The Plant Cell Culture Library

Gnaphalium uliginosum
Cell Line ID FU-13056
Media Type B105
Availability Low
Order Asterales
Family Compositae
Genus Gnaphalium
Antiviral Genus Level ➡ 36 citations
Common Names Cudweed, Everlasting
Culture Initiation Site Dusseldorf
Plant Habit Herb
Culture Start Material Seed
Native Range Genus : Cosmoplitan
Plant Supplier Botanical Garden Paris
Antiviral Citations
  1. Shah, R.C. et al., J. Chem. Soc., 1938, 1555- 1559 (Norwogonin, 8-Me ether, 5,8-di-Me ether, tri-Me ether, synth)
  2. Rao, K.V. et al., Proc. - Indian Acad. Sci., Sect. A, 1947, 25, 427- 431 (Norwogonin, synth)
  3. Pillon, D., Bull. Soc. Chim. Fr., 1954, 9- 25 (Norwogonin, synth)
  4. Katyal, M. et al., J. Indian Chem. Soc., 1963, 40, 191- 194 (Norwogonin, use, detn, U, Th)
  5. Popova, T.P. et al., Chem. Nat. Compd. (Engl. Transl.), 1973, 9, 699- 702 (Isowogonin,struct) [https://doi.org/10.1007/BF00565789]
  6. Escarria, S. et al., Phytochemistry, 1977, 16, 1618 (Gnaphalium pellitum constit, struct) [https://doi.org/10.1016/0031-9422(77)84045-4]
  7. Bohlmann, F. et al., Phytochemistry, 1978, 17, 1935- 1937 (Helichrysum mundii constit,synth) [https://doi.org/10.1016/S0031-9422(00)88737-3]
  8. Adinarayana, D. et al., Indian J. Chem., Sect. B, 1979, 18, 552 (5,7,8-Trimethoxyflavone,struct)
  9. Goudard, M. et al., Phytochemistry, 1979, 18, 186- 187 (7,8-di-Me ether, tri-Me ether, ms) [https://doi.org/10.1016/S0031-9422(00)90949-X]
  10. Iinuma, M. et al., Chem. Pharm. Bull., 1980, 28, 708- 716 (Norwogonin, cmr) [https://doi.org/10.1248/cpb.28.708]
  11. Torrenegra, G.R.D. et al., Rev. Latinoam. Quim., 1982, 13, 75- 76 (Achyrocline bogotensis constit, struct)
  12. Gupta, K.K. et al., Phytochemistry, 1983, 22, 314- 315 (7-O-Methylwogonin, pmr) [https://doi.org/10.1016/S0031-9422(00)80122-3]
  13. Tomimori, T. et al., Chem. Pharm. Bull., 1985, 33, 4457- 4463 (Norwogonin, isol) [https://doi.org/10.1248/cpb.33.4457]
  14. Tomimori, T. et al., Chem. Pharm. Bull., 1986, 34, 406- 408 (5-O-Methylwogonin, isol) [https://doi.org/10.1248/cpb.34.406]
  15. Mesquita, A.A.L. et al., Phytochemistry, 1986, 25, 1255- 1256 (Achyrocline satureoides constit, pmr) [https://doi.org/10.1016/S0031-9422(00)81599-X]
  16. Kuroyanagi, M. et al., Chem. Pharm. Bull., 1987, 35, 4429- 4435 (Andrographidin C, struct) [https://doi.org/10.1248/cpb.35.4429]
  17. Wang, Y.-Q. et al., Chem. Pharm. Bull., 1988, 36, 3206- 3209 (7-glucuronide, 8-glucuronide,cmr, pmr)
  18. Sakamoto, Y. et al., Bull. Chem. Soc. Jpn., 1989, 62, 2450- 2454 (Norwogonin, 5,8-di-Me ether, 7,8-di-Me ether, cAMP PDE inhibitor) [https://doi.org/10.1246/bcsj.62.2450]
  19. Tomimori, T. et al., Chem. Pharm. Bull., 1990, 38, 3488- 3490 (5,8-di-Me ether 7-glucuronide, struct) [https://doi.org/10.1248/cpb.38.3488]
  20. Ravanel, P. et al., Phytochemistry, 1990, 29, 441- 445 (Norwogonin, NADH dehydrogenase activity) [https://doi.org/10.1016/0031-9422(90)85093-U]
  21. Kikuchi, Y. et al., Chem. Pharm. Bull., 1991, 39, 1047- 1050 (Glychionide A, isol) [https://doi.org/10.1248/cpb.39.1047]
  22. Kikuchi, Y. et al., Chem. Pharm. Bull., 1991, 39, 1051- 1054 (Glychionide A: isol) [https://doi.org/10.1248/cpb.39.1051]
  23. Guha, P.K. et al., Phytochemistry, 1992, 31, 1833- 1834 (Pediflavone, struct) [https://doi.org/10.1016/0031-9422(92)83162-R]
  24. Parmar, V.S. et al., Indian J. Chem., Sect. B, 1993, 32, 244- 256 (7,8-di-Me ether, tri-Me ether, synth)
  25. Bilia, A.R. et al., Phytochemistry, 1993, 33, 1449- 1452 (5-glucoside, synth) [https://doi.org/10.1016/0031-9422(93)85108-4]
  26. Yuldashev, M.P. et al., Chem. Nat. Compd. (Engl. Transl.), 2001, 37, 428- 430 (Immaculoside, struct) [https://doi.org/10.1023/A:1014459023998]
  27. Yuldshaev, M.P. et al., Chem. Nat. Compd. (Engl. Transl.), 2001, 37, 431- 433 (Nepetoside A: struct) [https://doi.org/10.1023/A:1014411108068]
  28. Morimoto, M. et al., J. Agric. Food Chem., 2003, 51, 389- 393 (Norwogonin, 7-Me ether, 7,8-di-Me ether, synth, antifeedant activity) [https://doi.org/10.1021/jf025627a]
  29. Li, J.-R. et al., J. Asian Nat. Prod. Res., 2005, 7, 677- 680 (Glychionide A)
  30. Sagawa, T. et al., J. Nat. Prod., 2005, 68, 502- 505 (Achyrocline bogotensis constit, cytokine production inhibitor) [https://doi.org/10.1021/np040187y]
  31. Li, Z.-Y. et al., Org. Prep. Proced. Int., 2009, 41, 327- 330 (5-O-Methylwogonin)
  32. Wu, Q. et al., Fitoterapia, 2010, 81, 429- 433 (Mosla scabra constit, antiviral activity) [https://doi.org/10.1016/j.fitote.2009.12.005]
  33. Chao, W.-W. et al., J. Agric. Food Chem., 2010, 58, 2505- 2512 (7,8-di-Me ether,antiinflammatory activity) [https://doi.org/10.1021/jf903629j]
  34. Moriyasu, M. et al., J. Nat. Med. (Tokyo), 2011, 65, 313- 321 (Uvaria welwitschii constit)
  35. Jing, L.-L. et al., Nat. Prod. Commun., 2015, 10, 387- 388 (synth)
  36. Yuan, H. et al., Tetrahedron Lett., 2016, 57, 3389- 3391 (Norwogonin, synth) [https://doi.org/10.1016/j.tetlet.2016.06.085]
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Inquiries regarding the purchase of Plant cell lines or other PCCL services can be directed to Michael Daley mpdaley@umass.edu

Acknowledgements

The establishment of the PCCL has been sponsored by National Science Foundation (NSF/DBI-156 1572), United States Department of Agriculture Massachusetts Experiment Station Award (MAS00496), the Science and Technology fund from the President's office of the University of Massachusetts, and the 2016 UMass Amherst Armstrong Fund for Science.

National Science FoundationCenter for Agriculture, Food and the Environment

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