., J. Nat. Prod., 2005, 68, 1475- 1478 (Smilasides A-F) [https://doi.org/10.1021/np050109q]
  65. Georgopoulou, C. et al., Nat. Prod. Res., 2005, 19, 795- 799 (Acretoside)
  66. Kumagai, H. et al., Z. Naturforsch., C, 2005, 60, 39- 44 (Vanicosides A,B) [https://doi.org/10.1515/znc-2005-1-208]
  67. Li, J. et al., Chem. Pharm. Bull., 2006, 54, 1451- 1454 (3',4',6'-Triferuloylsucrose) [https://doi.org/10.1248/cpb.54.1451]
  68. Cheng, M.-C. et al., J. Nat. Prod., 2006, 69, 1305- 1309 (Polygalatenoside D) [https://doi.org/10.1021/np060207r]
  69. Maldonado, E. et al., J. Nat. Prod., 2006, 69, 1511- 1513 (Nicandroses A-E) [https://doi.org/10.1021/np060274l]
  70. Gouda, Y.G. et al., Nat. Prod. Res., 2006, 20, 935- 939 (6-Coumaroylsucrose)
  71. Wang, Y. et al., Chin. Chem. Lett., 2007, 18, 548- 550 (Parispolyside F) [https://doi.org/10.1016/j.cclet.2007.03.011]
  72. Chang, H.-T. et al., Helv. Chim. Acta, 2007, 90, 944- 950 (Telephiose F)
  73. Li, N. et al., J. Asian Nat. Prod. Res., 2007, 9, 373- 377 (Gastrodin A)
  74. Oliveira, P.E.S. et al., Biochem. Syst. Ecol., 2008, 36, 134- 137 (Vanicoside D, cmr) [https://doi.org/10.1016/j.bse.2007.06.001]
  75. Chen, H. et al., J. Asian Nat. Prod. Res., 2008, 10, 248- 251 (6,6'-Disinapoylsucrose)
  76. Xiong, Y. et al., J. Asian Nat. Prod. Res., 2008, 10, 425- 428 (Sparganium 3'-feruloyl acetates)
  77. Zhang, L. et al., Phytochemistry, 2008, 69, 1398- 1404 (Smilasides G-L) [https://doi.org/10.1016/j.phytochem.2008.01.002]
  78. Xiong, Y. et al., Arch. Pharmacal Res., 2009, 32, 717- 720 (1',2,3,6-Tetraacetyl-3'-cis-feruloylsucrose)
  79. Nhiem, N.X. et al., Arch. Pharmacal Res., 2009, 32, 1373- 1377 (Heterosmilaside) [https://doi.org/10.1007/s12272-009-2005-4]
  80. Tanaka, K. et al., Nat. Prod. Commun., 2009, 4, 1095- 1098 (Atractylodes esters)
  81. Wang, P. et al., Phytochemistry, 2009, 70, 430- 436 (Froelichia floridana ester) [https://doi.org/10.1016/j.phytochem.2009.01.017]
  82. Lee, S.Y. et al., Arch. Pharmacal Res., 2010, 33, 515- 521 (1'-Feruloylsucrose) [https://doi.org/10.1007/s12272-010-0404-1]
  83. Kim, K.H. et al., Can. J. Chem., 2010, 88, 519- 523 (Bistorosides A,B)
  84. Hasegawa, T. et al., Heterocycles, 2010, 81, 2763- 2770 (3',6-disinapoyl, 3',6-disinapoyl 3-Ac)
  85. Pérez-Castorena, A.-L. et al., J. Nat. Prod., 2010, 73, 1271- 1276 (Physordinoses A-D) [https://doi.org/10.1021/np100127k]
  86. Chang, C.-L. et al., J. Nat. Prod., 2010, 73, 1482- 1488 (Quiquesetinerviusides A-E) [https://doi.org/10.1021/np100181c]
  87. Wu, X.-Y. et al., Shenyang Yaoke Daxue Xuebao, 2010, 27, 788- 792 (Tenuifoliosides A,B,C)
  88. Lepore, L. et al., Fitoterapia, 2011, 82, 178- 183 (Monnina obtusifolia esters) [https://doi.org/10.1016/j.fitote.2010.08.018]
  89. Dong, L.B. et al., Nat. Prod. Bioprospect., 2011, 1, 41- 47 (1',2,3,4,6-Pentaacetyl-3'-coumaroylsucroses)
  90. Cheng, J.-T. et al., Helv. Chim. Acta, 2012, 95, 1158- 1163 (Equisetum hiemale esters)
  91. Sun, T.-T. et al., J. Asian Nat. Prod. Res., 2012, 14, 165- 170 (Smilasides M,N)
  92. Fan, P. et al., Nat. Prod. Res., 2012, 26, 1413- 1418 (2-Caffeoylsucrose)
  93. Wu, Q. et al., Carbohydr. Res., 2013, 372, 9- 14 (Brassica rapa triisovalerates) [https://doi.org/10.1016/j.carres.2012.09.015]
  94. Jia, C. et al., Carbohydr. Res., 2013, 372, 73- 77 (Komotini basma constit) [https://doi.org/10.1016/j.carres.2013.01.021]
  95. Fujimoto, K. et al., Chem. Pharm. Bull., 2013, 61, 445- 451 (Mumeoses F-J, activity) [https://doi.org/10.1248/cpb.c12-01068]
  96. Ren, Q. et al., Food Chem., 2013, 136, 1377- 1389 (Fagopyrum tataricum constits) [https://doi.org/10.1016/j.foodchem.2012.09.052]
  97. Nakamura, S. et al., J. Nat. Med. (Tokyo), 2013, 67, 799- 806 (Mumeoses K-O, activity)
  98. Zhao, J.-Q. et al., Nat. Prod. Bioprospect., 2013, 3, 61- 65 (Phyllanthus cochinchinensis constits)
  99. Nakamura, S. et al., Phytochemistry, 2013, 92, 128- 136 (Mumeoses A-E) [https://doi.org/10.1016/j.phytochem.2013.04.012]
  100. Zhao, W. et al., Bioorg. Med. Chem. Lett., 2014, 24, 2459- 2462 (Tomensides A-D, activity) [https://doi.org/10.1016/j.bmcl.2014.04.018]
  101. Wang, Y.-J. et al., Tetrahedron, 2014, 70, 3757- 3761 (Tenuifoliside B, synth)
  102. 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]
  103. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 1- 12 (Pinus constits) [https://doi.org/10.3891/acta.chem.scand.05-0001]
  104. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 121- 128 (Pinus constits, chromatogr) [https://doi.org/10.3891/acta.chem.scand.05-0121]
  105. Hasegawa, M. et al., JACS, 1957, 79, 450- 452 (Verecundin) [https://doi.org/10.1021/ja01559a059]
  106. Hasegawa, M. et al., JACS, 1957, 79, 1738- 1740 (Verecundin) [https://doi.org/10.1021/ja01564a056]
  107. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (Pinocembrin, abs config)
  108. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (Alpinetin, pmr) [https://doi.org/10.1071/CH9640428]
  109. Mongkolsuk, S. et al., JCS, 1964, 4654- 4655 ((±)-Pinostrobin, (±)-Alpinetin)
  110. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms)
  111. Aurnhammer, G. et al., Chem. Ber., 1970, 103, 3667- 3673 (Isosarotanoside, Sarotanoside)
  112. 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]
  113. Bick, I.R.C. et al., Aust. J. Chem., 1972, 25, 449- 451 (Eucalyptus sieberi constits) [https://doi.org/10.1071/CH9720449]
  114. The Flavonoids, (eds. Harborne, J.B. et al), Chapman and Hall, 1975, 563 (occur)
  115. Miyakado, M. et al., Phytochemistry, 1976, 15, 846- 847 (Pinocembrin, activity) [https://doi.org/10.1016/S0031-9422(00)94481-9]
  116. Wagner, H. et al., Tet. Lett., 1976, 17, 1799- 1802 (cmr) [https://doi.org/10.1016/S0040-4039(00)93787-0]
  117. Pomilio, A.B. et al., Phytochemistry, 1979, 18, 1410- 1411 (Sarotanoside) [https://doi.org/10.1016/0031-9422(79)83040-X]
  118. Tanaka, N. et al., Chem. Pharm. Bull., 1980, 28, 2843- 2845 (Pinocembroside) [https://doi.org/10.1248/cpb.28.2843]
  119. González, M.D. et al., Phytochemistry, 1981, 20, 1174- 1175 (7-(2'''-acetylneohesperidoside)) [https://doi.org/10.1016/0031-9422(81)83063-4]
  120. Ripperberger, H., Phytochemistry, 1981, 20, 1757- 1758 (4'''-Acetylsarotanoside) [https://doi.org/10.1016/S0031-9422(00)98578-9]
  121. Jaipetch, T. et al., Aust. J. Chem., 1982, 35, 351- 361 ((±)-Pinocembrin, (±)-Pinostrobin,Boesenbergia pandurata constit) [https://doi.org/10.1071/CH9820351]
  122. 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]
  123. The Flavonoids: Advances in Research, (eds. Harborne, J.B. et al), Chapman and Hall, 1982, 360 (occur)
  124. Bohlmann, F. et al., Phytochemistry, 1984, 23, 1338- 1339 (7-O-Prenylpinocembrin) [https://doi.org/10.1016/S0031-9422(00)80458-6]
  125. 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]
  126. Bohlmann, F. et al., Planta Med., 1984, 50, 271- 272 (5-Methoxy-7-prenyloxyflavanone) [https://doi.org/10.1055/s-2007-969699]
  127. Talapatra, B. et al., Indian J. Chem., Sect. B, 1985, 24, 561 (Pinocembrin, synth)
  128. Kaouadji, M. et al., J. Nat. Prod., 1986, 49, 153- 155 (7-O-Prenylpinocembrin) [https://doi.org/10.1021/np50043a023]
  129. Jakupovic, J. et al., Phytochemistry, 1987, 26, 803- 807 (hydroxyethylphenyl ether) [https://doi.org/10.1016/S0031-9422(00)84791-3]
  130. Fukui, H. et al., Chem. Pharm. Bull., 1988, 36, 4174- 4176 (Pinocembrin, activity) [https://doi.org/10.1248/cpb.36.4174]
  131. Kapetanidis, J. et al., Pharm. Acta Helv., 1988, 63, 206- 208 (7-rutinoside)
  132. Tomimori, T. et al., Shoyakugaku Zasshi, 1988, 42, 98- 101 (7-glucuronide)
  133. The Flavonoids: Advances in Research Since 1980, (ed. Harborne, J.B.), Chapman and Hall, 1988, 358 (occur)
  134. González, A.G. et al., Phytochemistry, 1989, 28, 2871- 2872 (Salvia texana constit) [https://doi.org/10.1016/S0031-9422(00)98114-7]
  135. Shoja, M., Z. Kristallogr., Kristallgeom., Kristallphys., Kristallchem., 1989, 189, 89- 93 (cryst struct, Pinostrobin)
  136. Krause, M. et al., J. Chromatogr., A, 1990, 502, 287- 296 (chiral hplc, Pinocembrin) [https://doi.org/10.1016/S0021-9673(01)89593-5]
  137. Jung, J.H. et al., Phytochemistry, 1990, 29, 1271- 1275 (cmr) [https://doi.org/10.1016/0031-9422(90)85441-H]
  138. Geibel, M. et al., Phytochemistry, 1991, 30, 1519- 1521 (Prunus cerasus constit) [https://doi.org/10.1016/0031-9422(91)84200-C]
  139. Randriaminahy, M. et al., Z. Naturforsch., C, 1992, 47, 10- 16 (neryl ether)
  140. Yuniong, X. et al., Phytochemistry, 1993, 33, 510- 511 (Onychin) [https://doi.org/10.1016/0031-9422(93)85552-3]
  141. 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]
  142. Hoeneison, M. et al., Phytochemistry, 1993, 34, 1653 (7-benzoyl) [https://doi.org/10.1016/S0031-9422(00)90867-7]
  143. Fukui, H. et al., Phytochemistry, 1993, 34, 1653 (Pinocembrin, activity)
  144. Houghton, P.J. et al., Pharm. Pharmacol. Lett., 1997, 7, 96- 98 (Pinocembrin, activity)
  145. Huang, Y.-L. et al., J. Nat. Prod., 1998, 61, 523- 524 (HHDP derivs) [https://doi.org/10.1021/np970428k]
  146. Meekes, M. et al., Phytomedicine, 1998, 5, 459- 463 (Pinostrobin, activity) [https://doi.org/10.1016/S0944-7113(98)80042-1]
  147. Tip-Pyang, S. et al., ACGC Chem. Res. Commun., 2000, 10, 21- 26 (Pinocembrin,Pinostrobin, Alpinetin, activity)
  148. Le Bail, J.-C. et al., Cancer Lett., 2000, 156, 37- 44 (Pinostrobin, activity) [https://doi.org/10.1016/S0304-3835(00)00435-3]
  149. Yuldashev, M.P., Chem. Nat. Compd. (Engl. Transl.), 2001, 37, 224- 225 (Pinocembroside) [https://doi.org/10.1023/A:1012505721054]
  150. Hodgetts, K.J. et al., Tet. Lett., 2001, 42, 3763- 3766 (Pinostrobin, synth) [https://doi.org/10.1016/S0040-4039(01)00567-6]
  151. Lin, J.-H. et al., J. Nat. Prod., 2002, 65, 638- 640 (7-apiosylapiosylglucoside) [https://doi.org/10.1021/np010548z]
  152. Gu, J.-Q. et al., J. Nat. Prod., 2002, 65, 1616- 1620 (±-7-Me ether)
  153. 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]
  154. Leu, Y.-L. et al., Chem. Pharm. Bull., 2004, 52, 858- 860 (Viscum articulatum glycosides) [https://doi.org/10.1248/cpb.52.858]
  155. He, W. et al., Bioorg. Med. Chem., 2005, 13, 1837- 1845 (Alpinetin, activity) [https://doi.org/10.1016/j.bmc.2004.11.038]
  156. 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]
  157. Urgaonkar, S. et al., Org. Lett., 2005, 7, 5609- 5612 ((±)-Pinocembrin, synth) [https://doi.org/10.1021/ol052269z]
  158. Ma, X.-M. et al., Chem. Biodiversity, 2007, 4, 2172- 2181 (isol, pmr, cmr)
  159. Matus-Cádiz, M.A. et al., J. Agric. Food Chem., 2008, 56, 1644- 1653 (7-rhamnoside, occur) [https://doi.org/10.1021/jf072970c]
  160. Yuan, Y. et al., J. Asian Nat. Prod. Res., 2008, 10, 999- 1002 (Pinocembrin, resoln)
  161. Drewes, S.E. et al., Phytochemistry, 2008, 69, 1745- 1749 (Dibenzylpinocembrin, activity) [https://doi.org/10.1016/j.phytochem.2008.02.022]
  162. Jeong, K.-W. et al., J. Nat. Prod., 2009, 72, 719- 724 (Pinocembrin, activity) [https://doi.org/10.1021/np800698d]
  163. Lotti, C. et al., J. Agric. Food Chem., 2010, 58, 2209- 2213 (Mexican propolis constit) [https://doi.org/10.1021/jf100070w]
  164. Chou, T.-S. et al., J. Nat. Prod., 2010, 73, 1470- 1475 (S-form, Pinostrobin, activity) [https://doi.org/10.1021/np100014j]
  165. 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]
  166. Xu, X. et al., J. Agric. Food Chem., 2011, 59, 1205- 1209 (7-neohesperidoside, 7-rutinoside,Litchioside D) [https://doi.org/10.1021/jf104387y]
  167. Allard, P.-M. et al., J. Nat. Prod., 2011, 74, 2446- 2453 (Cryptocarya chartacea constits) [https://doi.org/10.1021/np200715v]
  168. Korenaga, T. et al., Org. Lett., 2011, 13, 2022- 2025 ((-)-Pinostrobin, synth, bibl) [https://doi.org/10.1021/ol2004148]
  169. Katerere, D.R. et al., Fitoterapia, 2012, 83, 932- 940 (Alpinetin, Pinocembrin) [https://doi.org/10.1016/j.fitote.2012.04.011]
  170. Ullah, Z. et al., Nat. Prod. Commun., 2012, 7, 1011- 1014 (Pistacide A)
  171. Ukida, K. et al., Chem. Pharm. Bull., 2013, 61, 1136- 1142 (Schoepfiajasmin G) [https://doi.org/10.1248/cpb.c13-00466]
  172. Wang, M. et al., Nat. Prod. Res., 2014, 28, 70- 73 (S-form, 5-Me ether 7-glucoside)
  173. Vuppalapati, S.V.N. et al., Synthesis, 2014, 46, 465- 474 ((±)-di-Me ether)
  174. Bognár, R. et al., Chem. Ind. (London), 1954, 518 (Sophoricoside, synth)
  175. Rosler, H. et al., Chem. Ber., 1965, 98, 2193- 2196 (Sphaerobioside)
  176. Wagner, H. et al., Chem. Ber., 1967, 100, 101- 103 (Sphaerobioside, synth)
  177. Farkas, L. et al., Chem. Ber., 1968, 101, 2758- 2761 (Sophorabioside)
  178. Ganguly, A.K. et al., Chem. Ind. (London), 1970, 201 (Genistein)
  179. Umezawa, H. et al., J. Antibiot., 1975, 28, 947- 952 (Genistein, activity, microorganisms) [https://doi.org/10.7164/antibiotics.28.947]
  180. Pelter, A. et al., Synthesis, 1976, 326 (synth) [https://doi.org/10.1055/s-1976-24037]
  181. Wagner, H. et al., Tet. Lett., 1976, 17, 1799- 1802 (cmr) [https://doi.org/10.1016/S0040-4039(00)93787-0]
  182. Grayer-Barkmeijer, R.J. et al., Phytochemistry, 1978, 17, 829- 830 (7-Hydroxy-4',5-dimethoxyisoflavone) [https://doi.org/10.1016/S0031-9422(00)94255-9]
  183. Hazato, T. et al., J. Antibiot., 1979, 32, 217- 222 (Genistein, activity, microorganisms) [https://doi.org/10.7164/antibiotics.32.217]
  184. Ohta, N. et al., Agric. Biol. Chem., 1980, 44, 469- 470 (6''-O-Acetylgenistin)
  185. Asahi, K. et al., J. Antibiot., 1981, 34, 919- 920 (Differenol A) [https://doi.org/10.7164/antibiotics.34.919]
  186. Brum-Bousquet, M. et al., Tet. Lett., 1981, 22, 1223- 1226 (Sarothamnoside) [https://doi.org/10.1016/S0040-4039(01)90280-1]
  187. Ingham, J.L., Prog. Chem. Org. Nat. Prod., 1983, 43, 1- 266 (rev, occur)
  188. Sattikulov, A. et al., Uzb. Khim. Zh., 1983, 11- 15 (7-xylosylglucoside)
  189. Ho, L. et al., Shengzhi Yu Biyun, 1984, 4, 51- 53 (7-cellobioside, 7-diglucorhamnoside)
  190. Breytenbach, J.C., J. Nat. Prod., 1986, 49, 1003- 1009 (Ambocin, Neobacin) [https://doi.org/10.1021/np50048a006]
  191. Jain, A.C. et al., JCS Perkin 1, 1986, 215- 220 (synth) [https://doi.org/10.1039/p19860000215]
  192. Murthy, M.S.R. et al., Org. Magn. Reson., 1986, 24, 225- 230 (cmr)
  193. Goto, J. et al., Agric. Biol. Chem., 1987, 51, 3003- 3009 (K 254I, activity)
  194. Sekizaki, H. et al., Chem. Pharm. Bull., 1988, 36, 4876- 4880 (synth, derivs) [https://doi.org/10.1248/cpb.36.4876]
  195. Geibel, M. et al., Phytochemistry, 1990, 29, 1351- 1353 (5-glucoside) [https://doi.org/10.1016/0031-9422(90)85467-T]
  196. Anyanwutaku, I.O. et al., J. Nat. Prod., 1992, 55, 1498- 1504 (Streptomyces constit) [https://doi.org/10.1021/np50088a016]
  197. Nishiyama, K. et al., Biosci., Biotechnol., Biochem., 1993, 57, 107- 114 (synth)
  198. Moreira, I.C. et al., Phytochemistry, 1994, 35, 1567- 1572 (tri-Me ether) [https://doi.org/10.1016/S0031-9422(00)86895-8]
  199. Wang, T.T. et al., Carcinogenesis (London), 1996, 17, 271- 275 (pharmacol) [https://doi.org/10.1093/carcin/17.2.271]
  200. Saxena, V.K. et al., Fitoterapia, 1998, 69, 305- 306 (4'-rhamnoside)
  201. Lewis, P. et al., JCS Perkin 1, 1998, 2481- 2484 (Genistin, synth) [https://doi.org/10.1039/a804406f]
  202. Ma, W.G. et al., Phytochemistry, 1998, 49, 251- 254 (Ambocin)
  203. Johnson, E.L. et al., Z. Naturforsch., C, 1999, 54, 881- 888 (7-dirhamnoside 4'-glucoside) [https://doi.org/10.1515/znc-1999-1105]
  204. Shang-guan, D. et al., Zhongguo Kangshengsu Zazhi, 1999, 24, 254- 277, 299 (3'-nitro,3',5'-dinitro)
  205. Osterhage, C. et al., JOC, 2000, 65, 6412- 6417 (Ascochyta salicorniae constit) [https://doi.org/10.1021/jo000307g]
  206. Talukdar, A.C. et al., Phytochemistry, 2000, 53, 155- 157 (5-Hydroxy-4',7-dimethoxyisoflavone) [https://doi.org/10.1016/S0031-9422(99)00489-6]
  207. Balasubramanian, S. et al., Synth. Commun., 2000, 30, 469- 484 (synth)
  208. Hendrich, S. et al., Handbook of Nutraceuticals and Functional Foods, (ed. Wildman, R.E.C.), CRC Press, 2001, 55- 75 (occur, metab)
  209. Tang, Y. et al., J. Nat. Prod., 2001, 64, 1107- 1110 (Sophora japonica triglycosides) [https://doi.org/10.1021/np010081s]
  210. Dixon, R.A. et al., Phytochemistry, 2002, 60, 205- 211 (Genistein, rev) [https://doi.org/10.1016/S0031-9422(02)00116-4]
  211. Hu, J.-F. et al., Nat. Prod. Res., 2003, 17, 451- 458 (Genesteins G1,G2)
  212. Maskey, R.P. et al., Z. Naturforsch., B, 2003, 58, 686- 691 (4',7-dicymaroside, 4'-6-methylsalicylate)
  213. Xu, D. et al., Zhongcaoyao, 2003, 34, 1065- 1067 (7-arabinosylglucoside, 7-xylosylglucoside)
  214. Laupattarakasem, P. et al., Planta Med., 2004, 70, 496- 501 (Sphaerobioside) [https://doi.org/10.1055/s-2004-827147]
  215. Zhang, Z.-T. et al., Acta Cryst. C, 2005, 61, o29- o31 (4',7-di-Me ether, cryst struct)
  216. Wang, S.F. et al., Bioorg. Med. Chem., 2005, 13, 4880- 4890 (4',7-di-Me ether, tri-Me ether,synth) [https://doi.org/10.1016/j.bmc.2005.04.082]
  217. Deachathai, S. et al., Phytochemistry, 2005, 66, 2368- 2375 (Sphaerobioside heptacetate) [https://doi.org/10.1016/j.phytochem.2005.06.025]
  218. Yoon, T.M. et al., J. Antibiot., 2006, 59, 633- 639 (Talosins A,B, activity)
  219. Kim, W.-G. et al., J. Antibiot., 2006, 59, 640- 645 (Talosins A,B, activity)
  220. Li, H.-Q. et al., Acta Cryst. E, 2007, 63, o3953 (4',7-di-Me ether 5-Ac, synth, cryst struct)
  221. Al-Zereini, W. et al., J. Antibiot., 2007, 60, 301- 308 (3'-nitro, 3',5'-dinitro)
  222. Drenin, A.A. et al., Chem. Nat. Compd. (Engl. Transl.), 2008, 44, 178- 181 (7-galactoside)
  223. Pancharoen, O. et al., Chem. Pharm. Bull., 2008, 56, 835- 838 (4',7-Diprenylgenistein) [https://doi.org/10.1248/cpb.56.835]
  224. Al-Maharik, N. et al., Eur. J. Org. Chem., 2008, 5622- 5629 (4',5-di-Ac, 4',5,7-tri-Ac)
  225. Tang, Y.-P. et al., J. Asian Nat. Prod. Res., 2008, 10, 65- 70 (Sophora japonica triglycosides)
  226. Raynal, N.J.-M. et al., J. Nat. Prod., 2008, 71, 3- 7 (activity) [https://doi.org/10.1021/np070230s]
  227. Tang, Y. et al., J. Nat. Prod., 2008, 71, 448- 450 (Sophora japonica tetraglycosides) [https://doi.org/10.1021/np070396t]
  228. Shou, Q.-Y. et al., J. Agric. Food Chem., 2009, 57, 6712- 6719 (4'-geranyl, activity) [https://doi.org/10.1021/jf9009894]
  229. Al-Zereini, W. et al., J. Antibiot., 2009, 62, 453- 460 (3'-nitro, 3',5'-dinitro)
  230. Xiang, C. et al., Yaoxue Xuebao, 2009, 44, 158- 161 (Hirsutissimiside F, Sphaerobioside)
  231. Liu, X. et al., Zhongguo Kangshengsu Zazhi, 2009, 34, 654- 658 (5,7-dirhamnoside)
  232. Wu, Z. et al., Chin. J. Chem., 2010, 28, 1725- 1730 (Talosins A,B, synth)
  233. St. Denis, J.D. et al., Synthesis, 2010, 1590- 1592 (synth, pmr, cmr)
  234. Nara, K. et al., Food Chem., 2011, 124, 703- 710 (7-gentiobioside) [https://doi.org/10.1016/j.foodchem.2010.05.107]
  235. Huang, Z.-J. et al., Nat. Prod. Res., 2012, 26, 11- 15 (4'-O-Prenylprunetin)
  236. El-Shanawany, M.A. et al., Med. Chem. Res., 2013, 22, 2346- 2350 (7-6-caffeoylglucoside)
  237. Zhang, H.-X. et al., Fitoterapia, 2014, 95, 147- 153 (4'-prenyl) [https://doi.org/10.1016/j.fitote.2014.03.015]
  238. Fatima, A. et al., Nat. Prod. J., 2016, 6, 3- 12 (rev, chem, pharmacol)
  239. Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, GCM350
  240. Zemplén, G. et al., Ber., 1942, 75, 1043- 1047 (Glucohesperetin, Hesperidin, synth)
  241. Wan, L.-K. et al., Yakugaku Zasshi, 1942, 62, 466- 468 (Neohesperidin)
  242. Zemplen, G. et al., Ber., 1943, 76, 773- 775 (Hesperidin, synth)
  243. Arthur, H.R. et al., JCS, 1956, 632- 635 (Hesperetin, isol)
  244. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (abs config)
  245. Hardegger, E. et al., Helv. Chim. Acta, 1961, 44, 1413- 1417 (abs config)
  246. Horowitz, R.M. et al., Tetrahedron, 1963, 19, 773- 782 (Neohesperidin) [https://doi.org/10.1016/S0040-4020(01)99211-7]
  247. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (pmr) [https://doi.org/10.1071/CH9640428]
  248. Golovina, A.P. et al., Zh. Anal. Khim., 1966, 21, 163- 165 (detn, Al)
  249. Korkuć, A., Chem. Anal. (Warsaw), 1970, 15, 441- 444 (detn, Fe)
  250. Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhäuser Verlag, 1972, no. 1628 (occur, Hesperidin)
  251. Nevskaya, E.M. et al., Zh. Anal. Khim., 1972, 27, 1699- 1714 (use)
  252. Wagner, H. et al., Tet. Lett., 1976, 1799- 1802 (cmr) [https://doi.org/10.1016/S0040-4039(00)93787-0]
  253. Markham, K.R. et al., Tetrahedron, 1976, 32, 2607- 2712 (cmr) [https://doi.org/10.1016/0040-4020(76)88036-2]
  254. Sadykov, A.A., Chem. Nat. Compd. (Engl. Transl.), 1979, 15, 273- 278 (5-glucoside) [https://doi.org/10.1007/BF00566073]
  255. Tiwari, K.P. et al., Planta Med., 1979, 36, 191- 192 (rhamnoside) [https://doi.org/10.1055/s-0028-1097267]
  256. Shin, W. et al., Acta Cryst. C, 1987, 43, 1946- 1949 (Hesperitin, cryst struct) [https://doi.org/10.1107/S0108270187089510]
  257. Shen, C.-C. et al., Phytochemistry, 1993, 34, 843- 845 (pmr, cmr) [https://doi.org/10.1016/0031-9422(93)85370-7]
  258. Fujii, S. et al., Chem. Pharm. Bull., 1994, 42, 1143- 1145 (cryst struct) [https://doi.org/10.1248/cpb.42.1143]
  259. Emam, A.M. et al., Phytochemistry, 1998, 48, 739- 741 (7-2,6-dirhamnosylglucoside) [https://doi.org/10.1016/S0031-9422(97)01043-1]
  260. Singh, V.P. et al., Phytochemistry, 1999, 51, 587- 590 (Alhagidin) [https://doi.org/10.1016/S0031-9422(99)00010-2]
  261. Bae, E.-A. et al., Biol. Pharm. Bull., 2000, 23, 1122- 1124 (activity) [https://doi.org/10.1248/bpb.23.1122]
  262. Zhou, Y. et al., Indian J. Chem., Sect. B, 2001, 40, 1219- 1222 (7-glucosylrhamnoside)
  263. Garg, A. et al., Phytother. Res., 2001, 15, 655- 669 (Hesperidin, rev, chem, pharmacol)
  264. Tarun, E.I. et al., Russ. J. Bioorg. Chem. (Engl. Transl.), 2006, 32, 352- 359 (Hesperidin,activity) [https://doi.org/10.1134/S1068162006040054]
  265. Perveen, S. et al., Z. Naturforsch., B, 2007, 62, 863- 867 (Hesperidin) [https://doi.org/10.1515/znb-2007-0617]
  266. Di Donna, L. et al., J. Nat. Prod., 2009, 72, 1352- 1354 (Brutieridin) [https://doi.org/10.1021/np900096w]
  267. Fenaroli's Handbook of Flavor Ingredients, 6th edn., (ed. Burdock, G.A.), CRC Press, 2010, 441 (use)
  268. Pat. Coop. Treaty (WIPO), 2010, 2010 041 290 (Brutieridin, use)
  269. Xu, J. et al., Nat. Prod. Res., 2014, 28, 517- 521 (7-3-glucosylglucoside)
  270. Semwal, R.B. et al., Rec. Nat. Prod., 2014, 8, 66- 70 (7-Me ether 3',5-diglucoside, props)
  271. Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, HBU000
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Inquiries regarding the purchase of Plant cell lines or other PCCL services can be directed to Michael Daley mpdaley@umass.edu

Acknowledgements

The establishment of the PCCL has been sponsored by National Science Foundation (NSF/DBI-156 1572), United States Department of Agriculture Massachusetts Experiment Station Award (MAS00496), the Science and Technology fund from the President's office of the University of Massachusetts, and the 2016 UMass Amherst Armstrong Fund for Science.

National Science Foundation Center for Agriculture, Food and the Environment