Solanocapsine

Solanocapsine
Names

Other names (2S,4aS,4bS,6aS,6bR,7S,7aR,10R,11aS,12aR,13aS,13bR,15aS)- 2-Aminodocosahydro-4a,6a,7,10-tetramethylnaphth[2,1:4',5']indeno [1',2':5,6]pyrano[3,2-b]pyridin-11a(1H)-ol; 3β-Amino-22,26-epimino-16α,23-epoxy-5α,22αH,25βH-cholestan-23β-ol; (3β,5α,16α,22α,23β,25β)-3-Amino-16,23-epoxy-16,28-secosolanidan-23-ol
Identifiers
CAS Registry Number	639-86-1^Y
Jmol-3D images	Image
SMILES N[C@H]1CC[C@@]2(C)[C@](CC[C@]3([H])[C@]2([H])CC[C@@]4(C)[C@@]3([H])C[C@]5([H])[C@]4([H])[C@H](C)C6[C@@](C[C@@H](C)CN6)(O)O5)([H])C1
Properties
Chemical formula	C₂₇H₄₆N₂O₂
Molar mass	430.666
Appearance	long flat colorless prisms (ethanol-H₂O)^[1]
Melting point	222 °C (432 °F; 495 K) ^[1] 216-217 °C ^[2]
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Y verify (what is: Y/N?)
Infobox references

Solanocapsine is a toxic steroidal alkaloid from Solanum pseudocapsicum (Jerusalem cherry).

References

↑ 1.0 1.1 Barger, L. G.; Fraenkel-Conrat, H. L. (1936). "337. Alkaloids from Solanum pseudocapsicum, L.". Journal of the Chemical Society 1936: 1537–1542. doi:10.1039/JR9360001537.
↑ Schlittler, E.; Uehlinger, H. (1952). "Über das Sterinalkaloid Solanocapsin". Helvetica Chimica Acta (in German) 35 (6): 2034–2044. doi:10.1002/hlca.19520350633.