The Plant Cell Culture Library

Antirrhinum braun-blanquetii

Cell Line ID: AB-01752-R1

Media Type: B122

Lowest Tolerable USDA Zone: 5a

Drought Tolerance: Tolera

Availability: Medium

Order: Lamiales

Family: Plantaginaceae

Genus: Antirrhinum

Antiviral:

Genus Level ➡ 21 citations

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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