The Plant Cell Culture Library

Dalea purpurea
Cell Line ID DP-08164-R0 C2
Media Type M118
Availability Medium
Order Fabales
Family Fabaceae
Genus Dalea
Antibacterial Species Level ➡ 2 citations
Antifungal Species Level
Insecticidal Genus Level
Anticancer Genus Level ➡ 56 citations
Culture Initiation Site Taastrup
Plant Habit Herb Perennial
Culture Start Material Callus
Plant Supplier Comm/Alplains
Antibacterial Citations
  1. Wang Y, Jin L, Ominski KH, He M, Xu Z, Krause DO, Acharya SN, Wittenberg KM, Liu XL, Stanford K, McAllister TA. Screening of condensed tannins from Canadian prairie forages for anti-Escherichia coli O157:H7 with an emphasis on purple prairie clover (Dalea purpurea Vent). J Food Prot. 2013 Apr;76(4):560-7. [https://doi.org/10.4315/0362-028X.JFP-12-259.] PubMed PMID: 23575115.
  2. Liu XL, Hao YQ, Jin L, Xu ZJ, McAllister TA, Wang Y. Anti-Escherichia coli O157:H7 properties of purple prairie clover and sainfoin condensed tannins. Molecules. 2013 Feb 8;18(2):2183-99. [https://doi.org/10.3390/molecules18022183.] PubMed PMID: 23396143.
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Anticancer Citations
  1. Butenandt, A. et al., Annalen, 1932, 495, 172- 186 (struct)
  2. Clark, E.P. et al., JACS, 1933, 55, 422- 423 (Dehydrodeguelin) [https://doi.org/10.1021/ja01328a504]
  3. Merz, K.W. et al., Arch. Pharm. (Weinheim, Ger.), 1935, 273, 1- 21 (Dehydrodeguelin)
  4. Buchi, G. et al., Proc. Chem. Soc., London, 1960, 274- 276 (abs config)
  5. Fukami, H. et al., Agric. Biol. Chem., 1961, 25, 252- 256 (synth)
  6. Djerassi, C. et al., JCS, 1961, 1448- 1453 (abs config)
  7. Ollis, W.D. et al., Tetrahedron, 1967, 23, 4741- 4760 (Dehydrodeguelin) [https://doi.org/10.1016/S0040-4020(01)92572-4]
  8. Carlson, D.G. et al., Tetrahedron, 1973, 29, 2731- 2741 (pmr) [https://doi.org/10.1016/S0040-4020(01)93394-0]
  9. Omokawa, H. et al., Agric. Biol. Chem., 1974, 38, 1731- 1734 (synth)
  10. Anzeveno, P.B., JOC, 1979, 44, 2578- 2580 (synth) [https://doi.org/10.1021/jo01328a056]
  11. Ingham, J.L., Prog. Chem. Org. Nat. Prod., 1983, 43, 1- 266 (rev, occur)
  12. Crombie, L. et al., Chem. Comm., 1986, 352- 353 (biosynth) [https://doi.org/10.1039/c39860000352]
  13. Begley, M.J. et al., Chem. Comm., 1986, 353- 356 (biosynth) [https://doi.org/10.1039/C39860000353]
  14. Tahara, S. et al., Z. Naturforsch., C, 1990, 45, 154- 159 (Erythynone)
  15. Begley, M.J. et al., JCS Perkin 1, 1993, 21, 2605- 2614 ((±)-form, synth)
  16. Luyengi, L. et al., Phytochemistry, 1994, 36, 1523- 1526 (13-Hydroxydeguelin) [https://doi.org/10.1016/S0031-9422(00)89755-1]
  17. Manjary, F. et al., Planta Med., 1994, 60, 602 (Deguelin) [https://doi.org/10.1055/s-2006-959591]
  18. Gerhauser, C. et al., Cancer Res., 1997, 57, 3429- 3435 (activity)
  19. Crombie, L. et al., Phytochemistry, 1998, 49, 1479- 1507 (rev, biosynth) [https://doi.org/10.1016/S0031-9422(98)00178-2]
  20. Fang, N. et al., J. Agric. Food Chem., 1999, 47, 2130- 2136 (Didehydro-6-oxodeguelin) [https://doi.org/10.1021/jf981188x]
  21. Chun, K.H. et al., J. Natl. Cancer Inst., 2003, 95, 291- 302 (activity) [https://doi.org/10.1093/jnci/95.4.291]
  22. Pastine, S.J. et al., Org. Lett., 2003, 5, 4053- 4055 (synth) [https://doi.org/10.1021/ol035419j]
  23. Lee, H.Y., Biochem. Pharmacol., 2004, 68, 1119- 1124 (Deguelin, activity) [https://doi.org/10.1016/j.bcp.2004.05.033]
  24. Carboni, P. et al., Chem. Res. Toxicol., 2004, 17, 1540- 1548 (activity) [https://doi.org/10.1021/tx049867r]
  25. Yenesew, A. et al., Phytochemistry, 2005, 66, 653- 657 (Deguelin) [https://doi.org/10.1016/j.phytochem.2005.02.005]
  26. Ngandeu, F. et al., Phytochemistry, 2008, 69, 258- 263 (Millettia duchesnei constits) [https://doi.org/10.1016/j.phytochem.2007.05.038]
  27. Lu, H.-Y. et al., Chin. J. Nat. Med., 2009, 7, 24- 27 (Didehydro-7'-hydroxydeguelin) [https://doi.org/10.3724/SP.J.1009.2009.00024]
  28. Garcia, J. et al., Chem. - Eur. J., 2010, 16, 9767- 9771 (synth)
  29. Lawson, M.A. et al., Tet. Lett., 2010, 51, 6116- 6119 (15-Hydroxydeguelin) [https://doi.org/10.1016/j.tetlet.2010.09.057]
  30. Lee, S. et al., Chem. Comm., 2015, 51, 9026- 9029 (synth)
  31. Henrich, C.J. et al., J. Nat. Prod., 2015, 78, 2776- 2781 (activity) [https://doi.org/10.1021/acs.jnatprod.5b00753]
  32. Nayak, M. et al., JOC, 2015, 80, 11460- 11467 (synth) [https://doi.org/10.1021/acs.joc.5b02160]
  33. Deardorff, K. et al., J. Nat. Prod., 2016, 79, 2296- 2303 ((-)-Deguelin, activity) [https://doi.org/10.1021/acs.jnatprod.6b00444]
  34. Russell, D.A. et al., Org. Biomol. Chem., 2017, 15, 1593- 1596 (synth)
  35. Sax's Dangerous Properties of Industrial Materials, 10th edn., J. Wiley, 2000, DBH000
  36. Fujise, S. et al., Ber., 1933, 66, 929- 930 (synth)
  37. Fujise, S. et al., Ber., 1936, 69, 1893- 1896 (R-form, synth, struct, resoln)
  38. Arakawa, H. et al., Annalen, 1960, 636, 111- 117 (abs config)
  39. Mitscher, L.A. et al., J. Nat. Prod., 1973, 36, 422- 425 (Eugenia javanica constits)
  40. Joshi, B.S. et al., Indian J. Chem., Sect. B, 1974, 12, 1033- 1037 (7-Me ether)
  41. Cannon, J.R. et al., Aust. J. Chem., 1977, 30, 2099- 2101 (Agonis spathulata constit, bibl) [https://doi.org/10.1071/CH9772099]
  42. Hiraoka, A., Biochem. Syst. Ecol., 1978, 6, 171- 175 (glucoside) [https://doi.org/10.1016/0305-1978(78)90003-0]
  43. Wollenweber, E. et al., Z. Pflanzenphysiol., 1979, 94, 241- 246 (Pityrogramma pallida constit) [https://doi.org/10.1016/S0044-328X(79)80163-4]
  44. Hufford, C.D. et al., JOC, 1981, 46, 3073- 3078 (Uvaria afzelii constit) [https://doi.org/10.1021/jo00328a017]
  45. Tanrisever, N. et al., Phytochemistry, 1987, 26, 175- 179 (Ceratiola ericoides constit, cryst struct) [https://doi.org/10.1016/S0031-9422(00)81505-8]
  46. Kadota, S. et al., Chem. Pharm. Bull., 1994, 42, 1712- 1714 (Matteuorienate B) [https://doi.org/10.1248/cpb.42.1712]
  47. Basnet, P. et al., Chem. Pharm. Bull., 1995, 43, 1558- 1564 (Matteuccia orientalis constit) [https://doi.org/10.1248/cpb.43.1558]
  48. Wu, J.-H. et al., Bioorg. Med. Chem. Lett., 2003, 13, 1813- 1816 (S-form, activity) [https://doi.org/10.1016/S0960-894X(03)00197-5]
  49. Kuo, Y.-C. et al., Planta Med., 2004, 70, 1237- 1239 (5-Me ether) [https://doi.org/10.1055/s-2004-835859]
  50. Mustafa, K.A. et al., Biochem. Syst. Ecol., 2005, 33, 1049- 1059 (Metrosideros excelsa constit, cd, struct) [https://doi.org/10.1016/j.bse.2005.02.003]
  51. Salem, M.M. et al., J. Nat. Prod., 2005, 68, 108- 111 (S-form, activity) [https://doi.org/10.1021/np049682k]
  52. Boonphong, S. et al., J. Nat. Prod., 2007, 70, 795- 801 (Bauhinia purpurea constit, activity) [https://doi.org/10.1021/np070010e]
  53. Dacunha-Marinho, B. et al., Acta Cryst. C, 2008, 64, o353- o356 (5-Me ether, cryst struct)
  54. Lee, J.S. et al., Chem. Pharm. Bull., 2008, 56, 711- 714 (R-form, activity) [https://doi.org/10.1248/cpb.56.711]
  55. Zhang, D. et al., J. Asian Nat. Prod. Res., 2013, 15, 1163- 1167 (7-6-acetylglucoside, cd)
  56. Memon, A.H. et al., Molecules, 2015, 20, 14212- 14233 (cryst struct)
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