The University of Massachusetts Amherst

The Plant Cell Culture Library

Acer davidii
Cell Line ID AD-10602 C1
Media Type B39
Availability Low
Order Sapindales
Family Sapindaceae
Genus Acer
Antiviral Genus Level ➡ 16 citations
Antibacterial Genus Level ➡ 71 citations
Antifungal Genus Level
Anticancer Genus Level ➡ 14 citations
Culture Initiation Site Paris-Sud
Plant Habit Tree deciduous
Plant Habitat Temperate
Culture Start Material Shoot
Native Range Central China
Plant Supplier Botanical Garden Paris
Antiviral Citations
  1. Fischer, G. et al., CA, 1953, 47, 2827a (isol)
  2. Fischer, G. et al., Experientia, 1954, 10, 329- 330 (isol) [https://doi.org/10.1007/BF02160840]
  3. Haddock, E.A. et al., J. Chem. Soc., Perkin Trans. 1, 1982, 2515- 2524 (isol, struct, pmr,cmr, rev) [https://doi.org/10.1039/p19820002515]
  4. Nishizawa, M. et al., J. Chem. Soc., Perkin Trans. 1, 1982, 2963- 2968; 1983, 961 - 965 (Rhus semialata constits, Quercus infectaria constits) [https://doi.org/10.1039/p19820002963]
  5. Nishizawa, M. et al., Chem. Pharm. Bull., 1983, 31, 2593- 2600 (Paeonia lactiflora constits) [https://doi.org/10.1248/cpb.31.2593]
  6. Nishizawa, M. et al., Phytochemistry, 1985, 24, 2411- 2413 (Spirogyra constits) [https://doi.org/10.1016/S0031-9422(00)83053-8]
  7. Nonaka, G. et al., Chem. Pharm. Bull., 1987, 35, 3127- 3131 (struct, pmr, cmr) [https://doi.org/10.1248/cpb.35.3127]
  8. Kandil, F.E. et al., Phytochemistry, 1996, 42, 1243- 1245 (2-Trigalloyl-1,3,4,6-tetragalloylglucose, uv, pmr, cmr) [https://doi.org/10.1016/0031-9422(95)00924-8]
  9. Kandil, F.E. et al., Phytochemistry, 2001, 58, 611- 613 (Monacanthin A) [https://doi.org/10.1016/S0031-9422(01)00265-5]
  10. Duan, D. et al., Bioorg. Med. Chem. Lett., 2004, 14, 6041- 6044 (antiviral activity) [https://doi.org/10.1016/j.bmcl.2004.09.067]
  11. Zhang, J. et al., Pharm. Res., 2009, 26, 2066- 2080 (rev, activity)
  12. Cho, J.-Y. et al., Food Chem., 2010, 123, 501- 506 (isol, activity) [https://doi.org/10.1016/j.foodchem.2010.04.072]
  13. Baumgartner, R.R. et al., J. Nat. Prod., 2010, 73, 1578- 1581, 1742§ (isol, activity) [https://doi.org/10.1021/np100258e]
  14. Cryan, L.M. et al., J. Med. Chem., 2013, 56, 1940- 1945 (activity) [https://doi.org/10.1021/jm301558t]
  15. Cao, Y. et al., J. Nat. Med. (Tokyo), 2014, 68, 465- 472 (rev, activity)
  16. Tuominen, A. et al., Phytochemistry, 2015, 115, 239- 251 (Sylvatiins A,C) [https://doi.org/10.1016/j.phytochem.2015.01.005]
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Antibacterial Citations
  1. Fischer, G. et al., CA, 1953, 47, 2827a (isol)
  2. Fischer, G. et al., Experientia, 1954, 10, 329- 330 (isol) [https://doi.org/10.1007/BF02160840]
  3. Kipping, F.B. et al., JCS, 1935, 1145- 1147 (synth, bibl)
  4. Ruijgrok, H.W.L., Planta Med., 1963, 11, 338- 347 (occur) [https://doi.org/10.1055/s-0028-1100248]
  5. Moriarty, R.M. et al., JACS, 1965, 87, 3251- 3252 (cryst struct) [https://doi.org/10.1021/ja01092a047]
  6. Ju, Y. et al., CA, 1988, 109, 35250c (cryst struct)
  7. Yamamoto, M. et al., Chem. Comm., 1988, 560- 561 (synth) [https://doi.org/10.1039/c39880000560]
  8. Huang, Y.H. et al., J. Dermatol. Sci., 2008, 49, 115- 123 (activity) [https://doi.org/10.1016/j.jdermsci.2007.07.008]
  9. Lee, T.H. et al., J. Ethnopharmacol., 2008, 116, 518- 527 (activity) [https://doi.org/10.1016/j.jep.2007.12.019]
  10. Powers, J.L. et al., J. Am. Pharm. Assoc., 1940, 29, 209- 211 (Acertannin) [https://doi.org/10.1002/jps.3030290504]
  11. Fletcher, H.G., JACS, 1947, 69, 706- 707 (synth) [https://doi.org/10.1021/ja01195a504]
  12. Wiggins, L.F., Adv. Carbohydr. Chem., 1950, 5, 191- 228 (rev)
  13. Mackie, D.M. et al., Carbohydr. Res., 1972, 24, 67- 85 (synth, 2,3,4-tri-Ac) [https://doi.org/10.1016/S0008-6215(00)82260-0]
  14. Pitkanen, E., Clin. Chim. Acta, 1973, 48, 159 (occur) [https://doi.org/10.1016/0009-8981(73)90361-6]
  15. Que, L. Jr. et al., Biochemistry, 1974, 13, 146- 151 (cmr)
  16. Augé, J. et al., Carbohydr. Res., 1977, 59, 255- 257 (tetra-Ac) [https://doi.org/10.1016/S0008-6215(00)83312-1]
  17. Kondo, Y. et al., Carbohydr. Res., 1980, 82, 398- 403 (benzoyl, mesyl derivs) [https://doi.org/10.1016/S0008-6215(00)85717-1]
  18. Hong, S.H. et al., Chem. Nat. Prod., Proc. Sino-Am. Symp., 1980, 244- 247 (Ginnalin A,activity)
  19. Bock, K. et al., Phytochemistry, 1980, 19, 2033 (Aceritannin) [https://doi.org/10.1016/0031-9422(80)83034-2]
  20. Song, C. et al., Yaoxue Tongbao, 1981, 16, 756 (Cha Tiao Qi Sus A,B,C)
  21. Kocienski, P. et al., Carbohydr. Res., 1982, 110, 330- 332 (tetra-Ac, synth) [https://doi.org/10.1016/0008-6215(82)84016-0]
  22. Song, C et al., Huaxue Xuebao, 1982, 40, 1142- 1147 (Ginnalins)
  23. Haddock, E.A. et al., JCS Perkin 1, 1982, 2515- 2524 (Aceritannin, Acergallotannins) [https://doi.org/10.1039/p19820002515]
  24. Boeyens, J.C.A. et al., Phytochemistry, 1983, 22, 1959- 1960 (conformn, cryst struct) [https://doi.org/10.1016/0031-9422(83)80022-3]
  25. Witczak, Z.J. et al., Carbohydr. Res., 1986, 150, 121- 131 (6-mesyl, 6-tosyl, 6-trityl derivs) [https://doi.org/10.1016/0008-6215(86)80010-6]
  26. Hatano, T. et al., Chem. Pharm. Bull., 1990, 38, 1902- 1905 (Acergallotannins) [https://doi.org/10.1248/cpb.38.1902]
  27. Ikeya, Y. et al., Chem. Pharm. Bull., 1991, 39, 2600- 2605 (Tenuifoliside D) [https://doi.org/10.1248/cpb.39.2600]
  28. Elvebak, L.E. et al., Carbohydr. Res., 1995, 274, 85- 97 (partially methylated, acylated and benzoylated derivs) [https://doi.org/10.1016/0008-6215(95)00094-A]
  29. Murali, R. et al., Carbohydr. Res., 1996, 280, 351- 355 (synth) [https://doi.org/10.1016/0008-6215(95)00316-9]
  30. Pham, N.K.T. et al., Tap Chi Hoa Hoc, 2007, 45, 233- 236 (Hedyotis auricularia constit)
  31. Ogawa, A. et al., Chem. Pharm. Bull., 2011, 59, 672- 675 (1,5-Anhydro-3,6-digalloylglucitol) [https://doi.org/10.1248/cpb.59.672]
  32. Wan, C. et al., Bioorg. Med. Chem. Lett., 2012, 22, 597- 600 (Maplexins A-E) [https://doi.org/10.1016/j.bmcl.2011.10.073]
  33. Yuan, T. et al., Tetrahedron, 2012, 68, 959- 964 (Maplexins F-I, activity) [https://doi.org/10.1016/j.tet.2011.11.062]
  34. Zhou, Y.-H. et al., Chin. J. Nat. Med., 2014, 12, 225- 228 (Sibiricose A7)
  35. Powers, J.L. et al., J. Am. Pharm. Assoc., 1940, 29, 209- 211 (Acertannin) [https://doi.org/10.1002/jps.3030290504]
  36. Fletcher, H.G., JACS, 1947, 69, 706- 707 (synth) [https://doi.org/10.1021/ja01195a504]
  37. Wiggins, L.F., Adv. Carbohydr. Chem., 1950, 5, 191- 228 (rev)
  38. Mackie, D.M. et al., Carbohydr. Res., 1972, 24, 67- 85 (synth, 2,3,4-tri-Ac) [https://doi.org/10.1016/S0008-6215(00)82260-0]
  39. Pitkanen, E., Clin. Chim. Acta, 1973, 48, 159 (occur) [https://doi.org/10.1016/0009-8981(73)90361-6]
  40. Que, L. Jr. et al., Biochemistry, 1974, 13, 146- 151 (cmr)
  41. Augé, J. et al., Carbohydr. Res., 1977, 59, 255- 257 (tetra-Ac) [https://doi.org/10.1016/S0008-6215(00)83312-1]
  42. Kondo, Y. et al., Carbohydr. Res., 1980, 82, 398- 403 (benzoyl, mesyl derivs) [https://doi.org/10.1016/S0008-6215(00)85717-1]
  43. Hong, S.H. et al., Chem. Nat. Prod., Proc. Sino-Am. Symp., 1980, 244- 247 (Ginnalin A,activity)
  44. Bock, K. et al., Phytochemistry, 1980, 19, 2033 (Aceritannin) [https://doi.org/10.1016/0031-9422(80)83034-2]
  45. Song, C. et al., Yaoxue Tongbao, 1981, 16, 756 (Cha Tiao Qi Sus A,B,C)
  46. Kocienski, P. et al., Carbohydr. Res., 1982, 110, 330- 332 (tetra-Ac, synth) [https://doi.org/10.1016/0008-6215(82)84016-0]
  47. Song, C et al., Huaxue Xuebao, 1982, 40, 1142- 1147 (Ginnalins)
  48. Haddock, E.A. et al., JCS Perkin 1, 1982, 2515- 2524 (Aceritannin, Acergallotannins) [https://doi.org/10.1039/p19820002515]
  49. Boeyens, J.C.A. et al., Phytochemistry, 1983, 22, 1959- 1960 (conformn, cryst struct) [https://doi.org/10.1016/0031-9422(83)80022-3]
  50. Witczak, Z.J. et al., Carbohydr. Res., 1986, 150, 121- 131 (6-mesyl, 6-tosyl, 6-trityl derivs) [https://doi.org/10.1016/0008-6215(86)80010-6]
  51. Hatano, T. et al., Chem. Pharm. Bull., 1990, 38, 1902- 1905 (Acergallotannins) [https://doi.org/10.1248/cpb.38.1902]
  52. Ikeya, Y. et al., Chem. Pharm. Bull., 1991, 39, 2600- 2605 (Tenuifoliside D) [https://doi.org/10.1248/cpb.39.2600]
  53. Elvebak, L.E. et al., Carbohydr. Res., 1995, 274, 85- 97 (partially methylated, acylated and benzoylated derivs) [https://doi.org/10.1016/0008-6215(95)00094-A]
  54. Murali, R. et al., Carbohydr. Res., 1996, 280, 351- 355 (synth) [https://doi.org/10.1016/0008-6215(95)00316-9]
  55. Pham, N.K.T. et al., Tap Chi Hoa Hoc, 2007, 45, 233- 236 (Hedyotis auricularia constit)
  56. Ogawa, A. et al., Chem. Pharm. Bull., 2011, 59, 672- 675 (1,5-Anhydro-3,6-digalloylglucitol) [https://doi.org/10.1248/cpb.59.672]
  57. Wan, C. et al., Bioorg. Med. Chem. Lett., 2012, 22, 597- 600 (Maplexins A-E) [https://doi.org/10.1016/j.bmcl.2011.10.073]
  58. Yuan, T. et al., Tetrahedron, 2012, 68, 959- 964 (Maplexins F-I, activity) [https://doi.org/10.1016/j.tet.2011.11.062]
  59. Zhou, Y.-H. et al., Chin. J. Nat. Med., 2014, 12, 225- 228 (Sibiricose A7)
  60. Shaw, E., JACS, 1946, 68, 2510- 2513 (synth) [https://doi.org/10.1021/ja01216a024]
  61. Grundmann, C. et al., JACS, 1955, 77, 2332- 2333 (synth) [https://doi.org/10.1021/ja01613a092]
  62. Ruijgrok, H.W.L., Planta Med., 1963, 11, 338- 347 (occur) [https://doi.org/10.1055/s-0028-1100248]
  63. Suga, T. et al., Bull. Chem. Soc. Jpn., 1982, 55, 1584- 1587 (biosynth) [https://doi.org/10.1246/bcsj.55.1584]
  64. Mares, D. et al., Mycopathologia, 1987, 98, 133- 140 (activity)
  65. Yamamoto, M. et al., Chem. Comm., 1988, 560- 561 (synth) [https://doi.org/10.1039/c39880000560]
  66. Martin, M.L. et al., Planta Med., 1990, 56, 66- 69 (activity) [https://doi.org/10.1055/s-2006-960886]
  67. Alibés, R. et al., Synth. Commun., 1990, 20, 2607- 2615 (synth)
  68. Southwell, I.A. et al., Phytochemistry, 1993, 33, 1099 (Clematis constit, bibl) [https://doi.org/10.1016/0031-9422(93)85030-U]
  69. Crey, C. et al., Synth. Commun., 2003, 33, 3727- 3732 (synth)
  70. Sorg, A. et al., Synlett, 2005, 1286- 1290 (synth)
  71. Rambabu, D. et al., Tet. Lett., 2013, 54, 2151- 2155 (synth) [https://doi.org/10.1016/j.tetlet.2013.02.040]
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Anticancer Citations
  1. Haddock, E.A. et al., JCS Perkin 1, 1982, 2515- 2524 (isol, struct, pmr, cmr, rev) [https://doi.org/10.1039/p19820002515]
  2. Nishizawa, M. et al., JCS Perkin 1, 1982, 2963- 2968; 1983, 961 - 965 (Rhus semialata constits, Quercus infectaria constits) [https://doi.org/10.1039/p19820002963]
  3. Nishizawa, M. et al., Chem. Pharm. Bull., 1983, 31, 2593- 2600 (Paeonia lactiflora constits) [https://doi.org/10.1248/cpb.31.2593]
  4. Nishizawa, M. et al., Phytochemistry, 1985, 24, 2411- 2413 (Spirogyra constits) [https://doi.org/10.1016/S0031-9422(00)83053-8]
  5. Nonaka, G. et al., Chem. Pharm. Bull., 1987, 35, 3127- 3131 (struct, pmr, cmr) [https://doi.org/10.1248/cpb.35.3127]
  6. Kandil, F.E. et al., Phytochemistry, 1996, 42, 1243- 1245 (2-Trigalloyl-1,3,4,6-tetragalloylglucose, uv, pmr, cmr) [https://doi.org/10.1016/0031-9422(95)00924-8]
  7. Kandil, F.E. et al., Phytochemistry, 2001, 58, 611- 613 (Monacanthin A) [https://doi.org/10.1016/S0031-9422(01)00265-5]
  8. Duan, D. et al., Bioorg. Med. Chem. Lett., 2004, 14, 6041- 6044 (antiviral activity) [https://doi.org/10.1016/j.bmcl.2004.09.067]
  9. Zhang, J. et al., Pharm. Res., 2009, 26, 2066- 2080 (rev, activity)
  10. Cho, J.-Y. et al., Food Chem., 2010, 123, 501- 506 (isol, activity) [https://doi.org/10.1016/j.foodchem.2010.04.072]
  11. Baumgartner, R.R. et al., J. Nat. Prod., 2010, 73, 1578- 1581, 1742§ (isol, activity) [https://doi.org/10.1021/np100258e]
  12. Cryan, L.M. et al., J. Med. Chem., 2013, 56, 1940- 1945 (activity) [https://doi.org/10.1021/jm301558t]
  13. Cao, Y. et al., J. Nat. Med. (Tokyo), 2014, 68, 465- 472 (rev, activity)
  14. Tuominen, A. et al., Phytochemistry, 2015, 115, 239- 251 (Sylvatiins A,C) [https://doi.org/10.1016/j.phytochem.2015.01.005]
[top⬆]