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| Names | |
|---|---|
| IUPAC name (22R,25R)-Spirosol-5-en-3β-yl α-L-rhamnopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→4)]-β-D-glucopyranoside | |
| Systematic IUPAC name (2S,2′S,3R,3′R,4R,4′R,5R,5′R,6S,6′S)-2,2′-{[(2R,3S,4S,5R,6R)-4-Hydroxy-2-(hydroxymethyl)-6-{[(2S,2′R,4aR,4bS,5′R,6aS,6bR,7S,9aS,10aS,10bS)-4a,5′,6a,7-tetramethyl-1,2,3,4,4a,4b,5,6,6a,6b,7,9a,10,10a,10b,11-hexadecahydrospiro[naptho[2′,1′:4,5]indeno[2,1-b]furan-8,2′-piperidin]-2-yl]oxy}oxane-3,5-diyl]bis(oxy)}bis(6-methyloxane-3,4,5-triol) | |
| Other names Solamargin; δ-Solanigrine | |
| Identifiers | |
3D model (JSmol) | |
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| UNII | |
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| Properties | |
| C45H73NO15 | |
| Molar mass | 868.071 g·mol−1 |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Solamargine is acytotoxicchemical compound that occurs in plants of the familySolanaceae, such aspotatoes,tomatoes, andeggplants.[1][2] It has been also isolated fromSolanum nigrum fungalendophyteAspergillus flavus.[3] It is aglycoalkaloid derived from the steroidal alkaloidsolasodine.
Solamargine was one component of the unsuccessful experimental cancer drug candidateCoramsine.
Media related toSolamargine at Wikimedia Commons
