The University of Massachusetts Amherst

The Plant Cell Culture Library

Cirsium monspessulanum
Cell Line ID CM-04280-R0
Media Type M72
Availability Low
Order Asterales
Family Compositae
Genus Cirsium
Antibacterial Genus Level ➡ 8 citations
Anticancer Genus Level ➡ 31 citations
Culture Start Material Shoot
Plant Supplier Botanical Garden Chelsea Physic Garden
Antibacterial Citations
  1. Trivedi, B. et al., Tetrahedron Lett., 1964, 5, 1197- 1201 (Cyperene) [https://doi.org/10.1016/S0040-4039(00)90453-2]
  2. Nerali, S.B. et al., Tetrahedron Lett., 1967, 8, 2447- 2449 (Cyperenol) [https://doi.org/10.1016/S0040-4039(00)90829-3]
  3. Dreyfus, H. et al., Tetrahedron Lett., 1969, 10, 3757- 3760 (cryst struct, abs config) [https://doi.org/10.1016/S0040-4039(01)88506-3]
  4. Jacobs, H. et al., J. Nat. Prod., 1987, 50, 835- 842 (Cyperenol, Cyperenoic acid, pmr, cmr,struct) [https://doi.org/10.1021/np50053a010]
  5. Boonyaratavej, S. et al., J. Nat. Prod., 1988, 51, 769- 770 (Cyperenoic acid, cryst struct) [https://doi.org/10.1021/np50058a019]
  6. Takano, S. et al., Phytochemistry, 1988, 27, 1197- 1199 (Cyperenyl acetate, Cyperenal) [https://doi.org/10.1016/0031-9422(88)80302-9]
  7. Achenbach, H. et al., Eur. J. Pharm. Sci., 1994, 2, 128 (activity) [https://doi.org/10.1016/0928-0987(94)90211-9]
  8. Achenbach, H. et al., Phytochemistry, 1997, 45, 149- 157 (Methyl cyperenoate) [https://doi.org/10.1016/S0031-9422(96)00777-7]
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Anticancer Citations
  1. Robinson, R. et al., JCS, 1930, 822- 830 (synth)
  2. Merz, K.W. et al., Arch. Pharm. (Weinheim, Ger.), 1936, 274, 126- 148 (Linaria vulgaris constit)
  3. Zemplén, G. et al., Ber., 1942, 75, 489- 495 (Pectolinarin)
  4. Kupchan, S.M. et al., Tetrahedron, 1969, 25, 1603- 1615 (Pectolinarigenin, uv) [https://doi.org/10.1016/S0040-4020(01)82733-2]
  5. Kuptsova, L.P. et al., Chem. Nat. Compd. (Engl. Transl.), 1970, 6, 121- 122 (Pectolinarigenin 7-robinobioside)
  6. Farkas, L. et al., Tet. Lett., 1970, 11, 187- 190 (synth) [https://doi.org/10.1016/S0040-4039(01)97671-3]
  7. Smirnova, L.P. et al., Chem. Nat. Compd. (Engl. Transl.), 1973, 9, 114 (Pectolinarigenin 7-rutinoside) [https://doi.org/10.1007/BF00580915]
  8. Morita, N. et al., Phytochemistry, 1973, 12, 421- 423 (Pectolinarin) [https://doi.org/10.1016/0031-9422(73)80032-9]
  9. Smirnova, L.P. et al., Chem. Nat. Compd. (Engl. Transl.), 1974, 10, 259 (Linaroside) [https://doi.org/10.1007/BF00563634]
  10. Smirnova, L.P. et al., Chem. Nat. Compd. (Engl. Transl.), 1974, 10, 320- 324 (5-O-Acetylpectolinarin, isol, struct, di-Ac)
  11. Morita, N. et al., Yakugaku Zasshi, 1974, 94, 913- 916 (Linariin) [https://doi.org/10.1248/yakushi1947.94.8_913]
  12. Lin, C.N., Chem. Pharm. Bull., 1978, 26, 2036- 2039 (Pectolinarin) [https://doi.org/10.1248/cpb.26.2036]
  13. Goudard, M. et al., Phytochemistry, 1978, 17, 145- 146 (ms) [https://doi.org/10.1016/S0031-9422(00)89698-3]
  14. Arisawa, M. et al., Chem. Pharm. Bull., 1979, 27, 1252- 1254 (Comanthosides) [https://doi.org/10.1248/cpb.27.1252]
  15. Williams, C.A., Phytochemistry, 1979, 18, 803- 813 (7-glucoside) [https://doi.org/10.1016/0031-9422(79)80019-9]
  16. Voirin, B., Phytochemistry, 1983, 22, 2107- 2145 (uv) [https://doi.org/10.1016/S0031-9422(00)80133-8]
  17. Horie, T. et al., Yakugaku Zasshi, 1985, 105, 232- 239 (synth) [https://doi.org/10.1248/yakushi1947.105.3_232]
  18. Sing, M. et al., Pharmazie, 1987, 42, 490- 491 (7-rhamnoside)
  19. Otsuka, H., J. Nat. Prod., 1992, 55, 1252- 1255 (Isolinariins A,B) [https://doi.org/10.1021/np50087a011]
  20. Kraut, L. et al., Z. Naturforsch., C, 1992, 47, 794- 799 (7-galacturonoside)
  21. Mahoto, S.B. et al., Tetrahedron, 1994, 50, 9439- 9446 (Linaroside) [https://doi.org/10.1016/S0040-4020(01)85518-6]
  22. Hase, T. et al., Phytochemistry, 1995, 40, 287- 290 (Hortensin, struct) [https://doi.org/10.1016/0031-9422(95)00206-M]
  23. Begum, S. et al., J. Nat. Prod., 2000, 63, 765- 767 (Lantanoside, Linaroside, pmr, activity) [https://doi.org/10.1021/np9903548]
  24. Tundis, R. et al., Bioorg. Med. Chem. Lett., 2005, 15, 4757- 4760 (Linaria constits, activity) [https://doi.org/10.1016/j.bmcl.2005.07.029]
  25. Mou, M.-Y. et al., Acta Cryst. E, 2008, 64, o72 (cryst struct)
  26. Wetzel, S. et al., Angew. Chem., Int. Ed., 2010, 49, 3666- 3670 (activity)
  27. Murata, T. et al., Chem. Pharm. Bull., 2010, 58, 696- 702 (Meehania fargesii constit) [https://doi.org/10.1248/cpb.58.696]
  28. Peng, W.C., Chem. Nat. Compd. (Engl. Transl.), 2011, 47, 279- 280 (Cirsium japonicum constit)
  29. Samy, M.N. et al., Chem. Pharm. Bull., 2011, 59, 725- 729 (7-rhamnosylglucoside, 7-rhamnosylglucuronoside) [https://doi.org/10.1248/cpb.59.725]
  30. Al-Jaber, H.I. et al., J. Asian Nat. Prod. Res., 2012, 14, 618- 625 (Salvia syriaca constit)
  31. Phakeovilay, C. et al., J. Nat. Med. (Tokyo), 2013, 67, 228- 233 (7-2-rhamnosylglucuronoside, activity)
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