The Plant Cell Culture Library

Teucrium hircanicum
Cell Line ID TH-02979-R0
Media Type B112
Availability Low
Order Lamiales
Family Lamiaceae
Genus Teucrium
Antifungal Genus Level ➡ 51 citations
Insecticidal Genus Level ➡ 13 citations
Anticancer Genus Level
Culture Start Material Callus
Antifungal Citations
  1. Schopf, C. et al., Annalen, 1940, 544, 30- 62 (synth, 3-Me ether)
  2. Kelley, C.J. et al., JOC, 1975, 40, 1804; 1976, 41, 449-455 (Rosmarinic acid, pmr, cmr) [https://doi.org/10.1021/jo00900a028]
  3. Yahara, S. et al., Chem. Pharm. Bull., 1985, 33, 527- 531 (Coptis chinensis constits) [https://doi.org/10.1248/cpb.33.527]
  4. Parnham, M.J. et al., Drugs of the Future, 1985, 10, 756 (Rosmarinic acid, rev) [https://doi.org/10.1358/dof.1985.010.09.71743]
  5. Rao, N.N. et al., Arch. Pharm. (Weinheim, Ger.), 1988, 321, 179- 180 (enzymic synth)
  6. Englberger, W. et al., Int. J. Immunopharmacol., 1988, 10, 729 (Rosmarinic acid, pharmacol) [https://doi.org/10.1016/0192-0561(88)90026-4]
  7. Peake, P.W. et al., Int. J. Immunopharmacol., 1991, 13, 853 (Rosmarinic acid, pharmacol) [https://doi.org/10.1016/0192-0561(91)90036-7]
  8. Pabsch, K. et al., Recl. Trav. Chim. (J. R. Neth. Chem. Soc.), 1991, 110, 199 (Rosmarinic acid, synth)
  9. Mahmood, N., Antiviral Chem. Chemother., 1993, 4, 235 (Rosmarinic acid, anti-HIV activity,nmr, ms)
  10. Zou, Z.W. et al., Yaoxue Xuebao, 1993, 28, 241 (Rosmarinic acid, pharmacol)
  11. Zhao, L.M. et al., Chin. Chem. Lett., 1996, 7, 449- 452 (Salviaflaside)
  12. Abraham, S.K., Food Chem. Toxicol., 1996, 34, 15- 20 (Rosmarinic acid, activity) [https://doi.org/10.1016/0278-6915(95)00085-2]
  13. Huang, H. et al., J. Nat. Prod., 1996, 59, 1079- 1080 (Oresbiusins A,B) [https://doi.org/10.1021/np960430w]
  14. Binutu, O.A. et al., Planta Med., 1996, 62, 352- 353 (Rosmarinic acid, activity) [https://doi.org/10.1055/s-2006-957900]
  15. Robinson, W.E. et al., Proc. Natl. Acad. Sci. U.S.A., 1996, 93, 6326- 6331 (Rosmarinic acid,activity) [https://doi.org/10.1073/pnas.93.13.6326]
  16. Eicher, T. et al., Synthesis, 1996, 755- 762 (Rosmarinic acid, synth) [https://doi.org/10.1055/s-1996-4289]
  17. Bogucki, D.E. et al., Can. J. Chem., 1997, 75, 1783- 1794 (Rosmarinic acid, synth) [https://doi.org/10.1139/v97-612]
  18. Reimann, E. et al., Monatsh. Chem., 1997, 128, 995- 1008; 1998, 129, 187 - 193 (Rosmarinic acid, synth) [https://doi.org/10.1007/BF00806966]
  19. Kusano, G. et al., Biol. Pharm. Bull., 1998, 21, 997- 999 (Rosmarinic acid, activity) [https://doi.org/10.1248/bpb.21.997]
  20. Satake, T. et al., Chem. Pharm. Bull., 1999, 47, 1444- 1447 (glucosides, Isorinic acid) [https://doi.org/10.1248/cpb.47.1444]
  21. Huang, H. et al., Planta Med., 1999, 65, 92- 93 (Butyl rosmarinate) [https://doi.org/10.1055/s-2006-960451]
  22. Kuo, Y.-H. et al., J. Chin. Chem. Soc. (Taipei), 2000, 47, 241- 246 (Methyl rosmarinate)
  23. Choi, J.S. et al., Fitoterapia, 2001, 72, 30- 34 (amide) [https://doi.org/10.1016/S0367-326X(00)00248-3]
  24. Hou, Z.-F. et al., J. Chin. Chem. Soc. (Taipei), 2002, 49, 255- 258 (Ethyl rosmarinate)
  25. Petersen, M. et al., Phytochemistry, 2003, 62, 121- 125 (Rosmarinic acid, rev, biosynth) [https://doi.org/10.1016/S0031-9422(02)00513-7]
  26. Wei, X.-M. et al., J. Chin. Chem. Soc. (Taipei), 2004, 51, 1043- 1049 (Z-Rosmarinic acid)
  27. Ishii, T. et al., J. Nat. Prod., 2004, 67, 1764- 1766 (Tichocarpol B) [https://doi.org/10.1021/np0498509]
  28. Iqbal, K. et al., Chem. Biodiversity, 2005, 2, 104- 111 (Ehretia obtusifolia constit)
  29. Le Claire, E. et al., J. Agric. Food Chem., 2005, 53, 4367- 4372 (3'-Glucosylrosmarinic acid) [https://doi.org/10.1021/jf050024v]
  30. Tian, J.-K. et al., J. Asian Nat. Prod. Res., 2006, 8, 35- 39 (Ternatoside B)
  31. Vogelsang, K. et al., Planta, 2006, 223, 369- 373 (Anthoceros agrestis constits)
  32. Zhou, L.-Y. et al., Z. Naturforsch., B, 2006, 61, 607- 610 (Sanicula lamelligera constit)
  33. Choudhary, M.I. et al., Chem. Biodiversity, 2008, 5, 2676- 2683 (Lindelofia stylosa ester)
  34. Murata, T. et al., J. Nat. Prod., 2009, 72, 1379- 1384 (Clinopodic acids A,B) [https://doi.org/10.1021/np800781t]
  35. Petersen, M. et al., Phytochemistry, 2009, 70, 1663- 1679 (Rosmarinic acid, biosynth, rev) [https://doi.org/10.1016/j.phytochem.2009.05.010]
  36. Nan, Y.-F. et al., Acta Cryst. E, 2010, 66, o1105 (isopropyl ester, cryst struct)
  37. Zou, Y. et al., Chem. Nat. Compd. (Engl. Transl.), 2010, 46, 19- 21 (Ranunchinensin A,Oresbiusin A, Ternatoside B) [https://doi.org/10.1007/s10600-010-9515-7]
  38. Kim, J.-P. et al., Bioorg. Med. Chem. Lett., 2011, 21, 3483- 3487 (Glechoma hederacea constits) [https://doi.org/10.1016/j.bmcl.2011.02.002]
  39. Begum, S. et al., Chem. Biodiversity, 2011, 8, 850- 861 (Cordicilin)
  40. Murata, T. et al., Chem. Pharm. Bull., 2012, 60, 121- 128 (Shimobashiric acid B) [https://doi.org/10.1248/cpb.60.121]
  41. Hu, J. et al., Chin. Chem. Lett., 2012, 23, 1243- 1246 (Me ester 2-glucoside) [https://doi.org/10.1016/j.cclet.2012.08.001]
  42. Hwu, J.R. et al., Eur. J. Org. Chem., 2012, 4684- 4688 (Oresbiusins A,B, synth, config)
  43. Petersen, M., Phytochem. Rev., 2013, 12, 207- 227 (Rosmarinic acid, rev, occur, biosynth)
  44. Aziz, S. et al., Chem. Nat. Compd. (Engl. Transl.), 2014, 49, 1023- 1027 (Propyl rosmarinate, activity)
  45. Bloch, S.E. et al., ChemBioChem, 2014, 15, 2393- 2401 (biosynth)
  46. Zhou, X.-J. et al., Food Chem., 2014, 164, 150- 157 (Perilla frutescens constits) [https://doi.org/10.1016/j.foodchem.2014.05.062]
  47. Al-Qudah, M.A. et al., Phytochemistry, 2014, 99, 115- 120 (Salvia palaestina constit, activity) [https://doi.org/10.1016/j.phytochem.2014.01.001]
  48. Kim, G.-D. et al., Appl. Microbiol. Biotechnol., 2015, 99, 2083- 2092 (Rosmarinic acid, rev,prodn, use)
  49. Wang, B. et al., Planta, 2015, 241, 711- 725 (Rosmarinic acid, biosynth)
  50. Amoah, S.K.S. et al., Planta Med., 2016, 82, 388- 406 (Rosmarinic acid, rev, occur,biosynth, activity)
  51. Biotechnology of Natural Products, (eds. Schwab, W. et al), Springer, (eds. Schwab, W. et al), Springer, 2018, 25- 60 (Rosmarinic acid, rev, prodn)
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Insecticidal Citations
  1. Gács-Baitz, E. et al., Phytochemistry, 1978, 17, 1967- 1973; 1987, 26, 2110-2112 (Teucrin H3, Teupolin I, struct, bibl) [https://doi.org/10.1016/S0031-9422(00)88744-0]
  2. Malakov, P.Y. et al., Z. Naturforsch., B, 1978, 33, 789- 791; 1979, 34, 1570-1572 (Montanin C, Teupolin I, Teupolin II, struct)
  3. Savona, G. et al., Tet. Lett., 1979, 20, 379- 382 (Gnaphalin) [https://doi.org/10.1016/S0040-4039(01)85976-1]
  4. Miyase, T. et al., Chem. Pharm. Bull., 1981, 29, 3561- 3564 (Teucrium japonicum constits,synth) [https://doi.org/10.1248/cpb.29.3561]
  5. Gács-Baitz, E. et al., Heterocycles, 1982, 19, 539- 550 (cmr) [https://doi.org/10.3987/R-1982-03-0539]
  6. Fayos, J. et al., JOC, 1984, 49, 1789- 1793 (struct) [https://doi.org/10.1021/jo00184a023]
  7. Boneva, I.M. et al., Phytochemistry, 1988, 27, 295- 297 (12-Epiteupolin II) [https://doi.org/10.1016/0031-9422(88)80640-X]
  8. Lourenço, A. et al., Phytochemistry, 1991, 30, 613- 617 (abs config) [https://doi.org/10.1016/0031-9422(91)83737-6]
  9. Lopez-Olguin, J. et al., Phytochemistry, 1999, 50, 749- 753 (Teucrium constits, antifeedant activity, SAR) [https://doi.org/10.1016/S0031-9422(98)00642-6]
  10. Bruno, M. et al., J. Nat. Prod., 2000, 63, 1029- 1031 (12-Epiteucjaponin A) [https://doi.org/10.1021/np990510a]
  11. de la Torre, M.C. et al., Tetrahedron, 2000, 56, 8007- 8018 (Teucrium gnaphalodes constits,synth) [https://doi.org/10.1016/S0040-4020(00)00719-5]
  12. de las Heras, B. et al., Life Sci., 2001, 70, 269- 278 (6-ketone, 19-Ac, antiinflammatory,activity) [https://doi.org/10.1016/S0024-3205(01)01402-3]
  13. Fiorentino, A. et al., Phytochemistry, 2011, 72, 2037- 2044 (Teucrium polium constits, struct,tox) [https://doi.org/10.1016/j.phytochem.2011.07.006]
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