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Hippeastrine (Trispherine)

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Natural Compounds
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CAS Registry Number: 477-17-8

Taxonomy: Physicochemical and Pharmacological Properties of Alkaloids – Amaryllidaceae Alkaloids

Biological sources: Clivia miniata, Crinum amabile, C. giganteum, Galanthus nivalis, Hippeastrum equestre, Hymenocallis littoralis, Pancratium trianthum, Ungernia ferganica, U. sewertzowii, U.spiralis, U. tadshicorum, U. trisphaera, U. victoris, U. vvedenskyi

C17H17NO5: 315.1107

Mp: 209–210°C (MeOH) [1]

[α]D +122° (EtOH) [1], 267° (hydrobromide) [1], 218° (methiodide) [1], 258° (perchlorate) [1], 271° (nitrate) [1], 281° (hydrochloride) [1], 243° (picrate) [1]

Solubility: sol.MeOH, EtOH, CHCl3; spar. sol. Me2CO, Et2O; insol. H2O [1]

UV: 227, 267, 308 [2]

IR: 3600, 3015, 2960, 2920, 2860, 2790, 1715, 1618, 1508, 1484, 1453, 1400, 1387, 1354, 1338, 1318, 1293, 1252, 1190, 1152, 1121, 1058, 1041, 998, 983, 955, 943, 905, 888, 864, 841, 824 [2]

MS m/z: 315(M+, 0.7), 298(1), 297(2.3), 125(100), 124(13), 96(19) [3]

1 H NMR: 5.65 (H-4), 4.58 (H-5a), 4.38 (H-5), 7.43...

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References

  1. Kh. Allayarov, Kh.A. Abduazimov, S.Yu. Yunusov, DAN UzSSR (10), 25 (1961)

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(2013). Hippeastrine (Trispherine). In: Azimova, S.S., Yunusov, M.S. (eds) Natural Compounds. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0560-3_61

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