The University of Massachusetts Amherst

The Plant Cell Culture Library

Petroselinum crispum
Cell Line ID CP1027-R1
Media Type B6
Availability Low
Order Apiales
Family Apiaceae
Genus Petroselinum
Antifungal Species Level ➡ 35 citations
Insecticidal Species Level ➡ 9 citations
Culture Start Material Seed
Antifungal Citations
  1. Bohlmann, F. et al., Chem. Ber., 1961, 94, 958- 967 (Falcarindiol, Falcarindiones)
  2. Bohlmann, F. et al., Chem. Ber., 1961, 94, 3189- 3192 (Falcarindiol, Falcarindiones, synth)
  3. Bohlmann, F. et al., Chem. Ber., 1966, 99, 3552- 3558 (Falcaria vulgaris constits)
  4. Bohlmann, F. et al., Chem. Ber., 1967, 100, 3450- 3453 (Cotula coronopifolia constit)
  5. Bohlmann, F. et al., Chem. Ber., 1967, 100, 3454- 3456 (Apium graveolens constit)
  6. Bentley, R.K. et al., JCS(C), 1969, 685- 688 (Daucus corota constits)
  7. Bohlmann, F. et al., Chem. Ber., 1975, 108, 511- 514 (Centella constit)
  8. Schulte, K.E. et al., Arch. Pharm. (Weinheim, Ger.), 1977, 310, 945- 963 (Pituramthus tortuosus constit, synth)
  9. Tanaka, S. et al., Arzneim.-Forsch., 1977, 27, 2039- 2045 (pharmacol)
  10. Garrod, B. et al., Physiol. Plant Pathol., 1978, 13, 241- 246 (Falcarindiol) [https://doi.org/10.1016/0048-4059(78)90039-5]
  11. Lemmich, E., Phytochemistry, 1981, 20, 1419- 1420 (abs config) [https://doi.org/10.1016/0031-9422(81)80053-2]
  12. Fujimoto, Y. et al., Chem. Pharm. Bull., 1991, 39, 521- 522 (PQ 2) [https://doi.org/10.1248/cpb.39.521]
  13. Fujimoto, Y. et al., Phytochemistry, 1992, 31, 3499- 3501 (PQ 6) [https://doi.org/10.1016/0031-9422(92)83715-B]
  14. Satoh, A. et al., Biosci., Biotechnol., Biochem., 1996, 60, 152- 153 (Glehnia littoralis constit) [https://doi.org/10.1271/bbb.60.152]
  15. Bernart, M.W. et al., J. Nat. Prod., 1996, 59, 748- 753 (Dendropanax arboreus constit) [https://doi.org/10.1021/np960224o]
  16. Kobaisy, M. et al., J. Nat. Prod., 1997, 60, 1210- 1213 (Oplopandiol, abs config) [https://doi.org/10.1021/np970182j]
  17. Zheng, G. et al., J. Nat. Prod., 1999, 62, 626- 628 (synth) [https://doi.org/10.1021/np980418z]
  18. Xu, L. et al., Chin. Chem. Lett., 2000, 11, 213- 216 (synth, Oplopandiol, Ac)
  19. Lee, G. et al., J. Microbiol. Biotechnol., 2000, 10, 394- 398 (Falcarindiol, activity)
  20. Lechner, D. et al., Phytochemistry, 2004, 65, 331- 335 (Angelica dahurica constit, abs config) [https://doi.org/10.1016/j.phytochem.2003.11.010]
  21. Zidorn, C. et al., J. Agric. Food Chem., 2005, 53, 2518- 2523 (8-O-Methylfalcarindiol) [https://doi.org/10.1021/jf048041s]
  22. Yamazoe, S. et al., Nat. Prod. Commun., 2006, 1, 87- 94 (8-O-Acetylfalcarinolone)
  23. Yamazoe, S. et al., Phytochemistry, 2007, 68, 1706- 1711 (indole-3-acetate) [https://doi.org/10.1016/j.phytochem.2007.03.036]
  24. Sabitha, G. et al., Synthesis, 2008, 115- 121 (synth, ir, pmr, cmr) [https://doi.org/10.1055/s-2007-990944]
  25. Schmiech, L. et al., J. Agric. Food Chem., 2009, 57, 11030- 11040 (Daucus carota constits,synth) [https://doi.org/10.1021/jf9031475]
  26. Appendino, G. et al., J. Nat. Prod., 2009, 72, 962- 965 (9,10-Epoxyfalcarindiol) [https://doi.org/10.1021/np8007717]
  27. Yang, M.C. et al., J. Nat. Prod., 2010, 73, 801- 805 (Oploxyne A) [https://doi.org/10.1021/np900628j]
  28. Tamura, S. et al., Tet. Lett., 2010, 51, 1523- 1525 (synth, abs config) [https://doi.org/10.1016/j.tetlet.2010.01.047]
  29. Roman, M. et al., J. Nat. Prod., 2011, 74, 1757- 1763 (Falcarindiol, Raman, conformn) [https://doi.org/10.1021/np200265d]
  30. Yadav, J.S. et al., JOC, 2011, 76, 2568- 2576 (Oploxyne A, synth) [https://doi.org/10.1021/jo102445h]
  31. Bejjanki, N.K. et al., Helv. Chim. Acta, 2013, 96, 1571- 1578 (synth)
  32. Tan, K.W. et al., Eur. J. Pharmacol., 2014, 723, 346- 352 (activity) [https://doi.org/10.1016/j.ejphar.2013.11.005]
  33. Liu, X. et al., J. Nat. Prod., 2014, 77, 2513- 2521 (Notoincisol A) [https://doi.org/10.1021/np500605v]
  34. Wang, L. et al., Molecules, 2016, 21, 112:1- 12 (synth)
  35. Zhou, Y. et al., Tetrahedron: Asymmetry, 2017, 28, 288- 295 (9,10-Epoxyfalcarindiol, synth) [https://doi.org/10.1016/j.tetasy.2016.12.008]
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Insecticidal Citations
  1. Baker, W. et al., JCS, 1938, 1602- 1608 (synth)
  2. Kasting, R. et al., Phytochemistry, 1972, 11, 2277- 2282 (isol) [https://doi.org/10.1016/S0031-9422(00)88390-9]
  3. Sethi, M.L. et al., Phytochemistry, 1976, 15, 1773- 1775 (isol) [https://doi.org/10.1016/S0031-9422(00)97480-6]
  4. Goeckeritz, D. et al., Pharmazie, 1979, 34, 426- 429 (isol)
  5. MacLeod, A.J. et al., Phytochemistry, 1985, 24, 2623- 2627 (occur) [https://doi.org/10.1016/S0031-9422(00)80682-2]
  6. Santos, B.V. de O. et al., Phytochemistry, 1998, 49, 1381- 1384 (isol, pmr, cmr) [https://doi.org/10.1016/S0031-9422(98)00100-9]
  7. Benevides, P.J.C. et al., Phytochemistry, 1999, 52, 339- 343 (isol, pmr) [https://doi.org/10.1016/S0031-9422(99)00177-6]
  8. Atta-ur-Rahman, et al.Phytochemistry, 1999, 52, 495- 499 (isol, pmr, ms) [https://doi.org/10.1016/S0031-9422(99)00213-7]
  9. Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, AGE500
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