The University of Massachusetts Amherst

The Plant Cell Culture Library

Artemisia scoparia
Cell Line ID AS-05137
Media Type B105
Lowest Tolerable USDA Zone 3a
Drought Tolerance Tolerant
Availability medium
Order Asterales
Family Compositae
Genus Artemisia
Antiviral Genus Level ➡ 52 citations
Antibacterial Genus Level ➡ 282 citations
Antifungal Genus Level ➡ 296 citations
Trypanocidal Genus Level ➡ 8 citations
Anthelmintic Genus Level ➡ 15 citations
Insecticidal Genus Level ➡ 123 citations
Anticancer Genus Level ➡ 238 citations
Culture Initiation Site Lausanne
Plant Habit Herb biennial
Plant Habitat Temperate
Culture Start Material Seed
Native Range Central & East Europe, South West Asia, Siberia
Plant Supplier Botanical Garden Lausanne
Antiviral Citations
  1. Tu, Y.Y. et al., Yaoxue Xuebao, 1981, 16, 366- 370 (isol)
  2. Tu, Y.Y. et al., Planta Med., 1982, 44, 143- 145 (Artemisinin D)
  3. Jung, M. et al., JOC, 1986, 51, 5417- 5419 (synth, pmr, cryst struct, abs config) [https://doi.org/10.1021/jo00376a070]
  4. Xu, X.-X. et al., Tetrahedron, 1986, 42, 819- 826 (synth, ir)
  5. Brossi, A. et al., J. Med. Chem., 1988, 31, 645- 650 (synth, pmr) [https://doi.org/10.1021/jm00398a026]
  6. Liu, H.-J. et al., Heterocycles, 1996, 42, 493- 497 (Artemisinin D) [https://doi.org/10.3987/COM-95-S74]
  7. Agrawal, P.K. et al., J. Sci. Ind. Res., 1996, 55, 17- 26 (cmr)
  8. Haslam, E. et al., JCS, 1964, 2137- 2146 (coffee constit)
  9. Scarpati, M.L. et al., Tet. Lett., 1964, 5, 2851- 2853 (Isochlorogenic acid A) [https://doi.org/10.1016/S0040-4039(00)70434-5]
  10. Corse, J. et al., Phytochemistry, 1965, 4, 527- 529 (uv, pmr) [https://doi.org/10.1016/S0031-9422(00)86209-3]
  11. Nichiforescu, E.A. et al., Khim. Prir. Soedin., 1970, 7, 546 (Vaccinium arctostaphylos constit)
  12. Nichiforescu, E.A. et al., Plant. Med. Phytother., 1970, 4, 56- 62 (Cynara scolymus constit)
  13. Timmermann, B.N. et al., J. Nat. Prod., 1983, 46, 365- 368 (Chrysothamnus paniculatus constit, pmr, cmr, ms) [https://doi.org/10.1021/np50027a012]
  14. Nishizawa, M. et al., Chem. Pharm. Bull., 1988, 36, 87- 95 (4-3-hydroxy-3-methylglutarate) [https://doi.org/10.1248/cpb.36.87]
  15. Chen, M. et al., Yaoxue Xuebao, 1994, 29, 617- 620 (Macroantoin G)
  16. Tatefuji, T. et al., Biol. Pharm. Bull., 1996, 19, 966- 970 (propolis constit) [https://doi.org/10.1248/bpb.19.966]
  17. Chudo, Y. et al., J. Agric. Food Chem., 1996, 44, 2037- 2039 (4-succinate) [https://doi.org/10.1021/jf960182+]
  18. Kodoma, M. et al., Phytochemistry, 1998, 47, 371- 373 (Pyrus pyrifolia constit, activity) [https://doi.org/10.1016/S0031-9422(97)00621-3]
  19. Miketova, P. et al., J. Mass Spectrom., 1999, 34, 1240- 1252 (ms)
  20. Heilmann, J. et al., Phytochemistry, 1999, 51, 713- 718 (Dicaffeoyl-1-isobutyrylquinic acid) [https://doi.org/10.1016/S0031-9422(99)00082-5]
  21. Kwon, H.C. et al., Chem. Pharm. Bull., 2000, 48, 1796- 1798 (3,5-Dicaffeoylmucoquinic acid) [https://doi.org/10.1248/cpb.48.1796]
  22. Peng, L.Y. et al., Fitoterapia, 2000, 71, 713- 715 (butyl ester) [https://doi.org/10.1016/S0367-326X(00)00212-4]
  23. Zhang, W.-D. et al., J. Asian Nat. Prod. Res., 2000, 2, 283- 288 (Macroantoin G)
  24. Zhang, W.-D. et al., Yaoxue Xuebao, 2001, 36, 360- 363 (1-Me ether Me ester)
  25. Silva, B.M. et al., J. Agric. Food Chem., 2004, 52, 4705- 4712 (Cydonia oblonga constit) [https://doi.org/10.1021/jf040057v]
  26. Teramachi, F. et al., J. Nat. Prod., 2005, 68, 794- 796 (Dicaffeoyl-4-coumaroylquinic acid) [https://doi.org/10.1021/np0500631]
  27. Kim, H.J. et al., Planta Med., 2005, 71, 871- 876 (3,5-Dicaffeoylepiquinic acid) [https://doi.org/10.1055/s-2005-873115]
  28. Dini, I. et al., J. Agric. Food Chem., 2006, 54, 8733- 8737 (Ipomoea batatas constit) [https://doi.org/10.1021/jf061687v]
  29. Kim, H.J. et al., J. Nat. Prod., 2006, 69, 600- 603 (4-O-(4-carboxy-3-hydroxy-3-methylbutanoyl) Me ester, 5'-methoxy 3'-Me ether Et ester) [https://doi.org/10.1021/np050447r]
  30. Sprogøe, K. et al., J. Nat. Prod., 2007, 70, 1472- 1477 (Hubertia constits) [https://doi.org/10.1021/np0702741]
  31. Antognoni, F. et al., Fitoterapia, 2011, 82, 950- 954 (Irbic acid) [https://doi.org/10.1016/j.fitote.2011.05.008]
  32. Jaiswal, R. et al., J. Agric. Food Chem., 2011, 59, 4033- 4039 (Arnica montana constits) [https://doi.org/10.1021/jf103545k]
  33. Raheem, K.S. et al., Tet. Lett., 2011, 52, 7175- 7177 (synth) [https://doi.org/10.1016/j.tetlet.2011.10.127]
  34. Ela, M.A.A. et al., Helv. Chim. Acta, 2012, 95, 61- 66 (1-Me ether)
  35. Dahmani-Hamzaoui, N. et al., Helv. Chim. Acta, 2012, 95, 564- 576 (Artemisia herba-alba constit)
  36. Xiong, J. et al., Food Chem., 2013, 138, 327- 333 (activity) [https://doi.org/10.1016/j.foodchem.2012.10.127]
  37. Stojakowska, A. et al., Food Chem., 2013, 138, 1250- 1255 (Lactuca tuberosa constit) [https://doi.org/10.1016/j.foodchem.2012.11.062]
  38. Chen, J. et al., Fitoterapia, 2014, 99, 1- 6 (Gynura divaricata constits) [https://doi.org/10.1016/j.fitote.2014.08.015]
  39. Znati, M. et al., Molecules, 2014, 19, 16959- 16975 (Ferula lutea constit)
  40. Zou, X. et al., Phytochem. Lett., 2014, 7, 133- 136 (MTCQA, activity) [https://doi.org/10.1016/j.phytol.2013.11.002]
  41. Scarpati, M.L. et al., Tet. Lett., 1964, 5, 2851- 2853 (Isochlorogenic acid C) [https://doi.org/10.1016/S0040-4039(00)70434-5]
  42. Timmermann, B.N. et al., J. Nat. Prod., 1983, 46, 365- 368 (Chrysothamnus paniculatus constit) [https://doi.org/10.1021/np50027a012]
  43. Tatefuji, T. et al., Biol. Pharm. Bull., 1996, 19, 966- 970 (propolis constit) [https://doi.org/10.1248/bpb.19.966]
  44. Miketova, P. et al., J. Mass Spectrom., 1999, 34, 1240- 1252 (ms)
  45. Lin, L.C. et al., J. Nat. Prod., 1999, 62, 405- 408 (Dichrocephala bicoilor constit) [https://doi.org/10.1021/np980153o]
  46. Kwon, H.C. et al., Chem. Pharm. Bull., 2000, 48, 1796- 1798 (Aster scaber constit, activity) [https://doi.org/10.1248/cpb.48.1796]
  47. Zhang, W.-D. et al., J. Asian Nat. Prod. Res., 2000, 2, 283- 288 (Me ester)
  48. Farah, A. et al., J. Agric. Food Chem., 2005, 53, 1505- 1513 (1'→3-lactone) [https://doi.org/10.1021/jf048701t]
  49. Jaiswal, R. et al., J. Agric. Food Chem., 2011, 59, 4033- 4039 (Arnica montana constits) [https://doi.org/10.1021/jf103545k]
  50. Ela, M.A.A. et al., Helv. Chim. Acta, 2012, 95, 61- 66 (1-Me ether)
  51. Dahmani-Hamzaoui, N. et al., Helv. Chim. Acta, 2012, 95, 564- 576 (Atremisia herba-alba constit, activity)
  52. Chen, J. et al., Fitoterapia, 2014, 99, 1- 6 (Gynura divaricata constits) [https://doi.org/10.1016/j.fitote.2014.08.015]
[top⬆]
Antibacterial Citations
  1. Tu, Y.Y. et al., Planta Med., 1982, 44, 143- 145 (Artemisinic acid, isol)
  2. Wu, Z. et al., Huaxue Xuebao, 1984, 42, 596- 598 (4,5-Epoxyartemisinic acid)
  3. Zhou, W. et al., CA, 1985, 103, 160709 (config)
  4. Roth, R.J. et al., Planta Med., 1987, 53, 501- 502 (Artemisinic acid, isol) [https://doi.org/10.1055/s-2006-962787]
  5. Akhila, A. et al., Phytochemistry, 1990, 29, 2129- 2131 (biosynth) [https://doi.org/10.1016/0031-9422(90)83020-2]
  6. Misra, L.N. et al., J. Nat. Prod., 1993, 56, 215- 219 (Artemisinic acid, cryst struct, pmr, cmr) [https://doi.org/10.1021/np50092a005]
  7. Garbarino, J.A. et al., Phytochemistry, 1993, 32, 987- 989 (Nolana coelestris constits) [https://doi.org/10.1016/0031-9422(93)85241-I]
  8. Vonwiller, S.C. et al., Planta Med., 1993, 59, 562- 563 (Artemisinic acid, isol) [https://doi.org/10.1055/s-2006-959762]
  9. Vandenberghe, D.R. et al., J. Nat. Prod., 1995, 58, 798- 803 (Artemisinic acid, isol) [https://doi.org/10.1021/np50119a027]
  10. Sy, L.-K. et al., Phytochemistry, 1998, 48, 1207- 1211 (Methyl artemisinate)
  11. Bardón, A. et al., Phytochemistry, 1999, 52, 1323- 1329 (Rupestrenol, pmr, cmr, cryst struct) [https://doi.org/10.1016/S0031-9422(99)00452-5]
  12. Sy, L.-K. et al., Tetrahedron, 2001, 57, 8495- 8510 (synth)
  13. Kong, J. et al., RSC Adv., 2013, 3, 7622- 7641 (Artemisininc acid, rev)
  14. Barton, D.H.R. et al., Q. Rev., Chem. Soc., 1957, 11, 189 (rev) [https://doi.org/10.1039/qr9571100189]
  15. Corey, E.J. et al., JACS, 1964, 86, 485 (synth, bibl) [https://doi.org/10.1021/ja01057a040]
  16. Hill, H.C. et al., JCS(C), 1968, 93 (ms)
  17. Gollnick, K. et al., Tet. Lett., 1968, 689 (synth) [https://doi.org/10.1016/S0040-4039(00)75613-9]
  18. Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhäuser Verlag, 1972, no. 1929 (occur)
  19. Croteau, R. et al., Phytochemistry, 1972, 11, 1055 (biosynth) [https://doi.org/10.1016/S0031-9422(00)88453-8]
  20. Warnhoff, E.W. et al., Can. J. Chem., 1973, 51, 3955 (purifn) [https://doi.org/10.1139/v73-589]
  21. Opdyke, D.L.J., Food Cosmet. Toxicol., 1973, 11, 1059 (rev, tox) [https://doi.org/10.1016/0015-6264(73)90250-2]
  22. Morris, W.W., J. Assoc. Off. Anal. Chem., 1973, 56, 1037 (ir)
  23. Robertson, J., Int. Rev. Sci.: Phys. Chem., Ser. Two, 1975, 11, 57 (rev)
  24. Kumar, A. et al., Synthesis, 1976, 461 (synth) [https://doi.org/10.1055/s-1976-24082]
  25. Peyron, L., Riv. Ital. Essenze, Profumi, Piante Off., Aromi, Saponi, Cosmet., Aerosol, 1977,59, 603 (rev)
  26. Mauer, B. et al., Helv. Chim. Acta, 1983, 66, 2223 (epoxide)
  27. McMurry, J.E., Tet. Lett., 1983, 24, 1885 (synth) [https://doi.org/10.1016/S0040-4039(00)81797-9]
  28. Ohtsuka, Y. et al., JOC, 1984, 49, 2326 (synth) [https://doi.org/10.1021/jo00187a006]
  29. Berry, K.M. et al., Phytochemistry, 1985, 24, 2893 (2-Epicaryophyllene) [https://doi.org/10.1016/0031-9422(85)80022-4]
  30. Hinkley, S.F.R. et al., Phytochemistry, 1994, 35, 1489 (2-Epicaryophyllene, abs config) [https://doi.org/10.1016/S0031-9422(00)86882-X]
  31. Suginome, H. et al., JCS Perkin 1, 1995, 69 (synth)
  32. Fricke, C. et al., Phytochemistry, 1995, 39, 1119 ((+)-β-Caryophyllene) [https://doi.org/10.1016/0031-9422(95)00184-9]
  33. Encyclopedia of Food and Color Additives, (ed. Burdock, G.A.), CRC Press, 1997, 527- 528 (β-Caryophyllene, occur)
  34. Collado, I.G. et al., Nat. Prod. Rep., 1998, 15, 187- 204 (rev)
  35. Hampel, D. et al., Phytochemistry, 2005, 66, 305- 311 (biosynth) [https://doi.org/10.1016/j.phytochem.2004.12.010]
  36. Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, CCN000
  37. Haslam, E. et al., JCS, 1964, 2137- 2146 (coffee constit)
  38. Scarpati, M.L. et al., Tet. Lett., 1964, 5, 2851- 2853 (Isochlorogenic acid A) [https://doi.org/10.1016/S0040-4039(00)70434-5]
  39. Corse, J. et al., Phytochemistry, 1965, 4, 527- 529 (uv, pmr) [https://doi.org/10.1016/S0031-9422(00)86209-3]
  40. Nichiforescu, E.A. et al., Khim. Prir. Soedin., 1970, 7, 546 (Vaccinium arctostaphylos constit)
  41. Nichiforescu, E.A. et al., Plant. Med. Phytother., 1970, 4, 56- 62 (Cynara scolymus constit)
  42. Timmermann, B.N. et al., J. Nat. Prod., 1983, 46, 365- 368 (Chrysothamnus paniculatus constit, pmr, cmr, ms) [https://doi.org/10.1021/np50027a012]
  43. Nishizawa, M. et al., Chem. Pharm. Bull., 1988, 36, 87- 95 (4-3-hydroxy-3-methylglutarate) [https://doi.org/10.1248/cpb.36.87]
  44. Chen, M. et al., Yaoxue Xuebao, 1994, 29, 617- 620 (Macroantoin G)
  45. Tatefuji, T. et al., Biol. Pharm. Bull., 1996, 19, 966- 970 (propolis constit) [https://doi.org/10.1248/bpb.19.966]
  46. Chudo, Y. et al., J. Agric. Food Chem., 1996, 44, 2037- 2039 (4-succinate) [https://doi.org/10.1021/jf960182+]
  47. Kodoma, M. et al., Phytochemistry, 1998, 47, 371- 373 (Pyrus pyrifolia constit, activity) [https://doi.org/10.1016/S0031-9422(97)00621-3]
  48. Miketova, P. et al., J. Mass Spectrom., 1999, 34, 1240- 1252 (ms)
  49. Heilmann, J. et al., Phytochemistry, 1999, 51, 713- 718 (Dicaffeoyl-1-isobutyrylquinic acid) [https://doi.org/10.1016/S0031-9422(99)00082-5]
  50. Kwon, H.C. et al., Chem. Pharm. Bull., 2000, 48, 1796- 1798 (3,5-Dicaffeoylmucoquinic acid) [https://doi.org/10.1248/cpb.48.1796]
  51. Peng, L.Y. et al., Fitoterapia, 2000, 71, 713- 715 (butyl ester) [https://doi.org/10.1016/S0367-326X(00)00212-4]
  52. Zhang, W.-D. et al., J. Asian Nat. Prod. Res., 2000, 2, 283- 288 (Macroantoin G)
  53. Zhang, W.-D. et al., Yaoxue Xuebao, 2001, 36, 360- 363 (1-Me ether Me ester)
  54. Silva, B.M. et al., J. Agric. Food Chem., 2004, 52, 4705- 4712 (Cydonia oblonga constit) [https://doi.org/10.1021/jf040057v]
  55. Teramachi, F. et al., J. Nat. Prod., 2005, 68, 794- 796 (Dicaffeoyl-4-coumaroylquinic acid) [https://doi.org/10.1021/np0500631]
  56. Kim, H.J. et al., Planta Med., 2005, 71, 871- 876 (3,5-Dicaffeoylepiquinic acid) [https://doi.org/10.1055/s-2005-873115]
  57. Dini, I. et al., J. Agric. Food Chem., 2006, 54, 8733- 8737 (Ipomoea batatas constit) [https://doi.org/10.1021/jf061687v]
  58. Kim, H.J. et al., J. Nat. Prod., 2006, 69, 600- 603 (4-O-(4-carboxy-3-hydroxy-3-methylbutanoyl) Me ester, 5'-methoxy 3'-Me ether Et ester) [https://doi.org/10.1021/np050447r]
  59. Sprogøe, K. et al., J. Nat. Prod., 2007, 70, 1472- 1477 (Hubertia constits) [https://doi.org/10.1021/np0702741]
  60. Antognoni, F. et al., Fitoterapia, 2011, 82, 950- 954 (Irbic acid) [https://doi.org/10.1016/j.fitote.2011.05.008]
  61. Jaiswal, R. et al., J. Agric. Food Chem., 2011, 59, 4033- 4039 (Arnica montana constits) [https://doi.org/10.1021/jf103545k]
  62. Raheem, K.S. et al., Tet. Lett., 2011, 52, 7175- 7177 (synth) [https://doi.org/10.1016/j.tetlet.2011.10.127]
  63. Ela, M.A.A. et al., Helv. Chim. Acta, 2012, 95, 61- 66 (1-Me ether)
  64. Dahmani-Hamzaoui, N. et al., Helv. Chim. Acta, 2012, 95, 564- 576 (Artemisia herba-alba constit)
  65. Xiong, J. et al., Food Chem., 2013, 138, 327- 333 (activity) [https://doi.org/10.1016/j.foodchem.2012.10.127]
  66. Stojakowska, A. et al., Food Chem., 2013, 138, 1250- 1255 (Lactuca tuberosa constit) [https://doi.org/10.1016/j.foodchem.2012.11.062]
  67. Chen, J. et al., Fitoterapia, 2014, 99, 1- 6 (Gynura divaricata constits) [https://doi.org/10.1016/j.fitote.2014.08.015]
  68. Znati, M. et al., Molecules, 2014, 19, 16959- 16975 (Ferula lutea constit)
  69. Zou, X. et al., Phytochem. Lett., 2014, 7, 133- 136 (MTCQA, activity) [https://doi.org/10.1016/j.phytol.2013.11.002]
  70. Seikel, M.K. et al., Phytochemistry, 1966, 5, 439- 455 (Vitex lucens constit) [https://doi.org/10.1016/S0031-9422(00)82158-5]
  71. Gentili, B. et al., JOC, 1968, 33, 1571- 1577 (4'-Me ether) [https://doi.org/10.1021/jo01268a058]
  72. Ibrahim, R.K. et al., Phytochemistry, 1970, 9, 1855- 1858 (7-rhamnoside) [https://doi.org/10.1016/S0031-9422(00)85604-6]
  73. Zoll, A. et al., Plant. Med. Phytother., 1974, 8, 134- 140 (Stellarin 2)
  74. Osterdahl, B.G., Acta Chem. Scand., Ser. B, 1978, 32, 93- 97 (Lucenin 2, struct)
  75. Gaffield, W. et al., Tetrahedron, 1978, 34, 3089- 3096 (cd) [https://doi.org/10.1016/0040-4020(78)87004-5]
  76. Bouillant, M.-L. et al., Phytochemistry, 1979, 18, 1043- 1047 (Stellarin 2) [https://doi.org/10.1016/S0031-9422(00)91474-2]
  77. Numata, A. et al., Chem. Pharm. Bull., 1980, 28, 964- 965 (Lespedeza cuneata constit) [https://doi.org/10.1248/cpb.28.964]
  78. Salmenkallio, M. et al., Phytochemistry, 1982, 21, 2990- 2991 (Trichophorum cespitosum constit)
  79. Kumamoto, H. et al., CA, 1985, 103, 183426 (4'-Me ether)
  80. Saleh, N.A.M. et al., Phytochemistry, 1985, 24, 201- 203 (Artemisia monosperma constit) [https://doi.org/10.1016/S0031-9422(00)80845-6]
  81. Congora, C. et al., Helv. Chim. Acta, 1986, 69, 251- 254 (Passiflora incarnata constit)
  82. Basile, A. et al., Phytochemistry, 1999, 52, 1479- 1482 (Hedwigia ciliata constit, activity) [https://doi.org/10.1016/S0031-9422(99)00286-1]
  83. Silva, B.M. et al., J. Agric. Food Chem., 2004, 52, 4705- 4712 (Cydonia oblonga constit) [https://doi.org/10.1021/jf040057v]
  84. Simirgiotis, M.J. et al., Molecules, 2013, 18, 1672- 1692 (Lucenin 2, struct) [https://doi.org/10.3390/molecules18021672]
  85. 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]
  86. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 1- 12 (Pinus constits) [https://doi.org/10.3891/acta.chem.scand.05-0001]
  87. Linstedt, G. et al., Acta Chem. Scand., 1951, 5, 121- 128 (Pinus constits, chromatogr) [https://doi.org/10.3891/acta.chem.scand.05-0121]
  88. Hasegawa, M. et al., JACS, 1957, 79, 450- 452 (Verecundin) [https://doi.org/10.1021/ja01559a059]
  89. Hasegawa, M. et al., JACS, 1957, 79, 1738- 1740 (Verecundin) [https://doi.org/10.1021/ja01564a056]
  90. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (Pinocembrin, abs config)
  91. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (Alpinetin, pmr) [https://doi.org/10.1071/CH9640428]
  92. Mongkolsuk, S. et al., JCS, 1964, 4654- 4655 ((±)-Pinostrobin, (±)-Alpinetin)
  93. Audier, H., Bull. Soc. Chim. Fr., 1966, 2892- 2899 (ms)
  94. Aurnhammer, G. et al., Chem. Ber., 1970, 103, 3667- 3673 (Isosarotanoside, Sarotanoside)
  95. 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]
  96. Bick, I.R.C. et al., Aust. J. Chem., 1972, 25, 449- 451 (Eucalyptus sieberi constits) [https://doi.org/10.1071/CH9720449]
  97. The Flavonoids, (eds. Harborne, J.B. et al), Chapman and Hall, 1975, 563 (occur)
  98. Miyakado, M. et al., Phytochemistry, 1976, 15, 846- 847 (Pinocembrin, activity) [https://doi.org/10.1016/S0031-9422(00)94481-9]
  99. Wagner, H. et al., Tet. Lett., 1976, 17, 1799- 1802 (cmr) [https://doi.org/10.1016/S0040-4039(00)93787-0]
  100. Pomilio, A.B. et al., Phytochemistry, 1979, 18, 1410- 1411 (Sarotanoside) [https://doi.org/10.1016/0031-9422(79)83040-X]
  101. Tanaka, N. et al., Chem. Pharm. Bull., 1980, 28, 2843- 2845 (Pinocembroside) [https://doi.org/10.1248/cpb.28.2843]
  102. González, M.D. et al., Phytochemistry, 1981, 20, 1174- 1175 (7-(2'''-acetylneohesperidoside)) [https://doi.org/10.1016/0031-9422(81)83063-4]
  103. Ripperberger, H., Phytochemistry, 1981, 20, 1757- 1758 (4'''-Acetylsarotanoside) [https://doi.org/10.1016/S0031-9422(00)98578-9]
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[top⬆]
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[top⬆]
Trypanocidal Citations
  1. Naß J, Efferth T. The activity of Artemisia spp. and their constituents against Trypanosomiasis. Phytomedicine. 2018 Aug 1;47:184-191. [https://doi.org/10.1016/j.phymed.2018.06.002.] Epub 2018 Jun 9. Review. PubMed PMID: 30166103.
  2. Berrizbeitia de Morgado M, Cariaco Sifontes Y, Imery Buiza J, Lutgen P. Activity of Artemisia annua infusions on epimastigotes of Trypanosoma cruzi. Enferm Infecc Microbiol Clin. 2017 Jun - Jul;35(6):390-392. [https://doi.org/10.1016/j.eimc.2016.09.011.] Epub 2016 Nov 22. English, Spanish. PubMed PMID: 27884407.
  3. Martínez-Díaz RA, Ibáñez-Escribano A, Burillo J, Heras Lde L, Prado GD, Agulló-Ortuño MT, Julio LF, González-Coloma A. Trypanocidal, trichomonacidal and cytotoxic components of cultivated Artemisia absinthium Linnaeus (Asteraceae) essential oil.Mem Inst Oswaldo Cruz. 2015 Aug;110(5):693-9. [https://doi.org/10.1590/0074-02760140129.] Epub 2015 Jun 24. PubMed PMID: 26107187; PubMed Central PMCID: PMC4569837.
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[top⬆]
Anthelmintic Citations
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  3. Beshay EVN. Therapeutic efficacy of Artemisia absinthium against Hymenolepis nana: in vitro and in vivo studies in comparison with the anthelmintic praziquantel. J Helminthol. 2018 May;92(3):298-308. [https://doi.org/10.1017/S0022149X17000529.] Epub 2017 Jun 13. PubMed PMID: 28606189.
  4. de Almeida LM, de Carvalho LS, Gazolla MC, Silva Pinto PL, da Silva MP, de Moraes J, Da Silva Filho AA. Flavonoids and Sesquiterpene Lactones from Artemisia absinthium and Tanacetum parthenium against Schistosoma mansoni Worms. Evid Based Complement Alternat Med. 2016;2016:9521349. Epub 2016 Nov 17. PubMed PMID: 27980595; PubMed Central PMCID: PMC5131251.
  5. Irum S, Ahmed H, Mukhtar M, Mushtaq M, Mirza B, Donskow-Łysoniewska K, Qayyum M, Simsek S. Anthelmintic activity of Artemisia vestita Wall ex DC. and Artemisia maritima L. against Haemonchus contortus from sheep. Vet Parasitol. 2015 Sep 15;212(3-4):451-5. [https://doi.org/10.1016/j.vetpar.2015.06.028.] Epub 2015 Jul 2. PubMed PMID: 26194429.
  6. Khan S, Afshan K, Mirza B, Miller JE, Manan A, Irum S, Rizvi SS, Qayyum M. Anthelmintic properties of extracts from Artemisia plants against nematodes. Trop Biomed. 2015 Jun;32(2):257-68. PubMed PMID: 26691254.
  7. Akkari H, Rtibi K, B'chir F, Rekik M, Darghouth MA, Gharbi M. In vitro evidence that the pastoral Artemisia campestris species exerts an anthelmintic effect on Haemonchus contortus from sheep. Vet Res Commun. 2014 Sep;38(3):249-55. [https://doi.org/10.1007/s11259-014-9609-y.] Epub 2014 Jul 17. PubMed PMID: 25027867.
  8. Cala AC, Ferreira JF, Chagas AC, Gonzalez JM, Rodrigues RA, Foglio MA, Oliveira MC, Sousa IM, Magalhães PM, Barioni Júnior W. Anthelmintic activity of Artemisia annua L. extracts in vitro and the effect of an aqueous extract and artemisinin in sheep naturally infected with gastrointestinal nematodes. Parasitol Res. 2014 Jun;113(6):2345-53. [https://doi.org/10.1007/s00436-014-3891-z.] Epub 2014 May 7. PubMed PMID: 24802864.
  9. Zhu L, Dai JL, Yang L, Qiu J. In vitro ovicidal and larvicidal activity of the essential oil of Artemisia lancea against Haemonchus contortus (Strongylida). Vet Parasitol. 2013 Jul 1;195(1-2):112-7. [https://doi.org/10.1016/j.vetpar.2012.12.050.] Epub 2013 Jan 10. PubMed PMID: 23351974.
  10. Squires JM, Ferreira JF, Lindsay DS, Zajac AM. Effects of artemisinin and Artemisia extracts on Haemonchus contortus in gerbils (Meriones unguiculatus). Vet Parasitol. 2011 Jan 10;175(1-2):103-8. [https://doi.org/10.1016/j.vetpar.2010.09.011.] Epub 2010 Sep 16. PubMed PMID: 20943323.
  11. Tariq KA, Chishti MZ, Ahmad F, Shawl AS. Anthelmintic activity of extracts of Artemisia absinthium against ovine nematodes. Vet Parasitol. 2009 Mar 9;160(1-2):83-8. [https://doi.org/10.1016/j.vetpar.2008.10.084.] Epub 2008 Oct 28. PubMed PMID: 19070963.
  12. Iqbal Z, Lateef M, Ashraf M, Jabbar A. Anthelmintic activity of Artemisia brevifolia in sheep. J Ethnopharmacol. 2004 Aug;93(2-3):265-8. PubMed PMID: 15234763.
  13. Nakhare S, Garg SC. Anthelmintic activity of the essential oil of artemisia pallens wall. Anc Sci Life. 1991 Jan;10(3):185-6. PubMed PMID: 22556530; PubMed Central PMCID: PMC3331285.
  14. al-Waili NS. Artemisia herba-alba extract for treating Enterobius vermicularis infection. Trans R Soc Trop Med Hyg. 1988;82(4):626. PubMed PMID: 3256117.
  15. Idris UE, Adam SE, Tartour G. The anthelmintic efficacy of Artemisia herba-alba against Haemonchus contortus infection in goats.Natl Inst Anim Health Q (Tokyo). 1982 Fall;22(3):138-43. PubMed PMID: 7162537.
[top⬆]
Insecticidal Citations
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