The University of Massachusetts Amherst

The Plant Cell Culture Library

Ailanthus altissima
Cell Line ID AA-13605 C1
Media Type B50
Availability Low
Order Sapindales
Family Simaroubaceae
Genus Ailanthus
Antiviral Species Level ➡ 19 citations
Antifungal Genus Level ➡ 36 citations
Anthelmintic Genus Level ➡ 1 citations
Insecticidal Species Level ➡ 56 citations
Anticancer Species Level ➡ 56 citations
Common Names Tree Of Heaven
Culture Initiation Site Dusseldorf
Plant Habit Tree deciduous
Plant Habitat Temperate
Culture Start Material Seed
Native Range North China
Plant Supplier Comm/Chiltern Seeds
Antiviral Citations
  1. Sawabe, A. et al., Nippon Kagaku Kaishi, 1986, 60, 593- 599 (Citrusins) [https://doi.org/10.1271/nogeikagaku1924.60.593]
  2. Deyama, T. et al., Chem. Pharm. Bull., 1987, 35, 1803- 1807 (Citrusin B) [https://doi.org/10.1248/cpb.35.1803]
  3. Li, S. et al., Phytochemistry, 1998, 49, 2125- 2128 (synth, pmr, cmr) [https://doi.org/10.1016/S0031-9422(98)00449-X]
  4. Takara, K. et al., Biosci., Biotechnol., Biochem., 2002, 66, 29- 35 (cane sugar 3,3'-di-Me ether 7-glucosides)
  5. Su, B.-N. et al., J. Nat. Prod., 2002, 65, 163- 169 (Dadahols)
  6. Cutillo, F. et al., J. Agric. Food Chem., 2003, 51, 6165- 6172 (Brassica fruticulosa lignans,activity) [https://doi.org/10.1021/jf034644c]
  7. Zhu, H. et al., Z. Naturforsch., B, 2004, 59, 1063- 1066 (Ligularia veitchiana constit)
  8. Yuan, C.S. et al., Chin. Chem. Lett., 2005, 16, 781- 782 (Armaoside)
  9. Liao, S.-G. et al., Helv. Chim. Acta, 2006, 89, 73- 80 (Wikstroemol, Wikstroemone)
  10. Yuan, C.-S. et al., J. Asian Nat. Prod. Res., 2007, 9, 673- 677 (Armaoside, config)
  11. Gan, M. et al., J. Nat. Prod., 2008, 71, 647- 654 (Iodes cirrhosa glucoside) [https://doi.org/10.1021/np7007329]
  12. Liang, S. et al., J. Nat. Prod., 2008, 71, 1902- 1905 (Armaosigenin) [https://doi.org/10.1021/np8004166]
  13. Machida, K. et al., Magn. Reson. Chem., 2008, 46, 990- 994 (3,3',5-tri-Me ether 9'-glucosides)
  14. Machida, K. et al., J. Nat. Med. (Tokyo), 2009, 63, 227- 231 (3,3',5-tri-Me ether 7'-glucoside)
  15. Feng, X.-S. et al., Molecules, 2009, 14, 953- 958 (Syringa velutina glucoside)
  16. Liao, P.-Y. et al., Yunnan Zhiwu Yanjiu, 2010, 32, 183- 188 (Eupatorin A)
  17. Liu, Y.-B. et al., Helv. Chim. Acta, 2011, 94, 1685- 1691 (penta-Me ether)
  18. Lin, S. et al., Zhongguo Zhongyao Zazhi, 2011, 36, 1755- 1762 (5'-Methoxyligusinenoside B)
  19. Su, Y. et al., J. Braz. Chem. Soc., 2012, 23, 1925- 1932 (Chirita longgangensis aldehyde) [https://doi.org/10.1590/S0103-50532012005000068]
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Antifungal Citations
  1. Pinto, A.V. et al., Ann. Acad. Bras. Ciènc., 1982, 54, 1 (synth)
  2. Rao, M.M. et al., J. Nat. Prod., 1982, 45, 600- 604 (Tabebuia cassinoides constits) [https://doi.org/10.1021/np50023a014]
  3. Lopes, C.C. et al., J. Het. Chem., 1984, 21, 621- 622 (synth, uv, pmr, bibl)
  4. Wagner, H. et al., Helv. Chim. Acta, 1989, 72, 659- 667 (Tabebuia avellandae constits)
  5. Zani, C.L. et al., Phytochemistry, 1991, 30, 2379- 2381 (Tabebuia ochracea constits, 6-methoxy) [https://doi.org/10.1016/0031-9422(91)83653-3]
  6. Braga de Oliveira, A. et al., Phytochemistry, 1993, 34, 1409- 1412 (Tabebuia incana constits) [https://doi.org/10.1016/0031-9422(91)80039-4]
  7. Kosuge, K. et al., Chem. Pharm. Bull., 1994, 42, 1669- 1671 (Ailanthus integrifolia constits) [https://doi.org/10.1248/cpb.42.1669]
  8. Diaz, F. et al., J. Nat. Prod., 1996, 59, 423- 424 (5-hydroxy-1'ξ-alcohol, 7-methoxy, 7-methoxy-1'ξ-alcohol) [https://doi.org/10.1021/np9602022]
  9. Koyanagi, J. et al., J. Het. Chem., 1997, 34, 407- 412 (synth)
  10. Hagiwara, H. et al., Heterocycles, 1999, 51, 497- 500 (synth) [https://doi.org/10.3987/COM-98-8430]
  11. Moideen, S.V.K. et al., Planta Med., 1999, 65, 536- 540 (1'-alcohol, activity) [https://doi.org/10.1055/s-1999-14011]
  12. Rodriguez, E.C. et al., Rev. Latinoam. Quim., 2000, 27, 89
  13. Lee, Y.R. et al., Synth. Commun., 2001, 31, 381- 386 (1'-alcohol, synth, ir, pmr)
  14. Fotsing, M.T. et al., Planta Med., 2003, 69, 767- 770 (7-methoxy)
  15. Takano, A. et al., Anticancer Res., 2009, 29, 455- 464 (pharmacol)
  16. Fotsing, M.T. et al., Rasayan J. Chem., 2011, 4, 242- 244 (6,7-dimethoxy)
  17. Haynes, H.F. et al., Aust. J. Sci. Res., Ser. A, 1952, 5, 387- 400 (isol, uv, struct, oxide)
  18. Cannon, J.R. et al., Aust. J. Chem., 1956, 6, 86- 89 (isol) [https://doi.org/10.1071/CH9530086]
  19. Rosenkranz, H.J. et al., Annalen, 1966, 691, 159- 164 (synth, uv, ir)
  20. Mitscher, L.A. et al., Heterocycles, 1975, 3, 7- 14 (synth) [https://doi.org/10.3987/R-1975-01-0007]
  21. Oehl, R. et al., Chem. Ber., 1976, 109, 705- 709 (synth, uv, ir, ms)
  22. Ohmoto, T. et al., Chem. Pharm. Bull., 1976, 24, 1532- 1536; 1981, 29, 390 - 395 (isol, uv,ir, pmr, ms, synth, oxide) [https://doi.org/10.1248/cpb.24.1532]
  23. Campos, O. et al., Heterocycles, 1980, 14, 975- 984 (synth)
  24. Forgacs, P. et al., Planta Med., 1982, 46, 187- 189 (isol) [https://doi.org/10.1055/s-2007-971212]
  25. Anderson, L.A. et al., J. Nat. Prod., 1983, 46, 374- 378 (isol, biochem) [https://doi.org/10.1021/np50027a014]
  26. Cain, M. et al., JACS, 1983, 105, 907- 913 (synth) [https://doi.org/10.1021/ja00342a045]
  27. Aragozzini, F. et al., Plant Cell Rep., 1988, 7, 213- 215 (biosynth) [https://doi.org/10.1007/BF00269327]
  28. Ohmoto, T. et al., Alkaloids (Academic Press), 1989, 36, 135- 170 (rev)
  29. He, W. et al., Meded. Fac. Landbouwwet., Rijksuniv. Gent, 1998, 64, 565- 569 (activity)
  30. Rossler, U. et al., Tet. Lett., 1999, 40, 7075- 7078 (synth) [https://doi.org/10.1016/S0040-4039(99)01472-0]
  31. Czerwinski, K.M. et al., Synth. Commun., 2003, 33, 1225- 1231 (synth, pmr, cmr)
  32. Bröckelmann, M.G. et al., Eur. J. Org. Chem., 2004, 4856- 4863 (isol, pmr, cmr, ms)
  33. Soriano-Agatón, F. et al., J. Nat. Prod., 2005, 68, 1581- 1587 (synth, pmr, cmr) [https://doi.org/10.1021/np050250z]
  34. Suzuki, H. et al., Synthesis, 2005, 28- 31 (synth, ir, pmr, cmr)
  35. Gollner, A. et al., Org. Lett., 2010, 12, 1352- 1355 (synth, ir, pmr, cmr, ms) [https://doi.org/10.1021/ol100300s]
  36. Dai, J. et al., Molecules, 2016, 21, 493:1- 13 (Canthin-6-ones, rev, synth, biosynth, activity)
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Anthelmintic Citations
  1. Caboni P, Ntalli NG, Aissani N, Cavoski I, Angioni A. Nematicidal activity of (E,E)-2,4-decadienal and (E)-2-decenal from Ailanthus altissima against Meloidogyne javanica. J Agric Food Chem. 2012 Feb 1;60(4):1146-51. [https://doi.org/10.1021/jf2044586.] Epub 2012 Jan 19. PubMed PMID: 22224661.
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Insecticidal Citations
  1. Ham, A. et al., JACS, 1954, 76, 6066- 6068 (Glaucarubin, isol, ir) [https://doi.org/10.1021/ja01652a060]
  2. US Pat., 1958, 2 864 745 (Glaucarubin, amoebicidal activity)
  3. Polonsky, J. et al., Bull. Soc. Chim. Fr., 1964, 1818- 1826, 1827 - 1835; 1965, 2793 - 2799 (Glaucarubin, Glaucarubolone, pmr, struct)
  4. Kartha, G. et al., JACS, 1964, 86, 3630- 3634 (Glaucarubin, cryst struct) [https://doi.org/10.1021/ja01072a008]
  5. Polonsky, J. et al., Tet. Lett., 1964, 5, 3983- 3990 (Ailanthone, Ailanthinone) [https://doi.org/10.1016/S0040-4039(01)89352-7]
  6. Casinovi, G.G. et al., Tet. Lett., 1964, 5, 3991- 3997 (Ailanthinone, struct) [https://doi.org/10.1016/S0040-4039(01)89353-9]
  7. Polonsky, J. et al., Bull. Soc. Chim. Fr., 1965, 2793- 2799 (Chaparrinone)
  8. De Mayo, P. et al., Can. J. Chem., 1965, 43, 2996- 3007, 3008 - 3017 (Chaparrin)
  9. Nyburg, S.C. et al., Chem. Comm., 1965, 203- 204 (Glaucarubin, abs config)
  10. Moron, J. et al., Tet. Lett., 1965, 9, 385- 390 (Simaroubaceae terpenoids, biosynth) [https://doi.org/10.1016/S0040-4039(01)98767-2]
  11. Fourrey, J.L. et al., Org. Mass Spectrom., 1968, 1, 819- 833 (ms)
  12. Gaudemer, A. et al., Phytochemistry, 1968, 4, 149- 153 (Glaucarubolone, Glaucarubinone,struct) [https://doi.org/10.1016/S0031-9422(00)86157-9]
  13. Stöcklin, W. et al., Phytochemistry, 1969, 8, 1565- 1569 (Glaucarubol, struct) [https://doi.org/10.1016/S0031-9422(00)85931-2]
  14. Moron, J. et al., Phytochemistry, 1971, 10, 585- 592 (Glaucarubolone, Glaucarubinone,biosynth) [https://doi.org/10.1016/S0031-9422(00)94702-2]
  15. Kupchan, S.M. et al., JOC, 1975, 40, 654- 656 (Ailanthinone, Dehydroailanthinone, 2'S-Acetylglaucarubinone, struct) [https://doi.org/10.1021/jo00893a024]
  16. Polonsky, J. et al., JOC, 1975, 40, 2499- 2504 (cmr) [https://doi.org/10.1021/jo00905a017]
  17. Gottlieb, H.E. et al., JOC, 1975, 40, 2499- 2504 (Ailanthinone, Glaucarubinone, cmr)
  18. Kupchan, S.M. et al., J. Med. Chem., 1976, 19, 1130- 1133 (Glaucarubolone esters, sar) [https://doi.org/10.1021/jm00231a009]
  19. Ogura, M. et al., J. Nat. Prod., 1977, 40, 579- 584 (2'-Acetylglaucarubin)
  20. Polonsky, J. et al., Experientia, 1978, 34, 1122- 1123 (13,18-Dehydroglaucarubinone)
  21. Polonsky, J. et al., C. R. Seances Acad. Sci., Ser. C, 1979, 288, 269- 271 (Castelanone,struct)
  22. Khan, S.A. et al., Indian J. Chem., Sect. B, 1980, 19, 183- 184 (Excelsin, struct)
  23. Khan, S.A. et al., Phytochemistry, 1980, 19, 2484- 2485 (13,18-Dehydroexcelsin) [https://doi.org/10.1016/S0031-9422(00)91062-8]
  24. Tri, M.V. et al., J. Nat. Prod., 1981, 44, 279- 284 (Soularubinone, struct, activity)
  25. Naora, H. et al., Chem. Pharm. Bull., 1983, 56, 3694- 3698 (Shinjulactone A, Ailanthone,cryst struct)
  26. Handa, S.S. et al., J. Nat. Prod., 1983, 46, 359- 364 (Holacanthone, struct, activity) [https://doi.org/10.1021/np50027a011]
  27. Ishibashi, M. et al., Bull. Chem. Soc. Jpn., 1984, 57, 2484- 2489, 2496-2501 (Shinjulactone D, Shinjuglycosides)
  28. Waterman, P.G. et al., Planta Med., 1984, 50, 261- 263 (Odyendyea gabonensis constits) [https://doi.org/10.1055/s-2007-969694]
  29. Bhatnagar, S. et al., Tet. Lett., 1984, 25, 299- 302 (Simarouba glauca constits, cryst struct) [https://doi.org/10.1016/S0040-4039(00)99867-8]
  30. Bhatia, N. et al., J. Indian Chem. Soc., 1985, 62, 75- 76 (Excelsin, cmr)
  31. Lumonadio, L. et al., Phytochemistry, 1985, 24, 2387- 2389 (Hannoa klaineana constits) [https://doi.org/10.1016/S0031-9422(00)83047-2]
  32. Niimi, Y. et al., Bull. Chem. Soc. Jpn., 1986, 59, 1638- 1640 (Shinjulactone N) [https://doi.org/10.1246/bcsj.59.1638]
  33. O'Neill, M.F. et al., J. Ethnopharmacol., 1988, 22, 183- 190 (Simarouba amara constits) [https://doi.org/10.1016/0378-8741(88)90126-2]
  34. Hamburger, M.O. et al., Planta Med., 1988, 54, 352- 355 (pmr, cmr) [https://doi.org/10.1055/s-2006-962456]
  35. Gross, R.S. et al., JACS, 1990, 112, 9436- 9437; 1993, 115, 6078 - 6093 (Chaparrinone,synth) [https://doi.org/10.1021/ja00181a079]
  36. Chaudhuri, S.K. et al., Phytochemistry, 1992, 31, 3961- 3964 (Castelosides A,B) [https://doi.org/10.1016/S0031-9422(00)97563-0]
  37. Fleck, T.J. et al., Tet. Lett., 1992, 33, 1813- 1816 (Glaucarubolone, Holacanthone, synth) [https://doi.org/10.1016/S0040-4039(00)74149-9]
  38. Diakanamwa, C. et al., J. Nat. Prod., 1993, 56, 1817- 1820 (14-Hydroxychaparrenone) [https://doi.org/10.1021/np50100a024]
  39. Grieco, P.A. et al., JACS, 1993, 115, 6078- 6093 (Glaucarubol, synth) [https://doi.org/10.1021/ja00067a025]
  40. Grieco, P.A. et al., Phytochemistry, 1994, 37, 1451- 1454 (Peninsularinone, Glaucarubolone,Glaucarubinone, struct) [https://doi.org/10.1016/S0031-9422(00)90431-X]
  41. Dou, J. et al., J. Nat. Prod., 1996, 59, 73- 76 (Castela texana constit) [https://doi.org/10.1021/np960013j]
  42. Kubota, K. et al., J. Nat. Prod., 1996, 59, 683- 686 (Ailantinol B) [https://doi.org/10.1021/np960427c]
  43. Rodriguez Fo, E. et al., Phytochemistry, 1996, 43, 857- 862 (Glaucarubolone, pmr, cmr)
  44. Vieira, I.J.C. et al., Fitoterapia, 1998, 69, 88- 90 (Glaucarubol, Glaucarubolone, pmr, cmr)
  45. Francois, G. et al., Int. J. Parasitol., 1998, 28, 635- 640 (activity) [https://doi.org/10.1016/S0020-7519(98)00008-3]
  46. Ozeki, A. et al., J. Nat. Prod., 1998, 61, 776- 780 (Glaucarubolone, Glaucarubol, activity) [https://doi.org/10.1021/np980023f]
  47. Dayan, F.E. et al., Pestic. Biochem. Physiol., 1999, 65, 15- 24 (activity) [https://doi.org/10.1006/pest.1999.2432]
  48. Grieco, P.A. et al., Phytochemistry, 1999, 50, 637- 645 (Castela polyandra constits, cryst struct) [https://doi.org/10.1016/S0031-9422(98)00589-5]
  49. Kanchanapoom, T. et al., Phytochemistry, 2001, 57, 1205- 1208 (Iandonoside A, struct) [https://doi.org/10.1016/S0031-9422(01)00235-7]
  50. Joshi, B.C. et al., Phytochemistry, 2003, 62, 579- 584 (3,4-Dihydroexcelsin, struct) [https://doi.org/10.1016/S0031-9422(02)00493-4]
  51. Jacobs, H. et al., Biochem. Syst. Ecol., 2007, 35, 42- 44 (Castela macrophylla constits) [https://doi.org/10.1016/j.bse.2006.08.005]
  52. Beutler, J.A. et al., J. Nat. Prod., 2009, 72, 503- 506 (Holacanthone, activity) [https://doi.org/10.1021/np800732n]
  53. Usami, Y. et al., J. Nat. Prod., 2010, 73, 1553- 1558 (2'R-Acetylglaucarubinone) [https://doi.org/10.1021/np100406d]
  54. Wang, Y. et al., Bioorg. Med. Chem. Lett., 2013, 23, 654- 657 (Altissinols A,B) [https://doi.org/10.1016/j.bmcl.2012.11.116]
  55. Meng, D. et al., Fitoterapia, 2014, 92, 105- 110 (Δ4-14-Hydroxyglaucarubol, cryst struct) [https://doi.org/10.1016/j.fitote.2013.10.009]
  56. Sax's Dangerous Properties of Industrial Materials, 11th edn., J. Wiley, 2004, GEW700
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Anticancer Citations
  1. Ham, A. et al., JACS, 1954, 76, 6066- 6068 (Glaucarubin, isol, ir) [https://doi.org/10.1021/ja01652a060]
  2. US Pat., 1958, 2 864 745 (Glaucarubin, amoebicidal activity)
  3. Polonsky, J. et al., Bull. Soc. Chim. Fr., 1964, 1818- 1826, 1827 - 1835; 1965, 2793 - 2799 (Glaucarubin, Glaucarubolone, pmr, struct)
  4. Kartha, G. et al., JACS, 1964, 86, 3630- 3634 (Glaucarubin, cryst struct) [https://doi.org/10.1021/ja01072a008]
  5. Polonsky, J. et al., Tet. Lett., 1964, 5, 3983- 3990 (Ailanthone, Ailanthinone) [https://doi.org/10.1016/S0040-4039(01)89352-7]
  6. Casinovi, G.G. et al., Tet. Lett., 1964, 5, 3991- 3997 (Ailanthinone, struct) [https://doi.org/10.1016/S0040-4039(01)89353-9]
  7. Polonsky, J. et al., Bull. Soc. Chim. Fr., 1965, 2793- 2799 (Chaparrinone)
  8. De Mayo, P. et al., Can. J. Chem., 1965, 43, 2996- 3007, 3008 - 3017 (Chaparrin)
  9. Nyburg, S.C. et al., Chem. Comm., 1965, 203- 204 (Glaucarubin, abs config)
  10. Moron, J. et al., Tet. Lett., 1965, 9, 385- 390 (Simaroubaceae terpenoids, biosynth) [https://doi.org/10.1016/S0040-4039(01)98767-2]
  11. Fourrey, J.L. et al., Org. Mass Spectrom., 1968, 1, 819- 833 (ms)
  12. Gaudemer, A. et al., Phytochemistry, 1968, 4, 149- 153 (Glaucarubolone, Glaucarubinone,struct) [https://doi.org/10.1016/S0031-9422(00)86157-9]
  13. Stöcklin, W. et al., Phytochemistry, 1969, 8, 1565- 1569 (Glaucarubol, struct) [https://doi.org/10.1016/S0031-9422(00)85931-2]
  14. Moron, J. et al., Phytochemistry, 1971, 10, 585- 592 (Glaucarubolone, Glaucarubinone,biosynth) [https://doi.org/10.1016/S0031-9422(00)94702-2]
  15. Kupchan, S.M. et al., JOC, 1975, 40, 654- 656 (Ailanthinone, Dehydroailanthinone, 2'S-Acetylglaucarubinone, struct) [https://doi.org/10.1021/jo00893a024]
  16. Polonsky, J. et al., JOC, 1975, 40, 2499- 2504 (cmr) [https://doi.org/10.1021/jo00905a017]
  17. Gottlieb, H.E. et al., JOC, 1975, 40, 2499- 2504 (Ailanthinone, Glaucarubinone, cmr)
  18. Kupchan, S.M. et al., J. Med. Chem., 1976, 19, 1130- 1133 (Glaucarubolone esters, sar) [https://doi.org/10.1021/jm00231a009]
  19. Ogura, M. et al., J. Nat. Prod., 1977, 40, 579- 584 (2'-Acetylglaucarubin)
  20. Polonsky, J. et al., Experientia, 1978, 34, 1122- 1123 (13,18-Dehydroglaucarubinone)
  21. Polonsky, J. et al., C. R. Seances Acad. Sci., Ser. C, 1979, 288, 269- 271 (Castelanone,struct)
  22. Khan, S.A. et al., Indian J. Chem., Sect. B, 1980, 19, 183- 184 (Excelsin, struct)
  23. Khan, S.A. et al., Phytochemistry, 1980, 19, 2484- 2485 (13,18-Dehydroexcelsin) [https://doi.org/10.1016/S0031-9422(00)91062-8]
  24. Tri, M.V. et al., J. Nat. Prod., 1981, 44, 279- 284 (Soularubinone, struct, activity)
  25. Naora, H. et al., Chem. Pharm. Bull., 1983, 56, 3694- 3698 (Shinjulactone A, Ailanthone,cryst struct)
  26. Handa, S.S. et al., J. Nat. Prod., 1983, 46, 359- 364 (Holacanthone, struct, activity) [https://doi.org/10.1021/np50027a011]
  27. Ishibashi, M. et al., Bull. Chem. Soc. Jpn., 1984, 57, 2484- 2489, 2496-2501 (Shinjulactone D, Shinjuglycosides)
  28. Waterman, P.G. et al., Planta Med., 1984, 50, 261- 263 (Odyendyea gabonensis constits) [https://doi.org/10.1055/s-2007-969694]
  29. Bhatnagar, S. et al., Tet. Lett., 1984, 25, 299- 302 (Simarouba glauca constits, cryst struct) [https://doi.org/10.1016/S0040-4039(00)99867-8]
  30. Bhatia, N. et al., J. Indian Chem. Soc., 1985, 62, 75- 76 (Excelsin, cmr)
  31. Lumonadio, L. et al., Phytochemistry, 1985, 24, 2387- 2389 (Hannoa klaineana constits) [https://doi.org/10.1016/S0031-9422(00)83047-2]
  32. Niimi, Y. et al., Bull. Chem. Soc. Jpn., 1986, 59, 1638- 1640 (Shinjulactone N) [https://doi.org/10.1246/bcsj.59.1638]
  33. O'Neill, M.F. et al., J. Ethnopharmacol., 1988, 22, 183- 190 (Simarouba amara constits) [https://doi.org/10.1016/0378-8741(88)90126-2]
  34. Hamburger, M.O. et al., Planta Med., 1988, 54, 352- 355 (pmr, cmr) [https://doi.org/10.1055/s-2006-962456]
  35. Gross, R.S. et al., JACS, 1990, 112, 9436- 9437; 1993, 115, 6078 - 6093 (Chaparrinone,synth) [https://doi.org/10.1021/ja00181a079]
  36. Chaudhuri, S.K. et al., Phytochemistry, 1992, 31, 3961- 3964 (Castelosides A,B) [https://doi.org/10.1016/S0031-9422(00)97563-0]
  37. Fleck, T.J. et al., Tet. Lett., 1992, 33, 1813- 1816 (Glaucarubolone, Holacanthone, synth) [https://doi.org/10.1016/S0040-4039(00)74149-9]
  38. Diakanamwa, C. et al., J. Nat. Prod., 1993, 56, 1817- 1820 (14-Hydroxychaparrenone) [https://doi.org/10.1021/np50100a024]
  39. Grieco, P.A. et al., JACS, 1993, 115, 6078- 6093 (Glaucarubol, synth) [https://doi.org/10.1021/ja00067a025]
  40. Grieco, P.A. et al., Phytochemistry, 1994, 37, 1451- 1454 (Peninsularinone, Glaucarubolone,Glaucarubinone, struct) [https://doi.org/10.1016/S0031-9422(00)90431-X]
  41. Dou, J. et al., J. Nat. Prod., 1996, 59, 73- 76 (Castela texana constit) [https://doi.org/10.1021/np960013j]
  42. Kubota, K. et al., J. Nat. Prod., 1996, 59, 683- 686 (Ailantinol B) [https://doi.org/10.1021/np960427c]
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