The Plant Cell Culture Library

Ailanthus altissima
Cell Line ID AA-13605 C1
Media Type B50
Availability Medium
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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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 FoundationCenter for Agriculture, Food and the Environment

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