The University of Massachusetts Amherst

The Plant Cell Culture Library

Antirrhinum braun-blanquetii
Cell Line ID AB-01752-R1
Media Type B122
Lowest Tolerable USDA Zone 5a
Drought Tolerance Tolerant
Availability Low
Order Lamiales
Family Plantaginaceae
Genus Antirrhinum
Antiviral Genus Level ➡ 21 citations
Antibacterial Genus Level
Plant Habit Herb Perennial
Plant Habitat Warm Temperate
Culture Start Material Seed
Native Range Northwest Spain, Northeast Portugal
Antiviral Citations
  1. Seikel, M.K. et al., J. Am. Chem. Soc., 1950, 72, 5725- 5730 (Antirrhinum majus constits) [https://doi.org/10.1021/ja01168a095]
  2. Seikel, M.K. et al., J. Am. Chem. Soc., 1955, 77, 4622- 4624 (Cernuoside, Aureusin)
  3. Farkas, L. et al., Chem. Ber., 1961, 94, 2221- 2224 (Cernuoside, synth)
  4. Batterham, T.J. et al., Aust. J. Chem., 1964, 17, 428- 439 (pmr) [https://doi.org/10.1071/CH9640428]
  5. Farkas, L. et al., Chem. Ber., 1964, 97, 1044- 1046 (synth, struct, 6-glucoside, Rengasin)
  6. Harborne, J.B., Phytochemistry, 1966, 5, 111- 115 (Cernuoside, Aureusin, occur) [https://doi.org/10.1016/S0031-9422(00)85088-8]
  7. Harborne, J.B., Phytochemistry, 1967, 6, 1643- 1651 (occur, Cernuoside) [https://doi.org/10.1016/S0031-9422(00)82897-6]
  8. Clifford, H.T. et al., Phytochemistry, 1969, 8, 123- 126 (occur) [https://doi.org/10.1016/S0031-9422(00)85804-5]
  9. Hastings, J.S. et al., J. Chem. Soc., Perkin Trans. 1, 1972, 2128- 2132 (struct, 6-glucoside) [https://doi.org/10.1039/p19720002128]
  10. Deshmukh, S.W. et al., Indian J. Chem., 1974, 12, 893 (Rengasin, synth)
  11. Ogiyama, K. et al., Phytochemistry, 1976, 15, 2025 (Melanorrhoea constit, 4-Me ether)
  12. Markham, K.R. et al., Phytochemistry, 1978, 17, 159- 160 (6-glucuronoside) [https://doi.org/10.1016/S0031-9422(00)89707-1]
  13. Markham, K.R. et al., Phytochemistry, 1978, 17, 911- 913 (6-glucuronoside) [https://doi.org/10.1016/S0031-9422(00)88645-8]
  14. Harborne, J.B. et al., Phytochemistry, 1983, 22, 2741- 2742 (6-glucoside, 4,6-diglucoside) [https://doi.org/10.1016/S0031-9422(00)97685-4]
  15. Mohan, P. et al., Phytochemistry, 1989, 28, 2529- 2530 (6-rhamnoside) [https://doi.org/10.1016/S0031-9422(00)98027-0]
  16. Seabra, R.M. et al., Phytochemistry, 1997, 45, 839- 840 (Tetramethoxyaurone) [https://doi.org/10.1016/S0031-9422(97)00035-6]
  17. Bolek, D. et al., J. Heterocycl. Chem., 2005, 42, 1399- 1403 (synth, pmr, cmr)
  18. Kraus, G.A. et al., Synthesis, 2008, 2427- 2431 (tetra-Me ether) [https://doi.org/10.1055/s-2008-1078597]
  19. Detsi, A. et al., Bioorg. Med. Chem., 2009, 17, 8073- 8085 (synth, activity) [https://doi.org/10.1016/j.bmc.2009.10.002]
  20. Haudecoeur, R. et al., J. Med. Chem., 2011, 54, 5395- 5402 (Aureusidin, activity) [https://doi.org/10.1021/jm200242p]
  21. Zhao, X. et al., Synthesis, 2012, 2217- 2224 (synth)
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