Psilostachyin
Appearance
![]() Psilostachyin A
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![]() Psilostachyin B
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![]() Psilostachyin C
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3D model (JSmol)
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PubChem CID
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Psilostachyins are group of chemical compounds isolated from Ambrosia psilostachya.[1][2][3][4]
References
[edit]- ^ Kagan, H. B; Miller, H. E; Renold, Walter; Lakshmikantham, M. V; Tether, L. R; Herz, Werner; Mabry, T. J (1966). "The Structure of Psilostachyin C, a New Sesquiterpene Dilactone from Ambrosia psilostachya DC". The Journal of Organic Chemistry. 31 (5): 1629–1632. doi:10.1021/jo01343a072.
- ^ Da Silva, C. F.; Batista, D. d. G. J.; De Araujo, J. S.; Batista, M. M.; Lionel, J.; De Souza, E. M.; Hammer, E. R.; Da Silva, P. B.; De Mieri, M.; Adams, M.; Zimmermann, S.; Hamburger, M.; Brun, R.; Schuhly, W.; Soeiro, M. d. N. C. (2013). "Activities of Psilostachyin a and Cynaropicrin against Trypanosoma cruzi in Vitro and in Vivo". Antimicrobial Agents and Chemotherapy. 57 (11): 5307–14. doi:10.1128/AAC.00595-13. PMC 3811247. PMID 23939901.
- ^ Raszeja, W.; Gill, St. (2009). "Isolation and Identification of Psilostachyin B from Ambrosia Artemisiifolia L". Planta Medica. 32 (8): 319–22. doi:10.1055/s-0028-1097606. PMID 594205.
- ^ Sülsen, Valeria P.; Frank, Fernanda M.; Cazorla, Silvia I.; Barrera, Patricia; Freixa, Blanca; Vila, Roser; Sosa, Miguel A.; Malchiodi, Emilio L.; Muschietti, Liliana V.; Martino, Virginia S. (2011). "Psilostachyin C: A natural compound with trypanocidal activity". International Journal of Antimicrobial Agents. 37 (6): 536–43. doi:10.1016/j.ijantimicag.2011.02.003. hdl:11336/198521. PMID 21497061.