Chemistry:Psilostachyin

Psilostachyin
	; Psilostachyin A
	; Psilostachyin B
	; Psilostachyin C
Identifiers
CAS Number	A: 3533-47-9; B: 6995-02-4; C: 6466-67-7;
3D model (JSmol)	A: Interactive image; B: Interactive image; C: Interactive image;
ChEMBL	A: ChEMBL270060;
ChemSpider	A: 4478755; B: 4478756; C: 4478757;
PubChem CID	A: 5320767; B: 5320768; C: 5320769;
	InChI A: InChI=1S/C15H20O5/c1-8-4-5-10-9(2)13(17)19-12(10)14(3,18)15(8)7-6-11(16)20-15/h8,10,12,18H,2,4-7H2,1,3H3/t8-,10-,12+,14-,15+/m0/s1 Key: IRPFOXRBPHCCTG-JISBIHODSA-N; B: InChI=1S/C15H18O4/c1-8-4-5-10-9(2)14(17)18-13(10)15(3)11(8)6-7-12(16)19-15/h10,13H,2,4-7H2,1,3H3/t10-,13+,15+/m0/s1 Key: IOGFBFUSBVLQMS-PSOPSSQASA-N; C: InChI=1S/C15H20O4/c1-8-4-5-10-9(2)14(17)18-13(10)15(3)11(8)6-7-12(16)19-15/h8,10-11,13H,2,4-7H2,1,3H3/t8-,10-,11-,13+,15+/m0/s1 Key: FZYIWDQVFMUXPW-OEAYZANCSA-N;
	SMILES A: C[C@H]1CC[C@@H]2[C@H]([C@]([C@@]13CCC(=O)O3)(C)O)OC(=O)C2=C; B: CC1=C2CCC(=O)O[C@]2([C@H]3[C@@H](CC1)C(=C)C(=O)O3)C; C: C[C@H]1CC[C@@H]2[C@H]([C@]3([C@H]1CCC(=O)O3)C)OC(=O)C2=C;
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Psilostachyins are group of chemical compounds isolated from Ambrosia psilostachya.^[1]^[2]^[3]^[4]

References

↑ 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. et al. (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. 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. et al. (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. PMID 21497061.

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Identifiers
Psilostachyin A
Psilostachyin B
Psilostachyin C
CAS Number	A: 3533-47-9 B: 6995-02-4 C: 6466-67-7
3D model (JSmol)	A: Interactive image B: Interactive image C: Interactive image
ChEMBL	A: ChEMBL270060
ChemSpider	A: 4478755 B: 4478756 C: 4478757
PubChem CID	A: 5320767 B: 5320768 C: 5320769
InChI A: InChI=1S/C15H20O5/c1-8-4-5-10-9(2)13(17)19-12(10)14(3,18)15(8)7-6-11(16)20-15/h8,10,12,18H,2,4-7H2,1,3H3/t8-,10-,12+,14-,15+/m0/s1 Key: IRPFOXRBPHCCTG-JISBIHODSA-N B: InChI=1S/C15H18O4/c1-8-4-5-10-9(2)14(17)18-13(10)15(3)11(8)6-7-12(16)19-15/h10,13H,2,4-7H2,1,3H3/t10-,13+,15+/m0/s1 Key: IOGFBFUSBVLQMS-PSOPSSQASA-N C: InChI=1S/C15H20O4/c1-8-4-5-10-9(2)14(17)18-13(10)15(3)11(8)6-7-12(16)19-15/h8,10-11,13H,2,4-7H2,1,3H3/t8-,10-,11-,13+,15+/m0/s1 Key: FZYIWDQVFMUXPW-OEAYZANCSA-N
SMILES A: C[C@H]1CC[C@@H]2[C@H]([C@]([C@@]13CCC(=O)O3)(C)O)OC(=O)C2=C B: CC1=C2CCC(=O)O[C@]2([C@H]3[C@@H](CC1)C(=C)C(=O)O3)C C: C[C@H]1CC[C@@H]2[C@H]([C@]3([C@H]1CCC(=O)O3)C)OC(=O)C2=C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references