The University of Massachusetts Amherst

The Plant Cell Culture Library

Malus florentina
Cell Line ID MF-00763-R0
Media Type M72
Lowest Tolerable USDA Zone 4a
Drought Tolerance Average
Availability medium
Order Rosales
Family Rosaceae
Genus Malus
Antibacterial Genus Level ➡ 57 citations
Antifungal Genus Level ➡ 111 citations
Anticancer Genus Level
Culture Start Material Shoot
Antibacterial Citations
  1. Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 95C (ir)
  2. Aldrich Library of 13C and 1H FT-NMR Spectra, 1992, 2, 918C (nmr)
  3. Nadkarni, D.R. et al., JCS, 1938, 1320- 1322 (synth)
  4. Marsh, C.A., Biochem. J., 1955, 59, 58- 62 (7-glucuronopyranoside) [https://doi.org/10.1042/bj0590058]
  5. Katyal, M. et al., Proc. - Indian Acad. Sci., Sect. A, 1962, 56, 125 (detn, Th)
  6. Dev, B. et al., Fresenius' Z. Anal. Chem., 1963, 196, 178- 182 (7-Me ether, synth) [https://doi.org/10.1007/BF00636887]
  7. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms, Tectochrysin)
  8. Katyal, M. et al., Talanta, 1968, 15, 95- 106 (detn, U) [https://doi.org/10.1016/0039-9140(68)80012-8]
  9. Bowie, J.H. et al., JCS(B), 1969, 89- 93 (ms)
  10. Asakawa, Y., Bull. Chem. Soc. Jpn., 1971, 44, 2761- 2766 (Alnus sieboldiana constit) [https://doi.org/10.1246/bcsj.44.2761]
  11. Wagner, H. et al., Chem. Ber., 1972, 105, 257- 261 (7-glucuronoside, 7-rutinoside)
  12. Subramanian, S.S. et al., J. Indian Chem. Soc., 1972, 49, 1061- 1064 (7-rutinoside)
  13. Nevskaya, E.M. et al., Zh. Anal. Khim., 1972, 27, 1699- 1714 (reactions)
  14. Kingston, D.G.I. et al., Tetrahedron, 1973, 29, 4083- 4086 (ms) [https://doi.org/10.1016/0040-4020(73)80241-8]
  15. Thompson, M. et al., Anal. Chim. Acta, 1976, 85, 375- 381 (detn, Cu) [https://doi.org/10.1016/S0003-2670(01)84703-6]
  16. Gaydon, E.M. et al., Bull. Soc. Chim. Fr., Part II, 1978, 43- 47 (synth, uv, cmr)
  17. Garg, S.P. et al., Indian J. Chem., Sect. B, 1979, 17, 416- 417 (7-galactoside)
  18. Jain, P.K. et al., Synthesis, 1982, 221- 223 (synth, 5,7-Dimethoxyflavone) [https://doi.org/10.1055/s-1982-29755]
  19. Jaipetch, T. et al., Phytochemistry, 1983, 22, 625- 626 (Boesenbergia pandurata constit) [https://doi.org/10.1016/0031-9422(83)83075-1]
  20. De Rosa, S. et al., Phytochemistry, 1983, 22, 2323- 2324 (7-gentiobioside) [https://doi.org/10.1016/S0031-9422(00)80175-2]
  21. Agrawal, P.K. et al., Tet. Lett., 1983, 177- 180 (cmr) [https://doi.org/10.1016/S0040-4039(00)81359-3]
  22. Chauhan, J.S. et al., Phytochemistry, 1984, 23, 2404- 2405 (5-xyloside) [https://doi.org/10.1016/S0031-9422(00)80572-5]
  23. Saxena, S. et al., Synthesis, 1985, 697- 698 (synth) [https://doi.org/10.1055/s-1985-31319]
  24. Le Floc'h, Y. et al., Tet. Lett., 1986, 27, 5503- 5504 (synth) [https://doi.org/10.1016/S0040-4039(00)85249-1]
  25. Arriaga-Giner, F.J. et al., Z. Naturforsch., C, 1986, 41, 946- 948 (benzoate)
  26. Nikaido, T. et al., Chem. Pharm. Bull., 1988, 36, 654- 661 (7-glucuronoside, activity) [https://doi.org/10.1248/cpb.36.654]
  27. Yung-Qi, W. et al., Chem. Pharm. Bull., 1988, 36, 3206- 3209 (Citrus funadoko constit) [https://doi.org/10.1248/cpb.36.3206]
  28. The Flavonoids: Advances in Research Since 1980, (ed. Harborne, J.B.), Chapman and Hall, 1988
  29. Chantrapromma, K. et al., Aust. J. Chem., 1989, 42, 2289- 2293 (Uvaria rufas constit, cryst struct, Tectochrysin) [https://doi.org/10.1071/CH9892289]
  30. Jung, J.H. et al., Phytochemistry, 1990, 29, 1271- 1275 (pmr, cmr) [https://doi.org/10.1016/0031-9422(90)85441-H]
  31. Geibel, M. et al., Phytochemistry, 1990, 29, 1351- 1353 (Tectochrysin 5-glucoside) [https://doi.org/10.1016/0031-9422(90)85467-T]
  32. Liu, Q. et al., Phytochemistry, 1993, 34, 167- 170 (Aequinoctin)
  33. Shen, C.-C. et al., Phytochemistry, 1993, 34, 843- 845 (pmr, cmr) [https://doi.org/10.1016/0031-9422(93)85370-7]
  34. Mayer, R., Planta Med., 1993, 59, 269- 271 (5,7-Dimethoxyflavone) [https://doi.org/10.1055/s-2006-959667]
  35. Litkei, G. et al., Annalen, 1995, 1711- 1715 (synth, pmr)
  36. Hounghton, P.J. et al., Pharm. Pharmacol. Lett., 1997, 7, 96- 98 (activity)
  37. Rashad, M.A. et al., Phytomedicine, 1998, 5, 375- 381 (activity)
  38. Lee, J.-M. et al., Synthesis, 2001, 2247- 2254 (synth, pmr, cmr) [https://doi.org/10.1055/s-2001-18436]
  39. Montoro, P. et al., J. Agric. Food Chem., 2002, 49, 5156- 5160 (7-4-rhamnosylglucoside) [https://doi.org/10.1021/jf010318q]
  40. Pistelli, L. et al., Fitoterapia, 2003, 74, 417- 419 (Progenin, Calycotome villosa constit) [https://doi.org/10.1016/S0367-326X(03)00061-3]
  41. El Antri, A. et al., Molecules, 2004, 9, 568- 573 (7-6-acetylglucoside)
  42. Ahmed-Belkacem, A. et al., Cancer Res., 2005, 65, 4852- 4860 (Tectochrysin, pharmacol) [https://doi.org/10.1158/0008-5472.CAN-04-1817]
  43. Leu, S.J. et al., Biol. Pharm. Bull., 2006, 29, 740- 745 (Toringin, activity) [https://doi.org/10.1248/bpb.29.740]
  44. Park, Y. et al., Magn. Reson. Chem., 2007, 45, 674- 679, 1072 - 1075 (pmr, cmr)
  45. Berthier, A. et al., Planta Med., 2007, 73, 1447- 1451 (Progenin, activity) [https://doi.org/10.1055/s-2007-990248]
  46. Nallasivam, A. et al., Acta Cryst. E, 2008, 64, o2490- o2491 (dibenzyl ether, synth, cryst struct)
  47. Kraus, G.A. et al., Synthesis, 2008, 2427- 2431 (synth, pmr, cmr) [https://doi.org/10.1055/s-2008-1078597]
  48. Tashmatov, Z.O. et al., Chem. Nat. Compd. (Engl. Transl.), 2011, 47, 547- 549 (Schachristanoside)
  49. Uddin, N. et al., Phytochem. Lett., 2011, 4, 454- 458 (Lawsochrysinin) [https://doi.org/10.1016/j.phytol.2011.05.007]
  50. Chaipech, S. et al., Chem. Pharm. Bull., 2012, 60, 62- 69 (Kaempferia parviflora constit) [https://doi.org/10.1248/cpb.60.62]
  51. Senejoux, F. et al., Fitoterapia, 2012, 83, 377- 382 (Chrysin, Ziziphora clinopodioides constit,activity) [https://doi.org/10.1016/j.fitote.2011.11.023]
  52. Sermboonpaisarn, T. et al., Fitoterapia, 2012, 83, 780- 784 (Ficus foveolata constit, activity) [https://doi.org/10.1016/j.fitote.2012.03.009]
  53. Zhong, L. et al., Nat. Prod. Res., 2012, 26, 307- 313 (Chrysin, Populus nigra constits,activity)
  54. Ukida, K. et al., Chem. Pharm. Bull., 2013, 61, 1136- 1142 (Schoepfiajasmin H) [https://doi.org/10.1248/cpb.c13-00466]
  55. Dubrovskiy, A.V. et al., Tetrahedron, 2013, 69, 2789- 2798 (5,7-Dimethoxyflavone, synth) [https://doi.org/10.1016/j.tet.2013.01.078]
  56. Kim, K. et al., Org. Lett., 2015, 17, 2550- 2553 (synth, pmr, cmr) [https://doi.org/10.1021/acs.orglett.5b01138]
  57. Mani, R. et al., Phytochemistry, 2018, 145, 187- 196 (Chrysin, rev) [https://doi.org/10.1016/j.phytochem.2017.09.016]
[top⬆]
Antifungal Citations
  1. Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 95C (ir)
  2. Aldrich Library of 13C and 1H FT-NMR Spectra, 1992, 2, 918C (nmr)
  3. Nadkarni, D.R. et al., JCS, 1938, 1320- 1322 (synth)
  4. Marsh, C.A., Biochem. J., 1955, 59, 58- 62 (7-glucuronopyranoside) [https://doi.org/10.1042/bj0590058]
  5. Katyal, M. et al., Proc. - Indian Acad. Sci., Sect. A, 1962, 56, 125 (detn, Th)
  6. Dev, B. et al., Fresenius' Z. Anal. Chem., 1963, 196, 178- 182 (7-Me ether, synth) [https://doi.org/10.1007/BF00636887]
  7. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms, Tectochrysin)
  8. Katyal, M. et al., Talanta, 1968, 15, 95- 106 (detn, U) [https://doi.org/10.1016/0039-9140(68)80012-8]
  9. Bowie, J.H. et al., JCS(B), 1969, 89- 93 (ms)
  10. Asakawa, Y., Bull. Chem. Soc. Jpn., 1971, 44, 2761- 2766 (Alnus sieboldiana constit) [https://doi.org/10.1246/bcsj.44.2761]
  11. Wagner, H. et al., Chem. Ber., 1972, 105, 257- 261 (7-glucuronoside, 7-rutinoside)
  12. Subramanian, S.S. et al., J. Indian Chem. Soc., 1972, 49, 1061- 1064 (7-rutinoside)
  13. Nevskaya, E.M. et al., Zh. Anal. Khim., 1972, 27, 1699- 1714 (reactions)
  14. Kingston, D.G.I. et al., Tetrahedron, 1973, 29, 4083- 4086 (ms) [https://doi.org/10.1016/0040-4020(73)80241-8]
  15. Thompson, M. et al., Anal. Chim. Acta, 1976, 85, 375- 381 (detn, Cu) [https://doi.org/10.1016/S0003-2670(01)84703-6]
  16. Gaydon, E.M. et al., Bull. Soc. Chim. Fr., Part II, 1978, 43- 47 (synth, uv, cmr)
  17. Garg, S.P. et al., Indian J. Chem., Sect. B, 1979, 17, 416- 417 (7-galactoside)
  18. Jain, P.K. et al., Synthesis, 1982, 221- 223 (synth, 5,7-Dimethoxyflavone) [https://doi.org/10.1055/s-1982-29755]
  19. Jaipetch, T. et al., Phytochemistry, 1983, 22, 625- 626 (Boesenbergia pandurata constit) [https://doi.org/10.1016/0031-9422(83)83075-1]
  20. De Rosa, S. et al., Phytochemistry, 1983, 22, 2323- 2324 (7-gentiobioside) [https://doi.org/10.1016/S0031-9422(00)80175-2]
  21. Agrawal, P.K. et al., Tet. Lett., 1983, 177- 180 (cmr) [https://doi.org/10.1016/S0040-4039(00)81359-3]
  22. Chauhan, J.S. et al., Phytochemistry, 1984, 23, 2404- 2405 (5-xyloside) [https://doi.org/10.1016/S0031-9422(00)80572-5]
  23. Saxena, S. et al., Synthesis, 1985, 697- 698 (synth) [https://doi.org/10.1055/s-1985-31319]
  24. Le Floc'h, Y. et al., Tet. Lett., 1986, 27, 5503- 5504 (synth) [https://doi.org/10.1016/S0040-4039(00)85249-1]
  25. Arriaga-Giner, F.J. et al., Z. Naturforsch., C, 1986, 41, 946- 948 (benzoate)
  26. Nikaido, T. et al., Chem. Pharm. Bull., 1988, 36, 654- 661 (7-glucuronoside, activity) [https://doi.org/10.1248/cpb.36.654]
  27. Yung-Qi, W. et al., Chem. Pharm. Bull., 1988, 36, 3206- 3209 (Citrus funadoko constit) [https://doi.org/10.1248/cpb.36.3206]
  28. The Flavonoids: Advances in Research Since 1980, (ed. Harborne, J.B.), Chapman and Hall, 1988
  29. Chantrapromma, K. et al., Aust. J. Chem., 1989, 42, 2289- 2293 (Uvaria rufas constit, cryst struct, Tectochrysin) [https://doi.org/10.1071/CH9892289]
  30. Jung, J.H. et al., Phytochemistry, 1990, 29, 1271- 1275 (pmr, cmr) [https://doi.org/10.1016/0031-9422(90)85441-H]
  31. Geibel, M. et al., Phytochemistry, 1990, 29, 1351- 1353 (Tectochrysin 5-glucoside) [https://doi.org/10.1016/0031-9422(90)85467-T]
  32. Liu, Q. et al., Phytochemistry, 1993, 34, 167- 170 (Aequinoctin)
  33. Shen, C.-C. et al., Phytochemistry, 1993, 34, 843- 845 (pmr, cmr) [https://doi.org/10.1016/0031-9422(93)85370-7]
  34. Mayer, R., Planta Med., 1993, 59, 269- 271 (5,7-Dimethoxyflavone) [https://doi.org/10.1055/s-2006-959667]
  35. Litkei, G. et al., Annalen, 1995, 1711- 1715 (synth, pmr)
  36. Hounghton, P.J. et al., Pharm. Pharmacol. Lett., 1997, 7, 96- 98 (activity)
  37. Rashad, M.A. et al., Phytomedicine, 1998, 5, 375- 381 (activity)
  38. Lee, J.-M. et al., Synthesis, 2001, 2247- 2254 (synth, pmr, cmr) [https://doi.org/10.1055/s-2001-18436]
  39. Montoro, P. et al., J. Agric. Food Chem., 2002, 49, 5156- 5160 (7-4-rhamnosylglucoside) [https://doi.org/10.1021/jf010318q]
  40. Pistelli, L. et al., Fitoterapia, 2003, 74, 417- 419 (Progenin, Calycotome villosa constit) [https://doi.org/10.1016/S0367-326X(03)00061-3]
  41. El Antri, A. et al., Molecules, 2004, 9, 568- 573 (7-6-acetylglucoside)
  42. Ahmed-Belkacem, A. et al., Cancer Res., 2005, 65, 4852- 4860 (Tectochrysin, pharmacol) [https://doi.org/10.1158/0008-5472.CAN-04-1817]
  43. Leu, S.J. et al., Biol. Pharm. Bull., 2006, 29, 740- 745 (Toringin, activity) [https://doi.org/10.1248/bpb.29.740]
  44. Park, Y. et al., Magn. Reson. Chem., 2007, 45, 674- 679, 1072 - 1075 (pmr, cmr)
  45. Berthier, A. et al., Planta Med., 2007, 73, 1447- 1451 (Progenin, activity) [https://doi.org/10.1055/s-2007-990248]
  46. Nallasivam, A. et al., Acta Cryst. E, 2008, 64, o2490- o2491 (dibenzyl ether, synth, cryst struct)
  47. Kraus, G.A. et al., Synthesis, 2008, 2427- 2431 (synth, pmr, cmr) [https://doi.org/10.1055/s-2008-1078597]
  48. Tashmatov, Z.O. et al., Chem. Nat. Compd. (Engl. Transl.), 2011, 47, 547- 549 (Schachristanoside)
  49. Uddin, N. et al., Phytochem. Lett., 2011, 4, 454- 458 (Lawsochrysinin) [https://doi.org/10.1016/j.phytol.2011.05.007]
  50. Chaipech, S. et al., Chem. Pharm. Bull., 2012, 60, 62- 69 (Kaempferia parviflora constit) [https://doi.org/10.1248/cpb.60.62]
  51. Senejoux, F. et al., Fitoterapia, 2012, 83, 377- 382 (Chrysin, Ziziphora clinopodioides constit,activity) [https://doi.org/10.1016/j.fitote.2011.11.023]
  52. Sermboonpaisarn, T. et al., Fitoterapia, 2012, 83, 780- 784 (Ficus foveolata constit, activity) [https://doi.org/10.1016/j.fitote.2012.03.009]
  53. Zhong, L. et al., Nat. Prod. Res., 2012, 26, 307- 313 (Chrysin, Populus nigra constits,activity)
  54. Ukida, K. et al., Chem. Pharm. Bull., 2013, 61, 1136- 1142 (Schoepfiajasmin H) [https://doi.org/10.1248/cpb.c13-00466]
  55. Dubrovskiy, A.V. et al., Tetrahedron, 2013, 69, 2789- 2798 (5,7-Dimethoxyflavone, synth) [https://doi.org/10.1016/j.tet.2013.01.078]
  56. Kim, K. et al., Org. Lett., 2015, 17, 2550- 2553 (synth, pmr, cmr) [https://doi.org/10.1021/acs.orglett.5b01138]
  57. Mani, R. et al., Phytochemistry, 2018, 145, 187- 196 (Chrysin, rev) [https://doi.org/10.1016/j.phytochem.2017.09.016]
  58. Aldrich Library of FT-IR Spectra: Vapor Phase, 1989, 3, 1028A (ir)
  59. Aldrich Library of 13C and 1H FT-NMR Spectra, 1992, 2, 278A (nmr)
  60. Erdmann, F. et al., J. Prakt. Chem., 1897, 56, 143- 156 (synth) [https://doi.org/10.1002/prac.18970560112]
  61. Chaudhury, D.N. et al., JCS, 1949, 2054- 2057 (Gein, synth)
  62. Tamari, K. et al., Bull. Agric. Chem. Soc. Jpn., 1958, 21, 125- 126 (Oryzarol)
  63. Yamada, T. et al., Agric. Biol. Chem., 1967, 31, 85- 91 (Sasanquin)
  64. Yamada, T. et al., Agric. Biol. Chem., 1967, 31, 1076- 1078 (Sasanquin)
  65. Pšenák, M. et al., Planta Med., 1970, 19, 154- 159 (Gein)
  66. Sachdev, S.L. et al., Anal. Chim. Acta, 1972, 58, 141- 147 (detn, O3) [https://doi.org/10.1016/S0003-2670(00)86863-4]
  67. Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhäuser Verlag, 1972, nos. 185- 186 (Eugenol, Gein, occur)
  68. Popa, G. et al., Rev. Chim. (Bucharest), 1973, 24, 635- 638 (spectra)
  69. Manito, P. et al., JCS Perkin 1, 1974, 1727- 1731 (biosynth) [https://doi.org/10.1039/p19740001727]
  70. Klischies, M. et al., Chem. Comm., 1975, 879- 880 (biosynth) [https://doi.org/10.1039/C39750000879]
  71. Yamaguchi, H. et al., Chem. Pharm. Bull., 1975, 23, 1169- 1170 (pmr) [https://doi.org/10.1248/cpb.23.1169]
  72. Opdyke, D.L.J., Food Cosmet. Toxicol., 1975, 13, 545- 554 (rev, tox) [https://doi.org/10.1016/0015-6264(75)90011-5]
  73. Manito, P. et al., JCS Perkin 1, 1975, 1548- 1551 (biosynth) [https://doi.org/10.1039/p19750001548]
  74. Von Massow, F. et al., JCS Perkin 2, 1976, 977- 980 (cmr) [https://doi.org/10.1039/P29760000977]
  75. Bohlmann, F. et al., Phytochemistry, 1976, 15, 1318- 1319 (Felicia wrightii constit) [https://doi.org/10.1016/0031-9422(76)85104-7]
  76. Shibuya, M. et al., Chem. Pharm. Bull., 1978, 26, 2671- 2673 (O-prenyl) [https://doi.org/10.1248/cpb.26.2671]
  77. Wenkert, E. et al., Synthesis, 1983, 701- 703 (synth) [https://doi.org/10.1055/s-1983-30474]
  78. IARC Monogr., 1985, 36, 75; 1987, Suppl. 7, 63 (rev, tox)
  79. Lewis, R.J., Food Additives Handbook, Van Nostrand Reinhold International, New York, 1989, EQR500, EQS000
  80. Howes, A.J. et al., Food Chem. Toxicol., 1990, 28, 537- 542 (cytotoxicity) [https://doi.org/10.1016/0278-6915(90)90152-D]
  81. Yahara, S. et al., Shoyakugaku Zasshi, 1990, 44, 331- 334 (gentiobioside)
  82. Sashida, Y. et al., Chem. Pharm. Bull., 1991, 39, 2362- 2368 (6-rhamnosylglucoside) [https://doi.org/10.1248/cpb.39.2362]
  83. Machida, K. et al., Phytochemistry, 1991, 30, 2013- 2014 (apiosylglucoside) [https://doi.org/10.1016/0031-9422(91)85058-8]
  84. Fujita, T. et al., Phytochemistry, 1992, 31, 3265- 3269 (Citrusin C) [https://doi.org/10.1016/0031-9422(92)83490-P]
  85. Tanaka, T. et al., Chem. Pharm. Bull., 1993, 41, 1232- 1237 (6-galloylglucoside) [https://doi.org/10.1248/cpb.41.1232]
  86. Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 1368
  87. Encyclopedia of Food and Color Additives, (ed. Burdock, G.A.), CRC Press, 1997, 1052- 1058 (occur, props, esters)
  88. Takeda, Y. et al., Phytochemistry, 1998, 49, 787- 791 (6-apiofuranosylglucoside) [https://doi.org/10.1016/S0031-9422(98)00125-3]
  89. Zhao, W.M. et al., Fitoterapia, 1999, 70, 529- 531 (rutinoside, Sasanquin) [https://doi.org/10.1016/S0367-326X(99)00078-7]
  90. Straubinger, M. et al., Nat. Prod. Lett., 1999, 13, 5- 10 (arabinofuranosylglucoside)
  91. Sawabe, A. et al., Stud. Plant Sci., 1999, 6, 290- 296 (Celosia argentea constit, activity) [https://doi.org/10.1016/S0928-3420(99)80036-6]
  92. Yuwono, M. et al., Anal. Profiles Drug Subst., 2002, 29, 149- 177 (rev) [https://doi.org/10.1016/S0099-5428(08)60729-7]
  93. Nagatani, Y. et al., Chem. Pharm. Bull., 2002, 50, 583- 589 (Dracunculifoside N) [https://doi.org/10.1248/cpb.50.583]
  94. Plaza, A. et al., J. Agric. Food Chem., 2005, 53, 2853- 2858 (Tynanthus panurensis triglycoside) [https://doi.org/10.1021/jf0479867]
  95. Koeduka, T. et al., Proc. Natl. Acad. Sci. U.S.A., 2006, 103, 10129- 10133 (Eugenol,biosynth)
  96. Lin, C.-F. et al., Phytochemistry, 2007, 68, 2450- 2454 (2-methylbutanoate) [https://doi.org/10.1016/j.phytochem.2007.05.027]
  97. Murata, T. et al., J. Nat. Med. (Tokyo), 2009, 63, 402- 407 (6'-Malonylcitrusin C)
  98. Fenaroli's Handbook of Flavor Ingredients, 6th edn., (ed. Burdock, G.A.), CRC Press, 2010, 680- 683 (use, esters)
  99. Pramod, K. et al., Nat. Prod. Commun., 2010, 5, 1999- 2006 (rev, activity)
  100. Zeng, Q. et al., Arch. Pharmacal Res., 2011, 34, 2015- 2020 (6'-Acetylcitrusin C, 6'-Butenoylcitrusin C)
  101. Zhou, Z.-Y. et al., Fitoterapia, 2011, 82, 1309- 1312 (Lactarius deliciosus acetylrutinoside) [https://doi.org/10.1016/j.fitote.2011.09.002]
  102. Fontanelle, R.O.S. et al., Molecules, 2011, 16, 6422- 6431 (activity) [https://doi.org/10.3390/molecules16086422]
  103. Hu, J. et al., Chem. Nat. Compd. (Engl. Transl.), 2012, 48, 782- 784 (Conyza japonica glycoside)
  104. Kamatou, G.P. et al., Molecules, 2012, 17, 6953- 6981 (Eugenol, rev, activity) [https://doi.org/10.3390/molecules17066953]
  105. Pichika, M.R. et al., Acta Cryst. E, 2013, 69, o1088 (benzoyl, cryst struct)
  106. Kaufman, T.S., J. Braz. Chem. Soc., 2015, 26, 1055- 1085 (rev, use)
  107. Chowdhry, B.Z. et al., J. Phys. Chem. A, 2015, 119, 11280- 11292 (Eugenol, ir, Raman,conformn) [https://doi.org/10.1021/acs.jpca.5b07607]
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