The University of Massachusetts Amherst

The Plant Cell Culture Library

Rubus langei
Cell Line ID RL-09006-T4-R1-L1
Media Type M62
Lowest Tolerable USDA Zone 6a
Drought Tolerance Average
Availability Low
Order Rosales
Family Rosaceae
Genus Rubus
Antiviral Genus Level
Antifungal Genus Level ➡ 4 citations
Trypanocidal Genus Level
Anticancer Genus Level ➡ 14 citations
Culture Start Material Suspension Callus
Antifungal Citations
  1. Hajaji S, Jabri MA, Sifaoui I, López-Arencibia A, Reyes-Batlle M, B'chir F, Valladares B, Pinero JE, Lorenzo-Morales J, Akkari H. Amoebicidal, antimicrobial and in vitro ROS scavenging activities of Tunisian Rubus ulmifolius Schott, methanolic extract. Exp Parasitol. 2017 Dec;183:224-230. [https://doi.org/10.1016/j.exppara.2017.09.013.] Epub 2017 Sep 13. PubMed PMID: 28917707.
  2. Han B, Chen J, Yu YQ, Cao YB, Jiang YY. Antifungal activity of Rubus chingii extract combined with fluconazole against fluconazole-resistant Candida albicans. Microbiol Immunol. 2016 Feb;60(2):82-92. [https://doi.org/10.1111/1348-0421.12357.] PubMed PMID: 26891940.
  3. Thiem B, Goślińska O. Antimicrobial activity of Rubus chamaemorus leaves. Fitoterapia. 2004 Jan;75(1):93-5. PubMed PMID: 14693229.
  4. Panizzi L, Caponi C, Catalano S, Cioni PL, Morelli I. In vitro antimicrobial activity of extracts and isolated constituents of Rubus ulmifolius. J Ethnopharmacol. 2002 Feb;79(2):165-8. PubMed PMID: 11801377.
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Anticancer Citations
  1. Haddock, E.A. et al., JCS Perkin 1, 1982, 2515- 2524 (isol, struct, pmr, cmr, rev) [https://doi.org/10.1039/p19820002515]
  2. Nishizawa, M. et al., JCS Perkin 1, 1982, 2963- 2968; 1983, 961 - 965 (Rhus semialata constits, Quercus infectaria constits) [https://doi.org/10.1039/p19820002963]
  3. Nishizawa, M. et al., Chem. Pharm. Bull., 1983, 31, 2593- 2600 (Paeonia lactiflora constits) [https://doi.org/10.1248/cpb.31.2593]
  4. Nishizawa, M. et al., Phytochemistry, 1985, 24, 2411- 2413 (Spirogyra constits) [https://doi.org/10.1016/S0031-9422(00)83053-8]
  5. Nonaka, G. et al., Chem. Pharm. Bull., 1987, 35, 3127- 3131 (struct, pmr, cmr) [https://doi.org/10.1248/cpb.35.3127]
  6. Kandil, F.E. et al., Phytochemistry, 1996, 42, 1243- 1245 (2-Trigalloyl-1,3,4,6-tetragalloylglucose, uv, pmr, cmr) [https://doi.org/10.1016/0031-9422(95)00924-8]
  7. Kandil, F.E. et al., Phytochemistry, 2001, 58, 611- 613 (Monacanthin A) [https://doi.org/10.1016/S0031-9422(01)00265-5]
  8. Duan, D. et al., Bioorg. Med. Chem. Lett., 2004, 14, 6041- 6044 (antiviral activity) [https://doi.org/10.1016/j.bmcl.2004.09.067]
  9. Zhang, J. et al., Pharm. Res., 2009, 26, 2066- 2080 (rev, activity)
  10. Cho, J.-Y. et al., Food Chem., 2010, 123, 501- 506 (isol, activity) [https://doi.org/10.1016/j.foodchem.2010.04.072]
  11. Baumgartner, R.R. et al., J. Nat. Prod., 2010, 73, 1578- 1581, 1742§ (isol, activity) [https://doi.org/10.1021/np100258e]
  12. Cryan, L.M. et al., J. Med. Chem., 2013, 56, 1940- 1945 (activity) [https://doi.org/10.1021/jm301558t]
  13. Cao, Y. et al., J. Nat. Med. (Tokyo), 2014, 68, 465- 472 (rev, activity)
  14. Tuominen, A. et al., Phytochemistry, 2015, 115, 239- 251 (Sylvatiins A,C) [https://doi.org/10.1016/j.phytochem.2015.01.005]
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