CAS Registry Number: 56293-29-9
Taxonomy: Physicochemical and Pharmacological Properties of Alkaloids – Quinolizidine Alkaloids
Biological sources: Leptorhabdos parviflora, Sophora alopecuroides
C15H24N2: 232.194
Mp: 72°C (petr. ether), 265°C (dihydrochloride), 208°C (hydrochloride) [1]
[α]D +82° (c 0.854, EtOH)
MS m/z: 232(M+), 203, 189, 174, 148, 134, 98, 97, 96, 84, 83 [1]
1 H NMR: 1.79(1H, H-7), 2.26(1H, 2J15 = 13.5, J15,13e = 2.2, J15,14e = 2.2, He-15), 2.45(1H, q, J = 3.4, 12, Ha-10), 2.66(1H, J13,14a = 9, 2J13 = 12, Ha-13), 2.86(1H, q, J = 5.2, 12, He-10), 3.08(1H, 2J13 = 12, He-13), 3.11(1H, d, J = 6.3, H-11), 5.40(1H, d, J7,17 = 6.5, H-17) [1]
X-ray: [2]
Abs. Conf.: 6R7R9R11S [2]
HPLC, GC: [3]
Pharm./Biol.: Stimulating action. Raises arterial pressure and stimulates respiration [4]
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O.N. Tolkachev, T.E. Monakhova, V.I. Sheichenko, V.S. Kabanov, O.G. Fesenko, N.F. Proskurnina, Chem. Nat. Comp. 11, 29 (1975)
A.D. Brosius, J.W. Ziller, Q. Zhang, Acta Cryst. C. 53, 1510 (1997)
X. Chen, C.Q. Yi, X.Q. Yang, X. Wang, J. Chromatogr. B 812, 149 (2004)
T.E. Monakhova, Author’s Abstract of Candidate’s Dissertation, Moscow, 1975
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(2013). Aloperine. In: Azimova, S.S., Yunusov, M.S. (eds) Natural Compounds. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0560-3_1206
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DOI: https://doi.org/10.1007/978-1-4614-0560-3_1206
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